ArticleBMC genomics2008
Addition of the microchromosome GGA25 to the chicken genome sequence assembly through radiation hybrid and genetic mapping.
Article in BMC genomics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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7 citing papers in PubMed.
- Conservation and losses of non-coding RNAs in avian genomes.PloS one · 2015Article
- Mapping and genotypic analysis of the NK-lysin gene in chicken.Genetics, selection, evolution : GSE · 2014Article
- A duck RH panel and its potential for assisting NGS genome assembly.BMC genomics · 2012Article
- Epilepsy caused by an abnormal alternative splicing with dosage effect of the SV2A gene in a chicken model.PloS one · 2011Article
- Integrative mapping analysis of chicken microchromosome 16 organization.BMC genomics · 2010Article
- Genomic organization and molecular phylogenies of the beta (beta) keratin multigene family in the chicken (Gallus gallus) and zebra finch (Taeniopygia guttata): implications for feather evolution.BMC evolutionary biology · 2010Article
- Comparative genomics in chicken and Pekin duck using FISH mapping and microarray analysis.BMC genomics · 2009Article
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14 authors.
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Abstract
backgroundThe publication of the first draft chicken sequence assembly became available in 2004 and was updated in 2006. However, this does not constitute a definitive and complete sequence of the chicken genome, since the microchromosomes are notably under-represented. In an effort to develop maps for the microchromosomes absent from the chicken genome assembly, we developed radiation hybrid (RH) and genetic maps with markers isolated from sequence currently assigned to "chromosome Unknown" (chrUn). The chrUn is composed of sequence contigs not assigned to named chromosomes. To identify and map sequence belonging to the microchromosomes we used a comparative mapping strategy, and we focused on the small linkage group E26C13.
resultsIn total, 139 markers were analysed with the chickRH6 panel, of which 120 were effectively assigned to the E26C13 linkage group, the remainder mapping elsewhere in the genome. The final RH map is composed of 22 framework markers extending over a 245.6 cR distance. A corresponding genetic map was developed, whose length is 103 cM in the East Lansing reference population. The E26C13 group was assigned to GGA25 (Gallus gallus chromosome 25) by FISH (fluorescence in situ hybridisation) mapping.
conclusionThe high-resolution RH framework map obtained here covers the entire chicken chromosome 25 and reveals the existence of a high number of intrachromosomal rearrangements when compared to the human genome. The strategy used here for the characterization of GGA25 could be used to improve knowledge on the other uncharacterized small, yet gene-rich microchromosomes.
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