| status and transcriptional activity of a bovine-papillomavirus-i-based expression vector in a recombinant production cell line. | we have analysed the status and transcriptional activity of the bovine papillomavirus-i (complete bpv-i genome)-based expression vector pces in ci27i-cell-line-derived 3ti cells used for the industrial production of recombinant human erythropoietin (rhuepo). complete tandem head-to-tail integration of about 600 vector copies at a single site of the cellular genome was observed. deletions, insertions or rearrangements of pces-specific sequences or extrachromosomal copies of vector sequences were ... | 1996 | 8867900 |
| ebna1 and e2: a new paradigm for origin-binding proteins? | | 1996 | 8868083 |
| tumour suppressor gene p53 in the horse: identification, cloning, sequencing and a possible role in the pathogenesis of equine sarcoid. | the tumour suppressor protein p53 enhances the genetic stability of the cell and plays a critical role in tumour suppression. equine p53 was analysed by sequencing exons 5 to 9, a region which includes most known mutations and all the mutational hotspots in the species that have been investigated. the fragment was amplified, cloned and sequenced from genomic and complementary dna. a comparison of the predicted amino acid sequences between the horse and other species resulted in identities betwee ... | 1996 | 8880979 |
| the initiator protein e1 binds to the bovine papillomavirus origin of replication as a trimeric ring-like structure. | the replication initiator protein e1 binds to the origin of replication of bovine papillomavirus in several forms. e1 can bind to its recognition sequence as a monomer together with the viral transcription factor e2, or as a trimeric e1 complex. the trimerization of e1 is mediated by the sequence-specific binding of e1 to dna, and results in an e1 complex that is linked topologically to the dna because the three molecules of e1 form a ring-like structure that encircles the dna. these results dem ... | 1996 | 8890182 |
| enhanced transcriptional activation by e2 proteins from the oncogenic human papillomaviruses. | a systematic comparison of transcriptional activation by papillomavirus e2 proteins revealed that the e2 proteins from high-risk human papillomaviruses (human papillomavirus type 16 [hpv-16] and hpv-18) are much more active than are the e2 proteins from low-risk hpvs (hpv-6b and hpv-11). despite the tropism of hpvs for particular epithelial cell types, this difference in transcriptional activation was observed in a number of different epithelial and nonepithelial cells. the enhanced activities o ... | 1996 | 8892874 |
| e2 proteins: modulators of papillomavirus transcription and replication. | | 1996 | 8902804 |
| the e5 gene product of rhesus papillomavirus is an activator of endogenous ras and phosphatidylinositol-3'-kinase in nih 3t3 cells. | we examined the effect of two rhesus papillomavirus 1 (rhpv) oncogenes on cytokine-induced signal transduction pathways leading to the possible activation of ras protein (p21ras) and phosphatidylinositol kinase. p21ras in both the activated (gtp-bound) and inactivated (gdp-bound) states were quantitated. nih 3t3 cell lines expressing the rhpv 1 e5 gene or epidermal growth factor receptor cdna had about a sixfold higher ratio of p21ras-bound gtp to p21ras-bound gdp as compared with parental nih 3 ... | 1996 | 8917513 |
| bovine papillomavirus oncoprotein e5 induces the nf kappa b activation through superoxide radicals. | bovine papillomavirus type 1 (bpv-1) open reading frame e5 encodes the smallest known oncoprotein. this protein is involved in transforming cells during the early stage of infection. nuclear factor kappa b (nf kappa b) is activated in the host cells as a result of different virus infections. it has been shown that reactive oxygen intermediates activate nf kappa b which leads the activation of several cellular genes. we studied the effect of bpv-1 es protein on nf kappa b activation. we found tha ... | 1996 | 8950027 |
| conditional requirement for sequences distinct from the replication origin during episomal establishment of the bpv1 genome. | removal from bpv1 dna of a short segment (nt. 4786-5045) that contains several protein binding sites and is required for efficient replication in short term assays prevents its autonomous maintenance in cell lines established by selection in g418 medium after cotransfer of neo(r). in contrast, transformed cell lines established from foci, which express the viral genes at higher levels, maintain extrachromosomal copies of the deleted dna. two modes of maintenance of the viral genome are thus dist ... | 1996 | 8954917 |
| phenotypical characterization of lymphocytes infiltrating regressing papillomas. | papillomavirus-induced lesions often regress spontaneously in both humans and animals. papilloma regression is deemed to be due to a cell-mediated immune response, the nature of which is still ill defined, and is accompanied by immune cell infiltrates. to gain further information on the nature and role of the immune cells present in regressing papillomas, we have analyzed biopsies of papillomas induced in the soft palate of cattle by bovine papillomavirus type 4 (bpv-4) and have phenotypically c ... | 1996 | 8970967 |
| the bovine papillomavirus type 4 e8 protein binds to ductin and causes loss of gap junctional intercellular communication in primary fibroblasts. | the e8 open reading frame of bovine papillomavirus type 4 encodes a small hydrophobic polypeptide which contributes to cell transformation by conferring anchorage-independent growth. using an in vitro translation system, we show that the e8 polypeptide binds to ductin, the 16-kda proteolipid that forms transmembrane channels in both gap junctions and vacuolar h+-atpase. this association is not due to nonspecific hydrophobic interactions. ppa1, a saccharomyces cerevisiae polypeptide homologous (w ... | 1996 | 8971040 |
| dose-dependent regulation of the early promoter of human papillomavirus type 18 by the viral e2 protein. | the activity of the e6/e7 promoter of genital human papillomaviruses (hpvs) is positively and negatively modulated by a complex interplay between a variety of cellular transcription factors and the virally encoded e2 protein. the long control region of genital hpvs contains four e2 binding sites in conserved positions, two of which are very close to the tata box. binding of e2 to these two sites has been shown to repress the promoter. to carefully analyze the effect of e2 on the activity of the ... | 1997 | 8985322 |
| altered susceptibility to tumor necrosis factor alpha-induced apoptosis of mouse cells expressing polyomavirus middle and small t antigens. | infection with some virus types induces susceptibility to the cytotoxic effect of tumor necrosis factor alpha (tnf-alpha). to investigate whether expression of polyomavirus proteins has this effect on cells, the tnf-alpha sensitivity of c127 and l929 mouse cells transfected with viral dna was analyzed. expression of all three polyomavirus early proteins, the tumor (t) antigens, had no apparent effect. in contrast, middle t antigen by itself induced hypersensitivity to tnf-alpha. this effect was ... | 1997 | 8985347 |
