Chromosomal mapping of chicken mega-telomere arrays to GGA9, 16, 28 and W using a cytogenomic approach

• Published in: Cytogenetic and genome research Vol. 117; no. 1-4; pp. 54 - 63
• Main Authors: Delany, M.E., Gessaro, T.M., Rodrigue, K.L., Daniels, L.M.
• Format: Journal Article
• Language: English
• Published: Basel, Switzerland S. Karger AG 01.07.2007
• Subjects: Animals; Cell Lineage; Cells, Cultured; Chickens - genetics; Cytogenetic Analysis; Cytogenetics; Genomics; In Situ Hybridization; Physical Chromosome Mapping; Telomere - genetics
• ISBN: 3805583389; 9783805583381
• ISSN: 1424-8581; 1424-859X
• DOI: 10.1159/000103165

Four mega-telomere loci were mapped to chicken chromosomes 9, 16, 28, and the W sex chromosome by dual-color fluorescence in situ hybridization using a telomeric sequence probe and BAC clones previously assigned to chicken chromosomes. The in-common features of the mega-telomere chromosomes are that microchromosomes are involved rather than macrochromosomes; in three cases (9, 16, 28) acrocentrics are involved with the mega-telomeres mapping to the p arms. Three of the four chromosomes (9, 16, W) encode tandem repeats which in two cases (9 and 16) involve the ribosomal DNA arrays (the 5S and 18S-5.8S-28S gene repeats, respectively). All involved chromosomes have a typical-sized telomere on the opposite terminus. Intra- and interindividual variation for mega-telomere distribution are discussed in terms of karyotype abnormalities and the potential for mitotic instability of some telomeres. The diversity and distribution of telomere array quantity in the chicken genome should be useful in contributing to research related to telomere length regulation – how and by what mechanism genomes and individual chromosomes establish and maintain distinct sets of telomere array sizes, as well as for future studies related to stability of the chicken genome affecting development, growth, cellular lifespan and disease. An additional impact of this study includes the listing of BAC clones (26 autosomal and six W BACs tested) that were cytogenetically verified; this set of BACs provide a useful tool for future cytogenetic analyses of the microchromosomes.