[Screening and identification of key miRNAs in post-transcriptional regulation of CART in the bovine hypothalamus].

Q4 Biochemistry, Genetics and Molecular Biology
Junli Cheng, Junrong Yan, Shuning Hou, Zhiwei Zhu, Pengfei Li
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引用次数: 0

Abstract

This study aimed to explore the roles of microRNAs (miRNAs) in the post-transcriptional regulation of cocaine- and amphetamine-regulated transcript (CART) peptide in the bovine hypothalamus and to screen key regulatory miRNAs. Targetscan was used to predict the potential miRNAs binding to CART 3' untranslated regions (3'UTR). Bioinformatics analysis predicted 7 miRNA binding sites in the bovine CART 3'UTR, which were bta-miR-377, bta-miR-331-3p, bta-miR-491, bta-miR-493, bta-miR-758, bta-miR-877, and bta-miR-381, respectively. Reverse transcription-PCR (RT-PCR) was carried out to determine the endogenous expression of CART and target miRNAs in the bovine hypothalamus. All the 7 target miRNAs and CART were endogenously expressed in the bovine hypothalamus. The dual-luciferase reporter gene assay was employed to detect the targeted binding relationship between CART 3'UTR and target miRNAs obtained from bioinformatics analysis. The dual-luciferase reporter gene assay confirmed that the 3'UTR of CART had a targeted binding relationship with the 7 target miRNAs. Cell experiments were conducted to examine the effects of target miRNAs on the messenger RNA (mRNA) and protein levels of exogenous CART and screen for key regulatory miRNAs. The results of cell experiments showed that the 7 miRNAs downregulated the mRNA level of CART, with bta-miR-491 demonstrating the strongest downregulating effect. Bta-miR-377, bta-miR-331-3p, bta-miR-491, bta-miR-493, and bta-miR-381 downregulated the protein level of CART, with bta-miR-381 exerting the strongest downregulating effect. Animal experiments were conducted to explore the effects of key regulatory miRNAs on the mRNA and protein levels of CART in the hypothalamus and the CART concentration in the serum. The results from animal experiments showed that miR-491 and miR-381 regulated the endogenous expression of CART in the hypothalamus and the concentration in the serum by binding to the CART 3'UTR. These results suggest that miR-491 and miR-381 are the main miRNAs regulating CART expression in the bovine hypothalamus, which can affect serum CART concentration by modulating endogenous CART expression.

牛下丘脑CART转录后调控关键mirna的筛选与鉴定。
本研究旨在探讨microRNAs (miRNAs)在牛下丘脑可卡因和安非他明调节转录本(CART)肽转录后调控中的作用,并筛选关键调控miRNAs。Targetscan用于预测与CART 3‘非翻译区(3’ utr)结合的潜在mirna。生物信息学分析预测了牛CART 3'UTR中的7个miRNA结合位点,分别是bta-miR-377、bta-miR-331-3p、bta-miR-491、bta-miR-493、bta-miR-758、bta-miR-877和bta-miR-381。采用逆转录- pcr (RT-PCR)检测牛下丘脑中CART及靶mirna的内源性表达。这7种靶mirna和CART均在牛下丘脑内源性表达。采用双荧光素酶报告基因法检测CART 3’utr与生物信息学分析得到的靶mirna的靶向结合关系。双荧光素酶报告基因检测证实CART的3'UTR与7个靶mirna存在靶向结合关系。通过细胞实验检测靶mirna对外源CART信使RNA (mRNA)和蛋白水平的影响,筛选关键调控mirna。细胞实验结果显示,这7种miRNAs均下调了CART的mRNA水平,其中bta-miR-491的下调作用最强。Bta-miR-377、bta-miR-331-3p、bta-miR-491、bta-miR-493、bta-miR-381下调CART蛋白水平,其中bta-miR-381下调作用最强。通过动物实验探讨关键调控mirna对下丘脑中CART mRNA和蛋白水平及血清中CART浓度的影响。动物实验结果表明,miR-491和miR-381通过结合CART 3'UTR调节下丘脑内源性CART的表达和血清浓度。这些结果表明,miR-491和miR-381是调节牛下丘脑中CART表达的主要mirna,它们可以通过调节内源性CART表达来影响血清中CART的浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Sheng wu gong cheng xue bao = Chinese journal of biotechnology
Sheng wu gong cheng xue bao = Chinese journal of biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
1.50
自引率
0.00%
发文量
298
期刊介绍: Chinese Journal of Biotechnology (Chinese edition) , sponsored by the Institute of Microbiology, Chinese Academy of Sciences and the Chinese Society for Microbiology, is a peer-reviewed international journal. The journal is cited by many scientific databases , such as Chemical Abstract (CA), Biology Abstract (BA), MEDLINE, Russian Digest , Chinese Scientific Citation Index (CSCI), Chinese Journal Citation Report (CJCR), and Chinese Academic Journal (CD version). The Journal publishes new discoveries, techniques and developments in genetic engineering, cell engineering, enzyme engineering, biochemical engineering, tissue engineering, bioinformatics, biochips and other fields of biotechnology.
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