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本文引用的文献

1
SCL and associated proteins distinguish active from repressive GATA transcription factor complexes.SCL及相关蛋白可区分活性与抑制性GATA转录因子复合物。
Blood. 2009 Mar 5;113(10):2191-201. doi: 10.1182/blood-2008-07-169417. Epub 2008 Nov 14.
2
The role of the chromatin remodeler Mi-2beta in hematopoietic stem cell self-renewal and multilineage differentiation.染色质重塑因子Mi-2β在造血干细胞自我更新和多谱系分化中的作用。
Genes Dev. 2008 May 1;22(9):1174-89. doi: 10.1101/gad.1642808.
3
A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA-1 binding motif is associated with elevated hemoglobin F.位于HBG2上游核苷酸-567处GATA-1结合基序中的T到G颠换与血红蛋白F升高有关。
Mol Cell Biol. 2008 Jul;28(13):4386-93. doi: 10.1128/MCB.00071-08. Epub 2008 Apr 28.
4
Silencing of Agamma-globin gene expression during adult definitive erythropoiesis mediated by GATA-1-FOG-1-Mi2 complex binding at the -566 GATA site.在成人终末红细胞生成过程中,γ-珠蛋白基因表达的沉默由GATA-1-FOG-1-Mi2复合物结合于-566 GATA位点介导。
Mol Cell Biol. 2008 May;28(10):3101-13. doi: 10.1128/MCB.01858-07. Epub 2008 Mar 17.
5
Antagonism of FOG-1 and GATA factors in fate choice for the mast cell lineage.FOG-1与GATA因子在肥大细胞谱系命运选择中的拮抗作用。
J Exp Med. 2008 Mar 17;205(3):611-24. doi: 10.1084/jem.20070544. Epub 2008 Feb 25.
6
Exchange of GATA factors mediates transitions in looped chromatin organization at a developmentally regulated gene locus.GATA因子的交换介导了发育调控基因位点处环状染色质组织的转变。
Mol Cell. 2008 Feb 1;29(2):232-42. doi: 10.1016/j.molcel.2007.11.020.
7
Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex.非典型Mowat-Wilson患者证实了ZFHX1B/SIP1与NuRD共抑制复合物之间新关联的重要性。
Hum Mol Genet. 2008 Apr 15;17(8):1175-83. doi: 10.1093/hmg/ddn007. Epub 2008 Jan 8.
8
A shifting paradigm: histone deacetylases and transcriptional activation.一种转变的范式:组蛋白去乙酰化酶与转录激活
Bioessays. 2008 Jan;30(1):15-24. doi: 10.1002/bies.20687.
9
The zinc finger and C-terminal domains of MTA proteins are required for FOG-2-mediated transcriptional repression via the NuRD complex.MTA蛋白的锌指结构域和C末端结构域是FOG-2通过NuRD复合物介导转录抑制所必需的。
J Mol Cell Cardiol. 2008 Feb;44(2):352-60. doi: 10.1016/j.yjmcc.2007.10.023. Epub 2007 Nov 12.
10
Antagonistic interactions between Ikaros and the chromatin remodeler Mi-2beta determine silencer activity and Cd4 gene expression.Ikaro与染色质重塑因子Mi-2β之间的拮抗相互作用决定沉默子活性和Cd4基因表达。
Immunity. 2007 Nov;27(5):723-34. doi: 10.1016/j.immuni.2007.09.008. Epub 2007 Nov 1.

NuRD 介导 GATA-1 和 FOG-1 在血液发育过程中的激活和抑制功能。

NuRD mediates activating and repressive functions of GATA-1 and FOG-1 during blood development.

机构信息

Division of Hematology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

出版信息

EMBO J. 2010 Jan 20;29(2):442-56. doi: 10.1038/emboj.2009.336. Epub 2009 Nov 19.

DOI:10.1038/emboj.2009.336
PMID:19927129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2824460/
Abstract

GATA transcription factors interact with FOG proteins to regulate tissue development by activating and repressing transcription. FOG-1 (ZFPM1), a co-factor for the haematopoietic factor GATA-1, binds to the NuRD co-repressor complex through a conserved N-terminal motif. Surprisingly, we detected NuRD components at both repressed and active GATA-1/FOG-1 target genes in vivo. In addition, while NuRD is required for transcriptional repression in certain contexts, we show a direct requirement of NuRD also for FOG-1-dependent transcriptional activation. Mice in which the FOG-1/NuRD interaction is disrupted display defects similar to germline mutations in the Gata1 and Fog1 genes, including anaemia and macrothrombocytopaenia. Gene expression analysis in primary mutant erythroid cells and megakaryocytes (MKs) revealed an essential function for NuRD during both the repression and activation of select GATA-1/FOG-1 target genes. These results show that NuRD is a critical co-factor for FOG-1 and underscore the versatile use of NuRD by lineage-specific transcription factors to activate and repress gene transcription in the appropriate cellular and genetic context.

摘要

GATA 转录因子与 FOG 蛋白相互作用,通过激活和抑制转录来调节组织发育。FOG-1(ZFPM1)是造血因子 GATA-1 的辅助因子,通过保守的 N 端基序与 NuRD 共抑制复合物结合。令人惊讶的是,我们在体内检测到了被抑制和活跃的 GATA-1/FOG-1 靶基因都存在 NuRD 成分。此外,虽然在某些情况下 NuRD 是转录抑制所必需的,但我们还表明 NuRD 也直接需要 FOG-1 依赖性转录激活。FOG-1/NuRD 相互作用被破坏的小鼠表现出与 Gata1 和 Fog1 基因种系突变相似的缺陷,包括贫血和巨血小板减少症。在原发性突变红细胞和巨核细胞(MK)中的基因表达分析显示,NuRD 在选择的 GATA-1/FOG-1 靶基因的抑制和激活过程中都具有重要功能。这些结果表明 NuRD 是 FOG-1 的关键共因子,并强调了 NuRD 被谱系特异性转录因子在适当的细胞和遗传背景下激活和抑制基因转录的多功能性。