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Common variants in GNL3 gene contributed the susceptibility of hand osteoarthritis in Han Chinese population
Osteoarthritis (OA) is one of the most popular degenerative joint diseases. The nucleolar GTP binding protein 3 ( GNL3 ) gene encodes guanine nucleotide binding protein-like 3, which is related in cell proliferation, differentiation, and cell cycle regulation. Our study aimed to examine the contribu...
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Published in: | Scientific reports 2022-09, Vol.12 (1), p.16110-16110, Article 16110 |
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description | Osteoarthritis (OA) is one of the most popular degenerative joint diseases. The nucleolar GTP binding protein 3 (
GNL3
) gene encodes guanine nucleotide binding protein-like 3, which is related in cell proliferation, differentiation, and cell cycle regulation. Our study aimed to examine the contribution of
GNL3
gene polymorphisms to the risk of hand OA and its related clinical features. A total of 3387 study participants including 1160 patients with hand OA and 2227 controls were recruited in this study. Eleven SNPs in
GNL3
gene were selected for genotyping. Genetic association signals were examined using Plink. Relationships between significant SNPs and clinical features of hand OA were also explored. SNP rs11177 was found to be strongly associated with susceptibility of hand OA (
P
= 4.32 × 10
–5
). The minor allele of rs11177 was associated with increased susceptibility of hand OA. In addition, significant associations were also identified between genotypes of rs11177 and clinical features of hand OA patients including K-L grade (
P
|
doi_str_mv | 10.1038/s41598-022-20287-4 |
format | article |
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GNL3
) gene encodes guanine nucleotide binding protein-like 3, which is related in cell proliferation, differentiation, and cell cycle regulation. Our study aimed to examine the contribution of
GNL3
gene polymorphisms to the risk of hand OA and its related clinical features. A total of 3387 study participants including 1160 patients with hand OA and 2227 controls were recruited in this study. Eleven SNPs in
GNL3
gene were selected for genotyping. Genetic association signals were examined using Plink. Relationships between significant SNPs and clinical features of hand OA were also explored. SNP rs11177 was found to be strongly associated with susceptibility of hand OA (
P
= 4.32 × 10
–5
). The minor allele of rs11177 was associated with increased susceptibility of hand OA. In addition, significant associations were also identified between genotypes of rs11177 and clinical features of hand OA patients including K-L grade (
P
< 0.01) and categorized pain scores (
P
< 0.01). Significant eQTL signals for rs11177 on
GNL3
in multiple types of human tissues were also identified in GTEx database. Our results have established the link between
GNL3
gene and susceptibility of hand OA.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-022-20287-4</identifier><identifier>PMID: 36167888</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>692/308/53/2423 ; 692/499 ; Arthritis ; Cell cycle ; Cell differentiation ; Cell proliferation ; Gene polymorphism ; Genotypes ; Genotyping ; GTP-binding protein ; Guanine ; Guanine nucleotide-binding protein ; Humanities and Social Sciences ; Joint diseases ; multidisciplinary ; Nucleoli ; Osteoarthritis ; Patients ; Science ; Science (multidisciplinary) ; Single-nucleotide polymorphism ; Susceptibility</subject><ispartof>Scientific reports, 2022-09, Vol.12 (1), p.16110-16110, Article 16110</ispartof><rights>The Author(s) 2022</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c517t-231158a07f4778fc3e7c84b50ea19fff7bfb0dff06cfd991875e9513061d1b8a3</citedby><cites>FETCH-LOGICAL-c517t-231158a07f4778fc3e7c84b50ea19fff7bfb0dff06cfd991875e9513061d1b8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2718494430/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2718494430?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids></links><search><creatorcontrib>Wang, Xi</creatorcontrib><creatorcontrib>Xiao, Lin</creatorcontrib><creatorcontrib>Wang, Zhiyuan</creatorcontrib><creatorcontrib>Zhi, Liqiang</creatorcontrib><creatorcontrib>Li, Qiang</creatorcontrib><title>Common variants in GNL3 gene contributed the susceptibility of hand osteoarthritis in Han Chinese population</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><description>Osteoarthritis (OA) is one of the most popular degenerative joint diseases. The nucleolar GTP binding protein 3 (
GNL3
) gene encodes guanine nucleotide binding protein-like 3, which is related in cell proliferation, differentiation, and cell cycle regulation. Our study aimed to examine the contribution of
GNL3
gene polymorphisms to the risk of hand OA and its related clinical features. A total of 3387 study participants including 1160 patients with hand OA and 2227 controls were recruited in this study. Eleven SNPs in
GNL3
gene were selected for genotyping. Genetic association signals were examined using Plink. Relationships between significant SNPs and clinical features of hand OA were also explored. SNP rs11177 was found to be strongly associated with susceptibility of hand OA (
P
= 4.32 × 10
–5
). The minor allele of rs11177 was associated with increased susceptibility of hand OA. In addition, significant associations were also identified between genotypes of rs11177 and clinical features of hand OA patients including K-L grade (
P
< 0.01) and categorized pain scores (
P
< 0.01). Significant eQTL signals for rs11177 on
GNL3
in multiple types of human tissues were also identified in GTEx database. Our results have established the link between
