Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene LIPH

Author:

Kazantseva Anastasiya12345,Goltsov Andrey12345,Zinchenko Rena12345,Grigorenko Anastasia P.12345,Abrukova Anna V.12345,Moliaka Yuri K.12345,Kirillov Alexander G.12345,Guo Zhiru12345,Lyle Stephen12345,Ginter Evgeny K.12345,Rogaev Evgeny I.12345

Affiliation:

1. Brudnick Neuropsychiatric Research Institute, Department of Psychiatry, University of Massachusetts Medical School, 303 Belmont Street, Worcester, MA 01604, USA.

2. Laboratory of Molecular Brain Genetics, Research Center of Mental Health, Russian Academy of Medical Sciences (RAMS), 113152, Moscow, Russian Federation (RF).

3. Lomonosov Moscow State University, Faculty of Bioengineering and Bioinformatics, 119992, Moscow, RF.

4. National Research Center for Medical Genetics, RAMS, RF.

5. GUZ President's Prenatal Center of Chuvash Republic, Cheboksary, Uritsky Street 43, RF.

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 A1α), an enzyme that regulates the production of bioactive lipids. These results suggest that lipase H participates in hair growth and development.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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