Update on the Kelch-like (KLHL) gene family

被引:0
作者
Bajinder S Dhanoa
Tiziana Cogliati
Akhila G Satish
Elspeth A Bruford
James S Friedman
机构
[1] University of Colorado School of Medicine,Department of Ophthalmology
[2] National Institutes of Health,Neurobiology
[3] Wellcome Trust Genome Campus,Neurodegeneration and Repair Laboratory (N
来源
Human Genomics | / 7卷
关键词
KLHL; Kelch domain; BTB domain; Ubiquitination; Gene family; Evolution; Mendelian disease; Gene nomenclature; Cancer;
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学科分类号
摘要
The Kelch-like (KLHL) gene family encodes a group of proteins that generally possess a BTB/POZ domain, a BACK domain, and five to six Kelch motifs. BTB domains facilitate protein binding and dimerization. The BACK domain has no known function yet is of functional importance since mutations in this domain are associated with disease. Kelch domains form a tertiary structure of β-propellers that have a role in extracellular functions, morphology, and binding to other proteins. Presently, 42 KLHL genes have been classified by the HUGO Gene Nomenclature Committee (HGNC), and they are found across multiple human chromosomes. The KLHL family is conserved throughout evolution. Phylogenetic analysis of KLHL family members suggests that it can be subdivided into three subgroups with KLHL11 as the oldest member and KLHL9 as the youngest. Several KLHL proteins bind to the E3 ligase cullin 3 and are known to be involved in ubiquitination. KLHL genes are responsible for several Mendelian diseases and have been associated with cancer. Further investigation of this family of proteins will likely provide valuable insights into basic biology and human disease.
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