| sequences flanking the core dna-binding domain of bovine papillomavirus type 1 e2 contribute to dna-binding function. | we have compared a series of molecular constructs that contain the minimal dna-binding and dimerization domain of bovine papillomavirus type 1 (bpv-1) e2 alone or this binding domain plus the adjacent 16 or 40 amino acids to test the role of the flanking sequences in e2 function. the presence of these sequences resulted in an up to eightfold increase in the affinity of e2 for its target dna and stabilized the protein against denaturation both in the absence of dna and in the form of dna-protein ... | 1997 | 8985425 |
| isolation of an amino-terminal region of bovine papillomavirus type 1 e1 protein that retains origin binding and e2 interaction capacity. | in vitro dna binding results from a series of e1 proteins containing amino-terminal or carboxy-terminal truncations indicated that sequences between amino acids 121 and 284 were critical for origin binding. additional binding experiments with e1 proteins containing internal, in-frame insertions or deletions confirmed the importance of the region defined by truncated e1 proteins and also demonstrated that downstream sequences were not required for binding activity in the context of the full-lengt ... | 1997 | 8985429 |
| visualization of multicomponent transcription factor complexes on chromatin and nonnucleosomal templates in vivo. | there is increasing evidence that specific chromatin structures play an important role in the regulation of transcription in eukaryotes. the mouse mammary tumor virus (mmtv) promoter, which is reproducibly assembled into a phased array of six nucleosomes when introduced into cells, represents a particularly well-studied example. the second or b nucleosome of the phased array is disrupted in response to hormone stimulation, allowing the assembly of a preinitiation complex and the activation of tr ... | 1997 | 8993036 |
| casein kinase ii phosphorylates bovine papillomavirus type 1 e1 in vitro at a conserved motif. | the e1 protein of bovine papillomavirus type 1 (bpv-1) is a phosphoprotein which specifically binds and unwinds the virus replication origin by atp-dependent helicase activity. the el protein has been shown to be multiply phosphorylated in vivo, although the sites of modification are incompletely mapped. examination of the predicted amino acid sequence of all available e1 proteins revealed strong conservation between amino acids 25 and 60 of a motif consisting of a serine residue followed by a s ... | 1997 | 9010301 |
| sequence close to the n-terminus of l2 protein is displayed on the surface of bovine papillomavirus type 1 virions. | the bovine papillomavirus type 1 (bpv1) l2 protein purified from escherichia coli was used as an antigen to produce monoclonal antibodies (mabs). a total of 26 individual clones which recognized the bpv1 l2 protein were obtained. using infectious bpv1 virus particles, 3 of the mabs were found to interact with bpv1 virus particles. binding of the mabs to bpv1 was confirmed by immunoelectron microscopy. a set of 92 13-mer peptides overlapping by 8 amino acids spanning the entire bpv1 l2 protein wa ... | 1997 | 9018146 |
| age distribution of antibodies to human papillomavirus in children, women with cervical intraepithelial neoplasia and blood donors from south africa. | sera from 95 women with cervical intraepithelial neoplasia (cin), 95 age-matched female blood donors, and 155 children aged between 1 and 12 years were tested by enzyme-linked immunosorbent assay (elisa) for levels of serum igg to three human papillomavirus (hpv) peptides (hpv-16 e2 [e2-16], hpv-18 e2 (e2-18], hpv-16 l1 [l1-16]), as well as hpv-16 virus-like particles (vlp-16) and bovine papillomavirus type 1 virus-like particles (bpv-vlp). in the adult group antibodies to e2-16 and vlp-16 were ... | 1997 | 9021543 |
| modulation of bovine papillomavirus dna replication by phosphorylation of the viral e1 protein. | e1 is the dna replication origin recognition protein for bovine papillomavirus (bpv), and it carries out enzymatic functions required for initiation of viral dna replication. cellular mechanisms likely play a role in regulating bpv dna replication. we are investigating the role of phosphorylation of e1 on viral replication in vivo and on e1 activity in vitro. serine 109 is a phosphoacceptor in vivo and is targeted by protein kinase a and protein kinase c in vitro. a viral genome carrying a serin ... | 1997 | 9024804 |
| expression of the papillomavirus e2 protein in hela cells leads to apoptosis. | the papillomavirus e2 protein plays a central role in the viral life cycle as it regulates both transcription and replication of the viral genome. in this study, we showed that transient expression of bovine papillomavirus type 1 or human papillomavirus type 18 (hpv18) e2 proteins in hela cells activated the transcriptional activity of p53 through at least two pathways. the first one involved the binding of e2 to its recognition elements located in the integrated viral p105 promoter. e2 binding ... | 1997 | 9034333 |
| multiplicity of uses of monoclonal antibodies that define papillomavirus linear immunodominant epitopes. | during the last 10 yr, we have derived monoclonal antibodies from animals immunized with denatured bovine papillomaviruses type 1 major capsid (l1) protein, mapped their corresponding immunodominant epitopes to within a single amino acid (aa), and compared the reactivity of authentic l1 proteins to the predicted response by collinear analysis of the aa sequences of the same and other papillomaviruses (pvs). the data obtained from this approach has provided us with new insights into the sensitivi ... | 1997 | 9048212 |
| mutations in the human papillomavirus type 16 e2 protein identify a region of the protein involved in binding to e1 protein. | papillomavirus dna replication is primarily dependent upon two viral gene products, e1 and e2. work with bovine papillomavirus has shown that the e2 protein can bind directly to the e1 protein and enhance the binding of e1 to the viral origin of replication. however, little is known about the mechanism of interaction between e1 and e2 proteins. in this study we have analysed in detail the association between human papillomavirus type 16 (hpv-16) e1 and e2 proteins. using a purified glutathione s ... | 1995 | 9049327 |
| cell lines containing and expressing the human herpesvirus 6a ts gene are protected from both h-ras and bpv-1 transformation. | human herpesvirus 6a (hhv-6a) strain u1102 was previously shown to contain a 1473 bp transformation suppressor gene (ts) (araujo et al., 1995). ts inhibited transformation of nih3t3 cells by h-ras and transcription of the h-ras and human immunodeficiency type 1 (hiv-1) promoters in transient transfection experiments. in the current study, stable nih3t3 cell lines expressing ts protein were established by transfection with prc-ts containing the ts gene under the control of the rous sarcoma virus ... | 1997 | 9050993 |
| a mutation study of the dna binding domain of human papillomavirus type11 e2 protein. | a site-specific mutation study was performed on the c-terminal domain, containing a cloned dna binding region, of the human papillomavirus type11 (hpv11) e2 protein to determine the specific properties of residues directly involved in the dna binding. the effect of a point mutations on the dna binding was assessed by means of a gel mobility shift assay. the mutagenesis was concentrated on the residues in the third helix from the n-terminal, that is known as the "recognition helix," in the crysta ... | 1997 | 9058204 |
