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Nucleic Acids Research 2004 32(12):3615-3622; doi:10.1093/nar/gkh695
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Published online 7 July 2004

Nucleic Acids Research, Vol. 32 No. 12 © Oxford University Press 2004; all rights reserved

Rapid evolution of RNA editing sites in a small non-essential plastid gene

Andreas Fiebig1, Sandra Stegemann1 and Ralph Bock1,2,*

1 Westfälische Wilhelms-Universität Münster, Institut für Biochemie und Biotechnologie der Pflanzen, Hindenburgplatz 55, D-48143 Münster, Germany and 2 Max-Planck-Institut für Molekulare Pflanzenphysiologie, Am Mühlenberg 1, D-14476 Golm, Germany

* To whom correspondence should be addressed. Tel: +49 331 567 8700; Fax: +49 331 567 898700; Email: rbock{at}mpimp-golm.mpg.de
This publication is dedicated to our colleague and friend Professor Rainer Maier, co-discoverer of RNA editing in plastids, who sadly passed away on April 25,2004

Received June 4, 2004; Revised and Accepted June 21, 2004

Chloroplast RNA editing proceeds by C-to-U transitions at highly specific sites. Here, we provide a phylogenetic analysis of RNA editing in a small plastid gene, petL, encoding subunit VI of the cytochrome b6f complex. Analyzing representatives from most major groups of seed plants, we find an unexpectedly high frequency and dynamics of RNA editing. High-frequency editing has previously been observed in plastid ndh genes, which are remarkable in that their mutational inactivation does not produce an obvious mutant phenotype. In order to test the idea that reduced functional constraints allow for more flexible evolution of RNA editing sites, we have created petL knockout plants by tobacco chloroplast transformation. We find that, in the higher plant tobacco, targeted inactivation of petL does not impair plant growth under a variety of conditions markedly contrasting the important role of petL in photosynthesis in the green alga Chlamydomonas reinhardtii. Together with a low number of editing sites in plastid genes that are essential to gene expression and photosynthetic activity, these data suggest that RNA editing sites may evolve more readily in those genes whose transitory loss of function can be tolerated. Accumulated evidence for this ‘relative neutrality hypothesis for the evolution of plastid editing sites’ is discussed.


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