Highly prevalent LIPH founder mutations causing autosomal recessive woolly hair/hypotrichosis in Japan and the genotype/phenotype correlations

Kana Tanahashi, Kazumitsu Sugiura, Michihiro Kono, Hiromichi Takama, Nobuyuki Hamajima, Masashi Akiyama

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Mutations in LIPH cause of autosomal recessive woolly hair/hypotrichosis (ARWH), and the 2 missense mutations c.736T>A (p.Cys246Ser) and c.742C>A (p.His248Asn) are considered prevalent founder mutations for ARWH in the Japanese population. To reveal genotype/phenotype correlations in ARWH cases in Japan and the haplotypes in 14 Japanese patients from 14 unrelated Japanese families. 13 patients had woolly hair, and 1 patient had complete baldness since birth. An LIPH mutation search revealed homozygous c.736T>A mutations in 10 of the patients. Compound heterozygous c.736T>A and c.742C>A mutations were found in 3 of the patients, and homozygous c.742C>A mutation in 1 patient. The phenotype of mild hypotrichosis with woolly hair was restricted to the patients with the homozygous c.736T>A mutation. The severe phenotype of complete baldness was seen in only 1 patient with homozygous c.742C>A. Haplotype analysis revealed that the alleles containing the LIPH c.736T>A mutation had a haplotype identical to that reported previously, although 4 alleles out of 5 chromosomes containing the LIPH c.742C>A mutation had a different haplotype from the previously reported founder allele. These alleles with c.742C>A are thought to be the third founder LIPH mutation causing ARWH. To accurately determine the prevalence of the founder mutations, we investigated allele frequencies of those mutations in 819 Japanese controls. Heterozygous c.736T>A mutations were found in 13 controls (allele frequency: 0.0079; carrier rate: 0.016), and heterozygous c.742C>A mutations were found in 2 controls (allele frequency: 0.0012; carrier rate: 0.0024). In conclusion, this study confirms the more accurate allele frequencies of the pathogenic founder mutations of LIPH and shows that there is a third founder mutation in Japan. In addition, the present findings suggest that the mutation patterns of LIPH might be associated with hypotrichosis severity in ARWH.

Original languageEnglish
Article numbere89261
JournalPLoS One
Volume9
Issue number2
DOIs
Publication statusPublished - 19-02-2014
Externally publishedYes

Fingerprint

Hypotrichosis
Genetic Association Studies
hairs
Japan
mutation
Mutation
Chromosomes
Gene Frequency
Haplotypes
gene frequency
haplotypes
Alleles
alleles
Autosomal Recessive Woolly Hair
genotype-phenotype correlation
Alopecia
Hair
Phenotype

All Science Journal Classification (ASJC) codes

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)

Cite this

Tanahashi, Kana ; Sugiura, Kazumitsu ; Kono, Michihiro ; Takama, Hiromichi ; Hamajima, Nobuyuki ; Akiyama, Masashi. / Highly prevalent LIPH founder mutations causing autosomal recessive woolly hair/hypotrichosis in Japan and the genotype/phenotype correlations. In: PLoS One. 2014 ; Vol. 9, No. 2.
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Highly prevalent LIPH founder mutations causing autosomal recessive woolly hair/hypotrichosis in Japan and the genotype/phenotype correlations. / Tanahashi, Kana; Sugiura, Kazumitsu; Kono, Michihiro; Takama, Hiromichi; Hamajima, Nobuyuki; Akiyama, Masashi.

In: PLoS One, Vol. 9, No. 2, e89261, 19.02.2014.

Research output: Contribution to journalArticle

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AU - Tanahashi, Kana

AU - Sugiura, Kazumitsu

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