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泽布勒林和司立太显著改善了牦牛成纤维细胞的表观遗传重编程及克隆效率。

Zebularine and scriptaid significantly improve epigenetic reprogramming of yak fibroblasts and cloning efficiency.

作者信息

Xiong Xianrong, Lan Daoliang, Li Jian, Zhong Jincheng, Zi Xiangdong, Ma Li, Wang Yong

机构信息

College of Life Science and Technology, Southwest University for Nationalities, Chengdu, Sichuan 610041, China.

出版信息

Cell Reprogram. 2013 Aug;15(4):293-300. doi: 10.1089/cell.2012.0092. Epub 2013 Jun 22.

Abstract

Abnormal epigenetic reprogramming of the donor nucleus after somatic cell nuclear transfer (SCNT) is thought to be the main cause of low cloning efficiency. Following SCNT, the donor nucleus often fails to express early embryonic genes and establish a normal embryonic pattern of chromatin modification. Therefore, in this study, we have attempted to improve epigenetic reprogramming of the donor nucleus and cloned embryos with Zebularine and Scriptaid. Yak fibroblasts were treated with 20 μM Zebularine alone or 20 μM Zebularine plus 0.5 μM Scriptaid for 24 h, whereas yak cloned embryos were treated exclusively with 0.5 μM Scriptaid for 12 h. There was no effect on cellular viability and proliferation after drug treatment. The treatment of fibroblasts with Zebularine or Zebularine plus Scriptaid increased histone acetylation of histone 3 lysine 9 (H3K9), but decreased the level of DNA methylation of Oct-4 and Sox-2 promoter regions. When donor cells were used after Zebularine plus Scriptaid treatment to reconstruct cloned embryos and then treated with Scriptaid, the developmental competence and cryosurvival of embryos were improved significantly. In addition, the relative expression of Oct-4 and Sox-2 were increased significantly. The expression levels of Dnmt-1 and Hdac-1 were significantly decreased when fibroblasts and cloned embryos were treated with Zebularine or Scriptaid. This work provides functional evidence that treatment with Zebularine and Scriptaid modifies the epigenetic status of yak fibroblasts, subsequently enhancing in vitro developmental potential and the quality of yak cloned embryos.

摘要

体细胞克隆(SCNT)后供体细胞核异常的表观遗传重编程被认为是克隆效率低下的主要原因。SCNT后,供体细胞核常常无法表达早期胚胎基因并建立正常的染色质修饰胚胎模式。因此,在本研究中,我们尝试用泽布替尼和司立他汀改善供体细胞核和克隆胚胎的表观遗传重编程。牦牛成纤维细胞单独用20μM泽布替尼或20μM泽布替尼加0.5μM司立他汀处理24小时,而牦牛克隆胚胎仅用0.5μM司立他汀处理12小时。药物处理后对细胞活力和增殖没有影响。用泽布替尼或泽布替尼加司立他汀处理成纤维细胞增加了组蛋白3赖氨酸9(H3K9)的组蛋白乙酰化,但降低了Oct-4和Sox-2启动子区域的DNA甲基化水平。当用泽布替尼加司立他汀处理后的供体细胞用于重建克隆胚胎,然后用司立他汀处理时,胚胎的发育能力和冷冻存活率显著提高。此外,Oct-4和Sox-2的相对表达显著增加。当成纤维细胞和克隆胚胎用泽布替尼或司立他汀处理时,Dnmt-1和Hdac-1的表达水平显著降低。这项工作提供了功能证据,表明用泽布替尼和司立他汀处理可改变牦牛成纤维细胞的表观遗传状态,随后增强牦牛克隆胚胎的体外发育潜力和质量。

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