Tracing 100 million years of grass genome evolutionary plasticity.


Journal

The Plant journal : for cell and molecular biology
ISSN: 1365-313X
Titre abrégé: Plant J
Pays: England
ID NLM: 9207397

Informations de publication

Date de publication:
Jun 2023
Historique:
revised: 29 01 2023
received: 13 11 2022
accepted: 24 02 2023
medline: 19 6 2023
pubmed: 16 3 2023
entrez: 15 3 2023
Statut: ppublish

Résumé

Grasses derive from a family of monocotyledonous plants that includes crops of major economic importance such as wheat, rice, sorghum and barley, sharing a common ancestor some 100 million years ago. The genomic attributes of plant adaptation remain obscure and the consequences of recurrent whole genome duplications (WGD) or polyploidization events, a major force in plant evolution, remain largely speculative. We conducted a comparative analysis of omics data from ten grass species to unveil structural (inversions, fusions, fissions, duplications, substitutions) and regulatory (expression and methylation) basis of genome plasticity, as possible attributes of plant long lasting evolution and adaptation. The present study demonstrates that diverged polyploid lineages sharing a common WGD event often present the same patterns of structural changes and evolutionary dynamics, but these patterns are difficult to generalize across independent WGD events as a result of non-WGD factors such as selection and domestication of crops. Polyploidy is unequivocally linked to the evolutionary success of grasses during the past 100 million years, although it remains difficult to attribute this success to particular genomic consequences of polyploidization, suggesting that polyploids harness the potential of genome duplication, at least partially, in lineage-specific ways. Overall, the present study clearly demonstrates that post-polyploidization reprogramming is more complex than traditionally reported in investigating single species and calls for a critical and comprehensive comparison across independently polyploidized lineages.

Identifiants

pubmed: 36919199
doi: 10.1111/tpj.16185
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1243-1266

Subventions

Organisme : Institut Carnot Plant2Pro
ID : 0001455 project SyntenyViewer
Organisme : ISITE CAP2025
ID : 'Pack Ambition Recherche Project' TransBlé
Organisme : Région Auvergne-Rhône-Alpes
ID : #23000816

Informations de copyright

© 2023 Society for Experimental Biology and John Wiley & Sons Ltd.

Références

Acharya, D. & Ghosh, T.C. (2016) Global analysis of human duplicated genes reveals the relative importance of whole-genome duplicates originated in the early vertebrate evolution. BMC Genomics, 17, 1-14.
Akalin, A., Kormaksson, M., Li, S., Garrett-Bakelman, F.E., Figueroa, M.E., Melnick, A. et al. (2012) methylKit: a comprehensive R package for the analysis of genome-wide DNA methylation profiles. Genome Biology, 13(10), R87.
Alekseyev, M.A. & Pevzner, P.A. (2009) Breakpoint graphs and ancestral genome reconstructions. Genome Research, 19, 943-957.
Altschul, S.F., Gish, W., Miller, W., Myers, E.W. & Lipman, D.J. (1990) Basic local alignment search tool. Journal of Molecular Biology, 215, 403-410.
Aury, J.M., Jaillon, O., Duret, L., Noel, B., Jubin, C., Porcel, B.M. et al. (2006) Global trends of whole-genome duplications revealed by the ciliate Paramecium tetraurelia. Nature, 444, 171-178.
Bewick, A.J. & Schmitz, R.J. (2017) Gene body DNA methylation in plants. Current Opinion in Plant Biology, 36, 103-110.
Birchler, J.A. & Veitia, R.A. (2014) The gene balance hypothesis: dosage effects in plants. Methods in Molecular Biology, 1112, 25-32.
Birchler, J.A., Yao, H., Chudalayandi, S., Vaiman, D. & Veitia, R.A. (2010) Heterosis. Plant Cell, 22, 2105-2112.
Blanc, G., Hokamp, K. & Wolfe, K.H. (2003) A recent polyploidy superimposed on older large-scale duplications in the Arabidopsis genome. Genome Research, 13, 137-144.
Buggs, R.J.A., Elliott, N.M., Zhang, L., Koh, J., Viccini, L.F., Soltis, D.E. et al. (2010) Tissue-specific silencing of homoeologs in natural populations of the recent allopolyploid Tragopogon mirus. The New Phytologist, 186, 175-183.
