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Nuclear-localized Asunder regulates cytoplasmic dynein localization via its role in the Integrator complex

机译:核定位的Asunder通过其在整合子复合体中的作用调节细胞质动力蛋白的定位

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We previously reported that Asunder (ASUN) is essential for recruitment of dynein motors to the nuclear envelope (NE) and nucleus–centrosome coupling at the onset of cell division in cultured human cells and Drosophila spermatocytes, although the mechanisms underlying this regulation remain unknown. We also identified ASUN as a functional component of Integrator (INT), a multisubunit complex required for 3′-end processing of small nuclear RNAs. We now provide evidence that ASUN acts in the nucleus in concert with other INT components to mediate recruitment of dynein to the NE. Knockdown of other individual INT subunits in HeLa cells recapitulates the loss of perinuclear dynein in ASUN–small interfering RNA cells. Forced localization of ASUN to the cytoplasm via mutation of its nuclear localization sequence blocks its capacity to restore perinuclear dynein in both cultured human cells lacking ASUN and Drosophila asun spermatocytes. In addition, the levels of several INT subunits are reduced at G2/M when dynein is recruited to the NE, suggesting that INT does not directly mediate this step. Taken together, our data support a model in which a nuclear INT complex promotes recruitment of cytoplasmic dynein to the NE, possibly via a mechanism involving RNA processing.
机译:我们先前曾报道,在培养的人类细胞和果蝇精子细胞分裂开始时,Asunder(ASUN)对于将动力蛋白招募至核被膜(NE)和核-中心体偶联至关重要,尽管该调控的基本机制尚不清楚。我们还确定了ASUN是整合子(INT)的功能组件,这是小核RNA 3'末端加工所需的多亚基复合物。现在,我们提供证据表明ASUN与其他INT成分协同作用在细胞核中,以介导将动力蛋白招募至NE。剔除HeLa细胞中其他单个INT亚基,可以概括ASUN小干扰RNA细胞中核周动力蛋白的损失。通过其核定位序列的突变而将ASUN强制定位到细胞质会阻碍其在缺乏ASUN和果蝇Asun精母细胞的培养人细胞中恢复核周动力蛋白的能力。此外,当动力蛋白被募集到NE时,G2 / M时几个INT亚基的水平降低,这表明INT不直接介导这一步骤。综上所述,我们的数据支持一种模型,其中核INT复合物可能通过涉及RNA加工的机制促进细胞质动力蛋白向NE的募集。

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