Abstract:
:Antigen receptor gene assembly is regulated by transcriptional promoters and enhancers, which control the accessibility of gene segments to a lymphocyte-specific V(D)J recombinase. However, it remained unclear whether accessibility depends on the process of transcription itself or chromatin modifications that accompany transcription. By using T cell receptor beta substrates that integrate stably into nuclear chromatin, we show that promoter location, rather than germ-line transcription or histone acetylation, is a primary determinant of recombination efficiency. These spatial constraints on promoter positioning may reflect an RNA polymerase-independent mechanism to target adjacent gene segments for chromatin remodeling events that facilitate rearrangement.
journal_name
Proc Natl Acad Sci U S Aauthors
Sikes ML,Meade A,Tripathi R,Krangel MS,Oltz EMdoi
10.1073/pnas.182166699keywords:
subject
Has Abstractpub_date
2002-09-17 00:00:00pages
12309-14issue
19eissn
0027-8424issn
1091-6490pii
182166699journal_volume
99pub_type
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