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PLOS ONE  2012 

Analysis of Complete Nucleotide Sequences of 12 Gossypium Chloroplast Genomes: Origin and Evolution of Allotetraploids

DOI: 10.1371/journal.pone.0037128

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Abstract:

Background Cotton (Gossypium spp.) is a model system for the analysis of polyploidization. Although ascertaining the donor species of allotetraploid cotton has been intensively studied, sequence comparison of Gossypium chloroplast genomes is still of interest to understand the mechanisms underlining the evolution of Gossypium allotetraploids, while it is generally accepted that the parents were A- and D-genome containing species. Here we performed a comparative analysis of 13 Gossypium chloroplast genomes, twelve of which are presented here for the first time. Methodology/Principal Findings The size of 12 chloroplast genomes under study varied from 159,959 bp to 160,433 bp. The chromosomes were highly similar having >98% sequence identity. They encoded the same set of 112 unique genes which occurred in a uniform order with only slightly different boundary junctions. Divergence due to indels as well as substitutions was examined separately for genome, coding and noncoding sequences. The genome divergence was estimated as 0.374% to 0.583% between allotetraploid species and A-genome, and 0.159% to 0.454% within allotetraploids. Forty protein-coding genes were completely identical at the protein level, and 20 intergenic sequences were completely conserved. The 9 allotetraploids shared 5 insertions and 9 deletions in whole genome, and 7-bp substitutions in protein-coding genes. The phylogenetic tree confirmed a close relationship between allotetraploids and the ancestor of A-genome, and the allotetraploids were divided into four separate groups. Progenitor allotetraploid cotton originated 0.43–0.68 million years ago (MYA). Conclusion Despite high degree of conservation between the Gossypium chloroplast genomes, sequence variations among species could still be detected. Gossypium chloroplast genomes preferred for 5-bp indels and 1–3-bp indels are mainly attributed to the SSR polymorphisms. This study supports that the common ancestor of diploid A-genome species in Gossypium is the maternal source of extant allotetraploid species and allotetraploids have a monophyletic origin. G. hirsutum AD1 lineages have experienced more sequence variations than other allotetraploids in intergenic regions. The available complete nucleotide sequences of 12 Gossypium chloroplast genomes should facilitate studies to uncover the molecular mechanisms of compartmental co-evolution and speciation of Gossypium allotetraploids.

