Duplicate Gene Expression in Allopolyploid Gossypium Reveals Two Temporally Distinct Phases of Expression Evolution

dc.contributor.author Flagel, Lex
dc.contributor.author Udall, Joshua
dc.contributor.author Nettleton, Dan
dc.contributor.author Wendel, Jonathan
dc.contributor.department Department of Ecology, Evolution, and Organismal Biology (CALS)
dc.date 2018-02-17T02:40:25.000
dc.date.accessioned 2020-06-30T02:18:56Z
dc.date.available 2020-06-30T02:18:56Z
dc.date.copyright Tue Jan 01 00:00:00 UTC 2008
dc.date.issued 2008-04-01
dc.description.abstract <p>Polyploidy has played a prominent role in shaping the genomic architecture of the angiosperms. Through allopolyploidization, several modern Gossypium (cotton) species contain two divergent, although largely redundant genomes. Owing to this redundancy, these genomes can play host to an array of evolutionary processes that act on duplicate genes. We compared homoeolog (genes duplicated by polyploidy) contributions to the transcriptome of a natural allopolyploid and a synthetic interspecific F1 hybrid, both derived from a merger between diploid species from the Gossypium A-genome and D-genome groups. Relative levels of A- and D-genome contributions to the petal transcriptome were determined for 1,383 gene pairs. This comparison permitted partitioning of homoeolog expression biases into those arising from genomic merger and those resulting from polyploidy. Within allopolyploid Gossypium, approximately 24% of the genes with biased (unequal contributions from the two homoeologous copies) expression patterns are inferred to have arisen as a consequence of genomic merger, indicating that a substantial fraction of homoeolog expression biases occur instantaneously with hybridization. The remaining 76% of biased homoeologs reflect long-term evolutionary forces, such as duplicate gene neofunctionalization and subfunctionalization. Finally, we observed a greater number of genes biased toward the paternal D-genome and that expression biases have tended to increases during allopolyploid evolution. Our results indicate that allopolyploidization entails significant homoeolog expression modulation, both immediately as a consequence of genomic merger, and secondarily as a result of long-term evolutionary transformations in duplicate gene expression.</p>
dc.description.comments <p>This article is from <em>BMC Biology</em> 6 (2008): 16, doi:<a href="http://dx.doi.org/10.1186/1741-7007-6-16" target="_blank">10.1186/1741-7007-6-16</a>. Posted with permission.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/eeob_ag_pubs/61/
dc.identifier.articleid 1052
dc.identifier.contextkey 7705455
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath eeob_ag_pubs/61
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/23317
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/eeob_ag_pubs/61/2008_Wendel_DuplicateGene.pdf|||Sat Jan 15 01:16:04 UTC 2022
dc.source.uri 10.1186/1741-7007-6-16
dc.subject.disciplines Botany
dc.subject.disciplines Ecology and Evolutionary Biology
dc.subject.disciplines Genetics and Genomics
dc.subject.disciplines Plant Breeding and Genetics
dc.subject.keywords Polyploidy
dc.subject.keywords angiosperm
dc.subject.keywords cotton
dc.subject.keywords allopolyploid
dc.subject.keywords duplicate gene expression
dc.title Duplicate Gene Expression in Allopolyploid Gossypium Reveals Two Temporally Distinct Phases of Expression Evolution
dc.type article
dc.type.genre article
dspace.entity.type Publication
relation.isAuthorOfPublication 7d86677d-f28f-4ab1-8cf7-70378992f75b
relation.isAuthorOfPublication 6d2c458f-b99a-4af5-8869-8b7b2e304592
relation.isOrgUnitOfPublication 6fa4d3a0-d4c9-4940-945f-9e5923aed691
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