RNAseq Reveals Novel and Differentially Expressed Isoforms in Native and Commercial Poultry

A. S. Sadr, M. Nassiri, S. A. Salami, M. Bakhtiarizadeh, M. Tahmoorespur, A. Shafeinia
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Abstract

The poultry industry occupies an important position in the provision of animal protein. Recently, next generation sequencing technology (RNA-Seq) has become available as a powerful tool to investigate transcriptional profiles for gene expression analysis of many organisms. The main use of RNA-Seq in agriculture species are focusing on finding the immune related genes or pathways by comparison of the whole transcriptome following pathogen challenge. Alternative splicing (AS) is the major fundamental mechanism generating the protein diversity and regulating the gene expression in eukaryotic organism. Identifying genes that are differentially spliced between two groups of RNA-sequencing samples is interesting subject in transcriptome with next-generation sequencing technology in this study used RNA sequencing to comparison isoforms of two breeds. A total of 64,819 transcripts were identified by aligning sequence reads to genome among the evaluated isoforms for expression analysis, 310 were significantly differentially expressed between two breeds, including 251 up-regulated and 59 down-regulated. The KEGG results of up regulated isoforms showed that that no pathway was found significantly different (FDR ≤ 0.05). However, enrichment analysis suggested that seven were over-represented (P-value ≤ 0.05) within the up regulated isoforms. Only one of them functionally related to immune system, natural killer cell mediated cytotoxicity. The results showed genes which are breed-specific expression and the comparative transcriptome analysis help to understand the difference of genetic mechanism.
RNAseq在本地和商业家禽中揭示了新的和差异表达的亚型
家禽业在提供动物蛋白方面占有重要地位。近年来,下一代测序技术(RNA-Seq)已成为研究许多生物基因表达的转录谱的有力工具。RNA-Seq技术在农业物种中的应用主要集中在病原攻击后通过比较整个转录组来寻找与免疫相关的基因或途径。选择性剪接(Alternative splicing, AS)是真核生物产生蛋白质多样性和调控基因表达的重要机制。利用下一代测序技术鉴定两组RNA测序样本之间的差异剪接基因是转录组学中一个有趣的课题,本研究使用RNA测序来比较两个品种的同种异构体。通过序列reads与基因组比对,共鉴定出64,819个转录本进行表达分析,其中310个转录本在两个品种间表达显著差异,其中上调251个,下调59个。上调异构体的KEGG结果显示,没有发现明显的途径差异(FDR≤0.05)。然而,富集分析表明,在上调的亚型中,有7个过度代表(p值≤0.05)。其中只有一种与免疫系统有关,即自然杀伤细胞介导的细胞毒性。结果表明,品种特异性表达基因和比较转录组分析有助于了解遗传机制的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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