| identification of papillomaviruses in scrapings from bovine warts by use of the polymerase chain reaction. | | 1997 | 9060144 |
| binding of the e1 and e2 proteins to the origin of replication of bovine papillomavirus. | dna replication of bovine papillomavirus (bpv) requires two viral proteins encoded from the e1 and e2 open reading frames. e1 and e2 are sequence-specific dna binding proteins that bind to their cognate binding sites in the bpv origin of replication (ori). the e1 and e2 proteins can interact physically with each other, and this interaction results in cooperative binding when binding sites for both proteins are present. we have analyzed the binding of e1 to the ori in the absence and presence of ... | 1997 | 9060646 |
| virocrine transformation. | | 1997 | 9061007 |
| synergistic transcriptional-activation by the papillomavirus e2 protein occurs after dna binding and correlates with a change in chromatin structure. | the papillomavirus e2 protein only activates transcription strongly when two or more of its binding-sites, each of which bind an e2 dimer, are present upstream of a minimal promoter. such synergy has been observed both in mammalian and yeast cells. in an attempt to understand the molecular basis of this synergy we carried out genomic footprinting to monitor the binding in vivo of native or mutant e2 proteins to different templates in yeast. we show that in vivo e2 binds to its site even under co ... | 1997 | 9067604 |
| dna binding and bending by the human papillomavirus type 16 e2 protein. recognition of an extended binding site. | the human papillomavirus (hpv) 16 e2 protein (he2) binds to four sites present upstream of the p97 promoter and regulates transcription of the viral e6 and e7 oncogenes. we have determined the relative binding constants for the interaction of the full-length he2 protein with these sites. our results show that he2 binds tightly to site 4, less tightly to sites 1 and 2, and weakly to site 3. similar results have previously been obtained using a c-terminal fragment of the he2 protein suggesting tha ... | 1997 | 9079642 |
| a papillomavirus e2 phosphorylation mutant exhibits normal transient replication and transcription but is defective in transformation and plasmid retention. | papillomavirus dna persists in infected cells as a nuclear plasmid, causing epithelial lesions in many hosts, including humans. the viral protein e2 is required for both replication and transcription to facilitate this persistence. bovine papillomavirus e2 protein is phosphorylated at two predominant sites. phosphorylation of one of these sites (serine 301) inhibits replication of the genome. using mass spectrometry and edman sequencing, we have mapped additional phosphorylation sites in tryptic ... | 1997 | 9094639 |
| functional interactions between papillomavirus e1 and e2 proteins. | dna replication of papillomaviruses requires the viral e1 and e2 proteins. these proteins bind cooperatively to the viral origin of replication (ori), which contains binding sites for both proteins, forming an e1-e2-ori complex which is essential for initiation of dna replication. to map the domains in e2 that are involved in the interaction with e1, we have used chimeric bovine papillomavirus (bpv)/human papillomavirus type 11 (hpv-11) e2 proteins. the results from this study show that both the ... | 1997 | 9094661 |
| the bovine papillomavirus e6 oncoprotein interacts with paxillin and disrupts the actin cytoskeleton. | the e6 oncoprotein of bovine papillomavirus type 1 (bpv-1) has been shown to transform cells through a p53-independent pathway, but its transforming mechanism is unknown. here we demonstrate in vitro and in vivo interactions between bpv-1 e6 and the focal adhesion protein paxillin. the ability of bpv-1 e6 to complex with paxillin correlated with its ability to transform; e6 mutant proteins impaired in their transformation function also were impaired in their abilities to bind paxillin. e6 bindin ... | 1997 | 9114003 |
| diagnostic phase antibody response to the human papillomavirus type 16 e2 protein is associated with successful treatment of genital hpv lesions with systemic interferon alpha-2b. | systemic interferon alpha-2b treatment reduces relapses of genital human papillomavirus (hpv) lesions in some but not all females. the aim of the present study was to investigate possible predictive pretreatment factors for the outcome of therapy. | 1997 | 9126686 |
| novel structural features of bovine papillomavirus capsid revealed by a three-dimensional reconstruction to 9 a resolution. | the three-dimensional structure of bovine papillomavirus has been determined to 9 a resolution by reconstruction of high resolution, low dose cryo-electron micrographs of quench-frozen virions. although hexavalent and pentavalent capsomeres form star-shaped pentamers of the major capsid protein l1, they have distinct high-resolution structures. most prominently, a 25 a hole in the centre of hexavalent capsomeres is occluded in the pentavalent capsomeres. this raises the possibility that the l2 m ... | 1997 | 9145113 |
| transformation by bovine papillomavirus type 1 e6 is independent of transcriptional activation by e6. | we have generated mutants of bovine papillomavirus type 1 e6 (be6) that are defective for transcriptional activation and have analyzed these mutants for transformation of contact-inhibited cells and association with the mammalian protein e6-ap. these be6 mutants demonstrate that transformation by be6 does not require transcriptional activation and that association of be6 with e6-ap is a function separable from transcriptional activation by be6. association of be6 with e6-ap appears to be necessa ... | 1997 | 9151888 |
| vaccination against papillomavirus in cattle. | | 1997 | 9167911 |
| bovine papillomavirus e5 oncogene stimulates dna synthesis in c127 fibroblasts without general effects on growth factor responsive protein phosphorylations. | the bovine papillomavirus (bpv) transforming gene e5 is thought to modulate growth factor receptor function leading to a stimulation of growth factor signal transduction pathways. however, the influence of e5 on the range of receptor mediated changes in protein phosphorylation has not been addressed. we looked for the influence of e5 on dna synthesis as well as the phosphorylation of over 1000 cellular phosphoproteins in mouse c127 fibroblasts and subclones harboring wild type (id13)-, e5- mutan ... | 1997 | 9191860 |
| bovine papillomavirus type 1 dna replication: the transcriptional activator e2 acts in vitro as a specificity factor. | we previously devised cell-free conditions supporting efficient replication of bovine papillomavirus type 1 (bpv1) dna (c. bonne-andréa, s. santucci, and p. clertant, j. virol. 69:3201-3205, 1995): the use of highly active preparations of viral initiator protein e1, together with extract from a particular cell source, allowed the synthesis of complete dna circles through successive rounds of replication; this occurred in the absence of the viral transcriptional activator e2, required in vivo for ... | 1997 | 9261405 |
