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肽聚糖识别蛋白Pglyrp3和Pglyrp4由表皮分化复合体编码,是1号染色体1q21上银屑病相关基因座Psors4的候选基因。

Peptidoglycan recognition proteins Pglyrp3 and Pglyrp4 are encoded from the epidermal differentiation complex and are candidate genes for the Psors4 locus on chromosome 1q21.

作者信息

Sun Chao, Mathur Punam, Dupuis Josée, Tizard Rich, Ticho Barry, Crowell Tom, Gardner Humphrey, Bowcock Anne M, Carulli John

机构信息

Department of Genetics, BiogenIdec, Inc, 12 Cambridge Center, Cambridge, MA 02142, USA.

出版信息

Hum Genet. 2006 Mar;119(1-2):113-25. doi: 10.1007/s00439-005-0115-8. Epub 2005 Dec 17.

Abstract

Psoriasis is a common inflammatory skin disease caused by genetic and environmental factors, including bacterial and viral infections. Since the skin is in constant contact with commensal and pathogenic microorganisms, we examined well-supported psoriasis genetic linkage intervals to identify genes encoding innate immune pattern recognition proteins that may play a role in pathogenesis. Two peptidoglycan recognition proteins, Pglyrp3 and Pglyrp4, are localized to the Psors4 locus on chromosome 1q21 in a gene cluster known as the epidermal differentiation complex (EDC). We show that these genes are expressed in the skin as well as in germinal centers in the tonsil. We tested 13 SNPs in or near these genes for association with psoriasis in two independent patient collections: a family-based patient set comprised of 375 individuals from 101 families, and a case-control patient collection of 282 patients with moderate to severe psoriasis and 192 healthy controls. In the family-based analysis, several SNPs in the Pglyrp3-Pglyrp4 locus show association with psoriasis (0.01 < P < 0.05). Multiple-SNP haplotypes incorporating Pglyrp3 and Pglyrp4 SNPs also show significant association in the transmission disequilibrium test (TDT; P < 0.01). In the case-control test, none of the SNPs that we tested show association with psoriasis when analyzed in single-SNP or haplotype-based tests. The discordance between the TDT and case-control results suggests that the two populations are significantly different in disease etiology, that the polymorphism responsible for the Psors4 linkage is elsewhere in the Pglyrp locus, or that the causative Psors4 polymorphism is in a location near but not in the Pglyrp locus. These data are consistent with previous reports of association of psoriasis with genes on 1q21, and suggest a role for Pglyrps in skin biology.

摘要

银屑病是一种由遗传和环境因素引起的常见炎症性皮肤病,这些因素包括细菌和病毒感染。由于皮肤经常与共生微生物和致病微生物接触,我们研究了有充分证据支持的银屑病遗传连锁区间,以确定编码可能在发病机制中起作用的天然免疫模式识别蛋白的基因。两种肽聚糖识别蛋白Pglyrp3和Pglyrp4定位于1号染色体1q21上的Psors4位点,该位点位于一个称为表皮分化复合体(EDC)的基因簇中。我们发现这些基因在皮肤以及扁桃体生发中心均有表达。我们在两个独立的患者群体中检测了这些基因内部或附近的13个单核苷酸多态性(SNP)与银屑病的关联:一个基于家系的患者组,由来自101个家庭的375名个体组成;一个病例对照患者组,包括282例中度至重度银屑病患者和192名健康对照。在基于家系的分析中,Pglyrp3 - Pglyrp4位点的几个SNP与银屑病相关(0.01 < P < 0.05)。包含Pglyrp3和Pglyrp4 SNP的多个SNP单倍型在传递不平衡检验(TDT;P < 0.01)中也显示出显著关联。在病例对照检验中,我们检测的SNP在单SNP或基于单倍型的检验中均未显示与银屑病相关。TDT结果与病例对照结果之间的不一致表明,这两个群体在疾病病因上存在显著差异;导致Psors4连锁的多态性位于Pglyrp基因座的其他位置;或者导致Psors4多态性的原因位于Pglyrp基因座附近但不在该基因座内。这些数据与先前关于银屑病与1q21上基因关联的报道一致,并提示Pglyrps在皮肤生物学中发挥作用。

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