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Effects of HTR1B 3′ region polymorphisms and functional regions on gene expression regulation

BACKGROUND: The HTR1B gene encodes the 5-hydroxytryptamine (5-HT1B) receptor, which is involved in a variety of brain activities and mental disorders. The regulatory effects of non-coding regions on genomic DNA are one of many reasons for the cause of genetic-related diseases. Post-transcriptional r...

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Autores principales: Xia, Xi, Ding, Mei, Xuan, Jin-feng, Xing, Jia-xin, Pang, Hao, Yao, Jun, Wu, Xue, Wang, Bao-jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372893/
https://www.ncbi.nlm.nih.gov/pubmed/32689951
http://dx.doi.org/10.1186/s12863-020-00886-8
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author Xia, Xi
Ding, Mei
Xuan, Jin-feng
Xing, Jia-xin
Pang, Hao
Yao, Jun
Wu, Xue
Wang, Bao-jie
author_facet Xia, Xi
Ding, Mei
Xuan, Jin-feng
Xing, Jia-xin
Pang, Hao
Yao, Jun
Wu, Xue
Wang, Bao-jie
author_sort Xia, Xi
collection PubMed
description BACKGROUND: The HTR1B gene encodes the 5-hydroxytryptamine (5-HT1B) receptor, which is involved in a variety of brain activities and mental disorders. The regulatory effects of non-coding regions on genomic DNA are one of many reasons for the cause of genetic-related diseases. Post-transcriptional regulation that depends on the function of 3′ regulatory regions plays a particularly important role. This study investigated the effects, on reporter gene expression, of several haplotypes of the HTR1B gene (rs6297, rs3827804, rs140792648, rs9361234, rs76194807, rs58138557, and rs13212041) and truncated fragments in order to analyze the function of the 3′ region of HTR1B. RESULTS: We found that the haplotype, A-G-Del-C-T-Ins-A, enhanced the expression level compared to the main haplotype; A-G-Del-C-G-Ins-A; G-G-Del-C-G-Ins-G decreased the expression level. Two alleles, rs76194807T and rs6297G, exhibited different relative luciferase intensities compared to their counterparts at each locus. We also found that + 2440 ~ + 2769 bp and + 1953 ~ + 2311 bp regions both had negative effects on gene expression. CONCLUSIONS: The 3′ region of HTR1B has a regulatory effect on gene expression, which is likely closely associated with the interpretation of HTR1B-related disorders. In addition, the HTR1B 3′ region includes several effector binding sites that induce an inhibitory effect on gene expression.
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spelling pubmed-73728932020-07-21 Effects of HTR1B 3′ region polymorphisms and functional regions on gene expression regulation Xia, Xi Ding, Mei Xuan, Jin-feng Xing, Jia-xin Pang, Hao Yao, Jun Wu, Xue Wang, Bao-jie BMC Genet Research Article BACKGROUND: The HTR1B gene encodes the 5-hydroxytryptamine (5-HT1B) receptor, which is involved in a variety of brain activities and mental disorders. The regulatory effects of non-coding regions on genomic DNA are one of many reasons for the cause of genetic-related diseases. Post-transcriptional regulation that depends on the function of 3′ regulatory regions plays a particularly important role. This study investigated the effects, on reporter gene expression, of several haplotypes of the HTR1B gene (rs6297, rs3827804, rs140792648, rs9361234, rs76194807, rs58138557, and rs13212041) and truncated fragments in order to analyze the function of the 3′ region of HTR1B. RESULTS: We found that the haplotype, A-G-Del-C-T-Ins-A, enhanced the expression level compared to the main haplotype; A-G-Del-C-G-Ins-A; G-G-Del-C-G-Ins-G decreased the expression level. Two alleles, rs76194807T and rs6297G, exhibited different relative luciferase intensities compared to their counterparts at each locus. We also found that + 2440 ~ + 2769 bp and + 1953 ~ + 2311 bp regions both had negative effects on gene expression. CONCLUSIONS: The 3′ region of HTR1B has a regulatory effect on gene expression, which is likely closely associated with the interpretation of HTR1B-related disorders. In addition, the HTR1B 3′ region includes several effector binding sites that induce an inhibitory effect on gene expression. BioMed Central 2020-07-20 /pmc/articles/PMC7372893/ /pubmed/32689951 http://dx.doi.org/10.1186/s12863-020-00886-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Xia, Xi
Ding, Mei
Xuan, Jin-feng
Xing, Jia-xin
Pang, Hao
Yao, Jun
Wu, Xue
Wang, Bao-jie
Effects of HTR1B 3′ region polymorphisms and functional regions on gene expression regulation
title Effects of HTR1B 3′ region polymorphisms and functional regions on gene expression regulation
title_full Effects of HTR1B 3′ region polymorphisms and functional regions on gene expression regulation
title_fullStr Effects of HTR1B 3′ region polymorphisms and functional regions on gene expression regulation
title_full_unstemmed Effects of HTR1B 3′ region polymorphisms and functional regions on gene expression regulation
title_short Effects of HTR1B 3′ region polymorphisms and functional regions on gene expression regulation
title_sort effects of htr1b 3′ region polymorphisms and functional regions on gene expression regulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372893/
https://www.ncbi.nlm.nih.gov/pubmed/32689951
http://dx.doi.org/10.1186/s12863-020-00886-8
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