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

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...

Full description

Saved in:
Bibliographic Details
Published inNucleic acids research Vol. 31; no. 9; pp. 2344 - 2352
Main Authors Domitrovich, Angela M., Kunkel, Gary R.
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.05.2003
Oxford Publishing Limited (England)
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary: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.
Bibliography:ark:/67375/HXZ-40MRG588-1
local:gkg331
To whom correspondence should be addressed. Tel: +1 979 845 6257; Fax: +1 979 845 9274; Email: g‐kunkel@tamu.edu
istex:92C2DE135872DD97D118BE9701BA7BCDE181F56E
Received January 17, 2003; Revised and Accepted March 2, 2003
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
To whom correspondence should be addressed. Tel: +1 979 845 6257; Fax: +1 979 845 9274; Email: g-kunkel@tamu.edu
ISSN:0305-1048
1362-4962
1362-4962
DOI:10.1093/nar/gkg331