赖氨酸去甲基酶4A是中心体完整性和基因组稳定性所必需的中心体相关蛋白。

IF 4.2
Pratim Chowdhury, Xiaoli Wang, Richard I Han, Manga Motrapu, Ashley G Boice, Yuya Nakatani, Sofia Vargas-Hernandez, Julia F Love, Claude Chew, Sandra L Grimm, Dereck Mezquita, Frank M Mason, Elisabeth D Martinez, Cristian Coarfa, Cheryl L Walker, Anna-Karin Gustavsson, Ruhee Dere
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引用次数: 0

摘要

中心体在细胞的成核和微管的组织中起着至关重要的作用,对染色体的忠实分离和基因组稳定性的维持至关重要。中心体结构或功能完整性的丧失导致基因组不稳定,是肿瘤发生的驱动因素。在这里,我们确定赖氨酸去甲基酶4A (KDM4A),一种染色质甲基标记的表观遗传“擦除剂”,作为中心体定位的蛋白质,在纳米级分辨率下可视化。我们还发现,KDM4A去甲基酶活性是维持中心体稳态和完整性所必需的;一种先前未知的与调节中心体数目的基因表达改变无关的功能。我们发现KDM4A在有丝分裂的所有阶段都与中心体相互作用并定位于中心体,在有丝分裂期间维持中心体数量和中心粒接合。KDM4A的缺失会导致多余的中心体和染色体分离错误的累积,包括染色质桥和微核,这些都是基因组不稳定的标志。总之,这些数据强调了一个以前未知的调控中心体完整性、有丝分裂保真度和中心体基因组稳定性的表观遗传“橡皮擦”的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lysine demethylase 4A is a centrosome-associated protein required for centrosome integrity and genomic stability.

Centrosomes play a fundamental role in nucleating and organizing microtubules in the cell and are vital for faithful chromosome segregation and maintenance of genomic stability. Loss of structural or functional integrity of centrosomes causes genomic instability and is a driver of oncogenesis. Here we identify lysine demethylase 4A (KDM4A), an epigenetic 'eraser' of chromatin methyl marks, as a centrosome-localized protein, visualized at the nanometer-scale resolution. We additionally uncovered that KDM4A demethylase enzymatic activity is required to maintain centrosome homeostasis and integrity; a previously unknown functionality unlinked to altered expression of genes regulating centrosome number. We find that KDM4A interacts with and localizes to the centrosome in all stages of mitosis, where it maintains centrosome numbers and centriole engagement during mitosis. Loss of KDM4A results in supernumerary centrosomes and accrual of chromosome segregation errors including chromatin bridges and micronuclei, markers of genomic instability. In summary, these data highlight a previously unknown role for an epigenetic 'eraser' regulating centrosome integrity, mitotic fidelity, and genomic stability at the centrosome.

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