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17q12-q21 variants interact with early-life exposures to modify asthma risk in Black children.17号染色体长臂12区至21区的变异与儿童早期暴露因素相互作用,从而改变黑人儿童患哮喘的风险。
Clin Exp Allergy. 2022 Apr;52(4):565-568. doi: 10.1111/cea.14074. Epub 2021 Dec 12.
2
Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis.整合生物样本库资源揭示了调节特应性皮炎易感性的新遗传途径。
J Allergy Clin Immunol. 2022 Mar;149(3):1105-1112.e9. doi: 10.1016/j.jaci.2021.07.043. Epub 2021 Aug 27.
3
Prioritization of candidate causal genes for asthma in susceptibility loci derived from UK Biobank.基于英国生物库的易感性位点,对哮喘候选因果基因进行优先级排序。
Commun Biol. 2021 Jun 8;4(1):700. doi: 10.1038/s42003-021-02227-6.
4
Pathogenic ubiquitination of GSDMB inhibits NK cell bactericidal functions.GSDMB 的致病性泛素化抑制 NK 细胞的杀菌功能。
Cell. 2021 Jun 10;184(12):3178-3191.e18. doi: 10.1016/j.cell.2021.04.036. Epub 2021 May 21.
5
Genome-wide association study identifies TNFSF15 associated with childhood asthma.全基因组关联研究发现 TNFSF15 与儿童哮喘有关。
Allergy. 2022 Jan;77(1):218-229. doi: 10.1111/all.14952. Epub 2021 Jun 14.
6
Association of Gasdermin B Gene GSDMB Polymorphisms with Risk of Allergic Diseases.GSDMB 基因 GSDMB 多态性与过敏性疾病风险的关联。
Biochem Genet. 2021 Dec;59(6):1527-1543. doi: 10.1007/s10528-021-10073-8. Epub 2021 May 8.
7
Household mold exposure interacts with inflammation-related genetic variants on childhood asthma: a case-control study.家庭霉菌暴露与炎症相关的遗传变异在儿童哮喘中的相互作用:一项病例对照研究。
BMC Pulm Med. 2021 Apr 2;21(1):114. doi: 10.1186/s12890-021-01484-9.
8
Chromosome 17q12-21 Variants Are Associated with Multiple Wheezing Phenotypes in Childhood.染色体 17q12-21 变异与儿童多种喘息表型相关。
Am J Respir Crit Care Med. 2021 Apr 1;203(7):864-870. doi: 10.1164/rccm.202003-0820OC.
9
Emerging insights on the role of gasdermins in infection and inflammatory diseases.关于gasdermin蛋白在感染和炎症性疾病中作用的新见解。
Clin Transl Immunology. 2020 Oct 4;9(10):e1186. doi: 10.1002/cti2.1186. eCollection 2020.
10
Mapping the 17q12-21.1 Locus for Variants Associated with Early-Onset Asthma in African Americans.定位与非裔美国人早发性哮喘相关的 17q12-21.1 位点变异。
Am J Respir Crit Care Med. 2021 Feb 15;203(4):424-436. doi: 10.1164/rccm.202006-2623OC.

Gasdermin B 与儿童哮喘发病的新关联

New Insights Relating Gasdermin B to the Onset of Childhood Asthma.

机构信息

Department of Medicine and.

Department of Pediatrics and.

出版信息

Am J Respir Cell Mol Biol. 2022 Oct;67(4):430-437. doi: 10.1165/rcmb.2022-0043PS.

DOI:10.1165/rcmb.2022-0043PS
PMID:35580164
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9564923/
Abstract

Chromosome 17q12-q21 is the most replicated genetic locus for childhood-onset asthma. Polymorphisms in this locus containing ∼10 genes interact with a variety of environmental exposures in the home and outdoors to modify asthma risk. However, the functional basis for these associations and their linkages to the environment have remained enigmatic. Within this extended region, regulation of (gasdermin B) expression in airway epithelial cells has emerged as the primary mechanism underlying the 17q12-q21 genome-wide association study signal. Asthma-associated SNPs influence the abundance of transcripts as well as the functional properties of GSDMB protein in airway epithelial cells. GSDMB is a member of the gasdermin family of proteins, which regulate pyroptosis and inflammatory responses to microbial infections. The aims of this review are to synthesize recent studies on the relationship of 17q12-q21 SNPs to childhood asthma and the evidence pointing to gene expression or protein function as the underlying mechanism and to explore the potential functions of GSDMB that may influence the risk of developing asthma during childhood.

摘要

17q12-q21 染色体是儿童期起病哮喘最具复制性的遗传基因座。该基因座中包含约 10 个基因的多态性与家庭和户外的多种环境暴露相互作用,从而改变哮喘的风险。然而,这些关联的功能基础及其与环境的联系仍然是个谜。在这个扩展区域内,气道上皮细胞中 (gasdermin B)表达的调控已成为 17q12-q21 全基因组关联研究信号的主要机制。与哮喘相关的单核苷酸多态性影响 转录本的丰度以及气道上皮细胞中 GSDMB 蛋白的功能特性。GSDMB 是 gasdermin 蛋白家族的成员之一,可调节细胞焦亡和对微生物感染的炎症反应。本综述的目的是综合最近关于 17q12-q21 SNPs 与儿童哮喘的关系的研究,并提供指向基因表达或蛋白功能作为潜在机制的证据,并探讨 GSDMB 的潜在功能,这些功能可能影响儿童期哮喘的发病风险。