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使用冻干精子通过卵胞浆内单精子注射(ICSI)对猪卵母细胞受精前后DNA修复基因的表达

Expression of DNA repair genes in porcine oocytes before and after fertilization by ICSI using freeze-dried sperm.

作者信息

Men Nguyen Thi, Kikuchi Kazuhiro, Furusawa Tadashi, Dang-Nguyen Thanh Quang, Nakai Michiko, Fukuda Atsunori, Noguchi Junko, Kaneko Hiroyuki, Viet Linh Nguyen, Xuan Nguyen Bui, Tajima Atsushi

机构信息

Division of Animal Sciences, National Institute of Agrobiological Sciences, Tsukuba, Japan.

Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Japan.

出版信息

Anim Sci J. 2016 Nov;87(11):1325-1333. doi: 10.1111/asj.12554. Epub 2016 Mar 14.

Abstract

Boar sperm freeze-dried with trehalose showed a protective effect against sperm DNA fragmentation. However, normal fertilization and embryonic development were not improved. Damaged sperm may activate maternal DNA repair genes when injected into oocytes. Therefore, we investigated the expression profile of some DNA repair genes in porcine oocytes after intra-cytoplasmic sperm injection. First, the expression levels of MGMT, UDG, XPC, MSH2, XRCC6 and RAD51 genes that are concerned with different types of DNA repair were examined in in vitro mature (IVM) oocytes injected with ejaculated sperm, or freeze-dried sperm with or without trehalose. Quantitative reverse transcription polymerase chain reaction revealed that expression of six DNA repair genes in the oocytes at 4 h after injection did not differ among the four groups. Next, we investigated the gene expression levels of these genes at different stages of maturation. The relative expression levels of UDG and XPC were significantly up-regulated in mature oocytes compared with earlier stages. Furthermore, there was an increased tendency in relative expression of MSH2 and RAD51. These results suggested two possible mechanisms that messenger RNA of DNA repair genes are either accumulated during IVM to be ready for fertilization or increased expression levels of DNA repair genes in oocytes caused by suboptimal IVM conditions.

摘要

用海藻糖冻干的公猪精子对精子DNA片段化具有保护作用。然而,正常受精和胚胎发育并未得到改善。受损精子在注入卵母细胞时可能会激活母体DNA修复基因。因此,我们研究了胞浆内精子注射后猪卵母细胞中一些DNA修复基因的表达谱。首先,在注射射精精子或添加或不添加海藻糖的冻干精子的体外成熟(IVM)卵母细胞中,检测了与不同类型DNA修复相关的MGMT、UDG、XPC、MSH2、XRCC6和RAD51基因的表达水平。定量逆转录聚合酶链反应显示,注射后4小时卵母细胞中六个DNA修复基因的表达在四组之间没有差异。接下来,我们研究了这些基因在不同成熟阶段的基因表达水平。与早期阶段相比,成熟卵母细胞中UDG和XPC的相对表达水平显著上调。此外,MSH2和RAD51的相对表达有增加的趋势。这些结果提示了两种可能的机制,即DNA修复基因的信使RNA在IVM过程中积累以准备受精,或者IVM条件欠佳导致卵母细胞中DNA修复基因的表达水平增加。

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