首页> 美国卫生研究院文献>Iranian Journal of Basic Medical Sciences >Diagnosis of genetic defects through parallel assessment of PLCζ and CAPZA3 in infertile men with history of failed oocyte activation
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Diagnosis of genetic defects through parallel assessment of PLCζ and CAPZA3 in infertile men with history of failed oocyte activation

机译:通过平行评估PLCζ和CAPZA3对患有卵母细胞激活失败史的不育男性的遗传缺陷诊断

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摘要

Objective(s):Phospholipase C ζ (PLCζ) is considered as a nominee for sperm associated oocyte activating factors and is located back-to-back with CAPZA3, an actin-capping protein controlling actin polymerization during spermiogenesis. They contain a common bidirectional promoter. The objective of this study was to identify individuals with parallel low expression of PLCζ and CAPZA3 mRNA, in hope of detecting genetic defects in this bidirectional promoter.
机译:目的:磷脂酶Cζ(PLCζ)被认为是与精子相关的卵母细胞活化因子的代名词,并与CAPZA3背对背定位,CAPZA3是在生精过程中控制肌动蛋白聚合的肌动蛋白封端蛋白。它们包含共同的双向启动子。本研究的目的是鉴定具有平行表达的PLCζ和CAPZA3 mRNA低表达的个体,以期检测该双向启动子的遗传缺陷。

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