Literature DB >> 12021332

The human papillomavirus type 31 late 3' untranslated region contains a complex bipartite negative regulatory element.

Sarah A Cumming1, Claire E Repellin, Maria McPhillips, Jonathan C Radford, J Barklie Clements, Sheila V Graham.   

Abstract

The papillomavirus life cycle is tightly linked to epithelial cell differentiation. Production of virus capsid proteins is restricted to the most terminally differentiated keratinocytes in the upper layers of the epithelium. However, mRNAs encoding the capsid proteins can be detected in less-differentiated cells, suggesting that late gene expression is controlled posttranscriptionally. Short sequence elements (less than 80 nucleotides in length) that inhibit gene expression in undifferentiated epithelial cells have been identified in the late 3' untranslated regions (UTRs) of several papillomaviruses, including the high-risk mucosal type human papillomavirus type 16 (HPV-16). Here we show that closely related high-risk mucosal type HPV-31 also contains elements that can act to repress gene expression in undifferentiated epithelial cells. However, the HPV-31 negative regulatory element is surprisingly complex, comprising a major inhibitory element of approximately 130 nucleotides upstream of the late polyadenylation site and a minor element of approximately 110 nucleotides mapping downstream. The first 60 nucleotides of the major element have 68% identity to the negative regulatory element of HPV-16, and these elements bind the same cellular proteins, CstF-64, U2AF(65), and HuR. The minor inhibitory element binds some cellular proteins in common with the major inhibitory element, though it also binds certain proteins that do not bind the upstream element.

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Year:  2002        PMID: 12021332      PMCID: PMC136222          DOI: 10.1128/jvi.76.12.5993-6003.2002

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  47 in total

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2.  Transcriptional termination and coupled polyadenylation in vitro.

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Journal:  EMBO J       Date:  2000-07-17       Impact factor: 11.598

3.  Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure.

Authors:  D H Mathews; J Sabina; M Zuker; D H Turner
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4.  Regulation of human papillomavirus type 31 polyadenylation during the differentiation-dependent life cycle.

Authors:  S S Terhune; C Milcarek; L A Laimins
Journal:  J Virol       Date:  1999-09       Impact factor: 5.103

5.  The human papillomavirus type 16 negative regulatory RNA element interacts with three proteins that act at different posttranscriptional levels.

Authors:  M D Koffa; S V Graham; Y Takagaki; J L Manley; J B Clements
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-25       Impact factor: 11.205

6.  Early polyadenylation signals of human papillomavirus type 31 negatively regulate capsid gene expression.

Authors:  S S Terhune; W G Hubert; J T Thomas; L A Laimins
Journal:  J Virol       Date:  2001-09       Impact factor: 5.103

7.  hnRNP A/B proteins are required for inhibition of HIV-1 pre-mRNA splicing.

Authors:  M Caputi; A Mayeda; A R Krainer; A M Zahler
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8.  The carboxyl terminus of vertebrate poly(A) polymerase interacts with U2AF 65 to couple 3'-end processing and splicing.

Authors:  S Vagner; C Vagner; I W Mattaj
Journal:  Genes Dev       Date:  2000-02-15       Impact factor: 11.361

9.  A cellular 65-kDa protein recognizes the negative regulatory element of human papillomavirus late mRNA.

Authors:  W Dietrich-Goetz; I M Kennedy; B Levins; M A Stanley; J B Clements
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10.  Human papillomavirus type 16 DNA sequence.

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  18 in total

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Review 2.  Papillomavirus genome structure, expression, and post-transcriptional regulation.

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Journal:  Front Biosci       Date:  2006-09-01

3.  A downstream polyadenylation element in human papillomavirus type 16 L2 encodes multiple GGG motifs and interacts with hnRNP H.

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4.  A splicing enhancer in the E4 coding region of human papillomavirus type 16 is required for early mRNA splicing and polyadenylation as well as inhibition of premature late gene expression.

Authors:  Margaret Rush; Xiaomin Zhao; Stefan Schwartz
Journal:  J Virol       Date:  2005-09       Impact factor: 5.103

5.  A 57-nucleotide upstream early polyadenylation element in human papillomavirus type 16 interacts with hFip1, CstF-64, hnRNP C1/C2, and polypyrimidine tract binding protein.

Authors:  Xiaomin Zhao; Daniel Oberg; Margaret Rush; Joanna Fay; Helen Lambkin; Stefan Schwartz
Journal:  J Virol       Date:  2005-04       Impact factor: 5.103

6.  tRNASer(CGA) differentially regulates expression of wild-type and codon-modified papillomavirus L1 genes.

Authors:  Wenyi Gu; Mengrong Li; Wei Ming Zhao; Ning Xia Fang; Shurui Bu; Ian H Frazer; Kong-Nan Zhao
Journal:  Nucleic Acids Res       Date:  2004-08-19       Impact factor: 16.971

Review 7.  Regulation of human papillomavirus gene expression by splicing and polyadenylation.

Authors:  Cecilia Johansson; Stefan Schwartz
Journal:  Nat Rev Microbiol       Date:  2013-03-11       Impact factor: 60.633

8.  Identification of an hnRNP A1-dependent splicing silencer in the human papillomavirus type 16 L1 coding region that prevents premature expression of the late L1 gene.

Authors:  Xiaomin Zhao; Margaret Rush; Stefan Schwartz
Journal:  J Virol       Date:  2004-10       Impact factor: 5.103

9.  Polypyrimidine tract binding protein induces human papillomavirus type 16 late gene expression by interfering with splicing inhibitory elements at the major late 5' splice site, SD3632.

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10.  Activity of the human papillomavirus type 16 late negative regulatory element is partly due to four weak consensus 5' splice sites that bind a U1 snRNP-like complex.

Authors:  Sarah A Cumming; Maria G McPhillips; Thanaporn Veerapraditsin; Steven G Milligan; Sheila V Graham
Journal:  J Virol       Date:  2003-05       Impact factor: 5.103

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