GRK5 intronic (CA)n polymorphisms associated with type 2 diabetes in Chinese Hainan Island.

A genome-wide association study had showed G-protein-coupled receptor kinase 5 (GRK5) rs10886471 was related to the risk of type 2 diabetes mellitus (T2DM) through upregulated GRK5 mRNA expression. Rs10886471 is located in the intron region of GRK5. However, the mechanism by which intronic SNP affec...

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Main Authors: Zhenfang Xia, Tubao Yang, Zhuansuo Wang, Jianping Dong, Chunyan Liang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0090597&type=printable
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author Zhenfang Xia
Tubao Yang
Zhuansuo Wang
Jianping Dong
Chunyan Liang
author_facet Zhenfang Xia
Tubao Yang
Zhuansuo Wang
Jianping Dong
Chunyan Liang
author_sort Zhenfang Xia
collection DOAJ
description A genome-wide association study had showed G-protein-coupled receptor kinase 5 (GRK5) rs10886471 was related to the risk of type 2 diabetes mellitus (T2DM) through upregulated GRK5 mRNA expression. Rs10886471 is located in the intron region of GRK5. However, the mechanism by which intronic SNP affects gene expression remains unclear, whether the effect on gene expression depends on the intronic short tandem repeat (STR) (CA)n splicing regulator or not. Here we investigated the STR (CA)n polymorphism in rs10886471 and further discussed its role in the T2DM risk of Chinese Hainan Island individuals. A total of 1164 subjects were recruited and classified into a normal fasting glucose (NFG) group, an impaired fasting glucose (IFG) group, an impaired glucose tolerance (IGT) group, and a T2DM group. STR (CA)n polymorphisms were detected through polymerase chain reaction and sequencing. Five intronic (CA)n alleles, (CA)15 to (CA)19, were identified in GRK5 rs10886471. Only the (CA)16 allele was significantly associated with increased prediabetes and T2DM risk [odds ratio (OR)>1, P<0.05]. Conversely, multiple alleles without any (CA)16 protected against prediabetes and T2DM (0<OR<1, P<0.05). In summary, rs10886471 acts as both an SNP and an STR. The rs10886471 intronic SNP causes GRK5 overexpression the subsequent risk of T2DM may be due to the rs10886471 intronic STR (CA)n splicing enhancer. Further studies should focus on verifying these finding using a large sample size and analyzing the splicing mechanism of intronic (CA)n in rs10886471.
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spelling doaj-art-d62ad3437f9f455c95946d0963e596ab2025-08-20T02:15:23ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0193e9059710.1371/journal.pone.0090597GRK5 intronic (CA)n polymorphisms associated with type 2 diabetes in Chinese Hainan Island.Zhenfang XiaTubao YangZhuansuo WangJianping DongChunyan LiangA genome-wide association study had showed G-protein-coupled receptor kinase 5 (GRK5) rs10886471 was related to the risk of type 2 diabetes mellitus (T2DM) through upregulated GRK5 mRNA expression. Rs10886471 is located in the intron region of GRK5. However, the mechanism by which intronic SNP affects gene expression remains unclear, whether the effect on gene expression depends on the intronic short tandem repeat (STR) (CA)n splicing regulator or not. Here we investigated the STR (CA)n polymorphism in rs10886471 and further discussed its role in the T2DM risk of Chinese Hainan Island individuals. A total of 1164 subjects were recruited and classified into a normal fasting glucose (NFG) group, an impaired fasting glucose (IFG) group, an impaired glucose tolerance (IGT) group, and a T2DM group. STR (CA)n polymorphisms were detected through polymerase chain reaction and sequencing. Five intronic (CA)n alleles, (CA)15 to (CA)19, were identified in GRK5 rs10886471. Only the (CA)16 allele was significantly associated with increased prediabetes and T2DM risk [odds ratio (OR)>1, P<0.05]. Conversely, multiple alleles without any (CA)16 protected against prediabetes and T2DM (0<OR<1, P<0.05). In summary, rs10886471 acts as both an SNP and an STR. The rs10886471 intronic SNP causes GRK5 overexpression the subsequent risk of T2DM may be due to the rs10886471 intronic STR (CA)n splicing enhancer. Further studies should focus on verifying these finding using a large sample size and analyzing the splicing mechanism of intronic (CA)n in rs10886471.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0090597&type=printable
spellingShingle Zhenfang Xia
Tubao Yang
Zhuansuo Wang
Jianping Dong
Chunyan Liang
GRK5 intronic (CA)n polymorphisms associated with type 2 diabetes in Chinese Hainan Island.
PLoS ONE
title GRK5 intronic (CA)n polymorphisms associated with type 2 diabetes in Chinese Hainan Island.
title_full GRK5 intronic (CA)n polymorphisms associated with type 2 diabetes in Chinese Hainan Island.
title_fullStr GRK5 intronic (CA)n polymorphisms associated with type 2 diabetes in Chinese Hainan Island.
title_full_unstemmed GRK5 intronic (CA)n polymorphisms associated with type 2 diabetes in Chinese Hainan Island.
title_short GRK5 intronic (CA)n polymorphisms associated with type 2 diabetes in Chinese Hainan Island.
title_sort grk5 intronic ca n polymorphisms associated with type 2 diabetes in chinese hainan island
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0090597&type=printable
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