| cell-type-specific separate regulation of the e6 and e7 promoters of human papillomavirus type 6a by the viral transcription factor e2. | gene expression of human papillomaviruses (hpv) is tightly controlled by cellular factors and by the virally encoded e2 protein through binding to distinct sites within the regulatory noncoding region. while for the high-risk genital papillomaviruses a single promoter drives the expression of all early genes, a second promoter present in the e6 open reading frame of the low-risk hpv type 6 (hpv6) would allow an independent regulation of e6 and e7 oncogene expression. in this report, we provide t ... | 1997 | 9261424 |
| viral proteins of bovine papillomavirus type 4 during the development of alimentary canal tumours. | in cattle infection of the upper alimentary canal mucosa by bovine papillomavirus type 4 (bpv-4) results in the development of papillomas which can progress to cancer in animals fed on bracken fern. this paper describes a study of the cellular and subcellular distribution of a number of different bpv-4 products in experimentally-induced bpv-4 tumours. e8 and e4 proteins were detected solely as cytoplasmic antigens in the undifferentiated and differentiated layers of the papilloma, respectively; ... | 1997 | 9265855 |
| a peptide encoding a b-cell epitope from the n-terminus of the capsid protein l2 of bovine papillomavirus-4 prevents disease. | the first 200 n-terminus amino acids of the l2 capsid protein of bpv-4 (designated l2a) are an effective prophylactic vaccine against bpv-4 infection. vaccination with l2a induces the production of virus neutralizing antibodies, and when l2a antibodies are removed from immune sera, the sera lose their neutralization activity. l2a encodes three dominant b-cell epitopes, defined as epitope 1 (amino acids 101-120), epitope 2 (aa 131-151), and epitope 3 (aa 151-170). to investigate whether any of th ... | 1997 | 9268157 |
| adeno-associated virus rep78 inhibits oncogenic transformation of primary human keratinocytes by a human papillomavirus type 16-ras chimeric. | seroepidemiologic studies demonstrate that adeno-associated virus (aav) infection is negatively associated with cervical cancer. this inverse association may be due to an ability of aav to inhibit the role of human papillomavirus (hpv) in cervical carcinogenesis. in support of this hypothesis aav has been demonstrated to inhibit several papillomavirus types, including bovine papillomavirus type 1 and human papillomaviruses types 16 and 18 (hpv-16/18) in tissue culture. the aav-encoded rep78 prot ... | 1997 | 9299265 |
| mutational analysis of transcriptional activation by the bovine papillomavirus type 1 e6. | while the bovine papillomavirus type 1 (bpv-1) e6 induces tumorigenic transformation of murine c127 cells, it does not bind or promote the degradation of p53. we recently showed the cellular protein erc-55/e6bp binds bpv-1 e6 as well as the cancer-related human papillomavirus (hpv) e6 proteins. bpv-1 e6 also binds e6-ap, a ubiquitin ligase necessary for hpv e6-induced p53 degradation. we previously reported that the transforming activity of a set of bpv-1 e6 mutants correlated with their e6bp-bi ... | 1997 | 9299614 |
| linear b-cell epitopes in the n-terminus of l2 of bovine papillomavirus type 4. | the minor capsid protein l2 of bovine papillomavirus type 4 (bpv-4) is a very effective prophylactic vaccine which induces the production of virus neutralising antibodies and prevents virus-induced papillomatosis. the virus neutralising activity resides in the first 200 n-terminal amino acids of l2 (l2a). to further investigate the humoral immune response to l2, and the role it plays during infection and in prophylactic vaccination, the presentation of b-cell linear epitopes of l2a has been anal ... | 1997 | 9300551 |
| bovine papillomavirus type 5: partial sequence and comparison with other bovine papillomaviruses. | two restriction fragments of bovine papillomavirus type 5 (bpv5), of a genomic size of 1.6 and 1.2 kb were subcloned and sequenced. one of them seemed to correspond to the 3' end of the e1 open reading frame (orf) and the other to the region of the e7, e8 and 5' end of the e1 orf. alignments of these fragments with other bpvs showed that bpv5 is only distantly related to the other 5 bpvs. | 1997 | 9311560 |
| identification of amino acids in the transmembrane and juxtamembrane domains of the platelet-derived growth factor receptor required for productive interaction with the bovine papillomavirus e5 protein. | the bovine papillomavirus e5 protein forms a stable complex with the cellular platelet-derived growth factor (pdgf) beta receptor, resulting in receptor activation and cell transformation. amino acids in both the putative transmembrane domain and extracytoplasmic carboxyl-terminal domain of the e5 protein appear important for pdgf receptor binding and activation. previous analysis indicated that the transmembrane domain of the receptor was also required for complex formation and receptor activat ... | 1997 | 9311809 |
| bovine papillomavirus type 1 e1 and simian virus 40 large t antigen share regions of sequence similarity required for multiple functions. | the full-length product of the bovine papillomavirus type 1 (bpv-1) e1 translational open reading frame is required for viral dna replication in vivo and in vitro. e1 is a multifunctional protein whose properties include atp binding, acting as an atpase-dependent dna helicase, dna binding to the bpv-1 origin of viral dna replication, and association with the e2 transcriptional transactivator, e2ta, a second viral protein involved in dna replication. all of these properties are thought to be impo ... | 1997 | 9311841 |
| competitive binding of viral e2 protein and mammalian core-binding factor to transcriptional control sequences of human papillomavirus type 8 and bovine papillomavirus type 1. | the promoter p7535 of human papillomavirus type 8 and the promoter p7185 of bovine papillomavirus type 1 are negatively regulated by viral e2 proteins via the promoter proximal binding sites p2 and bs1, respectively. mutations of these e2 binding sites can reduce basal promoter activity. this suggests binding of a transcription-stimulating factor and may indicate that repression by e2 is due to competitive binding of viral and cellular proteins. a computer search revealed putative binding sites ... | 1997 | 9311900 |
| conserved interaction of the papillomavirus e2 transcriptional activator proteins with human and yeast tfiib proteins. | papillomavirus early gene expression is regulated by the virus gene-encoded e2 proteins. the best-characterized e2 protein, encoded by bovine papillomavirus type 1 (bpv-1), has been shown to interact with basal transcription factor iib (tfiib) and the tata binding protein basal transcription factor (n. m. rank and p. f. lambert, j. virol. 69:6323-6334, 1995). we demonstrate that the potent e2 transcriptional activator protein encoded by a gene of human pv type 16 also interacts with tfiib in vit ... | 1997 | 9311902 |
| papillomavirus is resistant to desiccation. | there is strong epidemiologic evidence for sexual transmission of high-risk genital human papillomavirus (hpv) types. however, it is unclear if infection may also be transmitted indirectly via fomites. to assess this possibility, the in vitro infectivity after desiccation was compared for pseudotype hpv-16 virions, a model for high-risk type genital hpv, and bovine papillomavirus type 1 (bpv-1), a papillomavirus known to be transmitted via fomites. the 2 viruses had similar resistance to desicca ... | 1997 | 9333171 |
