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先天性角化不良的遗传学

The genetics of dyskeratosis congenita.

作者信息

Mason Philip J, Bessler Monica

机构信息

Division of Hematology, Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, USA.

出版信息

Cancer Genet. 2011 Dec;204(12):635-45. doi: 10.1016/j.cancergen.2011.11.002.

Abstract

Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome associated with characteristic mucocutaneous features and a variable series of other somatic abnormalities. The disease is heterogeneous at the genetic and clinical levels. Determination of the genetic basis of DC has established that the disease is caused by a number of genes, all of which encode products involved in telomere maintenance, either as part of telomerase or as part of the shelterin complex that caps and protects telomeres. There is overlap at the genetic and clinical levels with other, more common conditions, including aplastic anemia (AA), pulmonary fibrosis (PF), and liver cirrhosis. Although part of the spectrum of disorders known to be associated with DC, it has emerged that mutations in telomere maintenance genes can lead to the development of AA and PF in the absence of other DC features. Here we discuss the genetics of DC and its relationship to disease presentation.

摘要

先天性角化不良(DC)是一种遗传性骨髓衰竭综合征,伴有特征性的黏膜皮肤表现以及一系列其他不同的躯体异常。该疾病在遗传和临床水平上具有异质性。对DC遗传基础的研究已确定,该疾病由多个基因引起,所有这些基因编码的产物都参与端粒维持,要么作为端粒酶的一部分,要么作为封端和保护端粒的 shelterin 复合体的一部分。在遗传和临床水平上,它与其他更常见的病症存在重叠,包括再生障碍性贫血(AA)、肺纤维化(PF)和肝硬化。虽然已知与DC相关的部分疾病谱中存在这种情况,但已发现端粒维持基因的突变可在没有其他DC特征的情况下导致AA和PF的发生。在此,我们讨论DC的遗传学及其与疾病表现的关系。

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