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常见 PAX9 变异与非综合征东亚人群恒牙大小变异的关联。

Association of common PAX9 variants with permanent tooth size variation in non-syndromic East Asian populations.

机构信息

Department of Orthodontics, Pusan National University Dental Hospital, Kyeongsangnamdo, Korea.

出版信息

J Hum Genet. 2012 Oct;57(10):654-9. doi: 10.1038/jhg.2012.90. Epub 2012 Jul 19.


DOI:10.1038/jhg.2012.90
PMID:22810112
Abstract

Studies on the heredity of dental characteristics in humans have indicated that the variance in many dental traits results from genetic variation. However, the genetic factors that influence commonly occurring dental variants are poorly understood. Paired domain box 9 (PAX9) codes a transcription factor that is important in tooth development. We investigated whether PAX9 polymorphisms are associated with normal variations in tooth agenesis and morphology. The study subjects were 273 Japanese and 223 Korean adults. Single-nucleotide polymorphisms (SNPs) in PAX9 (rs2295222, rs4904155, rs2073244, rs12881240 and rs4904210) were genotyped, and third molar agenesis and mesiodistal and buccolingual diameters were measured. We found that four of the five SNPs were significantly associated with the crown size. However, no SNP was associated with third molar agenesis. In additional analyses on non-metric dental traits, we found significant associations of PAX9 SNPs with shoveling of upper first incisors. In summary, common variants in PAX9 contributed to morphological variation in permanent teeth in humans.

摘要

人类牙齿特征遗传研究表明,许多牙齿特征的差异是由遗传变异引起的。然而,影响常见牙齿变异的遗传因素还了解甚少。配对盒基因 9(PAX9)编码一种在牙齿发育中起重要作用的转录因子。我们研究了 PAX9 多态性是否与牙齿缺失和形态的正常变异有关。研究对象为 273 名日本人和 223 名韩国成年人。对 PAX9 中的单核苷酸多态性(rs2295222、rs4904155、rs2073244、rs12881240 和 rs4904210)进行了基因分型,并测量了第三磨牙缺失情况以及近远中径和颊舌径。我们发现这 5 个 SNP 中的 4 个与牙冠大小显著相关。然而,没有 SNP 与第三磨牙缺失有关。在对非计量牙齿特征的进一步分析中,我们发现 PAX9 SNP 与上颌侧切牙铲形的发生显著相关。总之,PAX9 中的常见变异导致了人类恒牙形态的变异。

相似文献

[1]
Association of common PAX9 variants with permanent tooth size variation in non-syndromic East Asian populations.

J Hum Genet. 2012-7-19

[2]
PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China.

J Appl Oral Sci. 2013

[3]
Novel PAX9 gene polymorphisms and mutations and susceptibility to tooth agenesis in the Czech population.

Neuro Endocrinol Lett. 2015

[4]
Associations between the risk of tooth agenesis and single-nucleotide polymorphisms of MSX1 and PAX9 genes in nonsyndromic cleft patients.

Angle Orthod. 2013-5-29

[5]
Family-based association study of genetic analysis of paired box gene 9 polymorphisms in the peg-shaped teeth in the Jordanian Arab population.

Arch Oral Biol. 2021-1

[6]
Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis.

Eur J Med Genet. 2016-8

[7]
Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype.

J Dent Res. 2017-9-14

[8]
PAX-9 polymorphism may be a risk factor for hypodontia: a meta-analysis.

Genet Mol Res. 2014-11-28

[9]
Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.

Clin Genet. 2012-12-7

[10]
Study of rs12532, rs8670 Polymorphism of Msh Homeobox 1 (MSX1), rs61754301, rs4904155 Polymorphism of Paired Box Gene 9 (PAX9), and rs2240308 Polymorphism of Axis Inhibitor Protein 2 (AXIN2) Genes in Nonsyndromic Hypodontia.

Biomed Res Int. 2019-11-5

引用本文的文献

[1]
Detection of a rare AXIN2 variant in an Iranian family with hypodontia and oligodontia.

J Dent Res Dent Clin Dent Prospects. 2022

[2]
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J Dent Res. 2023-3

[3]
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Front Genet. 2022-3-25

[4]
The human EDAR 370V/A polymorphism affects tooth root morphology potentially through the modification of a reaction-diffusion system.

Sci Rep. 2021-3-4

[5]
Odontogenesis-related candidate genes involved in variations of permanent teeth size.

Clin Oral Investig. 2021-7

[6]
Genetic variants in tooth agenesis-related genes might be also involved in tooth size variations.

Clin Oral Investig. 2021-3

[7]
Molecular Insights Into the Causes of Human Thymic Hypoplasia With Animal Models.

Front Immunol. 2020

[8]
Assessment of Correlation of Growth Hormone Receptor Gene with Tooth Dimensions: A CBCT and Genotyping Study.

J Pharm Bioallied Sci. 2019-5

[9]
WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population.

J Genet. 2018-12

[10]
Growth hormone receptor gene is related to root length and tooth length in human teeth.

Angle Orthod. 2018-4-18

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