Rajput Neha, Gahlay Gagandeep Kaur
Department of Molecular Biology and Biochemistry, Guru Nanak Dev University, Amritsar, INDIA.
Front Cell Dev Biol. 2021 Nov 17;9:763166. doi: 10.3389/fcell.2021.763166. eCollection 2021.
ZP2, an important component of the zona matrix, surrounds mammalian oocytes and facilitates fertilization. Recently, some studies have documented the association of mutations in genes encoding the zona matrix with the infertile status of human females. Single nucleotide polymorphisms are the most common type of genetic variations observed in a population and as per the dbSNP database, around 5,152 SNPs are reported to exist in the human () gene. Although a wide range of computational tools are publicly available, yet no computational studies have been done to date to identify and analyze structural and functional effects of deleterious SNPs on . In this study, we conducted a comprehensive analysis of all the SNPs found in . Six different computational tools including SIFT and PolyPhen-2 predicted 18 common nsSNPs as deleterious of which 12 were predicted to most likely affect the structure/functional properties. These were either present in the N-term region crucial for sperm-zona interaction or in the zona domain. 31 additional SNPs in both coding and non-coding regions were also identified. Interestingly, some of these SNPs have been found to be present in infertile females in some recent studies.
ZP2是透明带基质的重要组成部分,围绕着哺乳动物的卵母细胞并促进受精。最近,一些研究记录了编码透明带基质的基因突变与人类女性不孕状态之间的关联。单核苷酸多态性是在人群中观察到的最常见的遗传变异类型,根据dbSNP数据库,据报道人类()基因中存在约5152个单核苷酸多态性。尽管有多种计算工具可供公众使用,但迄今为止尚未进行计算研究来识别和分析有害单核苷酸多态性对的结构和功能影响。在本研究中,我们对中发现的所有单核苷酸多态性进行了全面分析。包括SIFT和PolyPhen-2在内的六种不同计算工具预测18个常见的非同义单核苷酸多态性是有害的,其中12个被预测极有可能影响结构/功能特性。这些要么存在于对精子-透明带相互作用至关重要的N端区域,要么存在于透明带结构域中。在编码区和非编码区还鉴定出另外31个单核苷酸多态性。有趣的是,在最近的一些研究中发现其中一些单核苷酸多态性存在于不孕女性中。