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Expression Analysis of Ermin and Listerin E3 Ubiquitin Protein Ligase 1 Genes in Autistic Patients

Autism spectrum disorder (ASD) is a severe neurodevelopmental disorder that involves social interaction defects, impairment of non-verbal and verbal interactions, and limited interests along with stereotypic activities. Its incidence has been increasing rapidly in recent decades. Despite numerous at...

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Autores principales: Shiva, Shadi, Gharesouran, Jalal, Sabaie, Hani, Asadi, Mohammad Reza, Arsang-Jang, Shahram, Taheri, Mohammad, Rezazadeh, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326841/
https://www.ncbi.nlm.nih.gov/pubmed/34349621
http://dx.doi.org/10.3389/fnmol.2021.701977
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author Shiva, Shadi
Gharesouran, Jalal
Sabaie, Hani
Asadi, Mohammad Reza
Arsang-Jang, Shahram
Taheri, Mohammad
Rezazadeh, Maryam
author_facet Shiva, Shadi
Gharesouran, Jalal
Sabaie, Hani
Asadi, Mohammad Reza
Arsang-Jang, Shahram
Taheri, Mohammad
Rezazadeh, Maryam
author_sort Shiva, Shadi
collection PubMed
description Autism spectrum disorder (ASD) is a severe neurodevelopmental disorder that involves social interaction defects, impairment of non-verbal and verbal interactions, and limited interests along with stereotypic activities. Its incidence has been increasing rapidly in recent decades. Despite numerous attempts to understand the pathophysiology of ASD, its exact etiology is still unclear. Recent data shows the role of accurate myelination and translational regulation in ASD’s pathogenesis. In this study, we assessed Ermin (ERMN) and Listerin E3 Ubiquitin Protein Ligase 1 (LTN1) genes expression in Iranian ASD patients and age- and gender-matched healthy subjects’ peripheral blood using quantitative real-time PCR to recognize any probable dysregulation in the expression of these genes and propose this disorder’s mechanisms. Analysis of the expression demonstrated a significant ERMN downregulation in total ASD patients compared to the healthy individuals (posterior beta = −0.794, adjusted P-value = 0.025). LTN1 expression was suggestively higher in ASD patients in comparison with the corresponding control individuals. Considering the gender of study participants, the analysis showed that the mentioned genes’ different expression levels were significant only in male subjects. Besides, a significant correlation was found between expression of the mentioned genes (r = −0.49, P < 0.0001). The present study provides further supports for the contribution of ERMN and LTN1 in ASD’s pathogenesis.
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spelling pubmed-83268412021-08-03 Expression Analysis of Ermin and Listerin E3 Ubiquitin Protein Ligase 1 Genes in Autistic Patients Shiva, Shadi Gharesouran, Jalal Sabaie, Hani Asadi, Mohammad Reza Arsang-Jang, Shahram Taheri, Mohammad Rezazadeh, Maryam Front Mol Neurosci Neuroscience Autism spectrum disorder (ASD) is a severe neurodevelopmental disorder that involves social interaction defects, impairment of non-verbal and verbal interactions, and limited interests along with stereotypic activities. Its incidence has been increasing rapidly in recent decades. Despite numerous attempts to understand the pathophysiology of ASD, its exact etiology is still unclear. Recent data shows the role of accurate myelination and translational regulation in ASD’s pathogenesis. In this study, we assessed Ermin (ERMN) and Listerin E3 Ubiquitin Protein Ligase 1 (LTN1) genes expression in Iranian ASD patients and age- and gender-matched healthy subjects’ peripheral blood using quantitative real-time PCR to recognize any probable dysregulation in the expression of these genes and propose this disorder’s mechanisms. Analysis of the expression demonstrated a significant ERMN downregulation in total ASD patients compared to the healthy individuals (posterior beta = −0.794, adjusted P-value = 0.025). LTN1 expression was suggestively higher in ASD patients in comparison with the corresponding control individuals. Considering the gender of study participants, the analysis showed that the mentioned genes’ different expression levels were significant only in male subjects. Besides, a significant correlation was found between expression of the mentioned genes (r = −0.49, P < 0.0001). The present study provides further supports for the contribution of ERMN and LTN1 in ASD’s pathogenesis. Frontiers Media S.A. 2021-07-19 /pmc/articles/PMC8326841/ /pubmed/34349621 http://dx.doi.org/10.3389/fnmol.2021.701977 Text en Copyright © 2021 Shiva, Gharesouran, Sabaie, Asadi, Arsang-Jang, Taheri and Rezazadeh. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Shiva, Shadi
Gharesouran, Jalal
Sabaie, Hani
Asadi, Mohammad Reza
Arsang-Jang, Shahram
Taheri, Mohammad
Rezazadeh, Maryam
Expression Analysis of Ermin and Listerin E3 Ubiquitin Protein Ligase 1 Genes in Autistic Patients
title Expression Analysis of Ermin and Listerin E3 Ubiquitin Protein Ligase 1 Genes in Autistic Patients
title_full Expression Analysis of Ermin and Listerin E3 Ubiquitin Protein Ligase 1 Genes in Autistic Patients
title_fullStr Expression Analysis of Ermin and Listerin E3 Ubiquitin Protein Ligase 1 Genes in Autistic Patients
title_full_unstemmed Expression Analysis of Ermin and Listerin E3 Ubiquitin Protein Ligase 1 Genes in Autistic Patients
title_short Expression Analysis of Ermin and Listerin E3 Ubiquitin Protein Ligase 1 Genes in Autistic Patients
title_sort expression analysis of ermin and listerin e3 ubiquitin protein ligase 1 genes in autistic patients
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326841/
https://www.ncbi.nlm.nih.gov/pubmed/34349621
http://dx.doi.org/10.3389/fnmol.2021.701977
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