Qiu Meiyu, Li Tao, Wang Binhu, Gong Hongbin, Huang Tao
College of Animal Science and Technology, Shihezi University, Shihezi 832000, China.
Institute of Biotechnology, Xinjiang Academy of Animal Science, Urumqi 830000, China.
Protein Pept Lett. 2020;27(5):411-418. doi: 10.2174/0929866526666190911142926.
microRNAs (miRNAs) are a small, endogenous non-coding RNAs that are involved in post-transcriptional gene regulation of many biological processes, including embryo implantation and placental development. In our previous study, miR-146a-5p was found expressed higher in the serum exosomes of pregnant sows than non-pregnant. The research on miR-146a-5p has been mainly related to human diseases, but there are few studies on its effects on the reproduction of sows in early pregnancy.
In this article, our motivation is to study the role of miR-146a-5p in the early pregnancy of sows on the cell proliferetion and apoptosis by targeting SMAD3 and SMAD4.
Bioinformatics software was used to identify the target genes of miR-146a-5p. The wildtype and mutant-type recombinant plasmids of dual-luciferase reporter with 3'-UTR of Smad3 or 3'- UTR of Smad4 were constructed, and co-transfected in porcine kidney cell (PK-15 cell) with miR- 146a-5p mimic, mimic-NC(M-NC), inhibitor and inhibitor-NC(IN-NC), then dual-luciferase activity analysis, qRT-PCR and Western blot were performed to verify the target genes. After the transfection of BeWo choriocarcinoma cell (BeWo cell) with miR-146a-5p mimic, M-NC, inhibitor and IN-NC, the mRNA expression of Caspase-3, BAX and Bcl-2 was measured using qRT-PCR, and the cell proliferation was measured using CCK-8 kit.
The luciferase, mRNA and protein expression of Smad3 in PK-15 cells treated by Smad3- 3'-UTR-W co-transfected with miR-146a-5p mimic were significantly lower than that with miR- 146a-5p M-NC, and the results of Smad4 were similar to Smad3, but the protein expression had a trend to lower in mimic group. The expression level of Bcl-2 in the miR-146a-5p mimic group was significantly lower than that in the miR-146a-5p M-NC group, but the expression pattern of Caspase-3 was just opposite. The mimic of miR-146a-5p reduced the proliferation of BeWo cells, however the inhibitor increased.
Smad3 and Smad4 are the direct target genes of miR-146a-5p. The expression of Smad3 and Smad4 were affected by the mimic and inhibitor of miR-146a-5p. miR-146a-5p affects cell apoptosis and proliferation by regulating their target genes. This study provided new data to understand the regulation mechanism of early pregnancy in sows.
微小RNA(miRNA)是一类小的内源性非编码RNA,参与许多生物学过程的转录后基因调控,包括胚胎着床和胎盘发育。在我们之前的研究中,发现miR-146a-5p在妊娠母猪血清外泌体中的表达高于未妊娠母猪。关于miR-146a-5p的研究主要与人类疾病相关,但对其在妊娠早期母猪繁殖方面的影响研究较少。
在本文中,我们旨在研究miR-146a-5p通过靶向SMAD3和SMAD4在母猪早期妊娠中对细胞增殖和凋亡的作用。
使用生物信息学软件鉴定miR-146a-5p的靶基因。构建带有Smad3的3'-UTR或Smad4的3'-UTR的双荧光素酶报告基因的野生型和突变型重组质粒,并与miR-146a-5p模拟物、模拟物对照(M-NC)、抑制剂和抑制剂对照(IN-NC)共转染到猪肾细胞(PK-15细胞)中,然后进行双荧光素酶活性分析、qRT-PCR和蛋白质印迹以验证靶基因。用miR-146a-5p模拟物、M-NC、抑制剂和IN-NC转染BeWo绒毛膜癌细胞(BeWo细胞)后,使用qRT-PCR检测Caspase-3、BAX和Bcl-2的mRNA表达,并使用CCK-8试剂盒检测细胞增殖。
与miR-146a-5p M-NC共转染Smad3-3'-UTR-W处理的PK-15细胞中,Smad3的荧光素酶、mRNA和蛋白质表达明显低于miR-146a-5p M-NC处理组,Smad4的结果与Smad3相似,但模拟物组蛋白质表达有降低趋势。miR-146a-5p模拟物组中Bcl-2的表达水平明显低于miR-146a-5p M-NC组,但Caspase-3的表达模式相反。miR-146a-5p模拟物降低了BeWo细胞的增殖,而抑制剂则增加了增殖。
Smad3和Smad4是miR-146a-5p的直接靶基因。miR-146a-5p的模拟物和抑制剂影响Smad3和Smad4的表达。miR-146a-5p通过调节其靶基因影响细胞凋亡和增殖。本研究为理解母猪早期妊娠的调控机制提供了新数据。