Mutational dynamics and phylogenetic utility of noncoding chloroplast DNA

被引:157
作者
Borsch, Thomas [1 ,2 ]
Quandt, Dietmar [3 ]
机构
[1] Free Univ Berlin, Bot Garten & Bot Museum Berlin Dahlem, D-14195 Berlin, Germany
[2] Free Univ Berlin, Inst Biol Bot, D-14195 Berlin, Germany
[3] Univ Bonn, Nees Inst Biodiversitat Pflanzen, D-53115 Bonn, Germany
关键词
Spacers; Introns; Phylogenetic structure R; Molecular evolution; SSRs; Inversions; Mutational hotspots; DNA barcoding; GROUP-II INTRON; COMPLETE NUCLEOTIDE-SEQUENCE; PLASTID GENOME SEQUENCE; RBCL INTERGENIC SPACER; RIBOSOMAL-RNA GENES; TRNT-TRNF REGION; MOLECULAR EVOLUTION; RPS16; INTRON; MATK GENE; MICROSTRUCTURAL CHANGES;
D O I
10.1007/s00606-009-0210-8
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Introns and spacers are a rich and well-appreciated information source for evolutionary studies in plants. Compared to coding sequences, the mutational dynamics of introns and spacers is very different, involving frequent microstructural changes in addition to substitutions of individual nucleotides. An understanding of the biology of sequence change is required for correct application of molecular characters in phylogenetic analyses, including homology assessment, alignment coding, and tree inference. The widely used term "indel'' is very general, and different kinds of microstructural mutations, such as simple sequence repeats, short tandem repeats, homonucleotide repeats, inversions, inverted repeats, and deletions, need to be distinguished. Noncoding DNA has been indispensable for analyses at the species level because coding sequences usually do not offer sufficient variability. A variety of introns and spacers has been successfully applied for phylogeny inference at deeper levels (major lineages of angiosperms and land plants) in past years, and phylogenetic structure R in intron and spacer data sets usually outperforms that of coding-sequence data sets. In order to fully utilize their potential, the molecular evolution and applicability of the most important noncoding markers (the trnT-trnF region comprising two spacers and a group I intron; the trnS-G region comprising one spacer and a group II intron in trnG; the group II introns in petD, rpl16, rps16, and trnK; and the atpB-rbcL and psbA-trnG spacers) are reviewed. The study argues for the use of noncoding DNA in a spectrum of applications from deep-level phylogenetics to speciation studies and barcoding, and aims at outlining molecular evolutionary principles needed for effective analysis.
引用
收藏
页码:169 / 199
页数:31
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