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生物信息学分析和高通量测序以鉴定伴肌动蛋白基因(NEB)突变小鼠中的差异表达基因

Bioinformatics Analysis and High-Throughput Sequencing to Identify Differentially Expressed Genes in Nebulin Gene (NEB) Mutations Mice.

作者信息

Wang Haoyong, Nie Xiaoyue, Li Xin, Fang Yi, Wang Dandan, Wang William, Hu Yong, Liu Zijing, Cao Cheng

机构信息

School of Food Biological Engineering, Hubei University of Technology, Wuhan, Hubei, China (mainland).

Department of Endocrinology, The Fifth Medical Center, Chinese People's Liberation Army (PLA) General Hospital, Beijing, China (mainland).

出版信息

Med Sci Monit. 2020 May 11;26:e922953. doi: 10.12659/MSM.922953.

Abstract

BACKGROUND High-throughput sequencing of the pathological tissue of 59 patients with thyroid cancer was compared with the normal population. It was found that the mutation frequency of the Nebulin gene (NEB) at amino acid 1133 locus of thyroid cancer patients was much higher than that of the normal population, suggesting that NEB mutation may be related to thyroid cancer. Therefore, we constructed the NEB mutant mice for further investigation. MATERIAL AND METHODS The RNA extracted from the thyroid of wild-type and NEB mutant mice was analyzed by high-throughput sequencing, and the differential expression was analyzed by edgeR software. Several differentially expressed genes were selected for quantitative real-time PCR (qRT-PCR) verification, and these genes were analyzed with Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. RESULTS A total of 624 genes were significantly enriched. Analysis of GO function and pathway significant enrichment showed that differentially expressed genes were enriched in thyroid cancer, myocardial contraction, and autoimmune thyroid disease. The qRT-PCR results were consistent with the high-throughput sequencing results. CONCLUSIONS Our data indicate that the expression of some cancer-driving genes and cancer suppressor genes are significantly changed in NEB mutant mice compared to wild-type mice, which suggests that NEB function plays an important role in regulating the expression of cancer-related genes in the thyroid gland.

摘要

背景

对59例甲状腺癌患者的病理组织进行高通量测序,并与正常人群进行比较。发现甲状腺癌患者中肌动蛋白结合蛋白基因(NEB)第1133位氨基酸位点的突变频率远高于正常人群,提示NEB突变可能与甲状腺癌有关。因此,我们构建了NEB突变小鼠用于进一步研究。

材料与方法

对野生型和NEB突变小鼠甲状腺提取的RNA进行高通量测序分析,并用edgeR软件分析差异表达情况。选择几个差异表达基因进行定量实时PCR(qRT-PCR)验证,并用基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路分析这些基因。

结果

共624个基因显著富集。GO功能和通路显著富集分析表明,差异表达基因在甲状腺癌、心肌收缩和自身免疫性甲状腺疾病中富集。qRT-PCR结果与高通量测序结果一致。

结论

我们的数据表明,与野生型小鼠相比,NEB突变小鼠中一些癌症驱动基因和抑癌基因的表达发生了显著变化,这表明NEB功能在调节甲状腺中癌症相关基因的表达中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc2/7241215/7475f9e01b16/medscimonit-26-e922953-g001.jpg

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