WASHINGTON, Feb. 26 (Chinese media) -- The U.S. researchers
have discovered a new gene involved in determining hair texture in humans,
according to journal Nature Genetics to be published in March.
Their genetic analysis demonstrated that mutations in
a gene, known as P2RY5, cause hereditary "woolly hair" -- hair that is coarse,
dry, tightly curled and sparse. The paper about the findings will appear in the
March edition of journal Nature Genetics.
"Our findings indicate that mutations in the P2RY5
gene cause hereditary woolly hair. This is significant as it represents the
discovery of the first new gene whose primary function seems to be the
determination of hair texture in humans," said lead author Angela M. Christiano
at the Columbia University Medical Center.
"This genetic finding may inform the development of
new treatments for excessive or unwanted hair, or potentially hair growth,"
Christiano added.
The genetic causes of hair texture in humans are
largely unknown. Since research has shown that woolly hair was common among
Pakistani families, Christiano and her colleagues set out to determine why this
type of hair was specific to this group of people.
To identify a gene involved in controlling hair
texture, the research team performed a genetic analysis of six families of
Pakistani origin, who all shared hereditary woolly hair. The cause of hereditary
woolly hair was found to be a mutation in the P2RY5 gene.
"The bulb region of plucked hairs from woolly hair
patients showed irregular bending without attachment of the root sheath." the
authors said.
They propose that mutations in P2RY5 most likely
result in hair follicle disruptions, which then compromise its anchoring to the
hair shaft and cause the abnormal bending of the bulb region, leading to woolly
hair.
Christiano's discoveries have led to the
identification of several genes controlling human hair growth. It remains to be
determined whether common variants on the P2RY5 gene can also contribute to
naturally occurring variations in hair texture between different human
populations.
According to the researchers, P2RY5 is the first gene
of a type known as a G-protein coupled receptor (GPCR) implicated in a human
hair disorder, thereby making it possible to develop drugs that target this
receptor.

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