From Loops to Looks: Transcription Factors and Chromatin Organization Shaping Terminal B Cell Differentiation

被引:19
作者
Azagra, Alba [1 ]
Marina-Zarate, Ester [2 ]
Ramiro, Almudena R. [2 ]
Javierre, Biola M. [3 ]
Parra, Maribel [1 ]
机构
[1] Josep Carreras Leukaemia Res Inst IJC, Lymphocyte Dev & Dis Grp, Campus ICO Germans Trias & Pujol, Badalona, Spain
[2] Ctr Nacl Invest Cardiovasc, Cell Biol Lab B, Madrid 28029, Spain
[3] Josep Carreras Leukaemia Res Inst IJC, Chromatin Org Grp 3D, Campus ICO Germans Trias & Pujol, Badalona, Spain
关键词
GERMINAL CENTER B; PLASMA-CELLS; IMMUNOGLOBULIN GENES; TOPOLOGICAL DOMAINS; HIGH-RESOLUTION; FACTORS IRF8; 3D GENOME; MEMORY; CTCF; ARCHITECTURE;
D O I
10.1016/j.it.2019.11.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B lymphopoiesis is tightly regulated at the level of gene transcription. In recent years, investigators have shed light on the transcription factor networks and the epigenetic machinery involved at all differentiation steps of mammalian B cell development. During terminal differentiation, B cells undergo dramatic changes in gene transcriptional programs to generate germinal center E cells, plasma cells and memory B cells. Recent evidence indicates that mature B cell formation in volves an essential contribution from 3D chromatin conformations through its interplay with transcription factors and epigenetic machinery. Here, we provide an up-to-date overview of the coordination between transcription factors, epigenetic changes, and chromatin architecture during terminal B cell differentiation, focusing on recent discoveries and technical advances for studying 3D chromatin structures.
引用
收藏
页码:46 / 60
页数:15
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