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利用转基因拯救方法和 Cre-LoxP 系统对 PHGPx 基因敲除小鼠模型进行功能分析的新策略。

New Strategy of Functional Analysis of PHGPx Knockout Mice Model Using Transgenic Rescue Method and Cre-LoxP System.

机构信息

School of Pharmaceutical Sciences, Kitasato University, 5-9-1 Shirokane Minato-ku Tokyo 108-8641, Japan.

出版信息

J Clin Biochem Nutr. 2010 Jan;46(1):1-13. doi: 10.3164/jcbn.09-94R. Epub 2009 Dec 29.

DOI:10.3164/jcbn.09-94R
PMID:20104259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2803127/
Abstract

Phospholipid hydroperoxide glutathione peroxidase (PHGPx) is an intracellular antioxidant enzyme that directly reduces peroxidized phospholipids. PHGPx is transcribed from one gene into three types of mRNA, mitochondrial, non-mitochondrial and nucleolar PHGPx by alternative transcription. In this review, we focus on our recent experiments on the regulation of promoter activity of the types of PHGPx and on the novel strategy of functional analysis of a PHGPx knockout mice model using the transgenic rescue method and Cre-LoxP system. PHGPx is especially high in testis and spermatozoa. A deficiency is implicated in human infertility. We established spermatocyte-specific PHGPx knockout (KO) mice using a Cre-loxP system. Targeted disruption of all exons of the PHGPx gene in mice by homologous recombination caused embryonic lethality at 7.5 days post coitum. The PHGPx-loxP transgene rescued PHGPx KO mice from embryonic lethality. These rescued floxed PHGPx mice were mated with spermatocyte specific Cre expressing mice. All the spermatocyte-specific PHGPx KO male mice were infertile and displayed a significant decrease in the number of spermatozoa and significant reductions in forward motility by mitochondrial dysfunction of spermatozoa. These results demonstrate that depletion of PHGPx in spermatozoa may be one of the causes of male infertility in mice and humans.

摘要

磷脂氢过氧化物谷胱甘肽过氧化物酶(PHGPx)是一种细胞内抗氧化酶,可直接还原过氧化磷脂。PHGPx 通过选择性转录从一个基因转录为三种类型的 mRNA:线粒体、非线粒体和核仁 PHGPx。在这篇综述中,我们重点介绍了我们最近关于 PHGPx 各类型启动子活性调节的实验,以及使用转基因拯救方法和 Cre-LoxP 系统对 PHGPx 敲除小鼠模型进行功能分析的新策略。PHGPx 在睾丸和精子中含量特别高。缺乏 PHGPx 与人类不育有关。我们使用 Cre-loxP 系统建立了精母细胞特异性 PHGPx 敲除(KO)小鼠。通过同源重组靶向敲除 PHGPx 基因的所有外显子导致胚胎在受精后 7.5 天死亡。PHGPx-loxP 转基因拯救了 PHGPx KO 小鼠免于胚胎致死。这些被拯救的 PHGPx 基因敲除的 floxed 小鼠与精母细胞特异性表达 Cre 的小鼠交配。所有精母细胞特异性 PHGPx KO 雄性小鼠均不育,并显示精子线粒体功能障碍导致精子数量显著减少和前向运动能力显著降低。这些结果表明,精子中 PHGPx 的耗竭可能是小鼠和人类男性不育的原因之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6219/2803127/5efa90a52c4b/jcbn09-94Rf09.jpg
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