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牙周疾病中的调控元件与基因变异

Regulatory elements and genetic variations in periodontal diseases.

作者信息

Razzouk Sleiman

机构信息

Adjunct faculty, Department of Periodontology and Implant Dentistry, New York University College of Dentistry, New York, United States; Private Practice, Beirut, Lebanon.

出版信息

Arch Oral Biol. 2016 Dec;72:106-115. doi: 10.1016/j.archoralbio.2016.08.015. Epub 2016 Aug 17.

Abstract

OBJECTIVE

Current evidence suggests that many GWAS and IL1 SNPs are associated with periodontal diseases but their functional role remains ambiguous. Therefore, it is imperative to elucidate the molecular pathways through which these SNPs might act on the development of the disease. The purpose of this review was to highlight the regulatory elements of noncoding regions of the genome and provide insights on the functional role of periodontitis-associated GWAS and IL1 SNPs.

DESIGN

A search was performed using ENCODE data available on different browsers.

RESULTS

GWAS and IL1 SNPs overlap DNase I hypersensitivity sites, histone modifications and transcription binding sites. Some of these noncoding variants influenced the transcription activity of inflammatory genes.

CONCLUSION

SNPs associated with periodontal diseases may contribute to the development of the disorder through their functional roles. Unraveling the character of genetic components might explain the diversity of clinical phenotypes among population groups as well as disease susceptibility.

摘要

目的

目前的证据表明,许多全基因组关联研究(GWAS)和白细胞介素1(IL1)单核苷酸多态性(SNP)与牙周疾病相关,但其功能作用仍不明确。因此,阐明这些SNP可能作用于疾病发展的分子途径势在必行。本综述的目的是强调基因组非编码区的调控元件,并深入了解与牙周炎相关的GWAS和IL1 SNP的功能作用。

设计

使用不同浏览器上可用的ENCODE数据进行检索。

结果

GWAS和IL1 SNP与脱氧核糖核酸酶I超敏位点、组蛋白修饰和转录结合位点重叠。其中一些非编码变异影响炎症基因的转录活性。

结论

与牙周疾病相关的SNP可能通过其功能作用促进该疾病的发展。揭示遗传成分的特征可能解释人群组间临床表型的多样性以及疾病易感性。

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