Literature DB >> 2720783

A CCAAT box sequence in the adenovirus major late promoter functions as part of an RNA polymerase II termination signal.

S Connelly1, J L Manley.   

Abstract

Termination of transcription by RNA polymerase II has been shown in several cases to require a functional poly(A) addition site, although the actual termination event occurs further downstream. To define in more detail the sequences required for termination, we mapped the site at which transcription terminates on a chimeric plasmid template that contains the adenovirus MLP directing transcription of the SV40 early region. Termination in cells transfected with this plasmid occurs within a discrete promoter-proximal region that contains an inverted CCAAT-box sequence. This region of the MLP was also capable of directing termination, in an orientation-dependent manner, when inserted downstream of the poly(A) site in the plasmid template. In addition, in adenovirus-infected cells, transcription initiated from upstream promoters on the adenovirus chromosome terminates within the same MLP promoter-proximal region, both establishing the physiological relevance of the observed CCAAT-box dependent termination, and also suggesting a possible function for transcription termination in adenovirus infection.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2720783     DOI: 10.1016/0092-8674(89)90126-8

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  40 in total

1.  Mechanism of poly(A) signal transduction to RNA polymerase II in vitro.

Authors:  D P Tran; S J Kim; N J Park; T M Jew; H G Martinson
Journal:  Mol Cell Biol       Date:  2001-11       Impact factor: 4.272

2.  Map of cis-acting sequences that determine alternative pre-mRNA processing in the E3 complex transcription unit of adenovirus.

Authors:  H A Brady; A Scaria; W S Wold
Journal:  J Virol       Date:  1992-10       Impact factor: 5.103

3.  An RNA polymerase pause site is associated with the immunoglobulin mus poly(A) site.

Authors:  Martha L Peterson; Shannon Bertolino; Frankie Davis
Journal:  Mol Cell Biol       Date:  2002-08       Impact factor: 4.272

4.  Parameters that govern the regulation of immunoglobulin delta heavy-chain gene expression.

Authors:  R Tisch; N Kondo; N Hozumi
Journal:  Mol Cell Biol       Date:  1990-10       Impact factor: 4.272

5.  Termination of transcription in an 'in vitro' system is dependent on a polyadenylation sequence.

Authors:  V J Miralles
Journal:  Nucleic Acids Res       Date:  1991-07-11       Impact factor: 16.971

6.  Transcription termination by nuclear RNA polymerases.

Authors:  Patricia Richard; James L Manley
Journal:  Genes Dev       Date:  2009-06-01       Impact factor: 11.361

7.  An intact histone 3'-processing site is required for transcription termination in a mouse histone H2a gene.

Authors:  N Chodchoy; N B Pandey; W F Marzluff
Journal:  Mol Cell Biol       Date:  1991-01       Impact factor: 4.272

8.  Definition of transcriptional pause elements in fission yeast.

Authors:  A Aranda; N J Proudfoot
Journal:  Mol Cell Biol       Date:  1999-02       Impact factor: 4.272

9.  3' RNA processing efficiency plays a primary role in generating termination-competent RNA polymerase II elongation complexes.

Authors:  G Edwalds-Gilbert; J Prescott; E Falck-Pedersen
Journal:  Mol Cell Biol       Date:  1993-06       Impact factor: 4.272

10.  Promoter of the adenovirus polypeptide IX gene: similarity to E1B and inactivation by substitution of the simian virus 40 TATA element.

Authors:  L E Babiss; L D Vales
Journal:  J Virol       Date:  1991-02       Impact factor: 5.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.