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GANP regulates recruitment of AID to immunoglobulin variable regions by modulating transcription and nucleosome occupancy

机译:GANP通过调节转录和核小体的占用来调节AID向免疫球蛋白可变区的募集

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Somatic hypermutation in B cells is initiated by activation-induced cytidine deaminase -catalyzed C→U deamination at immunoglobulin variable regions. Here we investigate the role of the germinal centre-associated nuclear protein ( GANP ) in enhancing the access of activation-induced cytidine deaminase ( AID ) to immunoglobulin variable regions. We show that the nuclear export factor GANP is involved in chromatin modification at rearranged immunoglobulin variable loci, and its activity requires a histone acetyltransferase domain. GANP interacts with the transcription stalling protein Spt5 and facilitates RNA Pol-II recruitment to immunoglobulin variable regions. Germinal centre B cells from ganp -transgenic mice showed a higher AID occupancy at the immunoglobulin variable region, whereas B cells from conditional ganp -knockout mice exhibit a lower AID accessibility. These findings suggest that GANP -mediated chromatin modification promotes transcription complex recruitment and positioning at immunoglobulin variable loci to favour AID targeting.
机译:B细胞中的体细胞超突变是由免疫球蛋白可变区的活化诱导的胞苷脱氨酶催化的C→U脱氨作用引发的。在这里,我们调查生发中心相关的核蛋白(GANP)在增强激活诱导的胞苷脱氨酶(AID)进入免疫球蛋白可变区的作用。我们显示核出口因子GANP参与染色质修饰在重新排列的免疫球蛋白可变基因座,其活动需要一个组蛋白乙酰转移酶域。 GANP与转录停滞蛋白Spt5相互作用,并促进RNA Pol-II募集到免疫球蛋白可变区。来自ganp转基因小鼠的生发中心B细胞在免疫球蛋白可变区显示较高的AID占有率,而来自有条件ganp基因敲除小鼠的B细胞显示出较低的AID可及性。这些发现表明,GANP介导的染色质修饰促进转录复合物的募集和在免疫球蛋白可变基因座的定位,从而有利于AID靶向。

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