| reconstitution of a functional bovine papillomavirus type 1 origin of replication reveals a modular tripartite replicon with an essential at-rich element. | a functional replication origin was reconstituted using oligonucleotide cassettes corresponding to three sequence subelements within the bovine papillomavirus type 1 (bpv-1) replication origin: the 23-bp at-rich region (atr), the 18-bp binding site for the viral replication initiator protein e1 (e1bs), and a binding site for the viral transcriptional transactivator and replication enhancer protein e2 (e2bs). replication of the reconstituted origin depended on heterologous expression of both the ... | 1997 | 9356332 |
| the role of exogenous p53 and e6 oncoproteins in in vitro transformation by bovine papillomavirus type 4 (bpv-4): significance of the absence of an e6 orf in the bpv-4 genome. | bovine papillomavirus type 4 (bpv-4) does not possess an e6 orf. the e6 oncoprotein of human papillomavirus (hpv) binds and degrades the tumour suppressor protein p53, thus contributing to tumour progression. since bpv-4 lacks e6, it is unknown how the virus evades the tumour suppressor properties of p53 in the induction of tumours of the gastrointestinal tract. mutations in the p53 gene have been detected both in papillomas and carcinomas, suggesting that p53 dysfunction plays a part in these n ... | 1997 | 9367387 |
| structural, functional, and protein binding analyses of bovine papillomavirus type 1 exonic splicing enhancers. | alternative splicing plays an important role in regulation of bovine papillomavirus type 1 (bpv-1) gene expression. we have recently identified in bpv-1 late pre-mrnas two purine-rich exonic splicing enhancers (se1 and se2) which also stimulate splicing of a drosophila doublesex (dsx) pre-mrna containing a suboptimal 3' splice site. in vivo studies now demonstrate that both se1 and se2 are required for preferential use of the bpv-1 nucleotide (nt) 3225 3' splice site in nonpermissive cells. dele ... | 1997 | 9371566 |
| functional interaction of a novel cellular protein with the papillomavirus e2 transactivation domain. | the transactivation domain (ad) of bovine papillomavirus type 1 e2 stimulates gene expression and dna replication. to identify cellular proteins that interact with this 215-amino-acid domain, we used a transactivation-defective mutant as bait in the yeast two-hybrid screen. in vitro and in vivo results demonstrate that the cdna of one plasmid isolated in this screen encodes a 37-kda nuclear protein that specifically binds to an 82-amino-acid segment within the e2 ad. mutants with point mutations ... | 1997 | 9372953 |
| gene transfer of the cd80 costimulatory molecule into ocular melanoma cells using a novel episomal vector. | the cd80 (b7.1) molecule, which is a necessary costimulatory signal for t-cell activation and proliferation, is a powerful inducer of antitumor immunity. in this study, primary human ocular melanoma cells were transfected with a novel vector (b45-neo episomal vector) containing the complementary dna (cdna) for human cd80 to determine if this vector system is useful for stimulating cd8+ t cells. | 1997 | 9375572 |
| nmr-based discovery of lead inhibitors that block dna binding of the human papillomavirus e2 protein. | the e2 protein is required for the replication of human papillomaviruses (hpvs), which are responsible for anogenital warts and cervical carcinomas. using an nmr-based screen, we tested compounds for binding to the dna-binding domain of the hpv-e2 protein. three classes of compounds were identified which bound to two distinct sites on the protein. biphenyl and biphenyl ether compounds containing a carboxylic acid bind to a site near the dna recognition helix and inhibit the binding of e2 to dna. ... | 1997 | 9379433 |
| the bovine papillomavirus e6 protein binds to the ld motif repeats of paxillin and blocks its interaction with vinculin and the focal adhesion kinase. | the bovine papillomavirus type 1 (bpv-1) e6 oncoprotein can transform fibroblasts and induce anchorage-independent growth and disassembly of the actin stress fibers. we have previously shown that the e6 protein interacts with the focal adhesion protein, paxillin, suggesting a direct role of e6 in the disruption of the actin cytoskeleton. we have now mapped the e6 binding sites on paxillin to the ld motif repeats region, which has been implicated in mediating paxillin binding to two other focal a ... | 1997 | 9407131 |
| papillomaviruses: progress for human and veterinary medicine. | | 1997 | 9414949 |
| bovine papillomavirus and cancer. | bovine papillomavirus (bpv) induces papillomas of cutaneous or mucosal epithelia in cattle. the papillomas are benign tumours and generally regress, but occasionally persist and provide the focus for malignant transformation to squamous cell carcinoma, particularly in the presence of environmental cofactors. this has been experimentally demonstrated for bpv-2 and cancer of the urinary bladder, and bpv-4 and cancer of the upper alimentary canal in cattle feeding on bracken fern. in this review, s ... | 1997 | 9414951 |
| the papillomavirus minor capsid protein, l2, induces localization of the major capsid protein, l1, and the viral transcription/replication protein, e2, to pml oncogenic domains. | we have used immunofluorescent staining and confocal microscopy to examine the subcellular localization of structural and nonstructural bovine papillomavirus (bpv) proteins in cultured cells that produce infectious virions. when expressed separately, l1, the major capsid protein, showed a diffuse nuclear distribution while l2, the minor capsid protein, was found to localize to punctate nuclear regions identified as promonocytic leukemia protein (pml) oncogenic domains (pods). coexpression of l1 ... | 1998 | 9420209 |
| interaction of the bovine papillomavirus e6 protein with the clathrin adaptor complex ap-1. | the e6 gene of the bovine papillomavirus type 1 (bpv-1) is expressed in fibropapillomas caused by bpv-1 and in tissue culture cells transformed by bpv-1. it encodes one of the two major oncoproteins of bpv-1. in this study, we demonstrate an interaction between the bpv-1 e6 protein and ap-1, the tgn (trans-golgi network)-specific clathrin adaptor complex. ap-1 is a four-subunit protein complex required for clathrin-mediated cellular transport from the tgn. the ap-1/e6 interaction was observed in ... | 1998 | 9420248 |
| transient viral dna replication and repression of viral transcription are supported by the c-terminal domain of the bovine papillomavirus type 1 e1 protein. | the bovine papillomavirus type 1 e1 protein is important for viral dna replication and transcriptional repression. it has been proposed that the full-length e1 protein consists of a small n-terminal and a larger c-terminal domain. in this study, it is shown that an e1 polypeptide containing residues 132 to 605 (which represents the c-terminal domain) is able to support transient viral dna replication, although at a level lower than that supported by the wild-type protein. this domain can also re ... | 1998 | 9420289 |
