Accessibility of nucleosomal DNA to V(D)J cleavage is modulated by RSS positioning and HMG1.

Abstract:

:B and T cell receptor gene assembly by V(D)J recombination is tightly regulated during lymphoid development. The mechanisms involved in this regulation are poorly understood. Here we show that nucleosomal DNA is refractory to V(D)J cleavage. However, the presence of HMG1, a chromatin-associated nonhistone DNA-binding protein, stimulates V(D)J cleavage of nucleosomal templates. This HMG1 stimulation is differentially affected by the rotational or translational positioning of the recombination signal sequence on the histone octamer, with cleavage of the 12 bp spacer RSS showing sensitivity to rotational position and the 23 bp spacer RSS affected by its displacement from the dyad. These results suggest that V(D)J recombination can be modulated by controlling substrate accessibility and cleavage at the level of an individual nucleosome.

journal_name

Mol Cell

journal_title

Molecular cell

authors

Kwon J,Imbalzano AN,Matthews A,Oettinger MA

doi

10.1016/s1097-2765(00)80297-x

subject

Has Abstract

pub_date

1998-12-01 00:00:00

pages

829-39

issue

6

eissn

1097-2765

issn

1097-4164

pii

S1097-2765(00)80297-X

journal_volume

2

pub_type

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