Downregulation of TGIF2 is possibly correlated with neuronal apoptosis and autism‐like symptoms in mice

Abstract Background TGFB‐induced factor homeobox 2 (TGIF2) has been reported to exert essential functions in brain development. This study aimed to elucidate the correlation of TGIF2 with autism, a neurodevelopmental condition which presents with severe communication problems. Methods An autism‐rela...

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Main Authors: Jing Lei, Yijue Deng, Songdong Ma
Format: Article
Language:English
Published: Wiley 2022-06-01
Series:Brain and Behavior
Subjects:
Online Access:https://doi.org/10.1002/brb3.2610
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author Jing Lei
Yijue Deng
Songdong Ma
author_facet Jing Lei
Yijue Deng
Songdong Ma
author_sort Jing Lei
collection DOAJ
description Abstract Background TGFB‐induced factor homeobox 2 (TGIF2) has been reported to exert essential functions in brain development. This study aimed to elucidate the correlation of TGIF2 with autism, a neurodevelopmental condition which presents with severe communication problems. Methods An autism‐related gene expression dataset GSE36315 was used to analyze aberrantly expressed genes in autistic brain tissues. Maternal mice were treated with valproate (VPA), and their offspring were selected as model mice with autism. The functions of TGIF2 in autism‐like symptoms in mice were examined by behavioral tests and histological examination of their hippocampal tissues. Mouse hippocampal neurons were extracted for in vitro studies. A gene set enrichment analysis was performed to analyze the signaling pathways involved, and the upstream factors influencing TGIF2 expression were explored in the ENCODE database and validated by ChIP‐qPCR assays. Results TGIF2 was poorly expressed in autistic patients in the GSE36315 dataset as well as in the temporal cortex tissues of autistic mice. Adenovirus‐mediated overexpression of TGIF2 suppressed autism‐like symptoms and neuronal apoptosis in autistic mice. TGIF2 activated the Wnt/β‐catenin signaling pathway. TGIF2 could be regulated by monomethylation of histone H3 Lys4 (H3K4me1). The histone demethylase LSD1 was highly expressed in the tissues of autistic mice and bound to TGIF2 promoter, which was possibly responsible for TGIF2 downregulation. Conclusion This research suggests that the downregulation of TGIF2, possibly regulated by LSD1/H3K4me1, is correlated with neuronal apoptosis and development of autism in mice through the inactivation of the Wnt/β‐catenin pathway.
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spelling doaj.art-3bc650205e724742838e7383c080f9c12023-08-04T11:01:02ZengWileyBrain and Behavior2162-32792022-06-01126n/an/a10.1002/brb3.2610Downregulation of TGIF2 is possibly correlated with neuronal apoptosis and autism‐like symptoms in miceJing Lei0Yijue Deng1Songdong Ma2Department of the Ninth Pediatrics Hunan Provincial People's Hospital (the First‐Affiliated Hospital of Hunan Normal University) Changsha P. R. ChinaDepartment of Graduate School Hunan University of Chinese Medicine Changsha P. R. ChinaHunan Provincial Key Laboratory of Pediatric Respirology Hunan Provincial People's Hospital (the First‐Affiliated Hospital of Hunan Normal University) Changsha P. R. ChinaAbstract Background TGFB‐induced factor homeobox 2 (TGIF2) has been reported to exert essential functions in brain development. This study aimed to elucidate the correlation of TGIF2 with autism, a neurodevelopmental condition which presents with severe communication problems. Methods An autism‐related gene expression dataset GSE36315 was used to analyze aberrantly expressed genes in autistic brain tissues. Maternal mice were treated with valproate (VPA), and their offspring were selected as model mice with autism. The functions of TGIF2 in autism‐like symptoms in mice were examined by behavioral tests and histological examination of their hippocampal tissues. Mouse hippocampal neurons were extracted for in vitro studies. A gene set enrichment analysis was performed to analyze the signaling pathways involved, and the upstream factors influencing TGIF2 expression were explored in the ENCODE database and validated by ChIP‐qPCR assays. Results TGIF2 was poorly expressed in autistic patients in the GSE36315 dataset as well as in the temporal cortex tissues of autistic mice. Adenovirus‐mediated overexpression of TGIF2 suppressed autism‐like symptoms and neuronal apoptosis in autistic mice. TGIF2 activated the Wnt/β‐catenin signaling pathway. TGIF2 could be regulated by monomethylation of histone H3 Lys4 (H3K4me1). The histone demethylase LSD1 was highly expressed in the tissues of autistic mice and bound to TGIF2 promoter, which was possibly responsible for TGIF2 downregulation. Conclusion This research suggests that the downregulation of TGIF2, possibly regulated by LSD1/H3K4me1, is correlated with neuronal apoptosis and development of autism in mice through the inactivation of the Wnt/β‐catenin pathway.https://doi.org/10.1002/brb3.2610autismepigeneticsH3K4me1LSD1TGIF2Wnt/β‐catenin
spellingShingle Jing Lei
Yijue Deng
Songdong Ma
Downregulation of TGIF2 is possibly correlated with neuronal apoptosis and autism‐like symptoms in mice
Brain and Behavior
autism
epigenetics
H3K4me1
LSD1
TGIF2
Wnt/β‐catenin
title Downregulation of TGIF2 is possibly correlated with neuronal apoptosis and autism‐like symptoms in mice
title_full Downregulation of TGIF2 is possibly correlated with neuronal apoptosis and autism‐like symptoms in mice
title_fullStr Downregulation of TGIF2 is possibly correlated with neuronal apoptosis and autism‐like symptoms in mice
title_full_unstemmed Downregulation of TGIF2 is possibly correlated with neuronal apoptosis and autism‐like symptoms in mice
title_short Downregulation of TGIF2 is possibly correlated with neuronal apoptosis and autism‐like symptoms in mice
title_sort downregulation of tgif2 is possibly correlated with neuronal apoptosis and autism like symptoms in mice
topic autism
epigenetics
H3K4me1
LSD1
TGIF2
Wnt/β‐catenin
url https://doi.org/10.1002/brb3.2610
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