WD40-Repeat Proteins in Ciliopathies and Congenital Disorders of Endocrine System

被引:11
|
作者
Kim, Yeonjoo [1 ]
Kim, Soo-Hyun [1 ]
机构
[1] St Georges Univ London, Cell Biol Res Ctr, Mol & Clin Sci Res Inst, Cranmer Terrace, London SW17 0RE, England
基金
英国医学研究理事会;
关键词
WDR proteins; Ciliopathies; Congenital; hereditary; and neonatal diseases and abnormalities; Neuroendocrine; Kallmann syndrome; TRIPLE-A SYNDROME; MICROTUBULE-ASSOCIATED PROTEIN; GALLOWAY-MOWAT SYNDROME; WD-REPEAT PROTEIN; HYPOGONADOTROPIC HYPOGONADISM; JOUBERT-SYNDROME; INTRAFLAGELLAR TRANSPORT; PRIMARY CILIUM; PARKINSONS-DISEASE; KALLMANN-SYNDROME;
D O I
10.3803/EnM.2020.302
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
WD40-repeat (WDR)-containing proteins constitute an evolutionarily conserved large protein family with a broad range of biological functions. In human proteome, WDR makes up one of the most abundant protein-protein interaction domains. Members of the WDR protein family play important roles in nearly all major cellular signalling pathways. Mutations of WDR proteins have been associated with various human pathologies including neurological disorders, cancer, obesity, ciliopathies and endocrine disorders. This review provides an updated overview of the biological functions of WDR proteins and their mutations found in congenital disorders. We also highlight the significant role of WDR proteins in ciliopathies and endocrine disorders. The new insights may help develop therapeutic approaches targeting WDR motifs.
引用
收藏
页码:494 / 506
页数:13
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