| functional interaction of the bovine papillomavirus e2 transactivation domain with tfiib. | induction of gene expression by the papillomavirus e2 protein requires its approximately 220-amino-acid amino-terminal transactivation domain (tad) to interact with cellular factors that lead to formation of an activated rna polymerase complex. these interaction partners have yet to be identified and characterized. the e2 protein localizes the transcription complex to the target promoter through its carboxy-terminal sequence-specific dna binding domain. this domain has been reported to bind the ... | 1998 | 9444994 |
| polyomavirus large t can support dna replication in human cells. | human cells are generally thought to be nonpermissive for polyomavirus (py) dna replication. using transient transfection, we show that py large t-antigen (lt) was able to support replication of a py origin-containing plasmid in two human cell lines. replication supported by lt in human cells was specific for the py origin and required its enhancer sequences, as well as the previously reported critical phosphorylation sites within lt. py replication efficiency was comparable to that of papilloma ... | 1998 | 9448688 |
| papillomavirus virus-like particles can deliver defined ctl epitopes to the mhc class i pathway. | to evaluate an antigen delivery system in which exogenous antigen can target the major histocompatibility complex (mhc) class i pathway, a single human papillomavirus (hpv) 16 e7 cytotoxic t lymphocyte (ctl) epitope and a single hiv gp160 ctl epitope were separately fused to the c-terminus of bovine papillomavirus 1 (bpv1) l1 sequence to form hybrid bpv1l1 vlps. mice immunized with these hybrid vlps mounted strong ctl responses against the relevant target cells in the absence of any adjuvants. i ... | 1998 | 9448699 |
| association of bovine papillomavirus type 1 e6 oncoprotein with the focal adhesion protein paxillin through a conserved protein interaction motif. | we have found that the e6 oncoprotein of bovine papillomavirus type 1 (be6) as well as the e6 protein of the cancer associated hpv-16 (16e6) interact with the focal adhesion protein paxillin. mutational analysis of paxillin revealed that be6 binds paxillin through small protein interaction motifs called ld motifs that have been previously identified as important in regulating association of paxillin with vinculin and focal adhesion kinase (fak), and that be6 can interact with at least two separa ... | 1998 | 9467941 |
| an embryonic demethylation mechanism involving binding of transcription factors to replicating dna. | in vertebrates, transcriptionally active promoters are undermethylated. since the transcription factor sp1, and more recently nf-kappab, have been implicated in the demethylation process, we examined the effect of transcription factors on demethylation by injecting in vitro methylated plasmid dna into xenopus fertilized eggs. we found that various transactivation domains, including a strong acidic activation domain from the viral protein vp16, can enhance demethylation of a promoter region when ... | 1998 | 9482741 |
| human fibroblasts expressing the human papillomavirus e6 gene are deficient in global genomic nucleotide excision repair and sensitive to ultraviolet irradiation. | we investigated the role of wild-type p53 activity in modulating nucleotide excision repair after uv irradiation in normal and p53-deficient primary human fibroblasts created by expression of the human papillomavirus 16 e6 gene. compared with parental cells, the e6-expressing fibroblasts were deficient in global genomic repair of both uv-induced cyclobutane pyrimidine dimers and 6-4 photoproducts but exhibited normal transcription-coupled repair. the e6-expressing cells were also more sensitive ... | 1998 | 9485006 |
| screening for bovine papillomavirus in peripheral blood cells of donkeys with and without sarcoids. | papillomaviral dna has been identified in peripheral blood cells of both cattle and humans with and without associated disease and it has been suggested that such cells may act as sites of viral latency. in order to investigate the possibility of latent papillomaviral infection in the aetiopathogenesis of the equine sarcoid, peripheral blood derived dna samples from 20 healthy and 34 sarcoid-affected donkeys were subject to polymerase chain reaction (pcr) using papillomaviral specific primers. a ... | 1997 | 9491459 |
| competition for dna binding sites between the short and long forms of e2 dimers underlies repression in bovine papillomavirus type 1 dna replication control. | papillomaviruses establish a long-term latency in vivo by maintaining their genomes as nuclear plasmids in proliferating cells. bovine papillomavirus type 1 encodes two proteins required for viral dna replication: the helicase e1 and the positive regulator e2. the homodimeric e2 is known to cooperatively bind to dna with e1 to form a preinitiation complex at the origin of dna replication. the virus also codes for two short forms of e2 that can repress viral functions when overexpressed, and at l ... | 1998 | 9499046 |
| bovine papillomavirus type 1 genomes and the e2 transactivator protein are closely associated with mitotic chromatin. | the bovine papillomavirus type 1 e2 transactivator protein is required for viral transcriptional regulation and dna replication and may be important for long-term episomal maintenance of viral genomes within replicating cells (m. piirsoo, e. ustav, t. mandel, a. stenlund, and m. ustav, embo j. 15:1-11, 1996). we have evidence that, in contrast to most other transcriptional transactivators, the e2 transactivator protein is associated with mitotic chromosomes in dividing cells. the shorter e2-tr a ... | 1998 | 9499063 |
| intercapsomeric disulfide bonds in papillomavirus assembly and disassembly. | in order to analyze bonding contacts that stabilize the virion or promote capsid assembly, bovine papillomavirus (bpv) virions were subjected to buffer conditions known to disrupt polyomavirus virions. at physiologic ionic strength, incubation with dithiothreitol (dtt), egta, or dtt plus egta did not disrupt bpv virions as determined by electron microscopy. however, incubation of virions with dtt rendered the bpv l1 protein susceptible to trypsin cleavage at its carboxy terminus and rendered the ... | 1998 | 9499072 |
| dna structure and flexibility in the sequence-specific binding of papillomavirus e2 proteins. | the papillomavirus e2 proteins are transcriptional regulators that bind to a consensus dna sequence accg nnnn cggt. multiple copies of this binding site are found in the viral genomes. the affinities of the naturally occurring binding sites for the e2 proteins are predominantly dependent upon the sequence of the nnnn spacer. the hierarchies of binding site affinities among the sites present in the viral genomes result in differential occupancy during the viral life-cycle. in turn, this different ... | 1998 | 9500925 |
| subunit rearrangement accompanies sequence-specific dna binding by the bovine papillomavirus-1 e2 protein. | the 2.5 a crystal structures of the dna-binding domain of the e2 protein from bovine papillomavirus strain 1 and its complex with dna are presented. e2 is a transcriptional regulatory protein that is also involved in viral dna replication. it is the structural prototype for a novel class of dna-binding proteins: dimeric beta-barrels with surface alpha-helices that serve as recognition helices. these helices contain the amino-acid residues involved in sequence-specifying interactions. the e2 prot ... | 1998 | 9500927 |
