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Birth of Four Chimeric Plastid Gene Clusters in Japanese Umbrella Pine

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Date 2016 Jun 9
PMID 27269365
Citations 17
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Abstract

Many genes in the plastid genomes (plastomes) of plants are organized as gene clusters, in which genes are co-transcribed, resembling bacterial operons. These plastid operons are highly conserved, even among conifers, whose plastomes are highly rearranged relative to other seed plants. We have determined the complete plastome sequence of Sciadopitys verticillata (Japanese umbrella pine), the sole member of Sciadopityaceae. The Sciadopitys plastome is characterized by extensive inversions, pseudogenization of four tRNA genes after tandem duplications, and a unique pair of 370-bp inverted repeats involved in the formation of isomeric plastomes. We showed that plastomic inversions in Sciadopitys have led to shuffling of the remote conserved operons, resulting in the birth of four chimeric gene clusters. Our data also demonstrated that the relocated genes can be co-transcribed in these chimeric gene clusters. The plastome of Sciadopitys advances our current understanding of how the conifer plastomes have evolved toward increased diversity and complexity.

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References
1.
Wyman S, Jansen R, Boore J . Automatic annotation of organellar genomes with DOGMA. Bioinformatics. 2004; 20(17):3252-5. DOI: 10.1093/bioinformatics/bth352. View

2.
Sugiura M . The chloroplast genome. Plant Mol Biol. 1992; 19(1):149-68. DOI: 10.1007/BF00015612. View

3.
Wu C, Wang Y, Liu S, Chaw S . Chloroplast genome (cpDNA) of Cycas taitungensis and 56 cp protein-coding genes of Gnetum parvifolium: insights into cpDNA evolution and phylogeny of extant seed plants. Mol Biol Evol. 2007; 24(6):1366-79. DOI: 10.1093/molbev/msm059. View

4.
Wu C, Lin C, Hsu C, Wang R, Chaw S . Comparative chloroplast genomes of pinaceae: insights into the mechanism of diversified genomic organizations. Genome Biol Evol. 2011; 3:309-19. PMC: 5654405. DOI: 10.1093/gbe/evr026. View

5.
Guo W, Grewe F, Cobo-Clark A, Fan W, Duan Z, Adams R . Predominant and substoichiometric isomers of the plastid genome coexist within Juniperus plants and have shifted multiple times during cupressophyte evolution. Genome Biol Evol. 2014; 6(3):580-90. PMC: 3971597. DOI: 10.1093/gbe/evu046. View