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Elucidation of the Molecular Interaction between miRNAs and the HOXA9 Gene Involved in Acute Myeloid Leukemia by the Assistance of Argonaute Protein through a Computational Approach

机译:通过计算方法协助Argonaute蛋白阐明与急性髓性白血病有关的miRNA和HOXA9基因之间的分子相互作用

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摘要

Acute myeloid leukemia is a well characterized blood cancer in which the unnatural growth of immature white blood cell takes place, where several genes transcription is regulated by the micro RNAs (miRNAs). Argonaute (AGO) protein is a protein family that binds to the miRNAs and mRNA complex where a strong binding affinity is crucial for its RNA silencing function. By understanding pattern recognition between the miRNAs-mRNA complex and its binding affinity with AGO protein, one can decipher the regulation of a particular gene and develop suitable siRNA for the same in disease condition. In the current work, HOXA9 gene has been selected from literature, whose deregulation is well-established in acute myeloid leukemia. Four miRNAs (mir-145, mir-126, let-7a, and mir-196b) have been selected to target mRNA of HOXA9 (NCBI accession No. ). The binding interaction between mRNAs and mRNA of HOXA9 gene was studied computationally. From result, it was observed mir-145 has highest affinity for HOXA9 gene. Furthermore, the interaction between miRNAs-mRNA duplex of all chosen miRNAs are docked with AGO protein (PDB ID: 3F73, chain A) to study their interaction at molecular level through an in silico approach. The residual interaction and hydrogen bonding are inspected in Discovery Studio 3.5 suites. The current investigation throws light on understanding of AGO-assisted miRNA based gene silencing mechanism in HOXA9 gene associated in acute myeloid leukemia computationally.
机译:急性髓细胞性白血病是一种特征明确的血液癌,其中发生未成熟白细胞的不自然生长,其中一些基因的转录受微小RNA(miRNA)调节。 Argonaute(AGO)蛋白是一种与miRNA和mRNA复合物结合的蛋白家族,其中强大的结合亲和力对其RNA沉默功能至关重要。通过了解miRNAs-mRNA复合物之间的模式识别及其与AGO蛋白的结合亲和力,人们可以破译特定基因的调控,并针对疾病情况开发出适合其的siRNA。在当前的工作中,已从文献中选择了HOXA9基因,其在急性髓细胞性白血病中的失调作用已得到充分证实。已选择了四个miRNA(mir-145,mir-126,let-7a和mir-196b)靶向HOXA9的mRNA(NCBI登录号)。通过计算研究了HOXA9基因的mRNA与mRNA的结合相互作用。从结果可以看出,mir-145对HOXA9基因具有最高的亲和力。此外,所有选定miRNA的miRNA-mRNA双链体之间的相互作用都与AGO蛋白(PDB ID:3F73,链A)对接,以通过计算机方法研究它们在分子水平上的相互作用。在Discovery Studio 3.5套件中检查了残留的相互作用和氢键。当前的研究为计算急性髓细胞性白血病相关的HOXA9基因中基于AGO辅助miRNA的基因沉默机制提供了新的思路。

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