The molecular underpinnings of fertility: Genetic approaches in Caenorhabditis elegans

Xue Mei, Andrew W. Singson
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引用次数: 9

Abstract

The study of mutations that impact fertility has a catch-22. Fertility mutants are often lost since they cannot simply be propagated and maintained. This has hindered progress in understanding the genetics of fertility. In mice, several molecules are found to be required for the interactions between the sperm and egg, with JUNO and IZUMO1 being the only known receptor pair on the egg and sperm surface, respectively. In Caenorhabditis elegans, a total of 12 proteins on the sperm or oocyte have been identified to mediate gamete interactions. Majority of these genes were identified through mutants isolated from genetic screens. In this review, we summarize the several key screening strategies that led to the identification of fertility mutants in C. elegans and provide a perspective about future research using genetic approaches. Recently, advancements in new technologies such as high-throughput sequencing and Crispr-based genome editing tools have accelerated the molecular, cell biological, and mechanistic analysis of fertility genes. We review how these valuable tools advance our understanding of the molecular underpinnings of fertilization. We draw parallels of the molecular mechanisms of fertilization between worms and mammals and argue that our work in C. elegans complements fertility research in humans and other species.

Abstract Image

生殖能力的分子基础:秀丽隐杆线虫的遗传方法
对影响生育能力的突变的研究陷入了两难境地。由于不能简单地繁殖和维持,生育突变体经常丢失。这阻碍了理解生育遗传学的进展。在小鼠中,发现精子和卵子之间的相互作用需要几个分子,JUNO和IZUMO1分别是卵子和精子表面唯一已知的受体对。在秀丽隐杆线虫(Caenorhabditis elegans)中,精子或卵母细胞上共有12种蛋白被鉴定为介导配子相互作用。这些基因中的大多数是通过从遗传筛选中分离出的突变体来鉴定的。在这篇综述中,我们总结了几种导致秀丽隐杆线虫生育突变体鉴定的关键筛选策略,并对未来利用遗传方法进行研究提出了展望。最近,高通量测序和基于crispr的基因组编辑工具等新技术的进步加速了对生育基因的分子、细胞生物学和机制分析。我们回顾了这些有价值的工具如何促进我们对受精分子基础的理解。我们比较了蠕虫和哺乳动物受精的分子机制,认为秀丽隐杆线虫的研究补充了人类和其他物种的受精研究。
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