Genomics Inform.  2011 Sep;9(3):93-101.

The Hairless Gene: A Putative Navigator of Hair Follicle Development

Affiliations
  • 1Department of Medical Lifescience, The Catholic University of Korea, Seoul 137-701, Korea. sjkyoon@catholic.ac.kr
  • 2Department of Biomedical Sciences, The Catholic University of Korea, Seoul 137-701, Korea.

Abstract

The Hairless (HR) gene regulates the expression of several target genes as a transcriptional corepressor of nuclear receptors. The hair follicle (HF), a small independent organ of the skin, resides in the epidermis and undergoes regenerative cycling for normal hair formation. HF development requires many genes and signaling pathways to function properly in time and space, one of them being the HR gene. Various mutations of the HR gene have been reported to cause the hair loss phenotype in rodents and humans. In recent studies, it has been suggested that the HR gene is a critical player in the regulation of the hair cycle and, thus, HF development. Furthermore, the HR gene is associated with the Wnt signaling pathway, which regulates roliferation and differentiation of cells and plays an essential role in hair and skin development. In this review, we summarize the mutations responsible for human hair disorders and discuss the roles of the HR gene in HF development.

Keyword

hairless; corepressor; hair follicle; hair cycle; hair loss

MeSH Terms

Epidermis
Hair
Hair Follicle
Humans
Phenotype
Receptors, Cytoplasmic and Nuclear
Rodentia
Skin
Wnt Signaling Pathway
Receptors, Cytoplasmic and Nuclear
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