MBE Advance Access originally published online on January 12, 2008
Molecular Biology and Evolution 2008 25(3):603-615; doi:10.1093/molbev/msn009
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Research Articles |
The Mitochondrial Genome of the Gymnosperm Cycas taitungensis Contains a Novel Family of Short Interspersed Elements, Bpu Sequences, and Abundant RNA Editing Sites

,¶
* Research Center for Biodiversity, Academia Sinica, Taipei, Taiwan
Institute of Information Science, Academia Sinica, Taipei, Taiwan
Department of Informatics, Indiana University
Institute of Medical Biotechnology, Central Taiwan University of Science and Technology, Taichung City, Taiwan
E-mail: smchaw{at}sinica.edu.tw.
Accepted for publication January 6, 2008.
The mtDNA of Cycas taitungensis is a circular molecule of 414,903 bp, making it 2- to 6-fold larger than the known mtDNAs of charophytes and bryophytes, but similar to the average of 7 elucidated angiosperm mtDNAs. It is characterized by abundant RNA editing sites (1,084), more than twice the number found in the angiosperm mtDNAs. The A + T content of Cycas mtDNA is 53.1%, the lowest among known land plants. About 5% of the Cycas mtDNA is composed of a novel family of mobile elements, which we designated as "Bpu sequences." They share a consensus sequence of 36 bp with 2 terminal direct repeats (AAGG) and a recognition site for the Bpu 10I restriction endonuclease (CCTGAAGC). Comparison of the Cycas mtDNA with other plant mtDNAs revealed many new insights into the biology and evolution of land plant mtDNAs. For example, the noncoding sequences in mtDNAs have drastically expanded as land plants have evolved, with abrupt increases appearing in the bryophytes, and then in the seed plants. As a result, the genomic organizations of seed plant mtDNAs are much less compact than in other plants. Also, the Cycas mtDNA appears to have been exempted from the frequent gene loss observed in angiosperm mtDNAs. Similar to the angiosperms, the 3 Cycas genes nad1, nad2, and nad5 are disrupted by 5 group II intron squences, which have brought the genes into trans-splicing arrangements. The evolutionary origin and invasion/duplication mechanism of the Bpu sequences in Cycas mtDNA are hypothesized and discussed.
Key Words: mitochondrial genome Cycas RNA editing sites repeats mobile elements
William Martin, Associate Editor
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
F. Grewe, P. Viehoever, B. Weisshaar, and V. Knoop A trans-splicing group I intron and tRNA-hyperediting in the mitochondrial genome of the lycophyte Isoetes engelmannii Nucleic Acids Res., August 1, 2009; 37(15): 5093 - 5104. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. P. Mower The PREP suite: predictive RNA editors for plant mitochondrial genes, chloroplast genes and user-defined alignments Nucleic Acids Res., July 1, 2009; 37(suppl_2): W253 - W259. [Abstract] [Full Text] [PDF] |
||||
![]() |
S.-L. Liu, Y. Zhuang, P. Zhang, and K. L. Adams Comparative Analysis of Structural Diversity and Sequence Evolution in Plant Mitochondrial Genes Transferred to the Nucleus Mol. Biol. Evol., April 1, 2009; 26(4): 875 - 891. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. V. Sanchez-Puerta, Y. Cho, J. P. Mower, A. J. Alverson, and J. D. Palmer Frequent, Phylogenetically Local Horizontal Transfer of the cox1 Group I Intron in Flowering Plant Mitochondria Mol. Biol. Evol., August 1, 2008; 25(8): 1762 - 1777. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. R. Duvall, J. W. Robinson, J. G. Mattson, and A. Moore Phylogenetic analyses of two mitochondrial metabolic genes sampled in parallel from angiosperms find fundamental interlocus incongruence Am. J. Botany, July 1, 2008; 95(7): 871 - 884. [Abstract] [Full Text] [PDF] |
||||