| origin dna-binding proteins. | the first step in dna replication involves the recognition of origin dna sequences by origin-binding proteins. the three-dimensional structures of three different origin dna-binding proteins have recently been solved. these proteins form a structural class distinct from other dna-binding proteins. one of the origin-binding proteins, epstein-barr virus nuclear antigen 1, most likely has two modes of dna binding; the sequential use of these modes may be important for the initiation of dna replicat ... | 1998 | 9519296 |
| epithelial specific transcriptional regulation of the bovine papillomavirus 4 promoter by e2. | bovine papillomavirus 4 (bpv-4) is a mucosal epitheliotropic papillomavirus. it encodes a transcriptional regulator, e2, which acts on the bpv-4 transcriptional control region (the long control region or lcr) to regulate transcription. the distribution of e2 binding sites within the lcr of bpv-4 is identical to that of the human papillomaviruses hpv-16 and hpv-18, indicating that the mechanism of transcriptional control by e2 of mucosal epitheliotropic papillomaviruses is conserved. in this stud ... | 1998 | 9519828 |
| characterization of the dna-binding domain of the bovine papillomavirus replication initiator e1. | the bovine papillomavirus replication initiator protein e1 is an origin of replication (ori)-binding protein absolutely required for viral dna replication. in the presence of the viral transcription factor e2, e1 binds to the ori and initiates dna replication. to understand how the e1 initiator recognizes the ori and how e2 assists in this process, we have expressed and purified a 166-amino-acid fragment which corresponds to the minimal e1 dna-binding domain (dbd). dna binding studies using this ... | 1998 | 9525573 |
| stability without a centromere. | | 1998 | 9539691 |
| segregation of viral plasmids depends on tethering to chromosomes and is regulated by phosphorylation. | eukaryotic viruses can maintain latency in dividing cells as extrachromosomal nuclear plasmids. segregation and nuclear retention of dna is, therefore, a key issue in retaining copy number. the e2 enhancer protein of the papillomaviruses is required for viral dna replication and transcription. viral mutants that prevent phosphorylation of the bovine papillomavirus type 1 (bpv) e2 protein are transformation-defective, despite normal viral gene expression and replication function. cell colonies ha ... | 1998 | 9539738 |
| transactivation-competent bovine papillomavirus e2 protein is specifically required for efficient repression of human papillomavirus oncogene expression and for acute growth inhibition of cervical carcinoma cell lines. | the papillomavirus e2 proteins can function as sequence-specific transactivators or transrepressors of transcription and as cofactors in viral dna replication. we previously demonstrated that acute expression of the bovine papillomavirus type 1 (bpv1) e2 protein in hela and ht-3 cervical carcinoma cell lines greatly reduced cellular proliferation by imposing a specific g1/s phase growth arrest. in this report, we analyzed the effects of a panel of point mutations in the bpv1 e2 protein to identi ... | 1998 | 9557678 |
| dna packaging by l1 and l2 capsid proteins of bovine papillomavirus type 1. | encapsidation of circular dna by papillomavirus capsid protein was investigated in cos-1 cells. plasmids carrying both an sv40 origin of replication (ori) and an e. coli ori were introduced into cos-1 cells by dna transfection pv capsid proteins were supplied in trans by recombinant vaccinia viruses. pseudovirions were purified from infected cells and their packaged dna was extracted and used to transform e. coli as an indication of packaging efficacy. vlps assembled from bpv-1 l1 alone packaged ... | 1998 | 9568045 |
| calcium is required in reassembly of bovine papillomavirus in vitro. | papillomaviruses are small dna viruses which infect and induce benign warts and sometimes malignant tumours in the epithelium of the skin or mucosa. the viruses do not replicate in conventional tissue culture systems and little is known about the requirements for virus assembly. we investigated the effect of ethylene glycol-bis(aminoethyl ether)-tetraacetic acid (egta) and dithiothreitol (dtt) treatment on the stability of bovine papillomavirus type 1 (bpv-1) particles in vitro. removal of calci ... | 1998 | 9603328 |
| significant behavioral recovery in parkinson's disease model by direct intracerebral gene transfer using continuous injection of a plasmid dna-liposome complex. | as an alternative to virus-mediated gene transfer, we previously demonstrated a simple, safe, and efficient transfer of foreign gene into the central nervous system using continuous injection of a plasmid dna-cationic liposome complex. to explore whether this approach can be applied to the treatment of certain neurological disorders, we used an experimental model of parkinson's disease (pd) in the present study. following continuous injection for 7 days, tyrosine hydroxylase (th) and aromatic l- ... | 1998 | 9607420 |
| selective ablation of human t-cell lymphotropic virus type 1 p12i reduces viral infectivity in vivo. | human t-cell lymphotropic virus type 1 (htlv-1) is the etiologic agent of adult t-cell leukemia and htlv-1-associated myelopathy. novel, yet conserved rna transcripts encoded from open reading frames (orfs) i and ii of the viral px region are expressed both in vitro and in infected individuals. the orf i mrna encodes the protein p12(i), which has been shown to localize to cellular endomembranes, cooperate with bovine papillomavirus e5 in transformation, as well as bind to the il-2 receptor beta ... | 1998 | 9616168 |
| distinct roles of two binding sites for the bovine papillomavirus (bpv) e2 transactivator on bpv dna replication. | the modulation of dna replication by transcription factors was examined by using bovine papillomavirus type 1 (bpv). bpv replication in vivo requires two viral proteins: e1, an origin-binding protein, and e2, a transcriptional transactivator. in the origin, e1 interacts with a central region flanked by two binding sites for e2 (bs11 and bs12), of which only bs12 has been reported to be essential for replication in vivo. using chemical interference and electrophoretic mobility shift assays, we fo ... | 1998 | 9621032 |
| a high capacity assay for inhibitors of human papillomavirus dna replication. | the discovery of antiviral compounds against human papillomaviruses (hpv) has been hindered by the difficulties in culturing virus in vitro or assaying stable hpv dna replication. however, plasmids containing the hpv replication origin replicate transiently upon co-transfection with hpv e1 and e2 expression vectors. we have adapted this assay using secreted alkaline phosphatase (sap) as a reporter for rapid analysis of dna copy number. use of the sv40 early promoter in controlling sap expression ... | 1995 | 9636294 |
