生物
增强子
遗传学
基因座(遗传学)
染色质
体细胞突变
基因
轨迹控制区
细胞生物学
转录因子
B细胞
抗体
作者
Eric Pinaud,Marie Marquet,Rémi Fiancette,Sophie Péron,Christelle Vincent‐Fabert,Yves Denizot,Michel Cogné
标识
DOI:10.1016/b978-0-12-387663-8.00002-8
摘要
Antigen receptor gene loci are among the most complex in mammals. The IgH locus, encoding the immunoglobulin heavy chain (IgH) in B-lineage cells, undergoes major transcription-dependent DNA remodeling events, namely V(D)J recombination, Ig class-switch recombination (CSR), and somatic hypermutation (SHM). Various cis-regulatory elements (encompassing promoters, enhancers, and chromatin insulators) recruit multiple nuclear factors in order to ensure IgH locus regulation by tightly orchestrated physical and/or functional interactions. Among major IgH cis-acting regions, the large 3′ regulatory region (3′RR) located at the 3′ boundary of the locus includes several enhancers and harbors an intriguing quasi-palindromic structure. In this review, we report progress insights made over the past decade in order to describe in more details the structure and functions of IgH 3′RRs in mouse and human. Generation of multiple cellular, transgenic and knock-out models helped out to decipher the function of the IgH 3′ regulatory elements in the context of normal and pathologic B cells. Beside its interest in physiology, the challenge of elucidating the locus-wide cross talk between distant cis-regulatory elements might provide useful insights into the mechanisms that mediate oncogene deregulation after chromosomal translocations onto the IgH locus.
科研通智能强力驱动
Strongly Powered by AbleSci AI