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The SWI/SNF-like BAF Complex Is Essential for Early B Cell Development
Author(s) -
Jinwook Choi,
Myunggon Ko,
Shin Teo Jeon,
Yoon Jeon,
Kyungsoo Park,
Changjin Lee,
Ho Lee,
Rho Hyun Seong
Publication year - 2012
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1103390
Subject(s) - transcription factor , biology , microbiology and biotechnology , lineage (genetic) , smarca4 , b cell , chromatin , gene , swi/snf , protein subunit , lymphopoiesis , transcription (linguistics) , haematopoiesis , genetics , chromatin remodeling , stem cell , antibody , linguistics , philosophy
During the process of B cell development, transcription factors, such as E2A and Ebf1, have been known to play key roles. Although transcription factors and chromatin regulators work in concert to direct the expression of B lineage-specific genes, little is known about the involvement of regulators for chromatin structure during B lymphopoiesis. In this article, we show that deletion of Srg3/mBaf155, a scaffold subunit of the SWI/SNF-like BAF complex, in the hematopoietic lineage caused defects at both the common lymphoid progenitor stage and the transition from pre-pro-B to early pro-B cells due to failures in the expression of B lineage-specific genes, such as Ebf1 and Il7ra, and their downstream target genes. Moreover, mice that were deficient in the expression of Brg1, a subunit of the complex with ATPase activity, also showed defects in early B cell development. We also found that the expression of Ebf1 and Il7ra is directly regulated by the SWI/SNF-like BAF complex. Thus, our results suggest that the SWI/SNF-like BAF complex facilitates early B cell development by regulating the expression of B lineage-specific genes.

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