Predicting the possible effect of miR-203a-3p and miR-29a-3p on DNMT3B and GAS7 genes expression

Aberrant expression of genes involved in methylation, including DNA methyltransferase 3 Beta (DNMT3B), can cause hypermethylation of various tumor suppressor genes. In this regard, various molecular factors such as microRNAs can play a critical role in regulating these methyltransferase enzymes and...

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Main Authors: Ali Afgar, Mahla Sattarzadeh Bardsiri, Reza Vahidi, Alireza Farsinejad
Format: Article
Language:English
Published: De Gruyter 2021-12-01
Series:Journal of Integrative Bioinformatics
Subjects:
Online Access:https://doi.org/10.1515/jib-2021-0016
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author Ali Afgar
Mahla Sattarzadeh Bardsiri
Reza Vahidi
Alireza Farsinejad
author_facet Ali Afgar
Mahla Sattarzadeh Bardsiri
Reza Vahidi
Alireza Farsinejad
author_sort Ali Afgar
collection DOAJ
description Aberrant expression of genes involved in methylation, including DNA methyltransferase 3 Beta (DNMT3B), can cause hypermethylation of various tumor suppressor genes. In this regard, various molecular factors such as microRNAs can play a critical role in regulating these methyltransferase enzymes and eventually downstream genes such as growth arrest specific 7 (GAS7). Accordingly, in the present study we aimed to predict regulatory effect of miRNAs on DNMT3B and GAS7 genes expression in melanoma cell line. hsa-miR-203a-3p and hsa-miR-29a-3p were predicted and selected using bioinformatics software. The Real-time PCR technique was performed to investigate the regulatory effect of these molecules on the DNMT3B and GAS7 genes expression. Expression analysis of DNMT3B gene in A375 cell line showed that there was a significant increase compared to control (p value = 0.0015). Analysis of hsa-miR-203a-3p and hsa-miR-29a-3p indicated the insignificant decreased expression in melanoma cell line compared to control (p value < 0.05). Compared to control, the expression of GAS7 gene in melanoma cells showed a significant decrease (p value = 0.0323). Finally, our findings showed that the decreased expression of hsa-miR-203a-3p and hsa-miR-29a-3p can hypothesize that their aberrant expression caused DNMT3B dysfunction, possible methylation of the GAS7 gene, and ultimately decreased its expression. However, complementary studies are necessary to definite comment.
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spelling doaj.art-4bf562def10a40c784bac4372f4771a12022-12-21T23:15:00ZengDe GruyterJournal of Integrative Bioinformatics1613-45162021-12-011911121110.1515/jib-2021-0016Predicting the possible effect of miR-203a-3p and miR-29a-3p on DNMT3B and GAS7 genes expressionAli Afgar0Mahla Sattarzadeh Bardsiri1Reza Vahidi2Alireza Farsinejad3Research Center for Hydatid Disease in Iran, Kerman University of Medical Sciences, Kerman, IranStudent Research Committee, Faculty of Allied Medicine, Kerman University of Medical Sciences, Kerman, IranResearch Center for Hydatid Disease in Iran, Kerman University of Medical Sciences, Kerman, IranDepartment of Hematology and Medical Laboratory Sciences, Faculty of Allied Medicine, Kerman University of Medical Sciences, Kerman, IranAberrant expression of genes involved in methylation, including DNA methyltransferase 3 Beta (DNMT3B), can cause hypermethylation of various tumor suppressor genes. In this regard, various molecular factors such as microRNAs can play a critical role in regulating these methyltransferase enzymes and eventually downstream genes such as growth arrest specific 7 (GAS7). Accordingly, in the present study we aimed to predict regulatory effect of miRNAs on DNMT3B and GAS7 genes expression in melanoma cell line. hsa-miR-203a-3p and hsa-miR-29a-3p were predicted and selected using bioinformatics software. The Real-time PCR technique was performed to investigate the regulatory effect of these molecules on the DNMT3B and GAS7 genes expression. Expression analysis of DNMT3B gene in A375 cell line showed that there was a significant increase compared to control (p value = 0.0015). Analysis of hsa-miR-203a-3p and hsa-miR-29a-3p indicated the insignificant decreased expression in melanoma cell line compared to control (p value < 0.05). Compared to control, the expression of GAS7 gene in melanoma cells showed a significant decrease (p value = 0.0323). Finally, our findings showed that the decreased expression of hsa-miR-203a-3p and hsa-miR-29a-3p can hypothesize that their aberrant expression caused DNMT3B dysfunction, possible methylation of the GAS7 gene, and ultimately decreased its expression. However, complementary studies are necessary to definite comment.https://doi.org/10.1515/jib-2021-0016bioinformaticsdnmt3b genegas7 genemelanomamicrornas
spellingShingle Ali Afgar
Mahla Sattarzadeh Bardsiri
Reza Vahidi
Alireza Farsinejad
Predicting the possible effect of miR-203a-3p and miR-29a-3p on DNMT3B and GAS7 genes expression
Journal of Integrative Bioinformatics
bioinformatics
dnmt3b gene
gas7 gene
melanoma
micrornas
title Predicting the possible effect of miR-203a-3p and miR-29a-3p on DNMT3B and GAS7 genes expression
title_full Predicting the possible effect of miR-203a-3p and miR-29a-3p on DNMT3B and GAS7 genes expression
title_fullStr Predicting the possible effect of miR-203a-3p and miR-29a-3p on DNMT3B and GAS7 genes expression
title_full_unstemmed Predicting the possible effect of miR-203a-3p and miR-29a-3p on DNMT3B and GAS7 genes expression
title_short Predicting the possible effect of miR-203a-3p and miR-29a-3p on DNMT3B and GAS7 genes expression
title_sort predicting the possible effect of mir 203a 3p and mir 29a 3p on dnmt3b and gas7 genes expression
topic bioinformatics
dnmt3b gene
gas7 gene
melanoma
micrornas
url https://doi.org/10.1515/jib-2021-0016
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