Bukowski, R., Guo, X., Lu, Y., Zou, C., He, B., Rong, Z. et al. (2018) Construction of the third-generation Zea mays haplotype map. Gigascience, 7, 1-12.
Castresana, J. (2000) Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Molecular Biology and Evolution, 17, 540-552.
Chalhoub, B., Denoeud, F., Liu, S., Parkin, I.A.P., Tang, H., Wang, X. et al. (2014) Early allopolyploid evolution in the post-neolithic Brassica napus oilseed genome. Science, 345, 950-953.
Chang, F., Gu, Y., Ma, H. & Yang, Z. (2013) AtPRK2 promotes ROP1 activation via RopGEFs in the control of polarized pollen tube growth. Molecular Plant, 6, 1187-1201.
Chapman, B.A., Bowers, J.E., Feltus, F.A. & Paterson, A.H. (2006) Buffering of crucial functions by paleologous duplicated genes may contribute cyclicality to angiosperm genome duplication. Proceedings of the National Academy of Sciences of the United States of America, 103, 2730-2735.
Charif, D. & Lobry, J.R. (2007) SeqinR 1.0-2: a contributed Package to the R project for statistical computing devoted to biological sequences retrieval and analysis. In: Bastolla, U., Porto, M., Roman, H.E. & Vendruscolo, M. (Eds.) Structural approaches to sequence evolution. Biological and medical physics, biomedical engineering. Berlin, Heidelberg: Springer. Available from: https://doi.org/10.1007/978-3-540-35306-5_10
Chen, Y., Pal, B., Visvader, J.E., Smyth, G.K., Andrews, S. & Macdonald, J.W. (2018) Differential methylation analysis of reduced representation bisulfite sequencing experiments using edgeR, F1000Research, 1-40.
Cheng, F., Sun, R., Hou, X., Zheng, H., Zhang, F., Zhang, Y. et al. (2016) Subgenome parallel selection is associated with morphotype diversification and convergent crop domestication in Brassica rapa and Brassica oleracea. Nature Genetics, 48, 1218-1224.
Cheng, X.F., Wittich, P.E., Kieft, H., Angenent, G., XuHan, X. & Van Lammeren, A.A.M. (2000) Temporal and spatial expression of MADS box genes, FBP7 and FBP11, during initiation and early development of ovules in wild type and mutant Petunia hybrida. Plant Biology, 2, 693-702.
Cheng, F., Wu, J., Fang, L., Sun, S., Liu, B., Lin, K. et al. (2012) Biased gene fractionation and dominant gene expression among the subgenomes of Brassica rapa. PLoS One, 7(5), e36442.
Chuang, T.J., Chen, F.C. & Chen, Y.Z. (2012) Position-dependent correlations between DNA methylation and the evolutionary rates of mammalian coding exons. Proceedings of the National Academy of Sciences of the United States of America, 109, 15841-15846.
Chueasiri, C., Chunthong, K., Pitnjam, K., Chakhonkaen, S., Sangarwut, N., Sangsawang, K. et al. (2014) Rice ORMDL controls sphingolipid homeostasis affecting fertility resulting from abnormal pollen development. PLoS One, 9, e106386.
Coate, J.E., Farmer, A.D., Schiefelbein, J.W. & Doyle, J.J. (2020) Expression partitioning of duplicate genes at single cell resolution in Arabidopsis roots. Frontiers in Genetics, 11, 596150.
Colombo, L., Franken, J., Van der Krol, A.R., Wittich, P.E., Dons, H.J. & Angenent, G.C. (1997) Downregulation of ovule-specific MADS box genes from petunia results in maternally controlled defects in seed development. Plant Cell, 9, 703-715.
Conant, G.C., Birchler, J.A. & Pires, J.C. (2014) Dosage, duplication, and diploidization: clarifying the interplay of multiple models for duplicate gene evolution over time. Current Opinion in Plant Biology, 19, 91-98.
Darwin, C.R. (1859) On the origin of species by means of natural selection, or the preservation of favoured races in the struggle for life, 1st edition. London: John Murray.
Davis, M.P.A., van Dongen, S., Abreu-goodger, C., Bartonicek, N. & Enright, A.J. (2023) Kraken: a set of tools for quality control and analysis of high-throughput sequence data. Methods, 63, 41-49.
