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鉴定和描述一种卵母细胞因子,该因子对于猪核移植胚胎的发育是必需的。

Identification and characterization of an oocyte factor required for development of porcine nuclear transfer embryos.

机构信息

Laboratory of Reproductive Biology, Graduate School of Agriculture, Kyoto University, Kitashirakawa, Kyoto 606-8502, Japan.

出版信息

Proc Natl Acad Sci U S A. 2011 Apr 26;108(17):7040-5. doi: 10.1073/pnas.1013634108. Epub 2011 Apr 11.

Abstract

Nuclear reprogramming of differentiated cells can be induced by oocyte factors. Despite numerous attempts, these factors and mechanisms responsible for successful reprogramming remain elusive. Here, we identify one such factor, necessary for the development of nuclear transfer embryos, using porcine oocyte extracts in which some reprogramming events are recapitulated. After incubating somatic nuclei in oocyte extracts from the metaphase II stage, the oocyte proteins that were specifically and abundantly incorporated into the nuclei were identified by mass spectrometry. Among 25 identified proteins, we especially focused on a multifunctional protein, DJ-1. DJ-1 is present at a high concentration in oocytes from the germinal vesicle stage until embryos at the four-cell stage. Inhibition of DJ-1 function compromises the development of nuclear transfer embryos but not that of fertilized embryos. Microarray analysis of nuclear transfer embryos in which DJ-1 function is inhibited shows perturbed expression of P53 pathway components. In addition, embryonic arrest of nuclear transfer embryos injected with anti-DJ-1 antibody is rescued by P53 inhibition. We conclude that DJ-1 is an oocyte factor that is required for development of nuclear transfer embryos. This study presents a means for identifying natural reprogramming factors in mammalian oocytes and a unique insight into the mechanisms underlying reprogramming by nuclear transfer.

摘要

分化细胞的核重编程可被卵母细胞因子诱导。尽管已经进行了多次尝试,但这些因子和负责成功重编程的机制仍然难以捉摸。在这里,我们使用卵母细胞提取物来识别这样的一个因子,该因子对于核移植胚胎的发育是必需的,在卵母细胞提取物中可以重现一些重编程事件。在将体细胞核在来自 MII 期的卵母细胞提取物中孵育后,通过质谱法鉴定出特异性和丰富地掺入核中的卵母细胞蛋白。在鉴定出的 25 种蛋白质中,我们特别关注一种多功能蛋白 DJ-1。DJ-1 在从生发泡期到四细胞期的卵母细胞中浓度很高。抑制 DJ-1 功能会损害核移植胚胎的发育,但不会损害受精卵的发育。用抗 DJ-1 抗体抑制 DJ-1 功能的核移植胚胎的微阵列分析显示 P53 途径成分的表达失调。此外,用抗 DJ-1 抗体注射的核移植胚胎的胚胎停滞通过 P53 抑制得到挽救。我们得出结论,DJ-1 是卵母细胞中一种对于核移植胚胎发育所必需的因子。本研究提供了一种鉴定哺乳动物卵母细胞中天然重编程因子的方法,并为核移植的重编程机制提供了独特的见解。

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