ArticlePLoS genetics2015
Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation.
Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
11 citing papers in PubMed, 18 citations in OpenAlex.
- Functional impact of splicing variants in the elaboration of complex traits in cattle.Nature communications · 2025Article
- A large deletion encompassing exon 2 of the ectodysplasin A (EDA) gene in a British blue crossbred calf with hypohidrotic ectodermal dysplasia.Acta veterinaria Scandinavica · 2022Article
- AGenes · 2021Article
- Genomic and anatomical comparisons of skin support independent adaptation to life in water by cetaceans and hippos.Current biology : CB · 2021Article
- A Nonsense Variant in Hephaestin Like 1 (Genes · 2021Article
- A Large Deletion in theG3 (Bethesda, Md.) · 2017Article
- A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle.BMC genetics · 2017Article
- An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat Texture.G3 (Bethesda, Md.) · 2016Article
- A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle.BMC genomics · 2016Article
- Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1.BMC veterinary research · 2016Article
- Correction: Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation.PLoS genetics · 2016Article
Corrections and comments
- Erratum issued
Authors and funding
11 authors at 4 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Four related cows showed hairless streaks on various parts of the body with no correlation to the pigmentation pattern. The stripes occurred in a consistent pattern resembling the lines of Blaschko. The non-syndromic hairlessness phenotype observed occurred across three generations of a single family and was compatible with an X-linked mode of inheritance. Linkage analysis and subsequent whole genome sequencing of one affected female identified two perfectly associated non-synonymous sequence variants in the critical interval on bovine chromosome X. Both variants occurred in complete linkage disequilibrium and were absent in more than 3900 controls. An ERCC6L missense mutation was predicted to cause an amino acid substitution of a non-conserved residue. Analysis in mice showed no specific Ercc6l expression pattern related to hair follicle development and therefore ERCC6L was not considered as causative gene. A point mutation at the 5'-splice junction of exon 5 of the TSR2, 20S rRNA accumulation, homolog (S. cerevisiae), gene led to the production of two mutant transcripts, both of which contain a frameshift and generate a premature stop codon predicted to truncate approximately 25% of the protein. Interestingly, in addition to the presence of both physiological TSR2 transcripts, the two mutant transcripts were predominantly detected in the hairless skin of the affected cows. Immunohistochemistry, using an antibody against the N-terminal part of the bovine protein demonstrated the specific expression of the TSR2 protein in the skin and the hair of the affected and the control cows as well as in bovine fetal skin and hair. The RNA hybridization in situ showed that Tsr2 was expressed in pre- and post-natal phases of hair follicle development in mice. Mammalian TSR2 proteins are highly conserved and are known to be broadly expressed, but their precise in vivo functions are poorly understood. Thus, by dissecting a naturally occurring mutation in a domestic animal species, we identified TSR2 as a regulator of hair follicle development.
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