Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH

Science. 2006 Nov 10;314(5801):982-5. doi: 10.1126/science.1133276.

Abstract

The molecular mechanisms controlling human hair growth and scalp hair loss are poorly understood. By screening about 350,000 individuals in two populations from the Volga-Ural region of Russia, we identified a gene mutation in families who show an inherited form of hair loss and a hair growth defect. Affected individuals were homozygous for a deletion in the LIPH gene on chromosome 3q27, caused by short interspersed nuclear element-retrotransposon-mediated recombination. The LIPH gene is expressed in hair follicles and encodes a phospholipase called lipase H (alternatively known as membrane-associated phosphatidic acid-selective phospholipase A1alpha), an enzyme that regulates the production of bioactive lipids. These results suggest that lipase H participates in hair growth and development.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alu Elements
  • Amino Acid Sequence
  • Base Sequence
  • Chromosomes, Human, Pair 3 / genetics
  • Exons
  • Female
  • Gene Deletion
  • Gene Expression
  • Genetic Markers
  • Hair / growth & development*
  • Hair Follicle / enzymology
  • Heterozygote
  • Homozygote
  • Humans
  • Hypotrichosis / genetics*
  • Lipase / chemistry
  • Lipase / genetics*
  • Lipase / metabolism
  • Lipid Metabolism
  • Lod Score
  • Male
  • Molecular Sequence Data
  • Pedigree
  • Protein Structure, Tertiary
  • Recombination, Genetic
  • Retroelements
  • Russia
  • Tandem Repeat Sequences

Substances

  • Genetic Markers
  • LIPC protein, human
  • Retroelements
  • Lipase