DeSmet, R., Adams, K.L., Vandepoele, K., van Montagu, M.C.E., Maere, S. & van de Peer, Y. (2013) Convergent gene loss following gene and genome duplications creates single-copy families in flowering plants. Proceedings of the National Academy of Sciences of the United States of America, 110, 2898-2903.
Duarte, J.M., Cui, L., Wall, P.K., Zhang, Q., Zhang, X., Leebens-Mack, J. et al. (2006) Expression pattern shifts following duplication indicative of subfunctionalization and neofunctionalization in regulatory genes of Arabidopsis. Molecular Biology and Evolution, 23, 469-478.
Dvorak, J., Wang, L., Zhu, T., Jorgensen, C.M., Deal, K.R., Dai, X. et al. (2018) Structural variation and rates of genome evolution in the grass family seen through comparison of sequences of genomes greatly differing in size. The Plant Journal, 95, 487-503.
Edgar, R.C. (2004) MUSCLE: a multiple sequence alignment method with reduced time and space complexity. BMC Bioinformatics, 5, 1-19.
Edger, P.P., Poorten, T.J., Van Buren, R., Hardigan, M.A., Colle, M., McKain, M.R. et al. (2019) Origin and evolution of the octoploid strawberry genome. Nature Genetics, 51, 541-547.
Edger, P.P., Smith, R., McKain, M.R., Cooley, A.M., Vallejo-Marin, M., Yuan, Y. et al. (2017) Subgenome dominance in an interspecific hybrid, synthetic allopolyploid, and a 140-year-old naturally established neo-allopolyploid monkeyflower. Plant Cell, 29, 2150-2167.
El-Sharkawy, I., Mila, I., Bouzayen, M. & Jayasankar, S. (2010) Regulation of two germin-like protein genes during plum fruit development. Journal of Experimental Botany, 61, 1761-1770.
Escudero, M. & Wendel, J.F. (2020) The grand sweep of chromosomal evolution in angiosperms. The New Phytologist, 228, 805-808.
Favaro, R., Pinyopich, A., Battaglia, R., Kooiker, M., Borghi, L., Ditta, G. et al. (2003) MADS-box protein complexes control carpel and ovule development in Arabidopsis. Plant Cell, 15, 2603-2611.
Folta, K.M. & Barbey, C.R. (2019) The strawberry genome: a complicated past and promising future. Horticulture Research, 6, 19-21.
Fox, D.T., Soltis, D.E., Soltis, P.S., Ashman, T.L. & van de Peer, Y. (2020) Polyploidy: a biological force from cells to ecosystems. Trends in Cell Biology, 30, 688-694.
Freeling, M. (2009) Bias in plant gene content following different sorts of duplication: tandem, whole-genome, segmental, or by transposition. Annual Review of Plant Biology, 60, 433-453.
Freeling, M., Scanlon, M.J. & Fowler, J.F. (2015) Fractionation and subfunctionalization following genome duplications: mechanisms that drive gene content and their consequences. Current Opinion in Genetics & Development, 35, 110-118.
Glastad, K.M., Gokhale, K., Liebig, J. & Goodisman, M.A.D. (2016) The caste- and sex-specific DNA methylome of the termite Zootermopsis nevadensis. Scientific Reports, 6, 1-14.
Glémin, S., Scornavacca, C., Dainat, J., Burgarella, C., Viader, V., Ardisson, M. et al. (2019) Pervasive hybridizations in the history of wheat relatives. Science Advances, 5, 1-10.
Goidts, V., Szamalek, J.M., de Jong, P.J., Cooper, D.N., Chuzhanova, N., Hameister, H. et al. (2005) Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16. Genome Research, 15, 1232-1242.
Gordon, S.P., Contreras-Moreira, B., Woods, D.P., Des Marais, D.L., Burgess, D., Shu, S. et al. (2017) Extensive gene content variation in the Brachypodium distachyon pan-genome correlates with population structure. Nature Communications, 8, 2184.
Gu, Y.Q., Anderson, O.D., Londeorë, C.F., Kong, X., Chibbar, R.N. & Lazo, G.R. (2003) Structural organization of the barley D-hordein locus in comparison with its orthologous regions of wheat genomes. Genome, 46, 1084-1097.
Hannweg, K., Steyn, W. & Bertling, I. (2016) In vitro-induced tetraploids of Plectranthus esculentus are nematode-tolerant and have enhanced nutritional value. Euphytica, 207, 343-351.
