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H3 trimethyl K9 and H3 acetyl K9 chromatin modifications are associated with class switch recombination

机译:H3三甲基K9和H3乙酰K9染色质修饰与分类开关重组相关

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摘要

Class switch recombination (CSR) involves a DNA rearrangement in the Ig heavy chain (IgH) gene that allows the same variable (V) region to be expressed with any one of the downstream constant region (C) genes to encode antibodies with many different effector functions. One hypothesis for how CSR is targeted to different C region genes is that histone modifications increase accessibility and/or recruit activation-induced cytosine deaminase (AID) and its associated processes to particular donor and recipient switch regions. In this work, we identified H3 acetyl K9 and H3 trimethyl K9 as histone modifications that correlate with the recombining pair of donor and recipient switch regions. The appearance of H3 trimethyl K9 is surprising because usually it is thought to mark silent genes and heterochromatin. Nevertheless, the time course of appearance of these histone modifications, the regions in IgH they associate with, and their appearance independent of AID damage suggest that both modifications play a role in targeting CSR.
机译:类转换重组(CSR)涉及Ig重链(IgH)基因中的DNA重排,该基因重排可以使同一可变(V)区与任何下游恒定区(C)基因一起表达,从而编码具有许多不同效应子的抗体功能。关于CSR如何靶向不同C区基因的一种假设是,组蛋白修饰可增加可及性和/或将激活诱导的胞嘧啶脱氨酶(AID)及其相关过程募集到特定的供体和受体转换区。在这项工作中,我们确定H3乙酰K9和H3三甲基K9为组蛋白修饰,与供体和受体开关区域的重组对相关。 H3三甲基K9的出现令人惊讶,因为通常认为它可以标记沉默基因和异染色质。然而,这些组蛋白修饰的出现时间,它们与之结合的IgH区域以及它们的出现与AID损伤无关,这表明这两种修饰均在靶向CSR中起作用。

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