Regulation of T cell receptor-alpha gene recombination by transcription.

Abstract:

:Despite the longstanding correlation between transcription and variable-(diversity)-joining (V(D)J) recombination, it is unknown whether transcription itself can direct recombinase targeting. Here we show that blockade of transcriptional elongation through the mouse T cell receptor-alpha (Tcra) locus suppressed V(alpha)-to-J(alpha) recombination and chromatin remodeling of J(alpha) segments. Transcriptional blockade also derepressed cryptic J(alpha) promoters. Our results demonstrate two key functions for transcription in Tcra locus regulation. Transcription increases the recombination of J(alpha) segments located within several kilobases of a promoter and prevents the activation of downstream promoters through transcriptional interference. These influences promote an ordered progression of Tcra locus recombination events and selection of a robust Tcra repertoire.

journal_name

Nat Immunol

journal_title

Nature immunology

authors

Abarrategui I,Krangel MS

doi

10.1038/ni1379

subject

Has Abstract

pub_date

2006-10-01 00:00:00

pages

1109-15

issue

10

eissn

1529-2908

issn

1529-2916

pii

ni1379

journal_volume

7

pub_type

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