An RNA-Seq screen of the dithiothreitol-induced apoptosis response in chicken cardiomyocytes
文献类型: 外文期刊
作者: Wan, Chunyun 1 ; Xiang, Jinmei 2 ; Guo, Rui 4 ; Yang, Shijin 2 ; Li, Youwen 2 ; Guo, Dingzong 2 ;
作者机构: 1.Yangtze Univ, Coll Anim Sci, Jingzhou, Hubei, Peoples R China
2.Huazhong Agr Univ, Coll Vet Med, Wuhan 430070, Hubei, Peoples R China
3.Hubei Vocat Coll Biotechnol, Dept Anim Sci, Wuhan, Hubei, Peoples R China
4.Hubei Acad Agr Sci, Hubei Key Lab Embryo & Mol Breeding, Wuhan, Hubei, Peoples R China
关键词: RNA-Seq;apoptosis;cardiomyocytes;apoptosis inducer;DTT
期刊名称:INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY ( 影响因子:0.252; 五年影响因子:1.188 )
ISSN: 1936-2625
年卷期: 2017 年 10 卷 2 期
页码:
收录情况: SCI
摘要: Cardiomyocytes in postnatal heart are terminally differentiated and thus possess limited capacity to regenerate. Loss of cardiomyocytes through apoptosis and necrosis can lead to heart failure and other serious consequences. Compared to mammals, substantially less research has been conducted on chicken cardiomyocytes; thus, the apoptosis pathways and many relevant genes remain unknown. To elucidate the pathways and genes involved in chicken myocardial cell apoptosis, primary cultures of chicken embryo cardiomyocytes were sham-treated or exposed to the apoptosis inducer dithiothreitol (DTT), and RNA-Seq with technical replicates conducted to identify differentially expressed genes and transcripts. Relevant differentially expressed transcripts were used to construct a protein-protein interactive network for chicken apoptosis. Sequencing detected a total of 19,268 known genes and 2,160 novel genes. In the DTT treatment group, 6468 genes showed significant differential expression based on DEseq analysis, of which 47.99% were upregulated and 52.01% downregulated. The initiation of apoptosis was primarily dependent on caspase-8 and caspase-9, whereas the execution stage was dependent on caspase-3. Up-regulated genes also included many involved in the WNT and MAPK pathways. Repression of apoptosis was primarily dependent on Bcl-2, IAP, and SIVA. These results provide a foundation for detailed analysis of avian myocardial apoptosis, including genes and LncRNAs that constitute, regulate, or link various pro-and anti-apoptotic pathways.
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