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商业肉鸡木质胸和白条纹的遗传基础及候选基因鉴定。

Genetic basis and identification of candidate genes for wooden breast and white striping in commercial broiler chickens.

机构信息

Center for Bioinformatics and Computational Biology, University of Delaware, Newark, DE, USA.

Department of Animal and Food Sciences, University of Delaware, Newark, DE, USA.

出版信息

Sci Rep. 2021 Mar 24;11(1):6785. doi: 10.1038/s41598-021-86176-4.

Abstract

Wooden breast (WB) and white striping (WS) are highly prevalent and economically damaging muscle disorders of modern commercial broiler chickens characterized respectively by palpable firmness and fatty white striations running parallel to the muscle fiber. High feed efficiency and rapid growth, especially of the breast muscle, are believed to contribute to development of such muscle defects; however, their etiology remains poorly understood. To gain insight into the genetic basis of these myopathies, a genome-wide association study was conducted using a commercial crossbred broiler population (n = 1193). Heritability was estimated at 0.5 for WB and WS with high genetic correlation between them (0.88). GWAS revealed 28 quantitative trait loci (QTL) on five chromosomes for WB and 6 QTL on one chromosome for WS, with the majority of QTL for both myopathies located in a ~ 8 Mb region of chromosome 5. This region has highly conserved synteny with a portion of human chromosome 11 containing a cluster of imprinted genes associated with growth and metabolic disorders such as type 2 diabetes and Beckwith-Wiedemann syndrome. Candidate genes include potassium voltage-gated channel subfamily Q member 1 (KCNQ1), involved in insulin secretion and cardiac electrical activity, lymphocyte-specific protein 1 (LSP1), involved in inflammation and immune response.

摘要

木质胸(WB)和白条(WS)是现代商业肉鸡中高度流行且具有经济破坏性的肌肉疾病,其特征分别为可触及的硬度和与肌肉纤维平行的脂肪性白条。高饲料效率和快速生长,特别是胸肌的生长,被认为是导致这种肌肉缺陷的原因;然而,其病因仍知之甚少。为了深入了解这些肌肉疾病的遗传基础,对一个商业杂交肉鸡群体(n=1193)进行了全基因组关联研究。WB 和 WS 的遗传力估计分别为 0.5 和 0.88,两者之间具有高度遗传相关性。GWAS 揭示了 5 号染色体上与 WB 相关的 28 个数量性状位点(QTL)和 1 号染色体上与 WS 相关的 6 个 QTL,大多数与这两种肌肉疾病相关的 QTL都位于 5 号染色体的一个约 8 Mb 的区域。该区域与人类 11 号染色体的一部分具有高度同源性,该部分包含簇状印记基因,与生长和代谢紊乱有关,如 2 型糖尿病和贝克威思-威德曼综合征。候选基因包括与胰岛素分泌和心脏电活动有关的钾电压门控通道亚家族 Q 成员 1(KCNQ1),以及与炎症和免疫反应有关的淋巴细胞特异性蛋白 1(LSP1)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fba9/7990949/14a1bc012744/41598_2021_86176_Fig1_HTML.jpg

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