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Emerging Roles of PRDM Factors in Stem Cells and Neuronal System: Cofactor Dependent Regulation of PRDM3/16 and FOG1/2 (Novel PRDM Factors).PRDM 因子在干细胞和神经元系统中的新兴作用:共因子依赖性调节 PRDM3/16 和 FOG1/2(新型 PRDM 因子)。
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本文引用的文献

1
Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome.NBEAL2 基因突变导致灰色血小板综合征。
Nat Genet. 2011 Jul 17;43(8):738-40. doi: 10.1038/ng.884.
2
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules.NBEAL2 突变与灰色血小板综合征有关,是血小板α 颗粒生物发生所必需的。
Nat Genet. 2011 Jul 17;43(8):732-4. doi: 10.1038/ng.883.
3
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome.外显子组测序鉴定 NBEAL2 为灰色血小板综合征的致病基因。
Nat Genet. 2011 Jul 17;43(8):735-7. doi: 10.1038/ng.885.
4
Platelet protein kinase C-theta deficiency with human RUNX1 mutation: PRKCQ is a transcriptional target of RUNX1.血小板蛋白激酶 C-θ缺陷伴人类 RUNX1 突变:PRKCQ 是 RUNX1 的转录靶标。
Arterioscler Thromb Vasc Biol. 2011 Apr;31(4):921-7. doi: 10.1161/ATVBAHA.110.221879. Epub 2011 Jan 20.
5
Mechanism of platelet factor 4 (PF4) deficiency with RUNX1 haplodeficiency: RUNX1 is a transcriptional regulator of PF4.血小板因子 4(PF4)缺陷伴 RUNX1 杂合缺失的机制:RUNX1 是 PF4 的转录调节剂。
J Thromb Haemost. 2011 Feb;9(2):383-91. doi: 10.1111/j.1538-7836.2010.04154.x.
6
Filling a void in Gray Platelets.填补灰色血小板中的空白。
Blood. 2010 Dec 2;116(23):4738-40. doi: 10.1182/blood-2010-09-304378.
7
Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency.RUNX1 对血小板肌球蛋白轻链 (MYL9)的调控:对 RUNX1 杂合缺失所致血小板减少症和血小板功能障碍的影响。
Blood. 2010 Dec 23;116(26):6037-45. doi: 10.1182/blood-2010-06-289850. Epub 2010 Sep 27.
8
The platelet interior revisited: electron tomography reveals tubular alpha-granule subtypes.血小板内部再探:电子断层成像揭示管状α-颗粒亚型。
Blood. 2010 Aug 19;116(7):1147-56. doi: 10.1182/blood-2010-02-268680. Epub 2010 May 3.
9
Munc13-4 is a limiting factor in the pathway required for platelet granule release and hemostasis.Munc13-4 是血小板颗粒释放和止血所需途径中的一个限制因素。
Blood. 2010 Aug 12;116(6):869-77. doi: 10.1182/blood-2010-02-270934. Epub 2010 Apr 30.
10
NuRD mediates activating and repressive functions of GATA-1 and FOG-1 during blood development.NuRD 介导 GATA-1 和 FOG-1 在血液发育过程中的激活和抑制功能。
EMBO J. 2010 Jan 20;29(2):442-56. doi: 10.1038/emboj.2009.336. Epub 2009 Nov 19.

FOG1-NuRD 相互作用中断的小鼠中存在多效性血小板缺陷。

Pleiotropic platelet defects in mice with disrupted FOG1-NuRD interaction.

机构信息

Division of Hematology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

出版信息

Blood. 2011 Dec 1;118(23):6183-91. doi: 10.1182/blood-2011-06-363580. Epub 2011 Oct 11.

DOI:10.1182/blood-2011-06-363580
PMID:21989988
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3234671/
Abstract

Understanding platelet biology has been aided by studies of mice with mutations in key megakaryocytic transcription factors. We have shown that point mutations in the GATA1 cofactor FOG1 that disrupt binding to the nucleosome remodeling and deacetylase (NuRD) complex have erythroid and megakaryocyte lineages defects. Mice that are homozygous for a FOG1 point mutation (ki/ki), which ablates FOG1-NuRD interactions, have platelets that display a gray platelet syndrome (GPS)-like macrothrombocytopenia. These platelets have few α-granules and an increased number of lysosomal-like vacuoles on electron microscopy, reminiscent of the platelet in patients with GATA1-related X-linked GPS. Here we further characterized the platelet defect in ki/ki mice. We found markedly deficient levels of P-selectin protein limited to megakaryocytes and platelets. Other α-granule proteins were expressed at normal levels and were appropriately localized to α-granule-like structures. Treatment of ki/ki platelets with thrombin failed to stimulate Akt phosphorylation, resulting in poor granule secretion and platelet aggregation. These studies show that disruption of the GATA1/FOG1/NuRD transcriptional system results in a complex, pleiotropic platelet defect beyond GPS-like macrothrombocytopenia and suggest that this transcriptional complex regulates not only megakaryopoiesis but also α-granule generation and signaling pathways required for granule secretion.

摘要

研究表明,关键巨核细胞转录因子发生突变的小鼠有助于理解血小板生物学。我们已经表明,与核小体重塑和去乙酰化酶(NuRD)复合物结合的 GATA1 辅助因子 FOG1 的点突变会导致红系和巨核细胞谱系缺陷。FOG1 点突变(ki/ki)纯合子的小鼠(完全敲除 FOG1-NuRD 相互作用)的血小板表现出类似灰色血小板综合征(GPS)的巨血小板减少症。这些血小板α-颗粒较少,电子显微镜下溶酶体样空泡数量增加,与 GATA1 相关的 X 连锁 GPS 患者的血小板相似。在这里,我们进一步表征了 ki/ki 小鼠的血小板缺陷。我们发现 P-选择素蛋白的水平明显缺乏,仅限于巨核细胞和血小板。其他α-颗粒蛋白的表达水平正常,并适当定位于α-颗粒样结构。用凝血酶处理 ki/ki 血小板不能刺激 Akt 磷酸化,导致颗粒分泌和血小板聚集不良。这些研究表明,GATA1/FOG1/NuRD 转录系统的破坏导致复杂的、多效性的血小板缺陷,不仅仅是 GPS 样的巨血小板减少症,并表明该转录复合物不仅调节巨核细胞生成,还调节α-颗粒生成和颗粒分泌所需的信号通路。