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The mechanism of sperm-egg interaction and the involvement of IZUMO1 in fusion 被引量:3
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作者 Naokazu Inoue Masahito Ikawa Masaru Okabe 《Asian Journal of Andrology》 SCIE CAS CSCD 2011年第1期81-87,共7页
An average human ejaculate contains over 100 million sperm, but only a few succeed in accomplishing the journey to an egg by migration through the female reproductive tract. Among these few sperm, only one participate... An average human ejaculate contains over 100 million sperm, but only a few succeed in accomplishing the journey to an egg by migration through the female reproductive tract. Among these few sperm, only one participates in fertilization. There might be an ingenious molecular mechanism to ensure that the very best sperm fertilize an egg. However, recent gene disruption experiments in mice have revealed that many factors previously described as important for fertilization are largely dispensable. One could argue that the fertilization mechanism is made robust against gene disruptions. However, this is not likely, as there are already six different gene-disrupted mouse lines (Calmegin, Adam Ia, Adam2, Adam3, Ace and Pgapl), all of which result in male sterility. The sperm from these animals are known to have defective zona-binding ability and at the same time lose oviduct-migrating ability. Concerning spermzona binding, the widely accepted involvement of sugar moiety on zona pellucida 3 (ZP3) is indicated to be dispensable by gene disruption experiments. Thus, the landscape of the mechanism of fertilization is revolving considerably. In the sperm-egg fusion process, CD9 on egg and IZUMO1 on sperm have emerged as essential factors. This review focuses on the mechanism of fertilization elucidated by gene-manipulated animals. 展开更多
关键词 EGG FUSION gene-manipulation INTERACTION izumo1 SPERM zona pellucida
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绵羊Izumo1基因多态性及其与产羔数关联分析 被引量:2
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作者 胡文萍 董新龙 +8 位作者 田志龙 汤继顺 刘秋月 王翔宇 狄冉 张效生 张金龙 王金玉 储明星 《中国农业大学学报》 CAS CSCD 北大核心 2020年第1期95-104,共10页
为研究Izumo1基因多态性及与产羔数关系,本研究利用PCR和直接测序法对小尾寒羊和苏尼特羊的Izumo1基因DNA序列进行扩增、测序和BLAST分析,并和本课题组前期绵羊重测序数据进行比对,筛选出Izumo1基因SNP位点。同时,采用Sequenom MassARRA... 为研究Izumo1基因多态性及与产羔数关系,本研究利用PCR和直接测序法对小尾寒羊和苏尼特羊的Izumo1基因DNA序列进行扩增、测序和BLAST分析,并和本课题组前期绵羊重测序数据进行比对,筛选出Izumo1基因SNP位点。同时,采用Sequenom MassARRAY~?技术进行基因分型,并对其SNP位点的基因型和等位基因频率在各群体中的分布进行研究。结果表明:小尾寒羊Izumo1基因DNA全长序列3385 bp,苏尼特羊Izumo1基因DNA全长序列3382 bp;筛选出8个Izumo1基因SNP位点,经过初步筛选,将在小尾寒羊、苏尼特羊、滩羊、萨福克羊、杜泊羊、草原藏羊这6个绵羊品种中位点分布没有差异的SNP位点排除,最终筛选获得的g.54412135A>G和g.54412107C>A 2个位点。Izumo1基因g.54412135A>G位点在多羔和单羔绵羊品种中存在GG、GA和AA 3种基因型,G基因为优势等位基因;g.54412107C>A在多羔品种中存在CC和CA 2种基因型,而在单羔品种中存在CC、CA和AA 3种基因型,C基因为优势等位基因,其基因型频率和基因频率在单、多羔绵羊群体间的分布差异均极显著(P<0.01);群体遗传学分析得出g.54412135A>G多态位点在6个品种中的多态信息含量(PIC)都属于低度多态(PIC<0.25);g.54412107C>A多态位点在杜泊羊中属于中度多态(0.25<PIC<0.5),在其他5个品种中都属于低度多态(PIC<0.25),然而,关联分析发现Izumo1基因g.54412135A>G和g.54412107C>A位点的不同基因型与小尾寒羊不同胎次产羔数之间不存在显著关联(P>0.05)。 展开更多
关键词 绵羊 izumo1基因 克隆 多态性 SNP 产羔数
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