GNL3
gene and susceptibility of hand OA.</description><subject>692/308/53/2423</subject><subject>692/499</subject><subject>Arthritis</subject><subject>Cell cycle</subject><subject>Cell differentiation</subject><subject>Cell proliferation</subject><subject>Gene polymorphism</subject><subject>Genotypes</subject><subject>Genotyping</subject><subject>GTP-binding protein</subject><subject>Guanine</subject><subject>Guanine nucleotide-binding protein</subject><subject>Humanities and Social Sciences</subject><subject>Joint diseases</subject><subject>multidisciplinary</subject><subject>Nucleoli</subject><subject>Osteoarthritis</subject><subject>Patients</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Single-nucleotide polymorphism</subject><subject>Susceptibility</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kkFvFSEUhSdGY5vaP-CKxI2bUWBggI2JedG2yYtudE0Y5vKGlxl4AtOk_15806h1IRvI5dwvJyenaV4T_I7gTr7PjHAlW0xpSzGVomXPmkuKGW9pR-nzv94XzXXOR1wPp4oR9bK56HrSCynlZTPv4rLEgO5N8iaUjHxAN1_2HTpAAGRjKMkPa4ERlQlQXrOFU_GDn315QNGhyYQRxVwgmlSm5Is_I25NQLvJB8iATvG0zqb4GF41L5yZM1w_3lfN98-fvu1u2_3Xm7vdx31rORGlmiaES4OFY0JIZzsQVrKBYzBEOefE4AY8Ood760aliBQcFCcd7slIBmm6q-Zu447RHPUp-cWkBx2N1-dBTAdd3Xo7g7bjICgnjmE6MDMw1SmQ2IIzjGBDVWV92FindVhgtFATMfMT6NOf4Cd9iPe6OuJY8Ap4-whI8ccKuejF1xTn2QSIa9ZUEKl6ynlfpW_-kR7jmkKN6qxiirEOVxXdVDbFnBO432YI1r-6obdu6NoNfe6GZnWp25ZyFYcDpD_o_2z9BNhSvBU</recordid><startdate>20220927</startdate><enddate>20220927</enddate><creator>Wang, Xi</creator><creator>Xiao, Lin</creator><creator>Wang, Zhiyuan</creator><creator>Zhi, Liqiang</creator><creator>Li, Qiang</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><general>Nature Portfolio</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220927</creationdate><title>Common variants in GNL3 gene contributed the susceptibility of hand osteoarthritis in Han Chinese population</title><author>Wang, Xi ; Xiao, Lin ; Wang, Zhiyuan ; Zhi, Liqiang ; Li, Qiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c517t-231158a07f4778fc3e7c84b50ea19fff7bfb0dff06cfd991875e9513061d1b8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>692/308/53/2423</topic><topic>692/499</topic><topic>Arthritis</topic><topic>Cell cycle</topic><topic>Cell differentiation</topic><topic>Cell proliferation</topic><topic>Gene polymorphism</topic><topic>Genotypes</topic><topic>Genotyping</topic><topic>GTP-binding protein</topic><topic>Guanine</topic><topic>Guanine nucleotide-binding protein</topic><topic>Humanities and Social Sciences</topic><topic>Joint diseases</topic><topic>multidisciplinary</topic><topic>Nucleoli</topic><topic>Osteoarthritis</topic><topic>Patients</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Single-nucleotide polymorphism</topic><topic>Susceptibility</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Xi</creatorcontrib><creatorcontrib>Xiao, Lin</creatorcontrib><creatorcontrib>Wang, Zhiyuan</creatorcontrib><creatorcontrib>Zhi, Liqiang</creatorcontrib><creatorcontrib>Li, Qiang</creatorcontrib><collection>SpringerOpen</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals (Open Access)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Xi</au><au>Xiao, Lin</au><au>Wang, Zhiyuan</au><au>Zhi, Liqiang</au><au>Li, Qiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Common variants in GNL3 gene contributed the susceptibility of hand osteoarthritis in Han Chinese population</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><date>2022-09-27</date><risdate>2022</risdate><volume>12</volume><issue>1</issue><spage>16110</spage><epage>16110</epage><pages>16110-16110</pages><artnum>16110</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Osteoarthritis (OA) is one of the most popular degenerative joint diseases. The nucleolar GTP binding protein 3 (
GNL3
) gene encodes guanine nucleotide binding protein-like 3, which is related in cell proliferation, differentiation, and cell cycle regulation. Our study aimed to examine the contribution of
GNL3
gene polymorphisms to the risk of hand OA and its related clinical features. A total of 3387 study participants including 1160 patients with hand OA and 2227 controls were recruited in this study. Eleven SNPs in
GNL3
gene were selected for genotyping. Genetic association signals were examined using Plink. Relationships between significant SNPs and clinical features of hand OA were also explored. SNP rs11177 was found to be strongly associated with susceptibility of hand OA (
P
= 4.32 × 10
–5
). The minor allele of rs11177 was associated with increased susceptibility of hand OA. In addition, significant associations were also identified between genotypes of rs11177 and clinical features of hand OA patients including K-L grade (
P
< 0.01) and categorized pain scores (
P
< 0.01). Significant eQTL signals for rs11177 on
GNL3
in multiple types of human tissues were also identified in GTEx database. Our results have established the link between
GNL3
gene and susceptibility of hand OA.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>36167888</pmid><doi>10.1038/s41598-022-20287-4</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | PubMed (Medline); Full-Text Journals in Chemistry (Open access); Publicly Available Content (ProQuest); Springer Nature - nature.com Journals - Fully Open Access |
subjects | 692/308/53/2423 692/499 Arthritis Cell cycle Cell differentiation Cell proliferation Gene polymorphism Genotypes Genotyping GTP-binding protein Guanine Guanine nucleotide-binding protein Humanities and Social Sciences Joint diseases multidisciplinary Nucleoli Osteoarthritis Patients Science Science (multidisciplinary) Single-nucleotide polymorphism Susceptibility |
title | Common variants in GNL3 gene contributed the susceptibility of hand osteoarthritis in Han Chinese population |
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