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The nuclear import factor p10 regulates the functional size of the nuclear pore complex during oogenesis

机译:核输入因子p10调节卵子发生过程中核孔复合体的功能大小

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Previtellogenic, stage-1 Xenopus oocytes produce mainly 5S and tRNA, whereas vitellogenic oocytes, stages 2-6, synthesize predominantly 18S and 28S rRNA. Using nucleoplasmin-coated gold as a transport substrate, it was determined that the shift in synthesis from small to large RNAs during oogenesis is accompanied by an increase in both the rates of signal-mediated nuclear import and the functional size of nuclear pores. It was observed that, despite the reduction in transport capacity, gold still accumulated at the cytoplasmic surface of the pores in stage-1 oocytes. This suggested that transport in these cells is limited by translocation factors, rather than by cytoplasmic binding factors. Analysis of extracts prepared from stage-1 and vitellogenic oocytes revealed that the transport factor p10 is more abundant in stage-1 cells. Microinjection of purified p10 into stage-2 oocytes reduced the nuclear import of large gold particles to the level observed in stage-1 cells. It is concluded that p10 can modulate transport through the pores by regulating the functional size of the central transporter element. [References: 46]
机译:前玻璃体形成的第1阶段非洲爪蟾卵母细胞主要产生5S和tRNA,而卵母细胞的第2-6阶段卵母细胞主要合成18S和28S rRNA。使用涂有核纤溶酶的金作为转运底物,已确定在卵子发生过程中合成过程从小RNA转移到大RNA伴随着信号介导的核输入速率和核孔功能大小的增加。观察到,尽管转运能力降低,但金仍积累在1期卵母细胞的孔的细胞质表面。这表明这些细胞中的转运受到转运因子的限制,而不是受细胞质结合因子的限制。对从1期和卵黄母细胞制备的提取物的分析表明,转运因子p10在1期细胞中更为丰富。将纯化的p10显微注射到2期卵母细胞中,将大金颗粒的核输入降低到1期细胞中观察到的水平。结论是p10可通过调节中央转运蛋白元件的功能大小来调节通过孔的转运。 [参考:46]

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