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Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation
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 famil...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4512707/ https://www.ncbi.nlm.nih.gov/pubmed/26203908 http://dx.doi.org/10.1371/journal.pgen.1005427 |
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author | Murgiano, Leonardo Shirokova, Vera Welle, Monika Maria Jagannathan, Vidhya Plattet, Philippe Oevermann, Anna Pienkowska-Schelling, Aldona Gallo, Daniele Gentile, Arcangelo Mikkola, Marja Drögemüller, Cord |
author_facet | Murgiano, Leonardo Shirokova, Vera Welle, Monika Maria Jagannathan, Vidhya Plattet, Philippe Oevermann, Anna Pienkowska-Schelling, Aldona Gallo, Daniele Gentile, Arcangelo Mikkola, Marja Drögemüller, Cord |
author_sort | Murgiano, Leonardo |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4512707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45127072015-07-24 Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation Murgiano, Leonardo Shirokova, Vera Welle, Monika Maria Jagannathan, Vidhya Plattet, Philippe Oevermann, Anna Pienkowska-Schelling, Aldona Gallo, Daniele Gentile, Arcangelo Mikkola, Marja Drögemüller, Cord PLoS Genet Research Article 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. Public Library of Science 2015-07-23 /pmc/articles/PMC4512707/ /pubmed/26203908 http://dx.doi.org/10.1371/journal.pgen.1005427 Text en © 2015 Murgiano et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Murgiano, Leonardo Shirokova, Vera Welle, Monika Maria Jagannathan, Vidhya Plattet, Philippe Oevermann, Anna Pienkowska-Schelling, Aldona Gallo, Daniele Gentile, Arcangelo Mikkola, Marja Drögemüller, Cord Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation |
title | Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation |
title_full | Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation |
title_fullStr | Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation |
title_full_unstemmed | Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation |
title_short | Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation |
title_sort | hairless streaks in cattle implicate tsr2 in early hair follicle formation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4512707/ https://www.ncbi.nlm.nih.gov/pubmed/26203908 http://dx.doi.org/10.1371/journal.pgen.1005427 |
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