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首页> 外文期刊>Molecular human reproduction. >Sperm-borne small RNAs regulate α -tubulin acetylation and epigenetic modification of early bovine somatic cell nuclear transfer embryos
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Sperm-borne small RNAs regulate α -tubulin acetylation and epigenetic modification of early bovine somatic cell nuclear transfer embryos

机译:精子传播的小RNA调节α-丁蛋白乙酰化和早期牛体细胞核转移胚胎的表观遗传修饰

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摘要

Accumulated evidence indicates that sperm-borne small RNA plays a crucial role in embryonic development, especially the absence of the sperm-borne small RNA might be a major cause of the abnormal development of cloned embryos. In this study, we found that sperm-borne small RNA can affect abnormal pronuclear-like structures, postpone the timing of first embryo cleavage and enhance developmental competence of bovine somatic cell nuclear transfer (SCNT) embryos. In addition, the supplementation of sperm-borne small RNA can significantly increase live birth rates and decrease the birth weights of cloned offspring. To investigate the underlying mechanisms, the levels of a-tubulin K40 acetylation (Ac a-tubulin K40) and histone H3 lysine 9 trimethylation (H3K9me3) during early embryo development were investigated in SCNT embryos with sperm-borne small RNA supplementation (termed as T-NT), compared to those normal SCNT embryos and embryos obtained from standard IVF. The results showed that sperm-borne small RNA can significantly decrease the H3K9me3 levels at the pronuclear and two-cell stages, while significantly increase Ac a-tubulin K40 levels at anaphase and telophase of bovine SCNT embryos during the first cleavage. Collectively, our study for the first time demonstrates that sperm-borne small RNA plays a crucial role in the developmental competence of SCNT embryos by regulating H3K9me3 and Ac a-tubulin K40. Further studies will be required to determine how sperm small RNA regulate the H3K9me3 and Aca-tubulin K40. Our study suggests that the supplementation of sperm-borne small RNA is a potential application to improve the cloning efficiency.
机译:积累的证据表明,精子的小RNA在胚胎发育中发挥着至关重要的作用,特别是缺乏精子的小RNA可能是克隆胚胎异常发育的主要原因。在这项研究中,我们发现精子般的小RNA可以影响异常的核状结构,推迟第一胚胎切割的时序,增强牛体细胞核转移(SCNT)胚胎的发育能力。此外,补充精子的小RNA可以显着提高活速,降低克隆后代的出生权重。为了探讨潜在的机制,在SCNT胚胎中研究了在早期胚胎发育期间的α-微管蛋白K40乙酰化(AC A-TIMULIN K40)和组蛋白H3赖氨酸9的三甲基化(H3K9ME3)的水平,用精子传播的小RNA补充(称为T. -NT)与从标准IVF获得的正常SCNT胚胎和胚胎相比。结果表明,精子的小RNA可以显着降低经发核和双细胞阶段的H3K9ME3水平,而在第一次切割期间,在牛SCNT胚胎中的AC A-管蛋白K40水平显着增加。一致,我们第一次的研究表明,通过调节H3K9ME3和AC A-Timulin K40,精子的小RNA在SCNT胚胎的发育能力中起着至关重要的作用。进一步的研究将确定精子小RNA如何调节H3K9ME3和ACA-管蛋白K40。我们的研究表明,精子的小RNA的补充是提高克隆效率的潜在应用。

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