Epigenetic silencing of the c-fms locus during B-lymphopoiesis occurs in discrete steps and is reversible

被引:59
作者
Tagoh, H
Schebesta, A
Lefevre, P
Wilson, N
Hume, D
Busslinger, M
Bonifer, C [1 ]
机构
[1] Univ Leeds, St James Univ Hosp, Mol Med Unit, Leeds LS9 7TF, W Yorkshire, England
[2] Vienna Bioctr, Res Inst Mol Pathol, Vienna, Austria
[3] Univ Queensland, Inst Mol Biosci, St Lucia, Qld 4067, Australia
关键词
antisense RNA; c-fms locus; chromatin; gene silencing; Pax5;
D O I
10.1038/sj.emboj.7600421
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
The murine c-fms (Csf1r) gene encodes the macrophage colony-stimulating factor receptor, which is essential for macrophage development. It is expressed at a low level in haematopoietic stem cells and is switched off in all non-macrophage cell types. To examine the role of chromatin structure in this process we studied epigenetic silencing of c-fms during B-lymphopoiesis. c-fms chromatin in stem cells and multipotent progenitors is in the active conformation and bound by transcription factors. A similar result was obtained with specified common myeloid and lymphoid progenitor cells. In developing B cells, c-fms chromatin is silenced in distinct steps, whereby first the binding of transcription factors and RNA expression is lost, followed by a loss of nuclease accessibility. Interestingly, regions of de novo DNA methylation in B cells overlap with an intronic antisense transcription unit that is differently regulated during lymphopoiesis. However, even at mature B cell stages, c-fms chromatin is still in a poised conformation and c-fms expression can be re-activated by conditional deletion of the transcription factor Pax5.
引用
收藏
页码:4275 / 4285
页数:11
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