Profiling and characterization of a longissimus dorsi muscle microRNA dataset from an F2 Duroc × Pietrain pig resource population

Kaitlyn R. Daza , Juan P. Steibel , Deborah Velez-Irizarry , Nancy E. Raney , Ronald O. Bates , Catherine W. Ernst
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引用次数: 4

Abstract

To elucidate the effects of microRNA (miRNA) regulation in skeletal muscle of adult pigs, miRNA expression profiling was performed with RNA extracted from longissimus dorsi (LD) muscle samples from 174 F2 pigs (~ 5.5 months of age) from a Duroc × Pietrain resource population. Total RNA was extracted from LD samples, and libraries were sequenced on an Illumina HiSeq 2500 platform in 1 × 50 bp format. After processing, 232,826,977 total reads were aligned to the Sus scrofa reference genome (v10.2.79), with 74.8% of total reads mapping successfully. The miRDeep2 software package was utilized to quantify annotated Sus scrofa mature miRNAs from miRBase (Release 21) and to predict candidate novel miRNA precursors. Among the retained 295 normalized mature miRNA expression profiles ssc­miR­1, ssc­miR­133a­3p, ssc­miR­378, ssc­miR­206, and ssc­miR­10b were the most abundant, all of which have previously been shown to be expressed in pig skeletal muscle. Additionally, 27 unique candidate novel miRNA precursors were identified exhibiting homologous sequence to annotated human miRNAs. The composition of classes of small RNA present in this dataset was also characterized; while the majority of unique expressed sequence tags were not annotated in any of the queried databases, the most abundantly expressed class of small RNA in this dataset was miRNAs. This data provides a resource to evaluate miRNA regulation of gene expression and effects on complex trait phenotypes in adult pig skeletal muscle. The raw sequencing data were deposited in the Sequence Read Archive, BioProject PRJNA363073.

Abstract Image

Abstract Image

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来自F2 Duroc × Pietrain猪资源群体背最长肌microRNA数据集的分析和表征
为了阐明microRNA (miRNA)在成年猪骨骼肌中的调控作用,研究人员从杜洛克×皮特兰资源种群的174头F2猪(~ 5.5月龄)的背最长肌(LD)肌肉样本中提取RNA,进行了miRNA表达谱分析。提取LD样品的总RNA,在Illumina HiSeq 2500平台上以1 × 50 bp格式对文库进行测序。处理后,共有232,826,977条reads与Sus scrofa参考基因组(v10.2.79)对齐,其中74.8%的reads成功定位。使用miRDeep2软件包定量miRBase (Release 21)中已注释的su scrofa成熟miRNA,并预测候选的新型miRNA前体。在保留的295个标准化成熟miRNA表达谱中,ssc-miR-1、ssc-miR-133a-3p、ssc-miR-378、ssc-miR-206和ssc-miR-10b的表达量最为丰富,所有这些基因之前都被证明在猪骨骼肌中表达。此外,鉴定了27种独特的候选新型miRNA前体,它们与注释的人类miRNA具有同源序列。该数据集中存在的小RNA类别的组成也被表征;虽然大多数唯一表达的序列标签在任何查询的数据库中都没有注释,但该数据集中表达最丰富的小RNA类别是mirna。这些数据为评估miRNA调控成年猪骨骼肌基因表达及其对复杂性状表型的影响提供了资源。原始测序数据保存在Sequence Read Archive, BioProject PRJNA363073中。
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