Miranda P J, Vimalraj S, Selvamurugan N
Department of Biotechnology, School of Bioengineering, SRM University, Kattankulathur, Tamil Nadu, India.
Department of Biotechnology, School of Bioengineering, SRM University, Kattankulathur, Tamil Nadu, India.
Int J Biol Macromol. 2015 Jan;72:145-50. doi: 10.1016/j.ijbiomac.2014.07.051. Epub 2014 Aug 20.
MicroRNAs (miRNAs) are small non coding RNA molecules (∼ 23 nt) that are capable of regulating several physiological and pathological processes by targeting mRNAs post transcriptionally, and miRNAs are also known to be regulated by their own target gene(s) in a feedback manner. In this study, we analysed the expression of miRNAs (pre-mir-93, pre-mir-20b, pre-mir-520 c, pre-mir-143, pre-mir-154 and pre-mir-590) by body map, an in silico method and by qRT-PCR in MDA-MB231 (highly invasive and metastatic in nature), and MCF-7 (poor invasive and metastatic in nature) cells. These miRNAs were down regulated in MDA-MB231 cells, and among these, miR-590 was found to putatively target activating transcription factor-3 (ATF-3), a stress response gene. ATF-3 expression level was significantly increased in MDA-MB231 cells and inhibition of ATF-3 expression in these cells increased the expression of pre-mir-590. Thus, these results suggest that there is a negative feedback expression of pre-mir-590 and its putative target gene, ATF-3 in human breast cancer cells.
微小RNA(miRNA)是一类小的非编码RNA分子(约23个核苷酸),能够通过转录后靶向mRNA来调控多种生理和病理过程,并且已知miRNA也会以反馈方式受其自身靶基因的调控。在本研究中,我们通过人体图谱(一种计算机方法)以及在MDA-MB231细胞(本质上具有高侵袭性和转移性)和MCF-7细胞(本质上侵袭性和转移性较差)中进行定量逆转录聚合酶链反应(qRT-PCR),分析了miRNA(前体miR-93、前体miR-20b、前体miR-520c、前体miR-143、前体miR-154和前体miR-590)的表达。这些miRNA在MDA-MB231细胞中表达下调,其中,发现miR-590可能靶向激活转录因子3(ATF-3),一个应激反应基因。ATF-3的表达水平在MDA-MB231细胞中显著升高,并且抑制这些细胞中ATF-3的表达会增加前体miR-590的表达。因此,这些结果表明在人乳腺癌细胞中前体miR-590与其推定的靶基因ATF-3之间存在负反馈表达。