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鸡早羽和晚羽候选基因的鉴定

Identification of candidate genes for chicken early- and late-feathering.

作者信息

Zhao J, Yao J, Li F, Yang Z, Sun Z, Qu L, Wang K, Su Y, Zhang A, Montgomery S A, Geng T, Cui H

机构信息

College of Animal Science and Technology, Yangzhou University, Yangzhou, Jiangsu 225009, China; Institute of Epigenetics and Epigenomics, Yangzhou University, Yangzhou, Jiangsu 225009, China.

Institute of Poultry Science, Chinese Academy of Agricultural Science, Yangzhou, Jiangsu 225125, China.

出版信息

Poult Sci. 2016 Jul 1;95(7):1498-1503. doi: 10.3382/ps/pew131. Epub 2016 Apr 14.

Abstract

Previous studies suggest that prolactin receptor (Prlr) is a potential causative gene for chicken early- (EF) and late-feathering (LF) phenotypes. In this study, we evaluated candidate genes for this trait and determined the expression of 3 genes, including Prlr, sperm flagellar protein 2 (Spef2), and their fusion gene, in the skins of one-day-old EF and LF chicks using RT-qPCR. Data indicated that Prlr expression in the skin did not show significant difference between EF and LF chicks, suggesting Prlr may not be a suitable candidate gene. In contrast, Spef2 expression in the skin displayed a significant difference between EF and LF chicks (P < 0.01), suggesting that Spef2 may be a good candidate gene for chicken feathering. Moreover, dPrlr/dSpef2, the fusion gene, was also a good candidate gene as it was expressed only in LF chicks. However, the expression of the fusion gene was much lower than that of Prlr Additionally, using strand-specific primers, we found that the fusion gene was transcribed in 2 directions (one from dPrlr promoter, another from dSpef2 promoter), which could result in the formation of a double strand RNA. In conclusion, both Spef2 and the fusion gene are good candidate genes for chicken feathering, but Prlr is not. The research on the function and regulation of the candidate genes will help elucidate the molecular basis of the chicken feathering trait.

摘要

先前的研究表明,催乳素受体(Prlr)是鸡早羽(EF)和晚羽(LF)表型的潜在致病基因。在本研究中,我们评估了该性状的候选基因,并使用RT-qPCR测定了1日龄EF和LF雏鸡皮肤中3个基因的表达,包括Prlr、精子鞭毛蛋白2(Spef2)及其融合基因。数据表明,EF和LF雏鸡皮肤中Prlr的表达没有显著差异,这表明Prlr可能不是一个合适的候选基因。相比之下,EF和LF雏鸡皮肤中Spef2的表达存在显著差异(P < 0.01),这表明Spef2可能是鸡羽毛生长的一个良好候选基因。此外,融合基因dPrlr/dSpef2也是一个良好的候选基因,因为它仅在LF雏鸡中表达。然而,融合基因的表达远低于Prlr。此外,使用链特异性引物,我们发现融合基因以两个方向转录(一个来自dPrlr启动子,另一个来自dSpef2启动子),这可能导致双链RNA的形成。总之,Spef2和融合基因都是鸡羽毛生长的良好候选基因,但Prlr不是。对候选基因功能和调控的研究将有助于阐明鸡羽毛生长性状的分子基础。

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