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首页> 外文期刊>Royal Society Open Science >The histone H3K4 demethylase JARID1A directly interacts with haematopoietic transcription factor GATA1 in erythroid cells through its second PHD domain
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The histone H3K4 demethylase JARID1A directly interacts with haematopoietic transcription factor GATA1 in erythroid cells through its second PHD domain

机译:组蛋白H3K4去甲基酶JARID1A通过其第二族域通过其第二族域与红细胞细胞中的血包血转录因子GATA1直接相互作用

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Chromatin remodelling and transcription factors play important roles in lineage commitment and development through control of gene expression. Activation of selected lineage-specific genes and repression of alternative lineage-affiliated genes result in tightly regulated cell differentiation transcriptional programmes. However, the complex functional and physical interplay between transcription factors and chromatin-modifying enzymes remains elusive. Recent evidence has implicated histone demethylases in normal haematopoietic differentiation as well as in malignant haematopoiesis. Here, we report an interaction between H3K4 demethylase JARID1A and the haematopoietic-specific master transcription proteins SCL and GATA1 in red blood cells. Specifically, we observe a direct physical contact between GATA1 and the second PHD domain of JARID1A. This interaction has potential implications for normal and malignant haematopoiesis.
机译:染色质重塑和转录因子通过控制基因表达控制谱系承诺和发展的重要作用。选择谱系特异性基因的激活和替代谱系相关基因的抑制导致紧密调节的细胞分化转录程序。然而,转录因子和染色质修饰酶之间的复杂功能和物理相互作用仍然难以捉摸。最近的证据在正常的血包血分化以及恶性血液杂草中具有含有组蛋白脱甲基酶。在这里,我们在红细胞中报告了H3K4脱甲基酶JARID1A和血杂化特异性母血管转录蛋白SCL和GATA1之间的相互作用。具体地,我们观察GATA1和JARID1A的第二博物馆之间的直接物理接触。这种相互作用对正常和恶性血液缺血具有潜在的影响。

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