Multiple, dispersed human U6 small nuclear RNA genes with varied transcriptional efficiencies

被引:60
作者
Domitrovich, AM [1 ]
Kunkel, GR [1 ]
机构
[1] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
基金
美国国家科学基金会;
关键词
D O I
10.1093/nar/gkg331
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vertebrate U6 small nuclear RNA (snRNA) gene promoters are among the founding members of those recognized by RNA polymerase III in which all control elements for initiation are located in the 5'-flanking region. Previously, one human U6 gene (U6-1) has been studied extensively. We have identified a total of nine full-length U6 loci in the human genome. Unlike human U1 and U2 snRNA genes, most of the full-length U6 loci are dispersed throughout the genome. Of the nine full-length U6 loci, five are potentially active genes (U6-1, U6-2, U6-7, U6-8 and U6-9) since they are bound by TATA-binding protein and enriched in acetylated histone H4 in cultured human 293 cells. These five all contain OCT, SPH, PSE and TATA elements, although the sequences of these elements are variable. Furthermore, these five genes are transcribed to different extents in vitro or after transient transfection of human 293 cells. Of the nine full-length U6 loci, only U6-7 and U6-8 are closely linked and contain highly conserved 5'-flanking regions. However, due to a modest sequence difference in the proximal sequence elements for U6-7 and U6-8, these genes are transcribed at very different levels in transfected cells.
引用
收藏
页码:2344 / 2352
页数:9
相关论文
共 52 条
[1]   STABLE TRANSCRIPTION COMPLEXES OF XENOPUS 5S RNA GENES - A MEANS TO MAINTAIN THE DIFFERENTIATED STATE [J].
BOGENHAGEN, DF ;
WORMINGTON, WM ;
BROWN, DD .
CELL, 1982, 28 (02) :413-421
[2]   A system for stable expression of short interfering RNAs in mammalian cells [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
SCIENCE, 2002, 296 (5567) :550-553
[3]   Assembly of human small nuclear RNA gene-specific transcription factor IIIB complex de novo on and off promoter [J].
Cabart, P ;
Murphy, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (30) :26831-26838
[4]   Reconstitution of transcription from the human U6 small nuclear RNA promoter with eight recombinant polypeptides and a partially purified RNA polymerase III complex [J].
Chong, SS ;
Hu, P ;
Hernandez, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (23) :20727-20734
[5]  
Dahlberg JE, 1988, STRUCTURE FUNCTION M, P38
[6]   UPSTREAM REGULATORY ELEMENTS ARE NECESSARY AND SUFFICIENT FOR TRANSCRIPTION OF A U6-RNA GENE BY RNA POLYMERASE-III [J].
DAS, G ;
HENNING, D ;
WRIGHT, D ;
REDDY, R .
EMBO JOURNAL, 1988, 7 (02) :503-512
[7]   The Oct-1 POU domain activates snRNA gene transcription by contacting a region the SNAPc largest subunit that bears sequence similarities to the Oct-1 coactivator OBF-1 [J].
Ford, E ;
Strubin, M ;
Hernandez, N .
GENES & DEVELOPMENT, 1998, 12 (22) :3528-3540
[8]   Characterization of a trimeric complex containing Oct-1, SNAP(c), and DNA [J].
Ford, E ;
Hernandez, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (25) :16048-16055
[9]   THE TRANSCRIPTIONAL START SITE FOR A HUMAN U6 SMALL NUCLEAR-RNA GENE IS DICTATED BY A COMPOUND PROMOTER ELEMENT CONSISTING OF THE PSE AND THE TATA BOX [J].
GOOMER, RS ;
KUNKEL, GR .
NUCLEIC ACIDS RESEARCH, 1992, 20 (18) :4903-4912
[10]   Histone acetylation in chromatin structure and transcription [J].
Grunstein, M .
NATURE, 1997, 389 (6649) :349-352