Hao, Y., Zong, X., Ren, P., Qian, Y. & Fu, A. (2021) Basic Helix-Loop-Helix (bHLH) transcription factors regulate a wide range of functions in Arabidopsis. International Journal of Molecular Sciences, 22, 7152.
Hao, Y., Mabry, M.E., Edger, P.P., Freeling, M., Zheng, C., Jin, L. et al. (2021) The contributions from the progenitor genomes of the mesopolyploid Brassiceae are evolutionarily distinct but functionally compatible. Genome Research, 31, 799-810.
Hias, N., Svara, A. & Keulemans, J.W. (2018) Effect of polyploidisation on the response of apple (malus × domestica Borkh.) to Venturia inaequalis infection. European Journal of Plant Pathology, 151, 515-526.
Hidalgo, O., Pellicer, J., Christenhusz, M., Schneider, H., Leitch, A.R. & Leitch, I.J. (2017) Is there an upper limit to genome size? Trends in Plant Science, 22, 567-573.
Hoang, D.T., Vinh, L.S., Flouri, T., Stamatakis, A. & von Haeseler, A. (2018) MPBoot: fast phylogenetic maximum parsimony tree inference and bootstrap approximation. BMC Evolutionary Biology, 18, 1-11.
Ilyas, M., Rasheed, A. & Mahmood, T. (2016) Functional characterization of germin and germin-like protein genes in various plant species using transgenic approaches. Biotechnology Letters, 38, 1405-1421.
Joron, M., Frezal, L., Jones, R.T., Chamberlain, N.L., Lee, S.F., Haag, C.R. et al. (2011) Chromosomal rearrangements maintain a polymorphic supergene controlling butterfly mimicry. Nature, 477, 203-206.
Kim, D., Paggi, J.M., Park, C., Bennett, C. & Salzberg, S.L. (2019) Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype. Nature Biotechnology, 37, 907-915.
Landis, J.B., Soltis, D.E., Li, Z., Marx, H.E., Barker, M.S., Tank, D.C. et al. (2018) Impact of whole-genome duplication events on diversification rates in angiosperms. American Journal of Botany, 105, 348-363.
Leebens-Mack, J.H., Barker, M.S., Carpenter, E.J., Deyholos, M.K., Gitzendanner, M.A., Graham, S.W. et al. (2019) One thousand plant transcriptomes and the phylogenomics of green plants. Nature, 574, 679-685.
Leitch, A.R. & Leitch, I.J. (2008) Genomic plasticity and the diversity of polyploid plants. Science, 320, 481-483.
Leitch, I.J. & Bennett, M.D. (1997) Polyploidy in angiosperms. Trends in Plant Science, 2, 470-476.
Levin, D.A. & Soltis, D.E. (2018) ScienceDirect factors promoting polyploid persistence and diversification and limiting diploid speciation during the K - Pg interlude. Current Opinion in Plant Biology, 42, 1-7.
Li, B. & Dewey, C.N. (2011) RSEM: accurate transcript quantification from RNA-seq data with or without a reference genome. BMC Bioinformatics, 12, 1-16.
Li, H. & Durbin, R. (2009) Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics, 25, 1754-1760.
Li, L., Briskine, R., Schaefer, R., Schnable, P.S., Myers, C.L., Flagel, L.E. et al. (2016) Co-expression network analysis of duplicate genes in maize (Zea mays L.) reveals no subgenome bias. BMC Genomics, 17, 875.
Li, M., Wang, R., Wu, X. & Wang, J. (2020) Homoeolog expression bias and expression level dominance (ELD) in four tissues of natural allotetraploid Brassica napus. BMC Genomics, 21, 1-15.
Li, Q., Qiao, X., Yin, H., Zhou, Y., Dong, H., Qi, K. et al. (2019) Unbiased subgenome evolution following a recent whole-genome duplication in pear (Pyrus bretschneideri Rehd.). Horticulture Research, 6, 1-12.
Li, Z., Baniaga, A.E., Sessa, E.B., Scascitelli, M., Graham, S.W., Rieseberg, L.H. et al. (2015) Early genome duplications in conifers and other seed plants. Science Advances, 1, 1-7.
