Suppr超能文献

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。

相似文献

1
The genetics of dyskeratosis congenita.先天性角化不良的遗传学
Cancer Genet. 2011 Dec;204(12):635-45. doi: 10.1016/j.cancergen.2011.11.002.
2
Advances in the understanding of dyskeratosis congenita.先天性角化不良认识的进展
Br J Haematol. 2009 Apr;145(2):164-72. doi: 10.1111/j.1365-2141.2009.07598.x. Epub 2009 Feb 4.
5
Clinical utility gene card for: dyskeratosis congenita.先天性角化不良临床实用基因卡片
Eur J Hum Genet. 2011 Nov;19(11). doi: 10.1038/ejhg.2011.90. Epub 2011 May 25.
6
Dyskeratosis congenita as a disorder of telomere maintenance.先天性角化不良是一种端粒维持障碍。
Mutat Res. 2012 Feb 1;730(1-2):43-51. doi: 10.1016/j.mrfmmm.2011.06.008. Epub 2011 Jul 2.
7
Dyskeratosis congenita, stem cells and telomeres.先天性角化不良、干细胞与端粒
Biochim Biophys Acta. 2009 Apr;1792(4):371-9. doi: 10.1016/j.bbadis.2009.01.010. Epub 2009 Feb 7.

引用本文的文献

3
Telomerase-Mediated Anti-Ageing Interventions.端粒酶介导的抗衰老干预措施。
Subcell Biochem. 2024;107:1-20. doi: 10.1007/978-3-031-66768-8_1.

本文引用的文献

2
A role for heterochromatin protein 1γ at human telomeres.异染色质蛋白 1γ 在人类端粒上的作用。
Genes Dev. 2011 Sep 1;25(17):1807-19. doi: 10.1101/gad.17325211. Epub 2011 Aug 24.
3
Architecture of human telomerase RNA.人类端粒酶 RNA 的结构。
Proc Natl Acad Sci U S A. 2011 Dec 20;108(51):20325-32. doi: 10.1073/pnas.1100279108. Epub 2011 Aug 15.
4
Dyskeratosis congenita as a disorder of telomere maintenance.先天性角化不良是一种端粒维持障碍。
Mutat Res. 2012 Feb 1;730(1-2):43-51. doi: 10.1016/j.mrfmmm.2011.06.008. Epub 2011 Jul 2.
5
Clinical utility gene card for: dyskeratosis congenita.先天性角化不良临床实用基因卡片
Eur J Hum Genet. 2011 Nov;19(11). doi: 10.1038/ejhg.2011.90. Epub 2011 May 25.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验