首页> 美国卫生研究院文献>Molecular and Cellular Biology >Steroidogenic Factor 1 (NR5A1) Maintains Centrosome Homeostasis in Steroidogenic Cells by Restricting Centrosomal DNA-Dependent Protein Kinase Activation
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Steroidogenic Factor 1 (NR5A1) Maintains Centrosome Homeostasis in Steroidogenic Cells by Restricting Centrosomal DNA-Dependent Protein Kinase Activation

机译:类固醇形成因子1(NR5A1)通过限制中心体DNA依赖性蛋白激酶激活来维持类固醇细胞中心体稳态。

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摘要

Steroidogenic factor 1 (SF-1 or NR5A1) is a nuclear receptor that controls adrenogenital cell growth and differentiation. Adrenogenital primordial cells from SF-1 knockout mice die of apoptosis, but the mechanism by which SF-1 regulates cell survival is not entirely clear. Besides functioning in the nucleus, SF-1 also resides in the centrosome and controls centrosome homeostasis. Here, we show that SF-1 restricts centrosome overduplication by inhibiting aberrant activation of DNA-dependent protein kinase (DNA-PK) in the centrosome. SF-1 was found to be associated with Ku70/Ku80 only in the centrosome, sequestering them from the catalytic subunit of DNA-PK (DNA-PKcs). In the absence of SF-1, DNA-PKcs was recruited to the centrosome and activated, causing aberrant activation of centrosomal Akt and cyclin-dependent kinase 2 (CDK2)/cyclin A and leading to centrosome overduplication. Centrosome overduplication caused by SF-1 depletion was averted by the elimination of DNA-PKcs, Ku70/80, or cyclin A or by the inhibition of CDK2 or Akt. In the nucleus, SF-1 did not interact with Ku70/80, and SF-1 depletion did not activate a nuclear DNA damage response. Centriole biogenesis was also unaffected. Thus, centrosomal DNA-PK signaling triggers centrosome overduplication, and this centrosomal event, but not the nuclear DNA damage response, is controlled by SF-1.
机译:类固醇形成因子1(SF-1或NR5A1)是控制肾上腺生殖细胞生长和分化的核受体。来自SF-1基因敲除小鼠的肾上腺生殖原细胞死亡是凋亡,但SF-1调节细胞存活的机制尚不完全清楚。除了在细胞核中起作用外,SF-1还驻留在中心体中并控制中心体稳态。在这里,我们显示SF-1通过抑制中心体中DNA依赖性蛋白激酶(DNA-PK)的异常激活来限制中心体的重复复制。发现SF-1仅在中心体中与Ku70 / Ku80相关,将它们与DNA-PK的催化亚基(DNA-PKcs)隔离。在没有SF-1的情况下,DNA-PKcs被募集到中心体并被激活,从而导致中心体Akt和细胞周期蛋白依赖性激酶2(CDK2)/细胞周期蛋白A异常激活,并导致中心体过度复制。通过消除DNA-PKcs,Ku70 / 80或细胞周期蛋白A或抑制CDK2或Akt,避免了由SF-1耗竭引起的中心体重复复制。在细胞核中,SF-1不与Ku70 / 80相互作用,并且SF-1耗竭不激活核DNA损伤反应。质心生物发生也不受影响。因此,中心体DNA-PK信号触发了中心体的重复复制,并且该中心体事件(但不是核DNA损伤反应)由SF-1控制。

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