The B-cell identity factor Pax5 regulates distinct transcriptional programmes in early and late B lymphopoiesis

被引:171
作者
Revilla-i-Domingo, Roger [1 ]
Bilic, Ivan [1 ]
Vilagos, Bojan [1 ]
Tagoh, Hiromi [1 ]
Ebert, Anja [1 ]
Tamir, Ido M. [1 ]
Smeenk, Leonie [1 ]
Trupke, Johanna [1 ]
Sommer, Andreas [1 ]
Jaritz, Markus [1 ]
Busslinger, Meinrad [1 ]
机构
[1] Vienna Bioctr, Res Inst Mol Pathol, Dept Immunol, A-1030 Vienna, Austria
关键词
B-cell identity; cis-regulatory landscape; genome-wide Pax5 binding; Pax5-dependent target genes; pro-B and mature B cells; ACUTE LYMPHOBLASTIC-LEUKEMIA; GENOME-WIDE ANALYSIS; HISTONE MODIFICATIONS; GENE-EXPRESSION; PAIRED DOMAIN; TARGET GENES; CHIP-SEQ; IN-VIVO; SEQUENCE RECOGNITION; IMMUNE FUNCTION;
D O I
10.1038/emboj.2012.155
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pax5 controls the identity and development of B cells by repressing lineage-inappropriate genes and activating B-cell-specific genes. Here, we used genome-wide approaches to identify Pax5 target genes in pro-B and mature B cells. In these cell types, Pax5 bound to 40% of the cis-regulatory elements defined by mapping DNase I hypersensitive (DHS) sites, transcription start sites and histone modifications. Although Pax5 bound to 8000 target genes, it regulated only 4% of them in pro-B and mature B cells by inducing enhancers at activated genes and eliminating DHS sites at repressed genes. Pax5-regulated genes in pro-B cells account for 23% of all expression changes occurring between common lymphoid progenitors and committed pro-B cells, which identifies Pax5 as an important regulator of this developmental transition. Regulated Pax5 target genes minimally overlap in pro-B and mature B cells, which reflects massive expression changes between these cell types. Hence, Pax5 controls B-cell identity and function by regulating distinct target genes in early and late B lymphopoiesis. The EMBO Journal (2012) 31, 3130-3146. doi:10.1038/emboj.2012.155; Published online 5 June 2012
引用
收藏
页码:3130 / 3146
页数:17
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