References

[1]  Soltis D, Soltis P, Tate J (2004) Advances in the study of polyploidy since plant speciation. New Phytol 161: 173–191.
[2]  Fryxell P (1979) The natural history of the cotton tribe: Texas A and M University Press.
[3]  Wendel JF, Brubaker CL, Seelanan T (2010) The origin and evolution of Gossypium. In: Stewat J, Oosterhuis D, Heitholt JJ, Mauney J, editors. Physiology of cotton. Springer. 1–18.
[4]  Wendel JF, Cronn RC (2003) Polyploidy and the evolutionary history of cotton. Adv Agron 78: 139–186.
[5]  Flagel LE, Wendel JF (2010) Evolutionary rate variation, genomic dominance and duplicate gene expression evolution during allotetraploid cotton speciation. New Phytol 186: 184–193.
[6]  Wendel JF (1989) New World tetraploid cottons contain Old World cytoplasm. Proc Natl Acad Sci U S A 86: 4132–4136.
[7]  Brubaker CL, Paterson AH, Wendel JF (1999) Comparative genetic mapping of allotetraploid cotton and its diploid progenitors. Genome 42: 184–203.
[8]  Rong J, Abbey C, Bowers JE, Brubaker CL, Chang C, et al. (2004) A 3347-locus genetic recombination map of sequence-tagged sites reveals features of genome organization, transmission and evolution of cotton (Gossypium). Genetics 166: 389–417.
[9]  Grover CE, Kim HR, Wing RA, Paterson AH, Wendel JF (2007) Microcolinearity and genome evolution in the AdhA region of diploid and polyploid cotton (Gossypium). Plant J 50: 995–1006.
[10]  Small RL, Ryburn JA, Cronn RC, Seelanan T, Wendel JF (1998) The tortoise and the hare: choosing between noncoding plastome and nuclear Adh sequences for phylogeny reconstruction in a recently diverged plant group. Am J Bot 85: 1301–1315.
[11]  Cronn RC, Small RL, Wendel JF (1999) Duplicated genes evolve independently after polyploid formation in cotton. Proc Natl Acad Sci U S A 96: 14406–14411.
[12]  Endrizzi JE, Turcotte EL, Kohel RJ (1985) Genetics, cytology, and evolution of Gossypium. Adv Genet 23: 271–375.
[13]  Seelanan T, Schnabel A, Wendel JF (1997) Congruence and consensus in the cotton tribe (Malvaceae). Syst Bot 22: 259–290.
[14]  Cronn RC, Small RL, Haselkorn T, Wendel JF (2002) Rapid diversification of the cotton genus (Gossypium: Malvaceae) revealed by analysis of sixteen nuclear and chloroplast genes. Am J Bot 89: 707–725.
[15]  Senchina DS, Alvarez I, Cronn RC, Liu B, Rong J, et al. (2003) Rate variation among nuclear genes and the age of polyploidy in Gossypium. Mol Biol Evol 20: 633–643.
[16]  Grover CE, Yu Y, Wing RA, Paterson AH, Wendel JF (2008) A phylogenetic analysis of indel dynamics in the cotton genus. Mol Biol Evol 25: 1415–1428.
[17]  Turmel M, Gagnon MC, O'Kelly CJ, Otis C, Lemieux C (2009) The chloroplast genomes of the green algae Pyramimonas, Monomastix, and Pycnococcus shed new light on the evolutionary history of prasinophytes and the origin of the secondary chloroplasts of euglenids. Mol Biol Evol 26: 631–648.
[18]  Turmel M, Otis C, Lemieux C (2009) The chloroplast genomes of the green algae Pedinomonas minor, Parachlorella kessleri, and Oocystis solitaria reveal a shared ancestry between the Pedinomonadales and Chlorellales. Mol Biol Evol 26: 2317–2331.
[19]  Chan CX, Gross J, Yoon HS, Bhattacharya D (2011) Plastid origin and evolution: new models provide insights into old problems. Plant Physiol 155: 1552–1560.
[20]  Greiner S, Rauwolf U, Meurer J, Herrmann RG (2011) The role of plastids in plant speciation. Mol Ecol 20: 671–691.
[21]  Lee SB, Kaittanis C, Jansen RK, Hostetler JB, Tallon LJ, et al. (2006) The complete chloroplast genome sequence of Gossypium hirsutum: organization and phylogenetic relationships to other angiosperms. BMC Genomics 7: 61.
[22]  Ibrahim RIH, Azuma JI, Sakamoto M (2006) Complete nucleotide sequence of the cotton (Gossypium barbadense L.) chloroplast genome with a comparative analysis of sequences among 9 dicot plants. Genes Genet Syst 81: 311–321.
[23]  Wu FH, Kan DP, Lee SB, Daniell H, Lee YW, et al. (2009) Complete nucleotide sequence of Dendrocalamus latiflorus and Bambusa oldhamii chloroplast genomes. Tree Physiol 29: 847–856.
