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自身免疫性多内分泌腺病-念珠菌病-外胚层营养不良(APECED)基因的克隆为人类自身免疫性疾病提供了新的见解。

Cloning of the APECED gene provides new insight into human autoimmunity.

作者信息

Aaltonen J, Björses P

机构信息

National Public Health Institute, Department of Human Molecular Genetics, Helsinki, Finland.

出版信息

Ann Med. 1999 Apr;31(2):111-6. doi: 10.3109/07853899708998786.

Abstract

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is the only autoimmune disease characterized so far that is caused by a defect in a single gene. We have recently isolated the defective gene in this disease by positional cloning and have identified several different mutations in APECED patients. This novel gene, AIRE, contains two plant homeodomain (PHD)-type zinc finger motifs and a newly described putative DNA-binding domain SAND. We have further shown that the protein encoded by the AIRE gene is localized to the nuclear body-like structures of cell nuclei. Similar discrete speckles within the nucleus have been suggested to be involved in the regulation of transcription, oncogenesis and differentiation of cells. Together with the predicted structural features of the APECED protein the new data obtained both in vitro and ex vivo suggest that this protein participates in the regulation of gene expression in a restricted set of tissues and cells.

摘要

自身免疫性多内分泌腺病-念珠菌病-外胚层发育不良(APECED)是迄今为止唯一一种由单基因缺陷引起的自身免疫性疾病。我们最近通过定位克隆分离出了该疾病中的缺陷基因,并在APECED患者中鉴定出了几种不同的突变。这个新基因,AIRE,包含两个植物同源结构域(PHD)型锌指基序和一个新描述的假定DNA结合结构域SAND。我们进一步证明,由AIRE基因编码的蛋白质定位于细胞核的核体样结构。细胞核内类似的离散斑点被认为与细胞的转录、肿瘤发生和分化调节有关。结合APECED蛋白的预测结构特征,体外和体内获得的新数据表明,该蛋白在一组受限的组织和细胞中参与基因表达的调节。

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