尿微量RNA分析表明斯里兰卡不明病因慢性肾脏疾病的表观遗传学调控。

Thanuri Edirithilake, Nishantha Nanayakkara, Xiao Xiao Lin, Patrick J Biggs, Rohana Chandrajith, Sampath Lokugalappatti, Saumya Wickramasinghe
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引用次数: 0

摘要

背景:据报道,斯里兰卡干旱地区的男性稻农患有病因不明的慢性肾病。这种疾病的确切病因尚未确定。遗传易感性被确定为CKDu的主要危险因素目的:在本研究中,小尿RNA在CKDu患者、健康的地方病和非地方病对照中具有特征。在研究人群中发现了不同表达的尿miRNA及其相关途径。方法:从Girandurukote(地方病)和Mawanella(非地方病)地区招募健康和患病的男性志愿者(n=9)。使用Illumina MiSeqTM对尿液小RNA进行纯化和测序。对序列跟踪文件进行了汇编和分析。鉴定了这三组中不同的前压miRNA,并进行了通路分析。结果:尿液样本中含有130623个序列,被鉴定为非编码RNA、PIWI相互作用RNA(piRNA)和miRNA。大约4%的小RNA读数代表miRNA,29%代表piRNA。总共409种miRNA在尿液中被释放。有趣的是,患病和地方病对照人群都显示出miRNA和piRNA的显著低表达。无论健康状况如何,地方病人群的miR-10a、miR-21、miR-148a和miR-30a水平均显著较低,这些miR-10a和miR-148a与几种环境毒素有关。结论:在患病和健康的地方病样本中,miRNA和piRNA表达的显著下调表明CKDu的表观遗传调控涉及遗传和环境相互作用。需要对特定的miRNA物种进行进一步的研究,以开发miRNA小组来识别对CKDu敏感的个体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Urinary MicroRNA Analysis Indicates an Epigenetic Regulation of Chronic Kidney Disease of Unknown Etiology in Sri Lanka.
BACKGROUND Chronic kidney disease of unknown etiology (CKDu) is reported among male paddy farmers in the dry zone of Sri Lanka. The exact cause of this disease remains undetermined. Genetic susceptibility is identified as a major risk factor for CKDu. OBJECTIVES In this study, small urinary RNAs were characterized in CKDu patients, healthy endemic and non-endemic controls. Differently expressed urinary miRNAs and their associated pathways were identified in the study population. METHODS Healthy and diseased male volunteers (n=9) were recruited from Girandurukotte (endemic) and Mawanella (non-endemic) districts. Urinary small RNAs were purified and sequenced using Illumina MiSeqTM. The sequence trace files were assembled and analyzed. Differentially expressed miRNAs among these three groups were identified and pathway analysis was conducted. RESULTS The urine samples contained 130,623 sequence reads identified as non-coding RNAs, PIWI-interacting RNAs (piRNA), and miRNAs. Approximately four percent of the total small RNA reads represented miRNA, and 29% represented piRNA. A total of 409 miRNA species were expressed in urine. Interestingly, both diseased and endemic controls population showed significantly low expression of miRNA and piRNA. Regardless of the health status, the endemic population expressed significantly low levels of miR-10a, miR-21, miR-148a, and miR-30a which have been linked with several environmental toxins. CONCLUSION Significant downregulation of miRNA and piRNA expression in both diseased and healthy endemic samples indicates an epigenetic regulation of CKDu involving genetic and environmental interaction. Further studies of specific miRNA species are required to develop a miRNA panel to identify individuals susceptible to CKDu.
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