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Triple A patient cells suffering from mitotic defects fail to localize PGRMC1 to mitotic kinetochore fibers

机译:患有有丝分裂缺陷的Triple A患者细胞无法将PGRMC1定位于有丝分裂的动粒纤维

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摘要

BackgroundMembrane-associated progesterone receptors are restricted to the endoplasmic reticulum and are shown to regulate the activity of cytochrome P450 enzymes which are involved in steroidogenesis or drug detoxification. PGRMC1 and PGRMC2 belong to the membrane-associated progesterone receptor family and are of interest due to their suspected role during cell cycle. PGRMC1 and PGRMC2 are thought to bind to each other; thereby suppressing entry into mitosis. We could previously report that PGRMC2 interacts with the nucleoporin ALADIN which when mutated results in the autosomal recessive disorder triple A syndrome. ALADIN is a novel regulator of mitotic controller Aurora kinase A and depletion of this nucleoporin leads to microtubule instability.
机译:背景膜相关的孕激素受体仅限于内质网,并显示出可调节参与类固醇生成或药物排毒的细胞色素P450酶的活性。 PGRMC1和PGRMC2属于膜相关的孕激素受体家族,由于其在细胞周期中的可能作用而受到关注。 PGRMC1和PGRMC2被认为是相互绑定的。从而抑制进入有丝分裂。我们以前可能报道过,PGRMC2与核孔蛋白ALADIN相互作用,当突变时会导致常染色体隐性遗传性疾病Triple A综合征。 ALADIN是有丝分裂控制器Aurora激酶A的新型调节剂,这种核孔蛋白的消耗会导致微管不稳定。

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