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Effects of mutations in porcine miRNA-215 precursor sequences on miRNA-215 regulatory function

机译:miRNA-215前体序列突变对miRNA-215调节功能的影响

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MicroRNAs (miRNAs) play an important role in animal growth and disease development, and sequence variation in microRNAs can alter their functions. Herein, we explored the effects of mutations in the miRNA-215 precursor sequence on the miRNA-215 regulatory network and resistance to Escherichia coli (E. coli). Polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) was used to detect sequence variations in Sutai and Meishan pigs. The miR-192 precursor sequence was not mutated, but the miR-215 precursor included an AT insertion mutation at position 6 (start from the first base of the miR-215 precursor) and a C/T mutation at position 43. Wild-type (WT) and mutant miR-215 precursor expression vectors were constructed to investigate the effects of sequence variation on expression of miR-215 and its target genes DLG5 and ALCAM, cytokine levels and E. coli adhesion. Compared with the WT control group, cells harbouring the C/T mutant vector displayed reduced miR-215 expression, increased target gene expression, elevated cytokine levels and rising E. coli adhesion, whereas cells harbouring the AT insertion mutant vector were not significantly changed. The sequence variation in the miRNA-215 precursor may affect the miRNA-215 regulatory network, and alter the stability of intestinal epithelial cells (IPEC-J2 cells) and resistance to E. coli. Our findings provide guidance for future research on the regulatory mechanisms of miR-215 in porcine resistance to E. coli F18, and identifying effective genetic markers against this organism.
机译:MicroRNAS(miRNA)在动物生长和疾病开发中发挥着重要作用,MicroRNA的序列变异可以改变其功能。在此,我们探讨了MiRNA-215前体序列中的突变对miRNA-215调节网络和对大肠杆菌(大肠杆菌)的抗性的影响。聚合酶链反应 - 单链构象多态性(PCR-SSCP)用于检测Sutai和Meishan猪的序列变化。 miR-192前体序列未突变,但miR-215前体包括在位置6处的插入突变(从MiR-215前体的第一碱基开始)和在第43位的C / T突变。野生型(WT)和突变体MiR-215前体表达载体被构建以研究序列变异对miR-215表达的影响及其靶基因DLG5和Alcam,细胞因子水平和大肠杆菌粘附。与WT对照组相比,含C / T突变载体的细胞显示出降低的miR-215表达,增加靶基因表达,升高的细胞因子水平和升高的大肠杆菌粘附性,而携带AT插入突变体载体的细胞没有显着改变。 MiRNA-215前体的序列变异可能影响miRNA-215调节网络,并改变肠上皮细胞(IPEC-J2细胞)和抗大肠杆菌的稳定性。我们的调查结果为未来研究了对大肠杆菌F18的猪-215的调节机制的指导提供了指导,并鉴定了对该生物体的有效遗传标记。

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