[24]  Chen JQ, Wu Y, Yang H, Bergelson J, Kreitman M, et al. (2009) Variation in the ratio of nucleotide substitution and indel rates across genomes in mammals and bacteria. Mol Biol Evol 26: 1523–1531.
[25]  Matsuoka Y, Yamazaki Y, Ogihara Y, Tsunewaki K (2002) Whole chloroplast genome comparison of rice, maize, and wheat: implications for chloroplast gene diversification and phylogeny of cereals. Mol Biol Evol 19: 2084–2091.
[26]  Guisinger MM, Kuehl JV, Boore JL, Jansen RK (2008) Genome-wide analyses of Geraniaceae plastid DNA reveal unprecedented patterns of increased nucleotide substitutions. Proc Natl Acad Sci U S A 105: 18424–18429.
[27]  Greiner S, Wang X, Rauwolf U, Silber MV, Mayer K, et al. (2008) The complete nucleotide sequences of the five genetically distinct plastid genomes of Oenothera, subsection Oenothera: I. Sequence evaluation and plastome evolution. Nucleic Acids Res 36: 2366–2378.
[28]  Eric V, Bruce L (2007) Uncovering the mutation-fixation correlation in short lineages. BMC Evol Biol 7: 168.
[29]  Stoletzki N, Eyre-Walker A (2011) The positive correlation between dN/dS and dS in mammals is due to runs of adjacent substitutions. Mol Biol Evol 28: 1371–1380.
[30]  Greiner S, Wang X, Herrmann RG, Rauwolf U, Mayer K, et al. (2008) The complete nucleotide sequences of the 5 genetically distinct plastid genomes of Oenothera, subsection Oenothera: II. A microevolutionary view using bioinformatics and formal genetic data. Mol Biol Evol 25: 2019–2030.
[31]  Wendel JF, Rowley R, Stewart J (1994) Genetic diversity in and phylogenetic relationships of the Brazilian endemic cotton, Gossypium mustelinum (Malvaceae). Plant Syst Evol 192: 49–59.
[32]  Chaw SM, Chang CC, Chen HL, Li WH (2004) Dating the monocot-dicot divergence and the origin of core eudicots using whole chloroplast genomes. J Mol Evol 58: 424–441.
[33]  Leebens-Mack J, Raubeson L, Cui L, Kuehl J, Fourcade M, et al. (2005) Identifying the basal angiosperm node in chloroplast genome phylogenies: sampling one's way out of the Felsenstein zone. Mol Biol Evol 22: 1948–1963.
[34]  Bell CD, Soltis DE, Soltis PS (2010) The age and diversification of the angiosperms re-revisited. Am J Bot 97: 1296–1303.
[35]  Leseberg CH, Duvall MR (2009) The complete chloroplast genome of Coix lacryma-jobi and a comparative molecular evolutionary analysis of plastomes in cereals. J Mol Evol 69: 311–318.
[36]  Britten RJ, Rowen L, Williams J, Cameron RA (2003) Majority of divergence between closely related DNA samples is due to indels. Proc Natl Acad Sci U S A 100: 4661–4665.
[37]  Gu X, Li WH (1995) The size distribution of insertions and deletions in human and rodent pseudogenes suggests the logarithmic gap penalty for sequence alignment. J Mol Evol 40: 464–473.
[38]  Yamane K, Yano K, Kawahara T (2006) Pattern and rate of indel evolution inferred from whole chloroplast intergenic regions in sugarcane, maize and rice. DNA Res 13: 197–204.
[39]  McCluskey K, Wiest AE, Grigoriev IV, Lipzen A, Martin J, et al. (2011) Rediscovery by whole genome sequencing: classical mutations and genome polymorphisms in Neurospora crassa. G3: Genes, Genomes, Genetics 1: 303–316.
[40]  Ma J, Bennetzen JL (2004) Rapid recent growth and divergence of rice nuclear genomes. Proc Natl Acad Sci U S A 101: 12404–12410.
[41]  Baldauf SL, Palmer JD (1990) Evolutionary transfer of the chloroplast tufA gene to the nucleus. Nature 344: 262–265.
[42]  Sugiura C, Kobayashi Y, Aoki S, Sugita C, Sugita M (2003) Complete chloroplast DNA sequence of the moss Physcomitrella patens: evidence for the loss and relocation of rpoA from the chloroplast to the nucleus. Nucleic Acids Res 31: 5324–5331.
[43]  Jansen RK, Saski C, Lee SB, Hansen AK, Daniell H (2011) Complete plastid genome sequences of three rosids (Castanea, Prunus, Theobroma): evidence for at least two independent transfers of rpl22 to the nucleus. Mol Biol Evol 28: 835–847.
[44]  Grover CE, Kim HR, Wing RA, Paterson AH, Wendel JF (2004) Incongruent patterns of local and global genome size evolution in cotton. Genome Res 14: 1474–1482.
