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Sequence-based analysis of 5 ' UTR and coding regions of CASP3 in terms of miRSNPs and SNPs in targetting miRNAs

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dc.contributor.author Ergun, Sercan
dc.contributor.author Oztuzcu, Serdar
dc.date.accessioned 2022-08-16T11:55:08Z
dc.date.available 2022-08-16T11:55:08Z
dc.date.issued 2016
dc.identifier.uri http://doi.org/10.1016/j.compbiolchem.2016.04.003
dc.identifier.uri https://www.sciencedirect.com/science/article/pii/S1476927116301700?via%3Dihub
dc.identifier.uri http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2047
dc.description.abstract Apoptosis is described as a mechanism of cell death occurring after adequate cellular harm. Deregulation of apoptosis occurs in many human conditions such as autoimmune disorders, ischemic damage, neurodegenerative diseases and different cancer types. Information relating miRNAs to cancer is increasing. miRNAs can affect development of cancer via many different pathways, including apoptosis. Polymorphisms in miRNA genes or miRNA target sites (miRSNPs) can change miRNA activity. Although polymorphisms in miRNA genes are very uncommon, SNP5 in miRNA-binding sites of target genes are quite common. Many researches have revealed that SNP5 in miRNA target sites improve or decrease the efficacy of the interaction between miRNAs and their target genes. Our aim was to specify miRSNPs on CASP3 gene (caspase-3) and SNPs in miRNA genes targeting 5'UTR and coding exons of CASP3, and evaluate the effect of these miRSNPs and SNP5 of miRNA genes with respect to apoptosis. We detected 141 different miRNA binding sites (126 different miRNAs) and 7 different SNP5 in binding sites of miRNA in 5'UTR and CDS of CASP3 gene. Intriguingly, miR-339-3p's binding site on CASP3 has a SNP (rs35372903, G/A) on CASP3 5'UTR and its genomic sequence has a SNP (rs565188493, G/A) at the same nucleotide with rs35372903. Also, miR-339-3p has two other SNPs (rs373011663, C/T rs72631820, A/G) of which the first is positioned at the binding site. Here, miRSNP (rs35372903) at CASP3 5'UTR and SNP (rs565188493) at miR-339-3p genomic sequence cross-matches at the same site of binding region. Besides, miR-339-3p targets many apoptosis related genes (ZNF346, TAOK2, PIM2, HIP1, BBC3, TNFRSF25, CLCF1, IHPK2, NOL3) although it had no apoptosis related interaction proven before. This means that miR-339-3p may also have a critical effect on apoptosis via different pathways other than caspase-3. Hence, we can deduce that this is the first study demonstrating a powerful association between miR-339-3p and apoptosis upon computational analysis. (C) 2016 Elsevier Ltd. All rights reserved. en_US
dc.language.iso eng en_US
dc.publisher ELSEVIER SCI LTD, THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND en_US
dc.relation.isversionof 10.1016/j.compbiolchem.2016.04.003 en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Caspase-3; Apoptosis; miRSNP; 5 ' UTR region; Coding region en_US
dc.subject EMERGING ROLES; APOPTOSIS; MICRORNAS; CANCER; PROLIFERATION; EXPRESSION; RAT en_US
dc.title Sequence-based analysis of 5 ' UTR and coding regions of CASP3 in terms of miRSNPs and SNPs in targetting miRNAs en_US
dc.type article en_US
dc.relation.journal COMPUTATIONAL BIOLOGY AND CHEMISTRY en_US
dc.contributor.department Ordu Üniversitesi en_US
dc.contributor.authorID 0000-0002-6733-9848 en_US
dc.identifier.volume 62 en_US
dc.identifier.startpage 70 en_US
dc.identifier.endpage 74 en_US


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