A Small Deletion Hotspot in the Type II Keratin Gene mK6irs1/Krt2-6g on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (Ca) Mutation

Corresponding author: Hiromichi Yonekawa, The Tokyo Metropolitan Institute of Medical Science (Rinshoken), 3-18-22, Honkomagome Bunkyo-ku, Tokyo 113-8613, Japan., yonekawa{at}rinshoken.or.jp (E-mail)

Communicating editor: N. TAKAHATA

A new mutation has arisen in a colony of mice transgenic for human -galactosidase. The mutation is independent of the transgenic insertion, autosomal dominant, and morphologically very similar to the classical wavy coat mutation, caracul (Ca), on chromosome 15. Therefore, we designated this locus the caracul Rinshoken (Ca^Rin). Applying a positional cloning approach, we identified the mK6irs1/Krt2-6g gene as a strong candidate for Ca^Rin because among five Ca alleles examined mutations always occurred in the highly conserved positions of the -helical rod domain (1A and 2B subdomain) of this putative gene product. The most striking finding is that four independently discovered alleles, the three preexistent alleles Ca^J, Ca^9J, Ca^10J, and our allele Ca^Rin, all share one identical amino acid deletion (N 140 del) and the fifth, Ca^medJ, has an amino acid substitution (A 431 D). These findings indicate that a mutation hotspot exists in the Ca locus. Additionally, we describe a Ca mutant allele induced by ENU mutagenesis, which also possesses an amino acid substitution (L 424 W) in the mK6irs1/Krt2-6g gene. The identification of the Ca candidate gene enables us to further define the nature of the genetic pathway required for hair formation and provides an important new candidate that may be implicated in human hair and skin diseases.