Department of Ophthalmology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Hum Genomics. 2013 May 15;7(1):13. doi: 10.1186/1479-7364-7-13.
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.
Kelch 样(KLHL)基因家族编码一组通常具有 BTB/POZ 结构域、BACK 结构域和五个到六个 Kelch 基序的蛋白质。BTB 结构域促进蛋白质结合和二聚化。BACK 结构域目前还没有已知的功能,但它具有功能重要性,因为该结构域的突变与疾病有关。Kelch 结构域形成β-三叶桨轮的三级结构,在细胞外功能、形态和与其他蛋白质结合中起作用。目前,人类基因组组织(HUGO)基因命名委员会(HGNC)已经对 42 个 KLHL 基因进行了分类,它们分布在多个人类染色体上。KLHL 家族在进化过程中是保守的。KLHL 家族成员的系统发育分析表明,它可以分为三个亚组,其中 KLHL11 是最古老的成员,KLHL9 是最年轻的成员。一些 KLHL 蛋白与 E3 连接酶 cullin 3 结合,已知参与泛素化。KLHL 基因与几种孟德尔疾病有关,并与癌症有关。对这个蛋白质家族的进一步研究可能会为基础生物学和人类疾病提供有价值的见解。