4.5 Article

Multiple interaction partners for Cockayne syndrome proteins: Implications for genome and transcriptome maintenance

期刊

MECHANISMS OF AGEING AND DEVELOPMENT
卷 134, 期 5-6, 页码 212-224

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.mad.2013.03.009

关键词

Cockayne syndrome; Protein interactions; DNA repair deficiency; Transcription deficiency; Mitochondria

资金

  1. Intramural Program at the National Institutes on Aging, National Institutes of Health
  2. Velux Foundation
  3. NovoNordic Foundation

向作者/读者索取更多资源

Cockayne syndrome (CS) is characterized by progressive multisystem degeneration and is classified as a segmental premature aging syndrome. The majority of CS cases are caused by defects in the CS complementation group B (CSB) protein and the rest are mainly caused by defects in the CS complementation group A (CSA) protein. Cells from CS patients are sensitive to UV light and a number of other DNA damaging agents including various types of oxidative stress. The cells also display transcription deficiencies, abnormal apoptotic response to DNA damage, and DNA repair deficiencies. Herein we have critically reviewed the current knowledge about known protein interactions of the CS proteins. The review focuses on the participation of the CSB and CSA proteins in many different protein interactions and complexes, and how these interactions inform us about pathways that are defective in the disease. (c) 2013 Elsevier Ireland Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据