Publication:
Frequency of bovine congenital pseudomyotonia carriers in selected Italian Chianina sires

cris.virtual.author-orcid0000-0001-9773-522X
cris.virtualsource.author-orcid4f355f67-49ad-4eea-b71c-7496e5539155
cris.virtualsource.author-orcid478362cd-edc8-4f7e-a14f-4eedaf24c2c8
dc.contributor.authorMurgiano, Leonardo
dc.contributor.authorTestoni, S.
dc.contributor.authorDrögemüller, Cord
dc.contributor.authorBolcato, M.
dc.contributor.authorGentile, A.
dc.date.accessioned2024-10-14T16:15:37Z
dc.date.available2024-10-14T16:15:37Z
dc.date.issued2013-02
dc.description.abstractBovine congenital pseudomyotonia (PMT) is a genetic disease in Chianina and other breeds of cattle that induces muscular stiffness. PMT in the Chianina breed is caused by a missense mutation in exon 6 of the ATP2A1 gene, which encodes the SERCA1 pump. In this study, the prevalence of PMT carriers and the frequency of the deleterious PMT allele in selected subpopulations of the Chianina breed were estimated. The prevalence of PMT carriers among ranked Chianina sires used for artificial insemination in the years 2007-2011 was 13.6%. The frequency of PMT carriers in young bull calves born in the period January 2007 to June 2011 selected for a performance testing programme was 13.4%. Selective breeding against this genetic defect is restricted to males only and therefore is predicted to require at least seven generations to eradicate PMT.
dc.description.numberOfPages3
dc.description.sponsorshipInstitut für Genetik
dc.identifier.pmid22627047
dc.identifier.publisherDOI10.1016/j.tvjl.2012.04.021
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/114785
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofVeterinary journal
dc.relation.issn1090-0233
dc.relation.organizationDCD5A442C13CE17DE0405C82790C4DE2
dc.subject.ddc500 - Science::590 - Animals (Zoology)
dc.subject.ddc600 - Technology::630 - Agriculture
dc.titleFrequency of bovine congenital pseudomyotonia carriers in selected Italian Chianina sires
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage240
oaire.citation.issue2
oaire.citation.startPage238
oaire.citation.volume195
oairecerif.author.affiliationInstitut für Genetik
oairecerif.author.affiliationInstitut für Genetik
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unibe.description.ispublishedpub
unibe.eprints.legacyId43912
unibe.journal.abbrevTitleVET J
unibe.refereedTRUE
unibe.subtype.articlecontribution

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