Dai Qiu, Zhao Jue, Qi Xiaozhe, Xu Wentao, He Xiaoyun, Guo Mingzhang, Dweep Harsh, Cheng Wen-Hsing, Luo Yunbo, Xia Kai, Gretz Norbert, Huang Kunlun
Laboratory of food safety and molecular biology, College of Food Science and Nutritional Engineering, China Agricultural University, 302 box, No,17, Qinghua East Rd, Beijing, Haidian District 100083, P R China.
BMC Genomics. 2014 May 5;15(1):333. doi: 10.1186/1471-2164-15-333.
Nephrotoxicity is the most prominent one among the various toxicities of ochratoxin A (OTA). MicroRNAs (miRNAs) are small non-coding RNAs that have an impact on a wide range of biological processes by regulating gene expression at post-transcriptional level or protein systhesis level. The objective of this study is to analyze miRNA profiling in the kidneys of rats gavaged with OTA.
To profile miRNAs in the kidneys of rats with OTA nephrotoxicity, high-throughput sequencing and bioinformatics approaches were applied to analyze the miRNAs in the kidney of rats following OTA treatment. A total of 409 known miRNAs and 8 novel miRNAs were identified in the kidney and the levels of the novel miRNAs were varied in response to different doses of OTA. Expression of miR-129, miR-130a, miR-130b, miR-141, miR-218b and miR-3588 were uniquely suppressed in mid dose but then elevated in high dose, with opposite expression to their target genes. The expression pattern was closely related with the "MAPK signaling pathway". Dicer1 and Drosha were significantly suppressed, indicating an impairment of miRNA biogenesis in response to OTA.
The abrogation of miRNA maturation process suggests a new target of OTA toxicity. Moreover, the identification of the differentially expressed miRNAs provides us a molecular insight into the nephrtoxicity of OTA.
肾毒性是赭曲霉毒素A(OTA)多种毒性中最突出的一种。微小RNA(miRNA)是一类小的非编码RNA,通过在转录后水平或蛋白质合成水平调节基因表达,对广泛的生物学过程产生影响。本研究的目的是分析经OTA灌胃的大鼠肾脏中的miRNA谱。
为了分析OTA肾毒性大鼠肾脏中的miRNA,采用高通量测序和生物信息学方法分析OTA处理后大鼠肾脏中的miRNA。在肾脏中总共鉴定出409种已知的miRNA和8种新的miRNA,并且新miRNA的水平因不同剂量的OTA而有所变化。miR-129、miR-130a、miR-130b、miR-141、miR-218b和miR-3588的表达在中剂量时被独特地抑制,但在高剂量时升高,与其靶基因的表达相反。这种表达模式与“丝裂原活化蛋白激酶信号通路”密切相关。Dicer1和Drosha被显著抑制,表明OTA导致miRNA生物合成受损。
miRNA成熟过程的废除提示了OTA毒性的一个新靶点。此外,差异表达miRNA的鉴定为我们深入了解OTA的肾毒性提供了分子层面的认识。