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Positive Selection Within Sperm-Egg Adhesion Domains of Fertilin: An ADAM Gene with a Potential Role in Fertilization

机译:受精素精子-卵子粘附结构域内的正选择:具有受精潜在作用的ADAM基因

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摘要

Genes with a role in fertilization show a common pattern of rapid evolution. The role played by positive selection versus lack of selective constraints has been more difficult to establish. One problem arises from attempts to detect selection in an overall gene sequence analysis. I have analyzed the pattern of molecular evolution of fertilin, a gene coding for a heterodimeric sperm protein belonging to the ADAM (A disintegrin and A metalloprotease) gene family. A nonsynonymous to synonymous rate ratio (d_N/d_S) analysis for different protein domains of fertilin α and fertilin β showed d_N/d_S <1, suggesting that purifying selection has shaped fertilin's evolution. However, an analysis of the distribution of single positively selected codon sites using phylogentic analysis by maximum likelihood (PAML) showed sites within adhesion domains (disintegrin and cysteine-rich) of fertilin β evolving under positive selection. The region 3' to the EGF-like domain of fertilin α, whee the transmembrane and cytoplasmic tail regions are supposed to be localized, showed higher d_N and d_S than nay other fertilina α region. However, it was not possible to identify positively selected codon sites due to ambiguous alignments of the carboxy-end region (ClustalX vs. DiAlign2). When this region was excluded from the PAML analysis, most single positively selected codon sites were concentrated within adhesion domains (cysteine-rich and EGF-like). The use of an ancestral sequence prior to a recent duplication event of fertilin α among non-Hominidae primates (Macaca, Papio, and Saguinus) revealed that the duplication is partially responsible for masking the detection of positively selected sites within the disintegrin domain. Finally, most ADAM genes with a potential role in sperm maturation and/or fertilization showed significantly higher d_N estimates than other ADAM genes.
机译:在受精中起作用的基因显示出快速进化的共同模式。积极选择与缺乏选择性约束所起的作用更难确定。一个问题来自于试图在整个基因序列分析中检测选择。我分析了受精蛋白的分子进化模式,受精蛋白是编码属于 ADAM(A 解整合素和 A 金属蛋白酶)基因家族的异二聚体精子蛋白的基因。对受精α和受精β的不同蛋白质结构域的非同义与同义率比 (d_N/d_S) 分析显示 d_N/d_S <1,表明纯化选择塑造了肥蛋白的进化。然而,使用最大似然系统发育分析 (PAML) 对单个阳性选择密码子位点的分布进行分析表明,受精蛋白粘附域(富含解整合素和富含半胱氨酸)内的位点β正选择下进化。受精素α EGF样结构域的3'区域,跨膜和细胞质尾部区域应该是定位的,显示出比其他受精α区域更高的d_N和d_S。然而,由于羧基末端区域的不明确排列(ClustalX 与 DiAlign2),无法识别正选择的密码子位点。当该区域被排除在PAML分析之外时,大多数单个阳性选择的密码子位点集中在粘附结构域(富含半胱氨酸和EGF样)内。在非原始灵长类动物(Macaca、Papio 和 Saguinus)最近发生受精α复制事件之前使用祖先序列表明,复制部分原因掩盖了整合素结构域内阳性选择位点的检测。最后,大多数在精子成熟和/或受精中具有潜在作用的ADAM基因显示出明显高于其他ADAM基因的d_N估计值。

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