How transcription factors program chromatin - Lessons from studies of the regulation of myeloid-specific genes

被引:21
作者
Bonifer, Constanze [1 ]
Hoogenkamp, Maarten [1 ]
Krysinska, Hanna [1 ]
Tagoh, Hirorni [1 ]
机构
[1] Univ Leeds, St James Univ Hosp, Leeds Inst Mol Med, Leeds LS9 7TF, W Yorkshire, England
基金
英国生物技术与生命科学研究理事会;
关键词
chromatin; myelopoiesis; transcription factors; chromatin remodelling and modification; Pu.1 and csf1r;
D O I
10.1016/j.smim.2008.05.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hematopoietic stem cells exhibit a multi-lineage gene expression program, and this expression program is either maintained when these cells self-renew, or re-programmed when they differentiate. Both processes require the regulated expression of sequence-specific transcription factors and their interaction with the epigenetic regulatory machinery which programs the chromatin of hematopoietic genes in a cell type specific fashion. This article describes recent findings on the complexity of these molecular interactions and their consequences with respect to the regulation of cell fate decisions. We also describe recent findings from studies of genes expressed in the myeloid lineage (Pu.1 and csf1r) which highlight some of the molecular principles governing cell fate decisions at the epigenetic level. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:257 / 263
页数:7
相关论文
共 98 条
[1]   ETO, a target of t(8;21) in acute leukemia, makes distinct contacts with multiple histone deacetylases and binds mSin3A through its oligomerization domain [J].
Amann, JM ;
Nip, J ;
Strom, DK ;
Lutterbach, B ;
Harada, H ;
Lenny, N ;
Downing, JR ;
Meyers, S ;
Hiebert, SW .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (19) :6470-6483
[2]   Constitutive expression of PU.1 in fetal hematopoietic progenitors blocks T cell development at the pro-T cell stage [J].
Anderson, MK ;
Weiss, AH ;
Hernandez-Hoyos, G ;
Dionne, CJ ;
Rothenberg, EV .
IMMUNITY, 2002, 16 (02) :285-296
[3]  
Anderson MK, 1999, DEVELOPMENT, V126, P3131
[4]   Reciprocal activation of GATA-1 and PU.1 marks initial specification of hematopoietic stem cells into myeloerythroid and myelolymphoid lineages [J].
Arinobu, Yojiro ;
Mizuno, Shin-ichi ;
Chong, Yong ;
Shigematsu, Hirokazu ;
Lino, Tadafumi ;
Iwasaki, Hiromi ;
Graf, Thomas ;
Mayfield, Robin ;
Chan, Susan ;
Kastner, Philippe ;
Akashi, Koichi .
CELL STEM CELL, 2007, 1 (04) :416-427
[5]   Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain [J].
Bannister, AJ ;
Zegerman, P ;
Partridge, JF ;
Miska, EA ;
Thomas, JO ;
Allshire, RC ;
Kouzarides, T .
NATURE, 2001, 410 (6824) :120-124
[6]   Essential requirement of CCAAT/enhancer binding proteins in embryogenesis [J].
Bégay, V ;
Smink, J ;
Leutz, A .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (22) :9744-9751
[7]   A modular enhancer is differentially regulated by GATA and NFAT elements that direct different tissue-specific patterns of nucleosome positioning and inducible chromatin remodeling [J].
Bert, Andrew G. ;
Johnson, Brett V. ;
Baxter, Euan W. ;
Cockerill, Peter N. .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (08) :2870-2885
[8]   CREB-binding protein and p300: molecular integrators of hematopoietic transcription [J].
Blobel, GA .
BLOOD, 2000, 95 (03) :745-755
[9]   Lineage-specific transcription factors in multipotent hematopoietic progenitors - A little bit goes a long way [J].
Bottardi, Stefania ;
Ghiam, Alireza Fotouhi ;
Bergeron, Francois ;
Milot, Eric .
CELL CYCLE, 2007, 6 (09) :1035-1039
[10]   General transcription factors bind promoters repressed by Polycomb group proteins [J].
Breiling, A ;
Turner, BM ;
Bianchi, ME ;
Orlando, V .
NATURE, 2001, 412 (6847) :651-655