Proceedings of the National Academy of Sciences · 2014 · 209 citations · 35 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsQuantitative GeneticsDevelopmental MutationsGenetic DisordersGenetic Hair DisordersGenetics Of Growth DisordersHair DisordersMendelian DisordersAutosomal Recessive InheritanceCongenital Hair DisordersHair Growth DisordersMutations In Fibroblast Growth Factor Signaling PathwayQuantitative Trait GeneticsQuantitative Trait VariationSingle-gene InheritanceSingle-gene Mutations
Mechanisms that regulate the growth of eyelashes have remained obscure. We ascertained two families from Pakistan who presented with familial trichomegaly, or extreme eyelash growth. Using a combination of whole exome sequencing and homozygosity mapping, we identified distinct pathogenic mutations within fibroblast growth factor 5 (FGF5) that underlie the disorder. Subsequent sequencing of this gene in several additional trichomegaly families identified an additional mutation in FGF5. We further demonstrated that hair fibers from forearms of these patients were significantly longer than hairs from control individuals, with an increased proportion in the growth phase, anagen. Using hair follicle organ cultures, we show that FGF5 induces regression of the human hair follicle. We have identified FGF5 as a crucial regulator of hair growth in humans for the first time, to our knowledge, and uncovered a therapeutic target to selectively regulate eyelash growth.
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Fast and accurate short read alignment with Burrows–Wheeler transform
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A framework for variation discovery and genotyping using next-generation DNA sequencing data
Mark A. DePristo, Eric Banks, Ryan Poplin et al. · Nature Genetics · 2011 · 12.4K citations · Full text