Skip Navigation

This Article
Right arrow Print PDF (11218K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Tebb, G.
Right arrow Articles by Mattaj, l. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tebb, G.
Right arrow Articles by Mattaj, l. W.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1987, Vol. 15, No. 16 6437-6453
© 1987


Articles

Only two of the four sites of interaction with nuclear factors within the MXenopus U2 gene promoter are necessary for efficient transcription

Graham Tebb, Dirk Bohmann1,* and lain W. Mattaj

European Molecular Biology Laboratory (EMBL) D-6900 Heidelberg 1Division of Molecular Biology, Institute of Cell and Tumour Biology, German Cancer Research Centre D-6900 Heidelberg, FRG

Received May 11, 1987. Revised July 14, 1987. Accepted July 14, 1987.

An analysis, performed by DNase I footprinting, of the interactions between factors present in Molt-4 nuclear extracts and a Xenopus U2 snRNA gene promoter is presented. Four distinct regions of sequence-specific DNA-factor interaction are found. Two of these correspond to the previously identified proximal and distal sequence elements (PSE and DSE) of the promoter. Both of these elements are important in U2 transcription, indicating a functional role for the observed interactions. The other two sites of interaction correspond to a sequence element conserved in many, but not all, vertebrate U snRNA gene promoters (the MSE) and to a region adjacent to the site of transcription initiation (the "cap site"). Site-directed mutants of these latter two elements are constructed which no longer bind nuclear factors. Transcriptional analysis in Xenopus oocytes reveals that these mutants are transcribed as efficiently as wild-type U2. Other possible roles for the two factors are discussed.


*Present address: Department of Biochemistry, University of California, Berkeley, CA 94720, USA


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Genes Dev.Home page
P Weller, C Bark, L Janson, and U Pettersson
Transcription analysis of a human U4C gene: involvement of transcription factors novel to snRNA gene expression.
Genes & Dev., November 1, 1988; 2(11): 1389 - 1399.
[Abstract] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.