Literature DB >> 10629040

A composite polyadenylation signal with TATA box function.

N Paran1, A Ori, I Haviv, Y Shaul.   

Abstract

A variant polyadenylation signal, which is conserved and employed by mammalian hepadnaviruses, has a sequence resembling that of the TATA box. We report here that this composite box manifests all the promoter characteristics. It binds effectively TATA-binding protein with TFIIB and TFIIA in a synergistic manner. This capacity, however, is lost when the box is converted to a canonical and simple poly(A) signal. Furthermore, we show that it has promoter activity and supports transcription of reporter genes preferentially in liver-derived cells, a characteristic behavior of the hepatitis B virus (HBV) promoters. In addition, we show that the HBV noncanonical poly(A) signal supports transcription initiation from the viral genome, suggesting that it is a genuine promoter, possibly of the polymerase/reverse transcriptase gene. Finally, we found that this deviant poly(A) signal is crucial for HBV replication since a viral mutant with a canonical poly(A) box is impaired in replication. Our data, therefore, raise the interesting and novel possibility that a composite poly(A) box might have a dual function. At the level of DNA it functions as a promoter to initiate transcription, whereas at the level of RNA it serves as a poly(A) signal to process RNA. An interesting outcome of this strategy of gene expression is that it provides a novel mechanism for the synthesis of an approximately genome length transcript.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10629040      PMCID: PMC85200          DOI: 10.1128/MCB.20.3.834-841.2000

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  43 in total

1.  pX, the HBV-encoded coactivator, suppresses the phenotypes of TBP and TAFII250 mutants.

Authors:  I Haviv; Y Matza; Y Shaul
Journal:  Genes Dev       Date:  1998-04-15       Impact factor: 11.361

2.  Identification of a rat liver nuclear protein that binds to the enhancer core element of three animal viruses.

Authors:  P F Johnson; W H Landschulz; B J Graves; S L McKnight
Journal:  Genes Dev       Date:  1987-04       Impact factor: 11.361

3.  Liver-specific expression of hepatitis B virus is determined by the combined action of the core gene promoter and the enhancer.

Authors:  J Honigwachs; O Faktor; R Dikstein; Y Shaul; O Laub
Journal:  J Virol       Date:  1989-02       Impact factor: 5.103

4.  Hepatitis B virus (HBV) particles are produced in a cell culture system by transient expression of transfected HBV DNA.

Authors:  K Yaginuma; Y Shirakata; M Kobayashi; K Koike
Journal:  Proc Natl Acad Sci U S A       Date:  1987-05       Impact factor: 11.205

5.  Duck hepatitis B virus (DHBV) particles produced by transient expression of DHBV DNA in a human hepatoma cell line are infectious in vitro.

Authors:  J C Pugh; K Yaginuma; K Koike; J Summers
Journal:  J Virol       Date:  1988-09       Impact factor: 5.103

6.  Hepatitis B virus produced by transfected Hep G2 cells causes hepatitis in chimpanzees.

Authors:  G Acs; M A Sells; R H Purcell; P Price; R Engle; M Shapiro; H Popper
Journal:  Proc Natl Acad Sci U S A       Date:  1987-07       Impact factor: 11.205

7.  In vitro experimental infection of primary duck hepatocyte cultures with duck hepatitis B virus.

Authors:  J S Tuttleman; J C Pugh; J W Summers
Journal:  J Virol       Date:  1986-04       Impact factor: 5.103

8.  Regulation of hepatitis B virus S gene promoter in transfected cell lines.

Authors:  O Faktor; T De-Medina; Y Shaul
Journal:  Virology       Date:  1988-02       Impact factor: 3.616

9.  Expression and replication of the hepatitis B virus genome under foreign promoter control.

Authors:  M Junker; P Galle; H Schaller
Journal:  Nucleic Acids Res       Date:  1987-12-23       Impact factor: 16.971

10.  Multiple nuclear proteins in liver cells are bound to hepatitis B virus enhancer element and its upstream sequences.

Authors:  Y Shaul; R Ben-Levy
Journal:  EMBO J       Date:  1987-07       Impact factor: 11.598

View more
  6 in total

1.  Recombinant covalently closed circular hepatitis B virus DNA induces prolonged viral persistence in immunocompetent mice.

Authors:  Zhihua Qi; Gaiyun Li; Hao Hu; Chunhui Yang; Xiaoming Zhang; Qibin Leng; Youhua Xie; Demin Yu; Xinxin Zhang; Yueqiu Gao; Ke Lan; Qiang Deng
Journal:  J Virol       Date:  2014-05-07       Impact factor: 5.103

2.  Doubly Spliced RNA of Hepatitis B Virus Suppresses Viral Transcription via TATA-Binding Protein and Induces Stress Granule Assembly.

Authors:  Kuen-Nan Tsai; Chin-Liew Chong; Yu-Chi Chou; Chien-Chiao Huang; Yi-Ling Wang; Shao-Win Wang; Mong-Liang Chen; Chun-Hong Chen; Chungming Chang
Journal:  J Virol       Date:  2015-09-02       Impact factor: 5.103

Review 3.  Prospects for inhibiting the post-transcriptional regulation of gene expression in hepatitis B virus.

Authors:  Augustine Chen; Nattanan Panjaworayan T-Thienprasert; Chris M Brown
Journal:  World J Gastroenterol       Date:  2014-07-07       Impact factor: 5.742

4.  lnc-RHL, a novel long non-coding RNA required for the differentiation of hepatocytes from human bipotent progenitor cells.

Authors:  Bindu Prabhakar; Soowan Lee; Adara Bochanis; Wu He; José E Manautou; Theodore P Rasmussen
Journal:  Cell Prolif       Date:  2021-01-04       Impact factor: 6.831

5.  HBVRegDB: annotation, comparison, detection and visualization of regulatory elements in hepatitis B virus sequences.

Authors:  Nattanan Panjaworayan; Stephan K Roessner; Andrew E Firth; Chris M Brown
Journal:  Virol J       Date:  2007-12-17       Impact factor: 4.099

6.  Full-Length Isoform Sequencing Reveals Novel Transcripts and Substantial Transcriptional Overlaps in a Herpesvirus.

Authors:  Dóra Tombácz; Zsolt Csabai; Péter Oláh; Zsolt Balázs; István Likó; Laura Zsigmond; Donald Sharon; Michael Snyder; Zsolt Boldogkői
Journal:  PLoS One       Date:  2016-09-29       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.