Skip Navigation

This Article
Right arrow Print PDF (3217K)
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 Qian, L.
Right arrow Articles by Wilkinson, M. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Qian, L.
Right arrow Articles by Wilkinson, M. F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1992, Vol. 20, No. 20 5345-5350
© 1992


MOLECULAR BIOLOGY

A spliced intron accumulates as a lariat in the nucleus of T cells

Lian Qian, Minh N. Vu, Mark Carter and Miles F. Wilkinson*

Vollum Institute for Advanced Biomedical Research, Microbiology & Immunology Department, Oregon Health Sciences University L220, 3181 S.W. Sam Jackson Park Road, Portland, OR 97201, USA

* To whom correspondence should be addressed

Received July 20, 1992. Revised September 18, 1992. Accepted September 18, 1992.

The vast majority of mammalian genes are Interrupted by non-coding segments of DNA termed Introns. Introns are spliced out of RNA transcripts as lariat structures, and then are typically debranched and rapidly degraded. Here, we describe an unusual spliced intron from the constant region of the T cell receptor-ß (TCR-ß) locus that is relatively stable in mammalian cells. This intron, IVS1cß1, accumulates as a set of lariat RNA structures with different length talls in the nucleus of T cells. The accumulation of this spliced intron is developmentally regulated during murine thymocyte ontogeny. The property of stability appears to be evolutionary conserved since the human version of this intron also accumulates in T cells. The stability is selective since other spliced TCR-ß introns do not detectably accumulate in T cells. The unusual stability of this intron does not depend on T cell specific factors since non-T cells transfected with TCR-ß gene constructs also accumulate spliced IVSIcß1. The discovery of a mammalian intron that accumulates as a lariat in vivo provides an opportunity to elucidate mechanisms that regulate intron debranching, stability, and nuclear localization.


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
Mol Biol EvolHome page
J. S. Mattick and M. J. Gagen
Review ArticleThe Evolution of Controlled Multitasked Gene Networks: The Role of Introns and Other Noncoding RNAs in the Development of Complex Organisms
Mol. Biol. Evol., September 1, 2001; 18(9): 1611 - 1630.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Biol.Home page
C. Johnson, D. Primorac, M. McKinstry, J. McNeil, D. Rowe, and J. B. Lawrence
Tracking COL1A1 RNA in Osteogenesis Imperfecta: Splice-defective Transcripts Initiate Transport from the Gene but Are Retained within the SC35 Domain
J. Cell Biol., August 7, 2000; 150(3): 417 - 432.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
R. Dirks, F. van de Rijke, S Fujishita, M van der Ploeg, and A. Raap
Methodologies for specific intron and exon RNA localization in cultured cells by haptenized and fluorochromized probes
J. Cell Sci., January 4, 1993; 104(4): 1187 - 1197.
[Abstract] [PDF]


Home page
J. Biol. Chem.Home page
J. Q. Clement, S. Maiti, and M. F. Wilkinson
Localization and Stability of Introns Spliced from the Pem Homeobox Gene
J. Biol. Chem., May 11, 2001; 276(20): 16919 - 16930.
[Abstract] [Full Text] [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.