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骨关节炎软骨中II型胶原基因(COL2A1)的差异等位基因表达

Differential allelic expression of the type II collagen gene (COL2A1) in osteoarthritic cartilage.

作者信息

Loughlin J, Irven C, Athanasou N, Carr A, Sykes B

机构信息

University of Oxford, Institute of Molecular Medicine, John Radcliffe Hospital, United Kingdom.

出版信息

Am J Hum Genet. 1995 May;56(5):1186-93.

Abstract

Osteoarthritis (OA) is a common debilitating disease resulting from the degeneration of articular cartilage. The major protein of cartilage is type II collagen, which is encoded by the COL2A1 gene. Mutations at this locus have been discovered in several individuals with inherited disorders of cartilage. We have identified 27 primary OA patients who are heterozygous for sequence dimorphisms located in the coding region of COL2A1. These dimorphisms were used to distinguish the mRNA output from each of the two COL2A1 alleles in articular cartilage obtained from each patient. Three patients demonstrated differential allelic expression and produced < 12% of the normal level of mRNA from one of their COL2A1 alleles. The same allele shows reduced expression in all three patients, and this allele is more frequent in a well-defined OA population than in a control group, suggesting the possible existence of a rare COL2A1 allele that predisposes to OA.

摘要

骨关节炎(OA)是一种由关节软骨退变引起的常见致残性疾病。软骨的主要蛋白质是II型胶原蛋白,由COL2A1基因编码。在一些患有遗传性软骨疾病的个体中发现了该基因座的突变。我们鉴定出27例原发性OA患者,他们在COL2A1编码区的序列二态性上为杂合子。这些二态性用于区分从每位患者获得的关节软骨中两个COL2A1等位基因各自的mRNA产量。三名患者表现出等位基因差异表达,其两个COL2A1等位基因之一产生的mRNA水平低于正常水平的12%。在所有三名患者中,同一个等位基因的表达均降低,并且该等位基因在明确的OA人群中比在对照组中更常见,这表明可能存在一种易患OA的罕见COL2A1等位基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aad/1801477/1a4743dd7934/ajhg00031-0178-a.jpg

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