|
|
|
|
Genome Res. 15:1292-1297, 2005 ©2005 by Cold Spring Harbor Laboratory Press; ISSN 1088-9051/05 $5.00 Letter The evolutionary fate of MULE-mediated duplications of host gene fragments in riceDepartment of Biology, McGill University, Montreal, Quebec, H3A 1B1, Canada
DNA transposons are known to frequently capture duplicated fragments of host genes. The evolutionary impact of this phenomenon depends on how frequently the fragments retain protein-coding function as opposed to becoming pseudogenes. Gene fragment duplication by Mutator-like elements (MULEs) has previously been documented in maize, Arabidopsis, and rice. Here we present a rigorous genome-wide analysis of MULEs in the model plant Oryza sativa (domesticated rice). We identify 8274 MULEs with intact termini and target-site duplications (TSDs) and show that 1337 of them contain duplicated host gene fragments. Through a detailed examination of the 5% of duplicated gene fragments that are transcribed, we demonstrate that virtually all cases contain pseudogenic features such as fragmented conserved protein domains, frameshifts, and premature stop codons. In addition, we show that the distribution of the ratio of nonsynonymous to synonymous amino acid substitution rates for the duplications agrees with the expected distribution for pseudogenes. We conclude that MULE-mediated host gene duplication results in the formation of pseudogenes, not novel functional protein-coding genes; however, the transcribed duplications possess characteristics consistent with a potential role in the regulation of host gene expression.
1 These authors contributed equally to this work 2 Present address: Samuel Lunenfeld Research Institute, Toronto, Ontario, M5G 1X5, Canada.
3 Corresponding author. [Supplemental material is available online at www.genome.org. The following individuals kindly provided reagents, samples, or unpublished information as indicated in the paper: S.I. Wright and T. Sasaki.] Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.4064205.
This article has been cited by other articles:
|
|||||||||||||||||||||||||||||||||||||