| presence of papillomavirus-like dna sequences in cutaneous fibropapillomas of the goat udder. | papillomatous lesions were isolated from the mammary skin of goats and examined for evidence of papillomavirus (pv) infection by various criteria, including gross morphology, histology and dna hybridization. although some lesions showed gross papillomatous morphological and histological features similar to those caused by papillomavirus in other species, no viral particles were detected. reverse slot hybridization revealed cross-hybridization between dna extracted from goat mammary papillomas an ... | 1998 | 9646460 |
| the bpv-4 co-carcinogen quercetin induces cell cycle arrest and up-regulates transcription from the lcr of bpv-4. | bracken fern is the environmental co-carcinogen of bpv-4 in the induction of neoplasias of the upper alimentary canal of cattle. the flavonoid quercetin is one of the most potent and best characterised mutagens present in the fern. we have shown that transfection with bpv-4 dna and exposure to a single dose of quercetin leads to tumorigenic transformation of primary bovine cells. we now show that quercetin induces cell cycle arrest and up-regulates transcription from the bpv-4 long control regio ... | 1998 | 9652740 |
| p53 protein is a suppressor of papillomavirus dna amplificational replication. | p53 protein was able to block human and bovine papillomavirus dna amplificational replication while not interfering with epstein-barr virus orip once-per-cell cycle replication. oligomerization, intact dna-binding, replication protein a-binding, and proline-rich domains of the p53 protein were essential for efficient inhibition, while the n-terminal transcriptional activation and c-terminal regulatory domains were dispensable for the suppressor activity of the p53 protein. the inhibition of repl ... | 1998 | 9658131 |
| the papillomavirus e1 protein forms a dna-dependent hexameric complex with atpase and dna helicase activities. | the e1 protein from bovine papillomavirus has site-specific dna binding activity, dna helicase activity, and dna-dependent atpase activity consistent with the properties of an initiator protein. here we have identified and characterized a novel oligomeric form of e1 that is associated with the atpase and dna helicase activities and whose formation is strongly stimulated by single-stranded dna. this oligomeric form corresponds to a hexamer of e1. | 1998 | 9658141 |
| u1 snrnp inhibits pre-mrna polyadenylation through a direct interaction between u1 70k and poly(a) polymerase. | it has previously been shown in vivo that bovine papillomavirus represses its late gene expression via a 5' splice site sequence located upstream of the late polyadenylation signal. here, the mechanism of repression is determined by in vitro analysis. u1 snrnp binding to the 5' splice site results in inhibition of polyadenylation via a direct interaction with poly(a) polymerase (pap). although the inhibitory mechanism is similar to that used in u1a autoregulation, u1a within the u1 snrnp does no ... | 1998 | 9659922 |
| interaction of prion peptide huprp106-126 with nucleic acid. | synthetic prion peptide prp106-126 has been used as a model to understand prion diseases. the conformation of the peptide depends on the environmental conditions and it forms amyloid in vitro. the potential of this prion peptide to interact with nucleic acids has been studied using a fluorescent labelled nucleic acid by kinetic and equilibrium methods. a decrease in the fluorescence of the labelled dna induced by the peptide with time is observed which is ph, ionic strength and temperature depen ... | 1997 | 9672613 |
| two antibodies that neutralize papillomavirus by different mechanisms show distinct binding patterns at 13 a resolution. | complexes between bovine papillomavirus type 1 (bpv1) and examples of two sets of neutralizing, monoclonal antibodies (mab) to the major capsid protein (l1) were analyzed by low-dose cryo-electron microscopy and three-dimensional (3d) image reconstruction to 13 a resolution. mab #9 is representative of a set of neutralizing antibodies that can inhibit viral binding to the cell surface, while mab 5b6 is representative of a second set that efficiently neutralizes papillomaviruses without significa ... | 1998 | 9680478 |
| bpv-4 e8 transforms nih3t3 cells, up-regulates cyclin a and cyclin a-associated kinase activity and de-regulates expression of the cdk inhibitor p27kip1. | the e8 open reading frame of bovine papillomavirus type 4 (bpv-4) encodes a small (42 amino acid) hydrophobic polypeptide localized to cellular membranes and capable of conferring an anchorage-independent (ai) growth phenotype on primary bovine cells co-transfected with bpv-4 e7 orf and an activated ras gene. to further study the function of e8 independently of other viral gene products, we have expressed it in the murine fibroblast cell line, nih3t3. cells expressing e8 are capable of ai growth ... | 1998 | 9690511 |
| 1h, 15n, and 13c nmr resonance assignments for the dna-binding domain of the bpv-1 e2 protein. | | 1998 | 9691287 |
| functional interaction between the bovine papillomavirus virus type 1 replicative helicase e1 and cyclin e-cdk2. | we have found that the replicative helicase e1 of bovine papillomavirus type 1 (bpv-1) interacts with a key cell cycle regulator of s phase, the cyclin e-cdk2 kinase. the e1 helicase, which interacts with cyclin e and not with cdk2, presents the highest affinity for catalytically active kinase complexes. in addition, e1, cyclin e, and cdk2 expressed in xenopus egg extracts are quantitatively coimmunoprecipitated from crude extracts by either anti-cdk2 or anti-e1 antibodies. e1 protein is also a ... | 1998 | 9696820 |
| subpopulations of lymphocytes in cattle naturally infected with papillomavirus. | subpopulations of blood lymphocytes (cd2, cd4, cd8, wc1 and igm-mu chain) were evaluated in clinically manifested bovine papillomatosis. significantly lower numbers of cd2 (44.7%), cd4 (22.8%) and a lower ratio of cd4/cd8 (1.5) were found in animals with tumours compared to a group of cattle free of papillomas (62.3%, 34%, and 2.3, respectively). on the other hand, significantly higher numbers of gamma/delta+ t lymphocytes (9.6%) and of lymphocytes expressing igm molecules (35%) were observed in ... | 1998 | 9704506 |
| inhibition/stimulation of bovine papillomavirus by adeno-associated virus is time as well as multiplicity dependent. | infection by adeno-associated virus (aav) is associated with lower cervical cancer rates. we have been investigating the hypothesis that aav interacts with and inhibits the role of human papillomaviruses (hpv) in cervical cancer. we have been studying the response of bovine papillomavirus type 1 (bpv) oncogenic transformation and dna replication to aav as a prototype system. the aav rep 78 gene product is responsible for this inhibition. here, it is demonstrated that in two assay systems, focus ... | 1998 | 9705917 |
| the papillomavirus e6 proteins. | specific types of human papillomaviruses (hpv) are strongly associated with the development of cervical cancer. the e6 gene from cancer-related hpvs has exhibited functions in tumorigenesis, regulation of transcription, telomerase, and apoptosis. cancer-related hpvs e6 proteins bind the tumor suppressor p53 and promotes its degradation through an ubiquitin-dependent pathway. several additional cellular e6-binding proteins have recently been identified and implicated in playing roles in p53-indep ... | 1998 | 9739758 |