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PMID: 2497226 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Relative V beta transcript levels in thymus and peripheral lymphoid tissues from various mouse strains. Inverse correlation of I-E and Mls expression with relative abundance of several V beta transcripts in peripheral lymphoid tissues.

The Journal of experimental medicine ·Vol. 169 ·No. 5 ·1989-05-01 ·Pages 1703-19

Okada CY, Weissman IL

Abstract

We have measured the relative levels of transcripts for 15 of the 22 known V beta gene segments. The level of transcripts for the highest and lowest expressed V beta gene segment differed by greater than 20-fold in the thymus and an even larger difference was observed in the periphery. The levels of expressions were unrelated to the order of the V beta genes on the chromosome. For most of the V beta gene segments, the relative transcript levels were the same in the thymus and periphery, suggesting that thymic selection in general does not act solely upon the V beta gene segment. One V beta gene segment in the BALB and B10 mice strains was an exception to this rule. V beta 5.2 expression in the periphery of BALB and B10 mice inversely correlated with the expression of the MHC class II molecule I-E. Five V beta gene segments had reduced transcript levels in the periphery of Mls-1a mice compared with their thymic levels or to the levels found in Mls-1b mice. The peripheral level of V beta 3 transcripts vary with MHC and Mls-2 haplotypes. The observation that certain V beta transcript levels are reduced in the periphery when compared with the thymus favors the hypothesis that self tolerance at the T cell level results in the elimination of self-reactive T cells, rather than paralysis by a block at some post-transcriptional step. Finally, the wide variability of V beta gene segment expression in the thymus suggests mechanisms exist to import an early bias to the repertoire. Whether this bias results from differential V beta segment rearrangement rates, differential V beta expression rates, or events occurring after TCR-alpha/beta expression on immature/nonmature thymocyte cell surfaces is yet to be determined.

MeSH Terms
Animals Antigens, Surface/genetics Gene Expression Regulation Genes, Immunoglobulin Haplotypes Histocompatibility Antigens Class II/genetics Immunoglobulin Variable Region/genetics Lymphoid Tissue/immunology Major Histocompatibility Complex Membrane Glycoproteins Mice Mice, Inbred AKR Mice, Inbred BALB C Mice, Inbred C57BL Mice, Inbred CBA Minor Lymphocyte Stimulatory Antigens Receptors, Antigen, T-Cell/immunology Ribonucleases T-Lymphocytes/immunology Thymus Gland/immunology Transcription, Genetic
Chemicals
Antigens, Surface Histocompatibility Antigens Class II Immunoglobulin Variable Region Membrane Glycoproteins Minor Lymphocyte Stimulatory Antigens Receptors, Antigen, T-Cell Ribonucleases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Okada C Y
Department of Pathology, Stanford University School of Medicine, California 94305.
Weissman I L
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1989-05-01
Pages
1703-19
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2189317
Subset
IM
Grants
NIAID NIH HHS · AI-09072 · United States
NIAID NIH HHS · AI-18162 · United States
NIGMS NIH HHS · GM-07365 · United States
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