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通过放松基因表达调控来调节自身耐受性。

Regulating self-tolerance by deregulating gene expression.

作者信息

Gotter Jörn, Kyewski Bruno

机构信息

Tumour Immunology Program, Division of Developmental Immunology, German Cancer Research Centre (DKFZ), Im Neuenheimer Feld 280, D-69120 Heidelberg, Germany.

出版信息

Curr Opin Immunol. 2004 Dec;16(6):741-5. doi: 10.1016/j.coi.2004.08.004.

Abstract

Intrathymic expression of peripheral auto-antigens, termed promiscuous gene expression, extends the scope of central T-cell tolerance to peripheral organs and proves essential for the induction and maintenance of self-tolerance. The purification of antigen-presenting cells has been instrumental in identifying promiscuous gene expression as an inherent property of medullary epithelial cells. The pool of promiscuously expressed genes might encompass up to 10% of the whole genome. The remarkable diversity of this gene pool implies a complex mode of regulation, which cannot be solely explained by the action of a single factor, such as the transcriptional autoimmune regulator AIRE. Co-localization of promiscuously expressed genes in clusters also suggests epigenetic mechanisms (e.g. DNA methylation) to account for this unorthodox gene expression pattern. The identification of the molecular components controlling the expression of tissue-restricted genes in the thymus promises to add valuable new insights into the complex genetic regulation underlying most autoimmune diseases.

摘要

外周自身抗原在胸腺内的表达,即所谓的混杂基因表达,扩展了中枢T细胞对外周器官的耐受性范围,并被证明对自身耐受性的诱导和维持至关重要。抗原呈递细胞的纯化有助于将混杂基因表达鉴定为髓质上皮细胞的固有特性。混杂表达基因的库可能涵盖整个基因组的10%。这个基因库的显著多样性意味着一种复杂的调控模式,这不能仅由单一因素(如转录自身免疫调节因子AIRE)的作用来解释。混杂表达基因在簇中的共定位也提示表观遗传机制(如DNA甲基化)可解释这种非传统的基因表达模式。确定控制胸腺中组织限制性基因表达的分子成分,有望为大多数自身免疫性疾病背后复杂的基因调控增添有价值的新见解。

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