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首页> 外文期刊>Molecular reproduction and development >Altered expression of BRG1 and histone demethylases, and aberrant H3K4 methylation in less developmentally competent embryos at the time of embryonic genome activation
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Altered expression of BRG1 and histone demethylases, and aberrant H3K4 methylation in less developmentally competent embryos at the time of embryonic genome activation

机译:BRG1和组蛋白去甲基酶的改变表达,以及在胚胎基因组激活时在较少发育态胚胎中的异常H3K4甲基化

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摘要

Epigenetics is a fundamental regulator underlying many biological functions, such as development and cell differentiation. Epigenetic modifications affect key chromatin regulation, including transcription and DNA repair, which are critical for normal embryo development. In this study, we profiled the expression of epigenetic modifiers and patterns of epigenetic changes in porcine embryos around the period of embryonic genome activation (EGA). We observed that Brahma-related gene 1 (BRG1) and Lysine demethylase 1A (KDM1A), which can alter the methylation status of lysine 4 in histone 3 (H3K4), localize to the nucleus at Day 3-4 of development. We then compared the abundance of epigenetic modifiers between early- and late-cleaving embryos, which were classified based on the time to the first cell cleavage, to investigate if their nuclear localization contributes to developmental competence. The mRNA abundance of BRG1, KDM1A, as well as other lysine demethylases (KDM1B, KDM5A, KDM5B, and KDM5C), were significantly higher in late- compared to early-cleaving embryos near the EGA period, although these difference disappeared at the blastocyst stage. The abundance of H3K4 mono- (H3K4me) and di-methylation (H3K4me2) during the EGA period was reduced in late-cleaving and less developmentally competent embryos. By contrast, BRG1, KDM1A, and H3K4me2 abundance was greater in embryos with more than eight cells at Day 3-4 of development compared to those with fewer than four cells. These findings suggest that altered epigenetic modifications of H3K4 around the EGA period may affect the developmental capacity of porcine embryos to reach the blastocyst stage. Mol. Reprod. Dev. 84: 19-29, 2017. (c) 2016 Wiley Periodicals, Inc.
机译:表观遗传学是一种基本调节因素,潜在的许多生物学功能,如开发和细胞分化。表观遗传修饰影响关键染色质调控,包括转录和DNA修复,这对于正常胚胎发育至关重要。在这项研究中,我们在胚胎基因组活化期(EGA)周期内突出了猪胚胎的表观遗传改性剂和表观遗传变化的模式。我们观察到荆棘相关的基因1(BRG1)和赖氨酸脱甲基酶1A(KDM1A),其可以改变组蛋白3(H3K4)中赖氨酸4的甲基化状态,在发育的第3-4天定位于细胞核。然后,将早期和晚切割胚胎之间的表观遗传调节剂进行比较,这是基于第一种细胞切割的时间分类,以调查它们的核定情况是否有助于发育能力。 BRG1,KDM1A以及其他赖氨酸去甲基酶(KDM1B,KDM5A,KDM5B和KDM5C)的mRNA丰度与EGA时期附近的早期胚胎相比显着高,尽管这些差异在胚泡阶段消失。在EGA期间的H3K4单 - (H3K4ME)和二甲基化(H3K4ME2)的丰度降低了晚切割和较少发育致力的胚胎。相比之下,与具有少于四个细胞的胚胎,在3-4天的胚胎中,BRG1,KDM1A和H3K4ME2大量较大。这些发现表明,EGA周期周围H3K4的改变的表观遗传修饰可能影响猪胚胎到达胚泡阶段的发育能力。摩尔。装。开发。 84:19-29,2017。(c)2016 Wiley期刊,Inc。

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