Davoli R, Gaffo E, Zappaterra M, Bortoluzzi S, Zambonelli P
Department of Agricultural and-Food Sciences (DISTAL), University of Bologna, Viale G. Fanin 46, 40127, Bologna, Italy.
Department of Molecular Medicine, University of Padova, Viale G. Colombo 3, 35131, Padova, Italy.
Anim Genet. 2018 Jun;49(3):205-214. doi: 10.1111/age.12646. Epub 2018 Mar 23.
The identification of the molecular mechanisms regulating pathways associated with the potential for fat deposition in pigs can lead to the detection of key genes and markers for the genetic improvement of fat traits. Interactions of microRNAs (miRNAs) with target RNAs regulate gene expression and modulate pathway activation in cells and tissues. In pigs, miRNA discovery is far from saturation, and the knowledge of miRNA expression in backfat tissue and particularly of the impact of miRNA variations is still fragmentary. Using RNA-seq, we characterized the small RNA (sRNA) expression profiles in Italian Large White pig backfat tissue. Comparing two groups of pigs divergent for backfat deposition, we detected 31 significant differentially expressed (DE) sRNAs: 14 up-regulated (including ssc-miR-132, ssc-miR-146b, ssc-miR-221-5p, ssc-miR-365-5p and the moRNA ssc-moR-21-5p) and 17 down-regulated (including ssc-miR-136, ssc-miR-195, ssc-miR-199a-5p and ssc-miR-335). To understand the biological impact of the observed miRNA expression variations, we used the expression correlation of DE miRNA target transcripts expressed in the same samples to define a regulatory network of 193 interactions between DE miRNAs and 40 DE target transcripts showing opposite expression profiles and being involved in specific pathways. Several miRNAs and mRNAs in the network were found to be expressed from backfat-related pig QTL. These results are informative for the complex mechanisms influencing fat traits, shed light on a new aspect of the genetic regulation of fat deposition in pigs and facilitate the prospective implementation of innovative strategies of pig genetic improvement based on genomic markers.
鉴定调控猪脂肪沉积相关途径的分子机制,有助于发现关键基因和标记,从而对脂肪性状进行遗传改良。微小RNA(miRNA)与靶RNA的相互作用可调节基因表达,并调控细胞和组织中的途径激活。在猪中,miRNA的发现远未饱和,关于miRNA在背膘组织中的表达情况,尤其是miRNA变异的影响,目前仍知之甚少。我们利用RNA测序技术,对意大利大白猪背膘组织中的小RNA(sRNA)表达谱进行了特征分析。通过比较两组背膘沉积差异较大的猪,我们检测到31个显著差异表达的(DE)sRNA:14个上调(包括ssc-miR-132、ssc-miR-146b、ssc-miR-221-5p、ssc-miR-365-5p和moRNA ssc-moR-21-5p)和17个下调(包括ssc-miR-136、ssc-miR-195、ssc-miR-199a-5p和ssc-miR-335)。为了了解观察到的miRNA表达变异的生物学影响,我们利用相同样本中DE miRNA靶转录本的表达相关性,定义了一个由193个相互作用组成的调控网络,这些相互作用存在于DE miRNA和40个DE靶转录本之间,它们呈现相反的表达谱,并参与特定途径。该网络中的几个miRNA和mRNA被发现是从与背膘相关的猪数量性状位点(QTL)表达的。这些结果为影响脂肪性状的复杂机制提供了信息,揭示了猪脂肪沉积遗传调控的一个新方面,并有助于基于基因组标记的猪遗传改良创新策略的前瞻性实施。