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Evidence of Neutral Transcriptome Evolution in Plants

M. R. Broadley, P. J. White, J. P. Hammond, N. S. Graham, H. C. Bowen, Z. F. Emmerson, R. G. Fray, P. P. M. Iannetta, J. W. McNicol and S. T. May
The New Phytologist
Vol. 180, No. 3 (Nov., 2008), pp. 587-593
Published by: Wiley on behalf of the New Phytologist Trust
Stable URL: http://www.jstor.org/stable/25150609
Page Count: 7
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Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Evidence of Neutral Transcriptome Evolution in Plants
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Abstract

The transcriptome of an organism is its set of gene transcripts (mRNAs) at a defined spatial and temporal locus. Because gene expression is affected markedly by environmental and developmental perturbations, it is widely assumed that transcriptome divergence among taxa represents adaptive phenotypic selection. This assumption has been challenged by neutral theories which propose that stochastic processes drive transcriptome evolution. To test for evidence of neutral transcriptome evolution in plants, we quantified 18 494 gene transcripts in nonsenescent leaves of 14 taxa of Brassicaceae using robust cross-species transcriptomics which includes a two-step physical and in silico-based normalization procedure based on DNA similarity among taxa. Transcriptome divergence correlates positively with evolutionary distance between taxa and with variation in gene expression among samples. Results are similar for pseudogenes and chloroplast genes evolving at different rates. Remarkably, variation in transcript abundance among root-cell samples correlates positively with transcriptome divergence among root tissues and among taxa. Because neutral processes affect transcriptome evolution in plants, many differences in gene expression among or within taxa may be nonfunctional, reflecting ancestral plasticity and founder effects. Appropriate null models are required when comparing transcriptomes in space and time.

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