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Cytogenetic screening of a canadian pig breeding unit

TLDR
The cytogenetic study on the chromosomal makeup and breeding data of 29 boars housed in a Canadian pig farm revealed that three aberrations seemed to be responsible for ~35% decrease in prolificacy.
Abstract
A cytogenetic study was undertaken on the chromosomal makeup and breeding data of 29 boars housed in a Canadian pig farm. Blood cultures were made and chromosome spreads were examined, searching for carriers of chromosomal abnormalities. The investigation revealed that twenty-six individuals had a normal karyotype and 3 (10.3%) carried the following aberrations: (a) two 1/6 translocations in two - unrelated - individuals, (b) one reciprocal translocation rcp(10;13). The litter size of the two boars carrying the 1/6 translocation was, on average, 6.5 and 5.8, respectively. The mean size of the litter sired by the boar carrying the rcp(10;13) was 6.0. As compared with the average litter size (11.0) sired by the normal boars in the herd, the translocations described here seemed to be responsible for ~35% decrease in prolificacy.

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References
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Journal ArticleDOI

A rapid banding technique for human chromosomes

Marina Seabright
- 30 Oct 1971 - 
Journal ArticleDOI

Standard karyotype of the domestic pig. Committee for the Standardized Karyotype of the Domestic Pig.

TL;DR: Identification des bandes chromosomiques du porc en regions cytologiquement definies utilisables pour les descriptions de caryotypes normaux and aberrants.
Journal ArticleDOI

Nine new cases of reciprocal translocation in the domestic pig (Sus scrofa domestica L.)

TL;DR: Nine pigs with decreased litter size or sired by boars with decreases litter size were found to be reciprocal translocation carriers and a Gascon breed boar with reduced prolificacy also had an abnormal karyotype, namely 38 XY.
Journal ArticleDOI

Chromosomal rearrangements in cattle and pigs revealed by chromosome microdissection and chromosome painting

TL;DR: The results presented in this paper show the usefulness of the microdissection technique for characterising chromosomal rearrangements in species for which commercial probes are not available and confirmed that the main limiting factor of the technique is the quality of the chromosomal preparations, which does not allow the identification of target chromosomes or chromosome fragments in all cases.