Transfer of Chloroplast Genomic DNA to Mitochondrial Genome Occurred At Least 300 MYA
Author(s) -
Daryi Wang,
YuWei Wu,
Arthur Chun-Chieh Shih,
Chung-Shien Wu,
Yanan Wang,
ShuMiaw Chaw
Publication year - 2007
Publication title -
molecular biology and evolution
Language(s) - English
Resource type - Journals
eISSN - 1537-1719
pISSN - 0737-4038
DOI - 10.1093/molbev/msm133
Subject(s) - biology , chloroplast dna , mitochondrial dna , genome , phylogenetic tree , most recent common ancestor , horizontal gene transfer , transfer rna , genetics , gymnosperm , evolutionary biology , gene , botany , rna
With the completion of the first gymnosperm mitochondrial genome (mtDNA) from Cycas taitungensis and the availability of more mtDNA taxa in the past 5 years, we have conducted a systematic analysis of DNA transfer from chloroplast genomes (cpDNAs) to mtDNAs (mtpts) in 11 plants, including 2 algae, 1 liverwort, 1 moss, 1 gymnosperm, 3 monocots, and 3 eudicots. By using shared gene order and boundaries between different mtpts as the criterion, the timing of cpDNA transfer during plant evolution was estimated from the phylogenetic tree reconstructed independently from concatenated protein-coding genes of 11 available mtDNAs. Several interesting findings emerged. First, frequent DNA transfer from cpDNA to mtDNA occurred at least as far back as the common ancestor of extant gymnosperms and angiosperms, about 300 MYA. The oldest mtpt is trnV(uac)-trnM(cau)-atpE-atpB-rbcL. Three other mtpts--psaA-psaB, rps19-trnH(gug)-rpl2-rpl23, and psbE-psbF--were dated to the common ancestor of extant angiosperms, at least 150 MYA. However, all protein-coding genes of mtpts have degenerated since their first transfer. Therefore, mtpts contribute nothing to the functioning of mtDNA but junk sequences. We discovered that the cpDNA transfers have occurred randomly at any positions of the cpDNAs. We provide strong evidence that the cp-derived tRNA-trnM(cau) is the only mtpt (1 out of 3 cp-derived tRNA shared by seed plants) truly transferred from cpDNA to mtDNA since the time of the common ancestor of extant gymnosperms and angiosperms. Our observations support the proposition of Richly and Leister (2004) that "primary insertions of organellar DNAs are large and then diverge and fragment over evolutionary time."
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