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PMID: 11489996 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Distinct control of the frequency and allelic exclusion of the V beta gene rearrangement at the TCR beta locus.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 167 ·No. 4 ·2001-08-15 ·Pages 2121-9

Sieh P, Chen J

Abstract

Ag receptor gene loci contain many V gene segments, each of which is recombined and expressed at a different frequency and is subject to allelic exclusion. To probe the parameters that mediate the different levels of regulation of V gene rearrangement, a Vbeta gene segment together with 3.6-kb 5' and 0.7-kb 3' flanking sequences was inserted 6.8 kb upstream of the Dbeta1 gene segment in the murine TCRbeta locus. Despite its proximity to the Dbeta gene segments and the Ebeta enhancer, the inserted Vbeta segment underwent VDJ recombination at the same frequency as the natural copy located 470 kb upstream. However, the inserted Vbeta segment was no longer under allelic exclusion control as it recombined at a similar frequency in the presence of a TCRbeta transgene. These results suggest that while the inserted fragment contains the necessary cis-regulatory elements for determining the frequency of Vbeta rearrangement, additional cis-regulatory elements are required for mediating Vbeta allelic exclusion. Interestingly, most of the inserted Vbeta rearrangements were not transcribed and expressed in the presence of a TCRbeta transgene, suggesting that TCRbeta allelic exclusion can also be achieved by blocking the transcription of the rearranged gene segments. These findings provide strong evidence for distinct control of the frequency and allelic exclusion of Vbeta gene rearrangement.

MeSH Terms
Alleles Animals Gene Frequency/immunology Gene Rearrangement, beta-Chain T-Cell Antigen Receptor Gene Targeting Lymph Nodes/cytology Mice Mice, Knockout Mice, Transgenic Mutagenesis, Insertional/immunology Promoter Regions, Genetic/immunology Receptors, Antigen, T-Cell, alpha-beta/genetics,metabolism Recombination, Genetic/immunology T-Lymphocyte Subsets/immunology,metabolism Transgenes/immunology
Chemicals
Receptors, Antigen, T-Cell, alpha-beta
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Sieh P
Center for Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Chen J
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
2001-08-15
Pages
2121-9
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI40146 · United States
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