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A 3.7 Mb Deletion Encompassing ZEB2 Causes a Novel Polled and Multisystemic Syndrome in the Progeny of a Somatic Mosaic Bull

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Title
A 3.7 Mb Deletion Encompassing ZEB2 Causes a Novel Polled and Multisystemic Syndrome in the Progeny of a Somatic Mosaic Bull
Published in
PLOS ONE, November 2012
DOI 10.1371/journal.pone.0049084
Pubmed ID
Authors

Aurélien Capitan, Aurélie Allais-Bonnet, Alain Pinton, Brigitte Marquant-Le Guienne, Daniel Le Bourhis, Cécile Grohs, Stéphan Bouet, Laëtitia Clément, Laura Salas-Cortes, Eric Venot, Stéphane Chaffaux, Bernard Weiss, Arnaud Delpeuch, Guy Noé, Marie-Noëlle Rossignol, Sarah Barbey, Dominique Dozias, Emilie Cobo, Harmonie Barasc, Aurélie Auguste, Maëlle Pannetier, Marie-Christine Deloche, Emeline Lhuilier, Olivier Bouchez, Diane Esquerré, Gérald Salin, Christophe Klopp, Cécile Donnadieu, Céline Chantry-Darmon, Hélène Hayes, Yves Gallard, Claire Ponsart, Didier Boichard, Eric Pailhoux

Abstract

Polled and Multisystemic Syndrome (PMS) is a novel developmental disorder occurring in the progeny of a single bull. Its clinical spectrum includes polledness (complete agenesis of horns), facial dysmorphism, growth delay, chronic diarrhea, premature ovarian failure, and variable neurological and cardiac anomalies. PMS is also characterized by a deviation of the sex-ratio, suggesting male lethality during pregnancy. Using Mendelian error mapping and whole-genome sequencing, we identified a 3.7 Mb deletion on the paternal bovine chromosome 2 encompassing ARHGAP15, GTDC1 and ZEB2 genes. We then produced control and affected 90-day old fetuses to characterize this syndrome by histological and expression analyses. Compared to wild type individuals, affected animals showed a decreased expression of the three deleted genes. Based on a comparison with human Mowat-Wilson syndrome, we suggest that deletion of ZEB2, is responsible for most of the effects of the mutation. Finally sperm-FISH, embryo genotyping and analysis of reproduction records confirmed somatic mosaicism in the founder bull and male-specific lethality during the first third of gestation. In conclusion, we identified a novel locus involved in bovid horn ontogenesis and suggest that epithelial-to-mesenchymal transition plays a critical role in horn bud differentiation. We also provide new insights into the pathogenicity of ZEB2 loss of heterozygosity in bovine and humans and describe the first case of male-specific lethality associated with an autosomal locus in a non-murine mammalian species. This result sets PMS as a unique model to study sex-specific gene expression/regulation.

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Geographical breakdown

Country Count As %
United States 1 2%
Poland 1 2%
France 1 2%
Unknown 50 94%

Demographic breakdown

Readers by professional status Count As %
Researcher 11 21%
Student > Ph. D. Student 10 19%
Professor > Associate Professor 5 9%
Student > Master 5 9%
Student > Bachelor 3 6%
Other 8 15%
Unknown 11 21%
Readers by discipline Count As %
Agricultural and Biological Sciences 27 51%
Medicine and Dentistry 4 8%
Biochemistry, Genetics and Molecular Biology 4 8%
Neuroscience 2 4%
Psychology 1 2%
Other 1 2%
Unknown 14 26%