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dc.contributor.authorCheng, Yuanyuan
dc.contributor.authorStuart, Andrew
dc.contributor.authorMorris, Katrina
dc.contributor.authorTaylor, Robyn
dc.contributor.authorSiddle, Hannah
dc.contributor.authorDeakin, Janine
dc.contributor.authorJones, Menna
dc.contributor.authorAmemiya, Chris T
dc.contributor.authorBelov, Katherine
dc.date.accessioned2012-08-08T11:05:36Z
dc.date.available2012-08-08T11:05:36Z
dc.date.issued2012-03-12
dc.identifier.issn1471-2164
dc.identifier.urihttp://www.dspace.cam.ac.uk/handle/1810/243582
dc.descriptionRIGHTS : This article is licensed under the BioMed Central licence at http://www.biomedcentral.com/about/license which is similar to the 'Creative Commons Attribution Licence'. In brief you may : copy, distribute, and display the work; make derivative works; or make commercial use of the work - under the following conditions: the original author must be given credit; for any reuse or distribution, it must be made clear to others what the license terms of this work are.
dc.description.abstractBACKGROUND: The Tasmanian devil (Sarcophilus harrisii) is currently under threat of extinction due to an unusual fatal contagious cancer called Devil Facial Tumour Disease (DFTD). DFTD is caused by a clonal tumour cell line that is transmitted between unrelated individuals as an allograft without triggering immune rejection due to low levels of Major Histocompatibility Complex (MHC) diversity in Tasmanian devils. RESULTS: Here we report the characterization of the genomic regions encompassing MHC Class I and Class II genes in the Tasmanian devil. Four genomic regions approximately 960 kb in length were assembled and annotated using BAC contigs and physically mapped to devil Chromosome 4q. 34 genes and pseudogenes were identified, including five Class I and four Class II loci. Interestingly, when two haplotypes from two individuals were compared, three genomic copy number variants with sizes ranging from 1.6 to 17 kb were observed within the classical Class I gene region. One deletion is particularly important as it turns a Class Ia gene into a pseudogene in one of the haplotypes. This deletion explains the previously observed variation in the Class I allelic number between individuals. The frequency of this deletion is highest in the northwestern devil population and lowest in southeastern areas. CONCLUSIONS: The third sequenced marsupial MHC provides insights into the evolution of this dynamic genomic region among the diverse marsupial species. The two sequenced devil MHC haplotypes revealed three copy number variations that are likely to significantly affect immune response and suggest that future work should focus on the role of copy number variations in disease susceptibility in this species.
dc.language.isoen
dc.publisherSpringer Science and Business Media LLC
dc.rightsAll Rights Reserved
dc.rights.urihttps://www.rioxx.net/licenses/all-rights-reserved/
dc.titleAntigen-presenting genes and genomic copy number variations in the Tasmanian devil MHC.
dc.typeArticle
dc.type.versionPublished Version
dc.date.updated2012-08-08T11:05:36Z
dc.rights.holderYuanyuan Cheng et al.; licensee BioMed Central Ltd.
prism.publicationNameBMC Genomics
pubs.declined2017-10-11T13:54:30.472+0100
dcterms.dateAccepted2012-03-12
rioxxterms.versionofrecord10.1186/1471-2164-13-87
dc.identifier.eissn1471-2164
cam.issuedOnline2012-03-12


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