[45]  Heads M (2005) Dating nodes on molecular phylogenies: a critique of molecular biogeography. Cladistics 21: 62–78.
[46]  Li WH, Tanimura M (1987) The molecular clock runs more slowly in man than in apes and monkeys. Nature 326: 93–96.
[47]  Raubeson LA, Peery R, Chumley TW, Dziubek C, Fourcade HM, et al. (2007) Comparative chloroplast genomics: analyses including new sequences from the angiosperms Nuphar advena and Ranunculus macranthus. BMC Genomics 8: 174.
[48]  Muse SV (2000) Examining rates and patterns of nucleotide substitution in plants. Plant Mol Biol 42: 25–43.
[49]  Gaut BS (1998) Molecular clocks and nucleotide substitution rates in higher plants. In: al HMKe, editor. Evolutionary biology. New York: Plenum Press. 93–120.
[50]  Tajima F (1993) Simple methods for testing the molecular evolutionary clock hypothesis. Genetics 135: 599–607.
[51]  Gong X, Yan L (1991) Improvement of the purification of chloroplast DNA from higher plants. Chinese Sci Bull 36: 467–469.
[52]  Cronn R, Liston A, Parks M, Gernandt DS, Shen R, et al. (2008) Multiplex sequencing of plant chloroplast genomes using Solexa sequencing-by-synthesis technology. Nucleic Acids Res 36: e122.
[53]  Zerbino DR, Birney E (2008) Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 18: 821–829.
[54]  Wyman SK, Jansen RK, Boore JL (2004) Automatic annotation of organellar genomes with DOGMA. Bioinformatics 20: 3252–3255.
[55]  Lohse M, Drechsel O, Bock R (2007) OrganellarGenomeDRAW (OGDRAW): a tool for the easy generation of high-quality custom graphical maps of plastid and mitochondrial genomes. Curr Genet 52: 267–274.
[56]  Guindon S, Dufayard JF, Lefort V, Anisimova M, Hordijk W, et al. (2010) New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol 59: 307–321.
[57]  Argout X, Salse J, Aury JM, Guiltinan MJ, Droc G, et al. (2010) The genome of Theobroma cacao. Nature genetics 43: 101–108.
[58]  Ronquist F, Huelsenbeck JP (2003) MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics 19: 1572–1574.
[59]  Posada D, Buckley TR (2004) Model selection and model averaging in phylogenetics: advantages of Akaike information criterion and Bayesian approaches over likelihood ratio tests. Syst Biol 53: 793–808.
[60]  Tamura K, Peterson D, Peterson N, Stecher G, Nei M, et al. (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28: 2731–2739.
[61]  Sato S, Nakamura Y, Kaneko T, Asamizu E, Tabata S (1999) Complete structure of the chloroplast genome of Arabidopsis thaliana. DNA Res 6: 283–290.
[62]  Goremykin VV, Holland B, Hirsch-Ernst KI, Hellwig FH (2005) Analysis of Acorus calamus chloroplast genome and its phylogenetic implications. Mol Biol Evol 22: 1813–1822.
[63]  Guisinger MM, Chumley TW, Kuehl JV, Boore JL, Jansen RK (2010) Implications of the plastid genome sequence of Typha (Typhaceae, Poales) for understanding genome evolution in Poaceae. J Mol Evol 70: 149–166.
[64]  Maier RM, Neckermann K, Igloi GL, Kossel H (1995) Complete sequence of the maize chloroplast genome: gene content, hotspots of divergence and fine tuning of genetic information by transcript editing. J Mol Evol 251: 614–628.
[65]  Ogihara Y, Isono K, Kojima T, Endo A, Hanaoka M, et al. (2002) Structural features of a wheat plastome as revealed by complete sequencing of chloroplast DNA. Mol Genet Genomics 266: 740–746.
[66]  Goremykin VV, Hirsch-Ernst KI, W lfl S, Hellwig FH (2003) Analysis of the Amborella trichopoda chloroplast genome sequence suggests that Amborella is not a basal angiosperm. Mol Biol Evol 20: 1499–1505.
[67]  Wakasugi T, Tsudzuki J, Ito S, Nakashima K, Tsudzuki T, et al. (1994) Loss of all ndh genes as determined by sequencing the entire chloroplast genome of the black pine Pinus thunbergii. Proc Natl Acad Sci U S A 91: 9794–9798.
[68]  Yang Z (2007) PAML 4: phylogenetic analysis by maximum likelihood. Mol Biol Evol 24: 1586–1591.
[69]  Yang Z, Nielsen R (2000) Estimating synonymous and nonsynonymous substitution rates under realistic evolutionary models. Mol Biol Evol 17: 32–43.

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