Identification and bioinformatic analysis of target genes of lncRNA LOC102606465 induced by ionizing radiation

Q4 Medicine
Chang Yu, Qi Wang, Ruixue Liu, Jinfeng Huang, Zhi-dong Wang, Meijuan Zhou
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引用次数: 0

Abstract

Objective To screen the target genes of long non-coding RNA LOC102606465, which was previously identified to be induced by ionizing radiation, in order to examine its potential biological role. Methods The downstream differentially expressed genes (DEGs) of LOC102606465 were detected by microarray and partially verified by qRT-PCR. GO and KEGG enrichment analysis was performed, and PPI protein interaction network was constructed to screen significant modules and hub genes. Results The expression of LOC102606465 targeted by siRNA-447 and siRNA-541 was significantly lower than that of siRNA-NC (t=29.095, 13.751, P<0.01). A total of 374 common DEGs were identified(112 up-regulated/262 down-regulated) in both siRNA-447 and siRNA-541. The qRT-PCR was used to validate the expression of DEGs, which was consistent with the microarray result. In GO enrichment analysis, down-regulated DEGs were significantly enriched in " oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor" (molecular function), " basal lamina" (cellular component), " ammonium ion metabolic process" (biological process). Up-regulated DEGs were mainly enriched in " protein phosphatase inhibitor activity" (molecular function), " SNARE complex" (cellular component), " negative regulation of fibrinolysis" (biological process). In addition, the KEGG enrichment analysis revealed that DEGs were significantly enriched in " metabolism of xenobiotics by cytochrome P450" , " dorso-ventral axis formation" , " lysosome glycerophospholipid metabolism" and " p53 signaling pathway" . Based on the STRING database, the PPI network was constructed (including 194 nodes and 268 edges), and one significant module and five key hub genes ACTRT3, CDKN1A, DPYD, TMP4, and PRKACB were identified. Conclusions LOC102606465 could be a potential biomarker for the regulation of ionizing radiation sensitivity, and the down-regulation of LOC102606465 plays an important role in the response to radiation, which would be an important target for regulating radiation sensitivity. Key words: Bioinformatic analysis; Microarray; LOC102606465; Ionizing radiation
电离辐射诱导lncRNA LOC102606465靶基因的鉴定及生物信息学分析
目的筛选经鉴定为电离辐射诱导的长链非编码RNA LOC102606465的靶基因,探讨其潜在的生物学作用。方法采用芯片检测LOC102606465下游差异表达基因(DEGs),并采用qRT-PCR进行部分验证。进行GO和KEGG富集分析,构建PPI蛋白互作网络,筛选重要模块和枢纽基因。结果siRNA-447和siRNA-541靶向的LOC102606465表达量显著低于siRNA-NC (t=29.095、13.751,P<0.01)。在siRNA-447和siRNA-541中共鉴定出374个共同的deg(112个上调,262个下调)。使用qRT-PCR验证deg的表达,与芯片结果一致。在GO富集分析中,下调的DEGs在“氧化还原酶活性,作用于供体CH-CH基团,NAD或NADP作为受体”(分子功能),“基底层”(细胞成分),“铵离子代谢过程”(生物过程)中显著富集。上调的deg主要富集于“蛋白磷酸酶抑制剂活性”(分子功能)、“SNARE复合物”(细胞成分)、“纤维蛋白溶解负调控”(生物过程)。此外,KEGG富集分析显示,DEGs在“细胞色素P450代谢异种生物”、“背-腹轴形成”、“溶酶体甘油磷脂代谢”和“p53信号通路”中显著富集。基于STRING数据库构建PPI网络(包括194个节点和268条边),鉴定出1个重要模块和5个关键枢纽基因ACTRT3、CDKN1A、DPYD、TMP4和PRKACB。结论LOC102606465可能是调控电离辐射敏感性的潜在生物标志物,其下调在辐射应答中起重要作用,可能成为调控辐射敏感性的重要靶点。关键词:生物信息学分析;微阵列;LOC102606465;电离辐射
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来源期刊
中华放射医学与防护杂志
中华放射医学与防护杂志 Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
0.60
自引率
0.00%
发文量
6377
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