共 28 条
Visualization of looping involving the immunoglobulin heavy-chain locus in developing B cells
被引:148
作者:

Sayegh, C
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机构: Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA

Jhunjhunwala, S
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机构: Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA

Riblet, R
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机构: Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA

Murre, C
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机构:
Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
机构:
[1] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[2] Torrey Pines Inst Mol Studies, San Diego, CA 92121 USA
关键词:
D O I:
10.1101/gad.1254305
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The immunoglobulin heavy-chain (IgH) locus undergoes large-scale contraction in B cells poised to undergo IgH V(D)J recombination. We considered the possibility that looping of distinct IgH V regions plays a role in promoting long-range interactions. Here, we simultaneously visualize three subregions of the IgH locus, using three-dimensional fluorescence in situ hybridization. Looping within the IgH locus was observed in both B- and T-lineage cells. However, monoallelic looping of IgH V regions into close proximity of the IgH DJ cluster was detected in developing B cells with significantly higher frequency when compared with hematopoietic progenitor or CD8(+) T-lineage cells. Looping of a subset of IgH V regions, albeit at lower frequency, was also observed in RAG-deficient pro-B cells. Based on these observations, we propose that Ig loci are repositioned by a looping mechanism prior to IgH V(D)J rearrangement to facilitate the joining of Ig variable, diversity, and joining segments.
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页码:322 / 327
页数:6
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