Li, Y., Smith, C., Corke, F., Zheng, L., Merali, Z., Ryden, P. et al. (2007) Signaling from an altered cell wall to the nucleus mediates sugar-responsive growth and development in Arabidopsis thaliana. Plant Cell, 19(8), 2500-2515.
Li, Z., Tiley, G.P., Galuska, S.R., Reardon, C.R., Kidder, T.I., Rundell, R.J. et al. (2018) Multiple large-scale gene and genome duplications during the evolution of hexapods. Proceedings of the National Academy of Sciences of the United States of America, 115, 4713-4718.
Lian, S., Zhou, Y., Liu, Z., Gong, A. & Cheng, L. (2020) The differential expression patterns of paralogs in response to stresses indicate expression and sequence divergences. BMC Plant Biology, 20, 1-16.
Liao, B.Y. & Zhang, J. (2006) Low rates of expression profile divergence in highly expressed genes and tissue-specific genes during mammalian evolution. Molecular Biology and Evolution, 23, 1119-1128.
Lim, C.W., Baek, W., Han, S.W. & Lee, S.C. (2013) Arabidopsis PYl8 plays an important role for ABA signaling and drought stress responses. Plant Pathology Journal, 29, 471-476.
Liu, S., Liu, Y., Yang, X., Tong, C., Edwards, D., Parkin, I.A.P. et al. (2014) The brassica oleracea genome reveals the asymmetrical evolution of polyploid genomes. Nature Communications, 5, 1-11.
Liu, X.L., Jiang, F.F., Wang, Z.W., Li, X.Y., Li, Z., Zhang, X.J. et al. (2017a) Wider geographic distribution and higher diversity of hexaploids than tetraploids in Carassius species complex reveal recurrent polyploidy effects on adaptive evolution. Scientific Reports, 7, 1-10.
Liu, Y., Wang, J., Ge, W., Wang, Z., Li, Y., Yang, N. et al. (2017b) Two highly similar poplar paleo-subgenomes suggest an autotetraploid ancestor of salicaceae plants. Frontiers in Plant Science, 8, 1-11.
Lovell, J.T., MacQueen, A.H., Mamidi, S., Bonnette, J., Jenkins, J., Napier, J.D. et al. (2021) Genomic mechanisms of climate adaptation in polyploid bioenergy switchgrass. Nature, 590, 438-444.
Lu, K., Wei, L., Li, X., Wang, Y., Wu, J., Liu, M. et al. (2019) Whole-genome resequencing reveals Brassica napus origin and genetic loci involved in its improvement. Nature Communications, 10, 1-12.
Lynch, M. & Conery, J.S. (2000) The evolutionary fate and consequences of duplicate genes. Science, 290, 1151-1155.
Ma, Y.Q., Pu, Z.Q., Tan, X.M., Meng, Q., Zhang, K.L., Yang, L. et al. (2022) SEPALLATA-like genes of Isatis indigotica can affect the architecture of the inflorescences and the development of the floral organs. PeerJ, 10, e13034.
Marais, D.L.D. & Rausher, M.D. (2008) Escape from adaptive conflict after duplication in an anthocyanin pathway gene. Nature, 454, 762-765.
Maggiolini, F.A.M., Sanders, A.D., Shew, C.J., Sulovari, A., Mao, Y., Puig, M. et al. (2020) Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution. Genome Research, 30, 1680-1693.
Martin, M. (2011) Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet Journal, 17, 10-12.
McCarthy, D.J., Chen, Y. & Smyth, G.K. (2012) Differential expression analysis of multifactor RNA-seq experiments with respect to biological variation. Nucleic Acids Research, 40, 4288-4297.
McKenna, A., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A. et al. (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Research, 20(9), 1297-1303.
Miele, V., Penel, S., Daubin, V., Picard, F., Kahn, D. & Duret, L. (2012) High-quality sequence clustering guided by network topology and multiple alignment likelihood. Bioinformatics, 28, 1078-1085.
Miele, V., Penel, S. & Duret, L. (2011) Ultra-fast sequence clustering from similarity networks with SiLiX. BMC Bioinformatics, 12, 116.
Monroe, J.G., Srikant, T., Carbonell-Bejerano, P., Becker, C., Lensink, M., Exposito-Alonso, M. et al. (2022) Mutation bias reflects natural selection in Arabidopsis thaliana. Nature, 602, 101-105.
