Zhang Chunyan, Bruce Heather, Yang Tianfu, Charagu Patrick, Kemp Robert Alan, Boddicker Nicholas, Miar Younes, Wang Zhiquan, Plastow Graham
Department of Agricultural, Food and Nutritional Sciences, University of Alberta, Edmonton, AB, Canada.
Hypor Inc., Regina, SK, Canada.
PLoS One. 2016 Feb 22;11(2):e0145082. doi: 10.1371/journal.pone.0145082. eCollection 2016.
Of all the meat quality traits, tenderness is considered the most important with regard to eating quality and market value. In this study we have utilised genome wide association studies (GWAS) for peak shear force (PSF) of loin muscle as a measure of tenderness for 1,976 crossbred commercial pigs, genotyped for 42,721 informative SNPs using the Illumina PorcineSNP60 Beadchip. Four 1 Mb genomic regions, three on SSC2 (at 4 Mb, 5 Mb and 109 Mb) and one on SSC17 (at 20 Mb), were detected which collectively explained about 15.30% and 3.07% of the total genetic and phenotypic variance for PSF respectively. Markers ASGA0008566, ASGA0008695, DRGA0003285 and ASGA0075615 in the four regions were strongly associated with the effects. Analysis of the reference genome sequence in the region with the most important SNPs for SSC2_5 identified FRMD8, SLC25A45 and LTBP3 as potential candidate genes for meat tenderness on the basis of functional annotation of these genes. The region SSC2_109 was close to a previously reported candidate gene CAST; however, the very weak LD between DRGA0003285 (the best marker representing region SSC2_109) and CAST indicated the potential for additional genes which are distinct from, or interact with, CAST to affect meat tenderness. Limited information of known genes in regions SSC2_109 and SSC17_20 restricts further analysis. Re-sequencing of these regions for informative animals may help to resolve the molecular architecture and identify new candidate genes and causative mutations affecting this trait. These findings contribute significantly to our knowledge of the genomic regions affecting pork shear force and will potentially lead to new insights into the molecular mechanisms regulating meat tenderness.
在所有肉质性状中,就食用品质和市场价值而言,嫩度被认为是最重要的。在本研究中,我们利用全基因组关联研究(GWAS)对1976头杂交商品猪的腰大肌峰值剪切力(PSF)进行分析,以此作为嫩度的衡量指标,并使用Illumina PorcineSNP60 Beadchip对这些猪进行了42,721个信息性单核苷酸多态性(SNP)的基因分型。检测到四个1兆碱基的基因组区域,其中三个位于猪2号染色体(SSC2)上(分别位于4兆碱基、5兆碱基和109兆碱基处),一个位于猪17号染色体(SSC17)上(位于20兆碱基处),这些区域共同分别解释了PSF总遗传方差和表型方差的约15.30%和3.07%。这四个区域中的标记ASGA0008566、ASGA0008695、DRGA0003285和ASGA0075615与这些效应密切相关。基于对这些基因的功能注释,对SSC2_5最重要的SNP所在区域的参考基因组序列分析确定了FRMD8、SLC25A45和LTBP3作为肉质嫩度的潜在候选基因。SSC2_109区域靠近先前报道的候选基因CAST;然而,DRGA0003285(代表SSC2_109区域的最佳标记)与CAST之间非常弱的连锁不平衡表明,可能存在与CAST不同或与其相互作用的其他基因来影响肉质嫩度。SSC2_109和SSC17_20区域中已知基因的信息有限,限制了进一步的分析。对这些信息丰富的动物的这些区域进行重测序可能有助于解析分子结构,并识别影响该性状的新候选基因和致病突变。这些发现对我们了解影响猪肉剪切力的基因组区域有重大贡献,并可能为调节肉质嫩度的分子机制带来新的见解。