dc.creatorWang, Jianping 
dc.creatorRoe, Bruce 
dc.creatorMacmil, Simone 
dc.creatorYu, Qingyi 
dc.creatorMurray, Jan E
dc.creatorTang, Haibao 
dc.creatorChen, Cuixia 
dc.creatorNajar, Fares 
dc.creatorWiley, Graham 
dc.creatorBowers, John 
dc.creatorVan Sluys, Marie-Anne 
dc.creatorRokhsar, Daniel S
dc.creatorHudson, Matthew E
dc.creatorMoose, Stephen P
dc.creatorPaterson, Andrew H
dc.creatorMing, Ray 
dc.date.accessioned2013-08-26T16:57:42Z
dc.date.accessioned2018-07-04T16:26:41Z
dc.date.available2013-08-26T16:57:42Z
dc.date.available2018-07-04T16:26:41Z
dc.date.created2013-08-26T16:57:42Z
dc.date.issued2010-04
dc.identifier1471-2164
dc.identifierhttp://www.producao.usp.br/handle/BDPI/32773
dc.identifier10.1186/1471-2164-11-261
dc.identifierhttp://www.biomedcentral.com/1471-2164/11/261
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1635930
dc.description.abstractAbstract Background Sugarcane (Saccharum spp.) has become an increasingly important crop for its leading role in biofuel production. The high sugar content species S. officinarum is an octoploid without known diploid or tetraploid progenitors. Commercial sugarcane cultivars are hybrids between S. officinarum and wild species S. spontaneum with ploidy at ~12×. The complex autopolyploid sugarcane genome has not been characterized at the DNA sequence level. Results The microsynteny between sugarcane and sorghum was assessed by comparing 454 pyrosequences of 20 sugarcane bacterial artificial chromosomes (BACs) with sorghum sequences. These 20 BACs were selected by hybridization of 1961 single copy sorghum overgo probes to the sugarcane BAC library with one sugarcane BAC corresponding to each of the 20 sorghum chromosome arms. The genic regions of the sugarcane BACs shared an average of 95.2% sequence identity with sorghum, and the sorghum genome was used as a template to order sequence contigs covering 78.2% of the 20 BAC sequences. About 53.1% of the sugarcane BAC sequences are aligned with sorghum sequence. The unaligned regions contain non-coding and repetitive sequences. Within the aligned sequences, 209 genes were annotated in sugarcane and 202 in sorghum. Seventeen genes appeared to be sugarcane-specific and all validated by sugarcane ESTs, while 12 appeared sorghum-specific but only one validated by sorghum ESTs. Twelve of the 17 sugarcane-specific genes have no match in the non-redundant protein database in GenBank, perhaps encoding proteins for sugarcane-specific processes. The sorghum orthologous regions appeared to have expanded relative to sugarcane, mostly by the increase of retrotransposons. Conclusions The sugarcane and sorghum genomes are mostly collinear in the genic regions, and the sorghum genome can be used as a template for assembling much of the genic DNA of the autopolyploid sugarcane genome. The comparable gene density between sugarcane BACs and corresponding sorghum sequences defied the notion that polyploidy species might have faster pace of gene loss due to the redundancy of multiple alleles at each locus.
dc.languageeng
dc.relationBMC Genomics
dc.rightsWang et al; licensee BioMed Central Ltd. - This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.rightsopenAccess
dc.titleMicrocollinearity between autopolyploid sugarcane and diploid sorghum genomes
dc.typeArtículos de revistas


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