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RNA editing in an untranslated region of the Ginkgo chloroplast genome.
Authors:J Kudla  R Bock
Institution:1. Allgemeine Botanik, Universität Ulm, Albert-Einstein-Allee 11, D-89069 Ulm, Germany;2. Institut für Biologie III, Universität Freiburg, Schänzlestraße 1, D-79104 Freiburg, Germany;1. College of Horticulture and Plant Protection, Yangzhou University, Yangzhou, 225009, China;2. Resources & Environment College, Tibet Agriculture & Animal Husbandry University, Linzhi, 860000, China;1. College of Horticulture and Plant Protection, Yangzhou University, Yangzhou 225009, China;2. Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing 210037, China;1. Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, China;2. University of Chinese Academy of Sciences, Beijing, 100049, China
Abstract:mRNAs in plant cell organelles can be subject to RNA editing, an RNA processing step altering the identity of single nucleotide residues. In higher plant chloroplasts, editing proceeds by C-to-U conversions at highly specific sites. All known plastid RNA editing sites are located in protein-coding regions and, typically, change the coding properties of the mRNA. To gain more insight into the evolution of editing, we have determined the molecular structure and RNA editing pattern of the psbE operon of the primitive seed plant Ginkgo biloba. We report here the identification of altogether four sites of C-to-U editing, two of which are unique to Ginkgo and have not been found in other species. Surprisingly, one of the sites is located in an intercistronic spacer, thus being the first chloroplast editing site detected outside a protein-coding region. This indicates that the plastid editing machinery can operate also in untranslated regions and without having apparent functional consequences.
Keywords:
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