Murat, F., Armero, A., Pont, C., Klopp, C. & Salse, J. (2017) Reconstructing the genome of the most recent common ancestor of flowering plants. Nature Genetics, 49(4), 490-496.
Murat, F., Louis, A., Maumus, F., Armero, A., Cooke, R., Quesneville, H. et al. (2015) Understanding Brassicaceae evolution through ancestral genome reconstruction. Genome Biology, 16, 262.
Murat, F., Zhang, R., Guizard, S., Flores, R., Armero, A., Pont, C. et al. (2014) Shared subgenome dominance following polyploidization explains grass genome evolutionary plasticity from a seven protochromosome ancestor with 16K protogenes. Genome Biology and Evolution, 6, 12-33.
Murphy, W.J., Larkin, D.M., Everts-van der Wind, A., Bourque, G., Tesler, G., Auvil, L. et al. (2005) Evolution: dynamics of mammalian chromosome evolution inferred from multispecies comparative maps. Science, 309, 613-617.
Naser-Khdour, S., Quang Minh, B., Zhang, W., Stone, E.A. & Lanfear, R. (2019) The prevalence and impact of model violations in phylogenetic analysis. Genome Biology and Evolution, 11, 3341-3352.
Nguyen, L.T., Schmidt, H.A., von Haeseler, A. & Minh, B.Q. (2015) IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Molecular Biology and Evolution, 32(1), 268-274.
Ohno, S. (1970) Introduction. In: Ohno, S. (Ed.) Evolution by gene duplication. Berlin, Heidelberg: Springer, pp. 1-2. Available from: https://doi.org/10.1007/978-3-642-86659-3_1
Page, J.T., Liechty, Z.S., Alexander, R.H., Clemons, K., Hulse-Kemp, A.M., Ashrafi, H. et al. (2016) DNA sequence evolution and rare homoeologous conversion in tetraploid cotton. PLoS Genetics, 12, 1-22.
Parkin, I.A.P., Koh, C., Tang, H., Robinson, S.J., Kagale, S., Clarke, W.E. et al. (2014) Transcriptome and methylome profiling reveals relics of genome dominance in the mesopolyploid Brassica oleracea. Genome Biology, 15, 1-18.
Parks, M.B., Nakov, T., Ruck, E.C., Wickett, N.J. & Alverson, A.J. (2018) Phylogenomics reveals an extensive history of genome duplication in diatoms (Bacillariophyta). American Journal of Botany, 105, 330-347.
Paterson, A.H., Bowers, J.E., Bruggmann, R., Dubchak, I., Grimwood, J., Gundlach, H. et al. (2009) The Sorghum bicolor genome and the diversification of grasses. Nature, 457, 551-556.
Pham, S.K. & Pevzner, P.A. (2010) DRIMM-synteny: decomposing genomes into evolutionary conserved segments. Bioinformatics, 26, 2509-2516.
Pons, P. & Latapy, M. (2006) Computing communities in large networks using random walks. Journal of Graph Algorithms and Applications, 10, 191-218.
Pont, C., Leroy, T., Seidel, M., Tondelli, A., Duchemin, W., Armisen, D. et al. (2019a) Tracing the ancestry of modern bread wheats. Nature Genetics, 51, 905-911.
Pont, C., Murat, F., Guizard, S., Flores, R., Foucrier, S., Bidet, Y. et al. (2013) Wheat syntenome unveils new evidences of contrasted evolutionary plasticity between paleo- and neoduplicated subgenomes. The Plant Journal, 76, 1030-1044.
Pont, C., Wagner, S., Kremer, A., Orlando, L., Plomion, C. & Salse, J. (2019b) Paleogenomics: reconstruction of plant evolutionary trajectories from modern and ancient DNA. Genome Biology, 20, 1-17.
Qi, X., An, H., Hall, T.E., Di, C., Blischak, P.D., McKibben, M.T.W. et al. (2021) Genes derived from ancient polyploidy have higher genetic diversity and are associated with domestication in Brassica rapa. The New Phytologist, 230(1), 372-386.
Quinlan, A.R. & Hall, I.M. (2010) BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics, 26(6), 841-842.
Ramírez-González, R.H., Borrill, P., Lang, D., Harrington, S.A., Brinton, J., Venturini, L. et al. (2018) The transcriptional landscape of polyploid wheat. Science, 361, 1-12.
