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Complete chloroplast genome sequences of Solanum bulbocastanum, Solanum lycopersicum and comparative analyses with other Solanaceae genomes
Authors:Henry Daniell  Seung-Bum Lee  Justin Grevich  Christopher Saski  Tania Quesada-Vargas  Chittibabu Guda  Jeffrey Tomkins  Robert K. Jansen
Affiliation:(1) Department of Molecular Biology & Microbiology, Biomolecular Science, University of Central Florida, 4000 Central Florida Blvd, Bldg # 20, Room 336, Orlando, FL 32816-2364, USA;(2) Clemson University Genomics Institute, Biosystems Research Complex, Clemson University, 51 New Cherry Street, Clemson, SC 29634, USA;(3) Gen*NY*Sis Center for Excellence in Cancer Genomics, Department of Epidemiology & Biostatistics, University at Albany, State University of New York, 1 University Place, Rensselaer, NY 12144, USA;(4) Section of Integrative Biology and Institute of Cellular and Molecular Biology, Patterson Laboratories 141, University of Texas, Austin, TX 78712, USA
Abstract:Despite the agricultural importance of both potato and tomato, very little is known about their chloroplast genomes. Analysis of the complete sequences of tomato, potato, tobacco, and Atropa chloroplast genomes reveals significant insertions and deletions within certain coding regions or regulatory sequences (e.g., deletion of repeated sequences within 16S rRNA, ycf2 or ribosomal binding sites in ycf2). RNA, photosynthesis, and atp synthase genes are the least divergent and the most divergent genes are clpP, cemA, ccsA, and matK. Repeat analyses identified 33–45 direct and inverted repeats ≥30 bp with a sequence identity of at least 90%; all but five of the repeats shared by all four Solanaceae genomes are located in the same genes or intergenic regions, suggesting a functional role. A comprehensive genome-wide analysis of all coding sequences and intergenic spacer regions was done for the first time in chloroplast genomes. Only four spacer regions are fully conserved (100% sequence identity) among all genomes; deletions or insertions within some intergenic spacer regions result in less than 25% sequence identity, underscoring the importance of choosing appropriate intergenic spacers for plastid transformation and providing valuable new information for phylogenetic utility of the chloroplast intergenic spacer regions. Comparison of coding sequences with expressed sequence tags showed considerable amount of variation, resulting in amino acid changes; none of the C-to-U conversions observed in potato and tomato were conserved in tobacco and Atropa. It is possible that there has been a loss of conserved editing sites in potato and tomato.Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.
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