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Integration of chicken cytogenetic and genetic maps: 18 new polymorphic markers isolated from BAC and PAC clones
Author(s) -
Morisson M.,
Pitel F.,
Fillon V.,
Pouzadoux A.,
Bergé R.,
Vit J. P.,
Zoorob R.,
Auffray C.,
Gellin J.,
Vignal A.
Publication year - 1998
Publication title -
animal genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 81
eISSN - 1365-2052
pISSN - 0268-9146
DOI - 10.1046/j.1365-2052.1998.295348.x
Subject(s) - microchromosome , biology , genetics , gene mapping , genetic marker , microsatellite , bacterial artificial chromosome , chromosome , genetic linkage , fluorescence in situ hybridization , genome , karyotype , gene , allele
As an approach to integrate the chicken genetic and cytogenetic maps, bacterial artificial chromosome (BAC) and P1‐derived artificial chromosome (PAC) clones were localized by fluorescence in situ hybridization (FISH) on chromosomes and by genetic mapping on the East Lansing and Compton reference families. Some of the clones used in this study were previously selected for the presence of potentially polymorphic (CA)n repeats and a microsatellite marker was developed when possible for genetic mapping. For other clones, a single strand conformational polymorphism (SSCP) was developed and used for this purpose. Between the two approaches, 18 markers linking the cytogenetic and genetic maps, seven on macrochromosomes and 11 on microchromosomes, were generated. Our results enabled the assignment and orientation of a linkage group to chromosome 3, together with the assignment of linkage groups to eight different microchromosomes, a fraction of the genome lacking mapping data and for which the degree of coverage by the genetic map was not well estimated previously.