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© The Rockefeller University Press, 0021-9525/2001/8/619 $5.00
The Journal of Cell Biology, Volume 154, Number 3, August 6, 2001 619-630

Discovery of a novel murine keratin 6 (K6) isoform explains the absence of hair and nail defects in mice deficient for K6a and K6b

¹ Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030
² Department of Dermatology, Baylor College of Medicine, Houston, TX 77030

Address correspondence to Dennis R. Roop, Department of Molecular and Cellular Biology, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030. Tel.: (713) 798-4966. Fax: (713) 798-3800. E-mail: roopd{at}bcm.tmc.edu

The murine genome is known to have two keratin 6 (K6) genes, mouse K6 (MK6)a and MK6b. These genes display a complex expression pattern with constitutive expression in the epithelia of oral mucosa, hair follicles, and nail beds. We generated mice deficient for both genes through embryonic stem cell technology. The majority of MK6a/b^-/- mice die of starvation within the first two weeks of life. This is due to a localized disintegration of the dorsal tongue epithelium, which results in the build up of a plaque of cell debris that severely impairs feeding. However, 25% of MK6a/b^-/- mice survive to adulthood. Remarkably, the surviving MK6a/b^-/- mice have normal hair and nails. To our surprise, we discovered MK6 staining both in the hair follicle and the nail bed of MK6a/b^-/- mice, indicating the presence of a third MK6 gene. We cloned this previously unknown murine keratin gene and found it to be highly homologous to human K6hf, which is expressed in hair follicles. We therefore termed this gene MK6 hair follicle (MK6hf). The presence of MK6hf in the MK6a/b^-/- follicles and nails offers an explanation for the absence of hair and nail defects in MK6a/b^-/- animals.

Key Words: keratin; skin; tongue; hair follicle; pachyonychia congenita

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