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Analysis of Expression and Single Nucleotide Polymorphisms of INHA Gene Associated with Reproductive Traits in Chickens

机译:鸡INHA基因与生殖性状相关的表达及单核苷酸多态性分析

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摘要

Inhibin α (INHA) is a candidate gene controlling ovulation in poultry. As the functional center of inhibin, INHA is a molecular marker associated with egg-laying performance. The objective of the current study was to analyze the expression differences of INHA in reproductive system and single nucleotide polymorphisms (SNPs) associations with reproductive traits in chickens. A total of 260 LuHua chickens (barred-feather chicken) were adopted. Twelve SNPs were detected in INHA gene. Among the exonic SNPs, three (g. 22177991A>G, g. 22178249G>C, and g. 22178414G>A) were missense mutations, resulting in the amino acid substitutions Val→Ala, Ala→Gly, and Ala→Gly, respectively. Four SNPs in the 3' untranslated region of INHA were predicted to either disturb or create microRNA-target interactions. Five SNPs (g. 22176870T>C, g. 22177100T>C, g. 22177149T>C, g. 22177991A>G, and g. 22178975G>A) were significantly associated with the number of eggs at 300 d of age (EN) (P < 0.05). Birds carrying GA genotype exhibited more EN than those with AA genotype (P < 0.01). In addition, quantitative real-time PCR revealed that INHA is mainly expressed in follicles on d 300 in chickens. Firstly, INHA expression increased and then decreased. The highest INHA mRNA abundance was found in the fifth largest preovulatory follicle (F5) (P < 0.01). In the prehierarchical follicles, INHA mRNA expression increased dramatically in small yellow follicles (SYF) (P < 0.01). Western blotting analysis showed that the INHA protein expression profile in the follicle was similar to its mRNA counterpart with greater expression in F5 and SYF follicles and lowest expression in F1 follicles (P < 0.05). These results suggest that INHA is a potential candidate gene improving reproductive traits in chickens.
机译:抑制素α(INHA)是控制家禽排卵的候选基因。作为抑制素的功能中心,INHA是与产卵性能相关的分子标记。本研究的目的是分析INHA在鸡生殖系统中的表达差异以及单核苷酸多态性(SNPs)与鸡生殖特性的关系。总共采用了260只Lu花鸡(羽羽鸡)。在INHA基因中检测到12个SNP。在外显子SNP中,三个(g。22177991A> G,g。22178249G> C,和22178414G> A)是错义突变,分别导致氨基酸取代Val→Ala,Ala→Gly和Ala→Gly。 。预测INHA 3'非翻译区中的四个SNP会干扰或产生microRNA-靶标相互作用。五个SNP(g.22176870T> C,g.22177100T> C,g.22177149T> C,g.22177991A> G,g.22178975G> A)与300 d龄(EN)的卵数显着相关(P <0.05)。携带GA基因型的鸟类比具有AA基因型的鸟类表现出更多的EN(P <0.01)。另外,定量实时PCR显示INHA主要在鸡的第300天的卵泡中表达。首先,INHA表达升高然后降低。在排卵前第五大卵泡(F5)中发现最高的INHA mRNA丰度(P <0.01)。在等级前的卵泡中,小黄色卵泡(SYF)中的INHA mRNA表达显着增加(P <0.01)。蛋白质印迹分析表明,卵泡中的INHA蛋白表达谱与其mRNA相似,在F5和SYF卵泡中表达更高,在F1卵泡中表达最低(P <0.05)。这些结果表明,INHA是改善鸡生殖性状的潜在候选基因。

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