Renny-Byfield, S., Gallagher, J.P., Grover, C.E., Szadkowski, E., Page, J.T., Udall, J.A. et al. (2014) Ancient gene duplicates in Gossypium (cotton) exhibit near-complete expression divergence. Genome Biology and Evolution, 6, 559-571.
Renny-Byfield, S., Gong, L., Gallagher, J.P. & Wendel, J.F. (2015) Persistence of subgenomes in paleopolyploid cotton after 60 my of evolution. Molecular Biology and Evolution, 32, 1063-1071.
Renny-Byfield, S., Rodgers-Melnick, E. & Ross-Ibarra, J. (2017) Gene fractionation and function in the ancient subgenomes of maize. Molecular Biology and Evolution, 34, 1825-1832.
Renny-Byfield, S. & Wendel, J.F. (2014) Doubling down on genomes: polyploidy and crop plants. American Journal of Botany, 101, 1711-1725.
Robinson, M.D., Mccarthy, D.J. & Smyth, G.K. (2010) edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics, 26, 139-140.
Rohart, F., Gautier, B., Singh, A. & Lê Cao, K.A. (2017) mixOmics: An R package for 'omics feature selection and multiple data integration. PLoS Computational Biology, 13(11), e1005752.
Salman-Minkov, A., Sabath, N. & Mayrose, I. (2016) Whole-genome duplication as a key factor in crop domestication. Nature Plants, 2, 1-4.
Salse, J. (2016) Deciphering the evolutionary interplay between subgenomes following polyploidy: a paleogenomics approach in grasses. American Journal of Botany, 103, 1167-1174.
Salse, J., Abrouk, M., Murat, F., Quraishi, U.M. & Feuillet, C. (2009) Improved criteria and comparative genomics tool provide new insights into grass paleogenomics. Briefings in Bioinformatics, 10(6), 619-630.
Sarda, S., Zeng, J., Hunt, B.G. & Yi, S.V. (2012) The evolution of invertebrate gene body methylation. Molecular Biology and Evolution, 29, 1907-1916.
Schmid, M., Evans, B.J. & Bogart, J.P. (2015) Polyploidy in amphibia. Cytogenet. Genome Research, 145, 315-330.
Schmutz, J., Cannon, S.B., Schlueter, J., Ma, J., Mitros, T., Nelson, W. et al. (2010) Genome sequence of the palaeopolyploid soybean. Nature, 463, 178-183.
Schnable, J.C., Freeling, M. & Lyons, E. (2012) Genome-wide analysis of syntenic gene deletion in the grasses. Genome Biology and Evolution, 4, 265-277.
Schnable, J.C., Springer, N.M. & Freeling, M. (2011) Differentiation of the maize subgenomes by genome dominance and both ancient and ongoing gene loss. Proceedings of the National Academy of Sciences of the United States of America, 108, 4069-4074.
Scornavacca, C., Jacox, E. & Szöllosi, G.J. (2015) Joint amalgamation of most parsimonious reconciled gene trees. Bioinformatics, 31, 841-848.
Shi, J., Ma, X., Zhang, J., Zhou, Y., Liu, M., Huang, L. et al. (2019) Chromosome conformation capture resolved near complete genome assembly of broomcorn millet. Nature Communications, 10, 1-9.
Shi, T., Rahmani, R.S., Gugger, P.F., Wang, M., Li, H., Zhang, Y. et al. (2020) Distinct expression and methylation patterns for genes with different fates following a single whole-genome duplication in flowering plants. Molecular Biology and Evolution, 37, 2394-2413.
Slane, D., Reichardt, I., El Kasmi, F., Bayer, M. & Jürgens, G. (2017) Evolutionarily diverse SYP1 Qa-SNAREs jointly sustain pollen tube growth in Arabidopsis. The Plant Journal, 92, 375-385.
Song, K., Li, L. & Zhang, G. (2018) Relationship among intron length, gene expression, and nucleotide diversity in the Pacific oyster Crassostrea gigas. Marine Biotechnology, 20, 676-684.
Stamatakis, A. (2014) RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics, 30, 1312-1313.
Stein, A., Coriton, O., Rousseau-Gueutin, M., Samans, B., Schiessl, S.V., Obermeier, C. et al. (2017) Mapping of homoeologous chromosome exchanges influencing quantitative trait variation in Brassica napus. Plant Biotechnology Journal, 15, 1478-1489.
