Yurikova O Yu, Aisina D E, Niyazova R E, Atambayeva Sh A, Labeit S, Ivashchenko A T
Scientific Research Institute of Biology and Biotechnology Problems, al-Farabi Kazakh National University, Almaty, 050040 Kazakhstan.
Institute for Anaesthesiology and Intensive Operative Care Medical Faculty Mannheim, Mannheim, 68135 Germany.
Mol Biol (Mosk). 2019 Jul-Aug;53(4):692-704. doi: 10.1134/S0026898419040189.
miRNAs regulate the expression of many genes and are involved in the development of diseases. We studied miRNAs that interact partly or fully complementarily with the 5'UTR, CDS and 3'UTR of mRNAs of target genes. The MirTarget program used in this study allows for the discovery of miRNA binding sites (BS) in the entire nucleotide sequence of the mRNA and for determining the characteristics of the interactions of miRNAs with mRNAs. We identified five pairs of fully complementary BS for miR-127-5p and miR-127-3p, miR-136-5p and miR-136-3p, miR-431-5p and miR-431-3p, miR-432-5p and miR-432-3p, and miR-433-5p and miR-433-3p in the CDS of the human and animal mRNA of RTL1 gene. The fully complementary BS for miR-6720-5p, miR-6720-3p were identified in the CDS of the FOXF2 gene; BS for miR-3187-5p, miR-3187-3p were found in the CDS of the PLPPR3 gene; BS for miR-4665-5p, miR-4665-3p were found in the 5'UTR of the KIAA2026 gene; BS for miR-135a-5p, miR-135a-3p were found in the 3'UTR of the GLYCTK gene; BS for miR-7106-5p, miR-7106-3p were found in the 3'UTR of the CCDC42B gene. The miRNA-5p and miRNA-3p associated with the RTL1 gene have BS in the mRNAs of 32 target human genes. The miRNA-5p and miRNA-3p associated with the FOXF2, PLPPR3, KIAA2026, GLYCTK and CCDC42B genes have BS in the mRNAs of 27 target genes, involved in development of several diseases. Nucleotide sequences of miRNA-5p and miRNA-3p and BS are conserved over tens of millions of years of divergence of the studied animal species. Binding characteristics of miR-3120-3p and miR-3120-5p, miR-196b-3p and miR-196b-5p, miR-125a-3p and miR-125a-3p, let-7e-3p and let-7e-5p, miR-99b-3p in fully complementary BS of non-coding DMN3OS, HOXA10-AS, SPACA6P-AS genes have been established.
微小RNA(miRNA)调控许多基因的表达,并参与疾病的发生发展。我们研究了与靶基因mRNA的5'非翻译区(UTR)、编码区(CDS)和3'UTR部分或完全互补相互作用的miRNA。本研究中使用的MirTarget程序可在mRNA的整个核苷酸序列中发现miRNA结合位点(BS),并确定miRNA与mRNA相互作用的特征。我们在RTL1基因的人类和动物mRNA的编码区中鉴定出五对完全互补的miR-127-5p与miR-127-3p、miR-136-5p与miR-136-3p、miR-431-5p与miR-431-3p、miR-432-5p与miR-432-3p以及miR-433-5p与miR-433-3p的结合位点。在FOXF2基因的编码区中鉴定出miR-6720-5p与miR-6720-3p的完全互补结合位点;在PLPPR3基因的编码区中发现miR-3187-5p与miR-3187-3p的结合位点;在KIAA2026基因的5'UTR中发现miR-4665-5p与miR-4665-3p的结合位点;在GLYCTK基因的3'UTR中发现miR-135a-5p与miR-135a-3p的结合位点;在CCDC42B基因的3'UTR中发现miR-7106-5p与miR-7106-3p的结合位点。与RTL1基因相关的miRNA-5p和miRNA-3p在32个靶人类基因的mRNA中有结合位点。与FOXF2、PLPPR3、KIAA2026、GLYCTK和CCDC42B基因相关的miRNA-5p和miRNA-3p在27个靶基因的mRNA中有结合位点,这些靶基因参与多种疾病的发生发展。在所研究的动物物种经过数千万年分化后,miRNA-5p和miRNA-3p的核苷酸序列以及结合位点是保守的。已确定了miR-3120-3p与miR-3120-5p、miR-196b-3p与miR-196b-5p、miR-125a-3p与miR-125a-3p、let-7e-3p与let-7e-5p、miR-99b-3p在非编码DMN3OS、HOXA10-AS、SPACA6P-AS基因的完全互补结合位点中的结合特性。