Skip Navigation

This Article
Right arrow Print PDF (819K)
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 Klein, S.
Right arrow Articles by Schaffner, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Klein, S.
Right arrow Articles by Schaffner, W.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1985, Vol. 13, No. 24 8901-8912
© 1985


Articles

Evidence for transient requirement of the IgH enhancer

Sigrid Klein*, Thomas Gerster1, Didier Picard1, Andreas Radbruch and Walter Schaffner1

Institut für Genetik der Univeisität zu Köln Weyertal 121, D-5000 Köln 41, FRG 1Institut für Molekularbiologie II der Universität Zürich Hönggerberg, CH-8093 Zürich, Switzerland

*To whom reprint requests should be sent

Received October 21, 1985. Accepted November 19, 1985.

A transcriptional enhancer is thought to play a major role in determining tissue-specific expression of the immaunoglobulin heavy chain (IgH) gene (1–3). However in three B-lymaphoid cell lines the Ig enhancer has been lost due to a spontaneous deletion, yet heavy chain synthesis persists at a high level (4–6). In the case of the enhancerless delta chain gene (5) we wanted to test whether the IgH enhancer is no longer necessary for maintenance of transcription or whether perhaps a new enhancer was created de novo by the deletion process. To this end we have cloned the relevant portion of the variant IgH gene and transfected it into myeloma and hybridoma cells. We find that the reintroduced gene segment is not expressed unless it is linked again to an enhancer. The results suggest that the IgH enhancer is necessary for the onset of transcription, presumably by organizing the gene into stable transcription complexes, but is dispensable at later stages once the transcription unit is activated.


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
JEMHome page
J. P. Manis, N. van der Stoep, M. Tian, R. Ferrini, L. Davidson, A. Bottaro, and F. W. Alt
Class Switching in B Cells Lacking 3' Immunoglobulin Heavy Chain Enhancers
J. Exp. Med., October 19, 1998; 188(8): 1421 - 1431.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
J K Liu, Y Bergman, and K S Zaret
The mouse albumin promoter and a distal upstream site are simultaneously DNase I hypersensitive in liver chromatin and bind similar liver-abundant factors in vitro.
Genes & Dev., May 1, 1988; 2(5): 528 - 541.
[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.