Literature DB >> 2834065

Sequence requirements for premature termination of transcription in the human c-myc gene.

D L Bentley1, M Groudine.   

Abstract

We have used the Xenopus oocyte injection system to investigate the sequence requirements of premature termination of transcription within the human c-myc gene. We show that in the oocyte, truncated RNAs are produced by RNA polymerase II with 5' ends at the P1 and P2 promoters and 3' ends at two T stretches (sites I and II) near the exon 1/intron 1 junction. The location of these 3' ends is consistent with the site of the block to c-myc transcription identified by nuclear runoff assays in human cells and confirmed in dissected nuclei of injected oocytes. Evidence is presented that transcriptional termination rather than RNA processing produces these short c-myc RNAs. Deletion analysis of site I reveals that sequences upstream of the T stretch determine the site of 3' end formation, and that the stretch of T's on the sense DNA strand is not required for termination. The sequences specifying termination reside within a 95 base region located -130 to -35 relative to the exon 1/intron 1 boundary. The termination activity of these sequences is orientation-dependent and functions downstream of the HSV-TK promoter.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 2834065     DOI: 10.1016/0092-8674(88)90386-8

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


  97 in total

1.  Coiled bodies preferentially associate with U4, U11, and U12 small nuclear RNA genes in interphase HeLa cells but not with U6 and U7 genes.

Authors:  E Y Jacobs; M R Frey; W Wu; T C Ingledue; T C Gebuhr; L Gao; W F Marzluff; A G Matera
Journal:  Mol Biol Cell       Date:  1999-05       Impact factor: 4.138

2.  cis-Acting Elements for Light Regulation of Pea Ferredoxin I Gene Expression Are Located within Transcribed Sequences.

Authors:  R. C. Elliott; L. F. Dickey; M. J. White; W. F. Thompson
Journal:  Plant Cell       Date:  1989-07       Impact factor: 11.277

3.  A 10 residue motif at the C-terminus of the RNA pol II CTD is required for transcription, splicing and 3' end processing.

Authors:  Nova Fong; Gregory Bird; Marc Vigneron; David L Bentley
Journal:  EMBO J       Date:  2003-08-15       Impact factor: 11.598

4.  Elongation factor-dependent transcript shortening by template-engaged RNA polymerase II.

Authors:  D Reines
Journal:  J Biol Chem       Date:  1992-02-25       Impact factor: 5.157

5.  In vitro analysis of a transcription termination site for RNA polymerase II.

Authors:  D K Wiest; D K Hawley
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

6.  A cis-acting element in the promoter region of the murine c-myc gene is necessary for transcriptional block.

Authors:  H Miller; C Asselin; D Dufort; J Q Yang; K Gupta; K B Marcu; A Nepveu
Journal:  Mol Cell Biol       Date:  1989-12       Impact factor: 4.272

7.  Control of formation of two distinct classes of RNA polymerase II elongation complexes.

Authors:  N F Marshall; D H Price
Journal:  Mol Cell Biol       Date:  1992-05       Impact factor: 4.272

8.  RNA polymerase II elongation complex. Elongation complexes purified using an anti-RNA antibody do not contain initiation factor alpha.

Authors:  D Reines
Journal:  J Biol Chem       Date:  1991-06-05       Impact factor: 5.157

9.  Galectin-3: differential accumulation of distinct mRNAs in serum-stimulated mouse 3T3 fibroblasts.

Authors:  P G Voss; Y G Tsay; J L Wang
Journal:  Glycoconj J       Date:  1994-08       Impact factor: 2.916

10.  Loss of Marek's disease virus tumorigenicity is associated with truncation of RNAs transcribed within BamHI-H.

Authors:  G Bradley; G Lancz; A Tanaka; M Nonoyama
Journal:  J Virol       Date:  1989-10       Impact factor: 5.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.