Department of Animal Genetics, Centre for Research in Agricultural Genomics (CRAG) CSIC-IRTA-UAB-UB, Campus de la Universitat Autònoma de Barcelona, Bellaterra, 08193, Barcelona, Spain.
Dipartimento di Medicina Veterinaria, Università degli Studi di Sassari, via Vienna, 2, 07100, Sassari, Italy.
Sci Rep. 2018 Jul 11;8(1):10486. doi: 10.1038/s41598-018-28760-9.
The goal of the current study is to analyse the gene expression profile of the ovine skeletal muscle as well as to characterize the genetic variation of transcripts expressed in such tissue. This aim has been achieved by sequencing the longissimus dorsi transcriptomes of 50 sheep distributed in five pools representing the Canaria de Pelo, Roja Mallorquina, Gallega, Xisqueta and Ripollesa Spanish autochthonous breeds. Approximately, 363 million reads per pool have been produced and 71.9-82.9% have been successfully mapped to the ovine genome in a paired-end mode (2 × 75 bp). The 200 most expressed muscle transcripts (≈1% of the total transcript count) account for 51% (Canaria de Pelo) to 67% (Gallega) of the total ovine skeletal muscle mRNA expression. These highly expressed genes play key roles in pathways related with striated muscle contraction, gluconeogenesis, glycolysis, citric acid cycle and respiratory electron transport. RNA-Sequencing of muscle transcripts has also revealed that ~72% of the SNPs detected with this approach are shared by at least two pools, and 10% of them segregate in the five pools under analysis. Most of the substitutions detected by RNA-Seq are synonymous or missense and only a minority are predicted to have consequences on protein function.
本研究的目的是分析绵羊骨骼肌的基因表达谱,并对该组织中表达的转录本的遗传变异进行特征分析。为了实现这一目标,我们对分布在五个群体中的 50 只绵羊的背最长肌转录组进行了测序,这些群体代表了西班牙本土品种 Canaria de Pelo、Roja Mallorquina、Gallega、Xisqueta 和 Ripollesa。每个群体大约产生了 3.63 亿条读长,并且在配对末端模式(2×75bp)下有 71.9-82.9%成功映射到绵羊基因组上。200 个表达量最高的肌肉转录本(约占总转录本数的 1%)占绵羊骨骼肌 mRNA 总表达量的 51%(Canaria de Pelo)到 67%(Gallega)。这些高表达的基因在与横纹肌收缩、糖异生、糖酵解、柠檬酸循环和呼吸电子传递相关的途径中发挥着关键作用。肌肉转录本的 RNA-Seq 还表明,通过这种方法检测到的大约 72%的 SNP 至少被两个群体共享,其中 10%在分析的五个群体中分离。RNA-Seq 检测到的大多数取代是同义或错义的,只有少数被预测会对蛋白质功能产生影响。