Stupar, R.M., Bhaskar, P.B., Yandell, B.S., Rensink, W.A., Hart, A.L., Ouyang, S. et al. (2007) Phenotypic and transcriptomic changes associated with potato autopolyploidization. Genetics, 176, 2055-2067.
Sun, H., Wu, S., Zhang, G., Jiao, C., Guo, S., Ren, Y. et al. (2017) Karyotype stability and unbiased fractionation in the paleo-allotetraploid Cucurbita genomes. Molecular Plant, 10, 1293-1306.
Sun, Y., Zhong, M., Li, Y., Zhang, R., Su, L., Xia, G. et al. (2021) GhADF6-Mediated Actin reorganization is associated with defence against verticillium dahliae infection in cotton. Molecular Plant Pathology, 22, 1656-1667.
Suyama, M., Torrents, D., Bork, P. & Delbru, M. (2006) PAL2NAL: robust conversion of protein sequence alignments into the corresponding codon alignments. Nucleic Acids Research, 34, 609-612.
Suzuki, M.M. & Bird, A. (2008) DNA methylation landscapes: provocative insights from epigenomics. Nature Reviews. Genetics, 9, 465-476.
Szöllosi, G.J., Rosikiewicz, W., Boussau, B., Tannier, E. & Daubin, V. (2013) Efficient exploration of the space of reconciled gene trees. Systematic Biology, 62, 901-912.
Takuno, S. & Gaut, B.S. (2012) Body-methylated genes in arabidopsis thaliana are functionally important and evolve slowly. Molecular Biology and Evolution, 29, 219-227.
Thomas, B.C., Pedersen, B. & Freeling, M. (2006) Following tetraploidy in an Arabidopsis ancestor, genes were removed preferentially from one homeolog leaving clusters enriched in dose-sensitive genes. Genome Research, 16(7), 934-946.
Throude, M., Bolot, S., Bosio, M., Pont, C., Sarda, X., Quraishi, U.M. et al. (2009) Structure and expression analysis of rice paleo duplications. Nucleic Acids Research, 37, 1248-1259.
Ulrich, D. & Olbricht, K. (2013) Diversity of volatile patterns in sixteen Fragaria vesca L. accessions in comparison to cultivars of Fragaria xananassa. Journal of Applied Botany and Food Quality, 86, 37-46.
Van de Peer, Y., Mizrachi, E. & Marchal, K. (2017) The evolutionary significance of polyploidy. Nature Reviews. Genetics, 18, 411-424.
VanBuren, R., Man Wai, C., Wang, X., Pardo, J., Yocca, A.E., Wang, H. et al. (2020) Exceptional subgenome stability and functional divergence in the allotetraploid Ethiopian cereal teff. Nature Communications, 11, 1-11.
Vanneste, K., Baele, G., Maere, S. & van de Peer, Y. (2014) Analysis of 41 plant genomes supports a wave of successful genome duplications in association with the cretaceous − Paleogene boundary. Genome Research, 32, 1334-1347.
Wang, Z., Li, Y., Sun, P., Zhu, M., Wang, D., Lu, Z. et al. (2022) A high-quality Buxus austro-yunnanensis (Buxales) genome provides new insights into karyotype evolution in early eudicots. BMC Biology, 20, 216.
Wang, M., Tu, L., Lin, M., Lin, Z., Wang, P., Yang, Q. et al. (2017a) Asymmetric subgenome selection and cis-regulatory divergence during cotton domestication. Nature Genetics, 49, 579-587.
Wang, X., Zhang, Z., Fu, T., Hu, L., Xu, C., Gong, L. et al. (2017b) Gene-body CG methylation and divergent expression of duplicate genes in rice. Scientific Reports, 7, 1-11.
Wang, Y., Wang, X., Lee, T.H., Mansoor, S. & Paterson, A.H. (2013) Gene body methylation shows distinct patterns associated with different gene origins and duplication modes and has a heterogeneous relationship with gene expression in Oryza sativa (rice). The New Phytologist, 198, 274-283.
Wang, Y., Wang, X. & Paterson, A.H. (2012) Genome and gene duplications and gene expression divergence: a view from plants. Annals of the New York Academy of Sciences, 1256, 1-14.
Wickland, D.P. & Hanzawa, Y. (2015) The FLOWERING LOCUS T/TERMINAL FLOWER 1 gene family: functional evolution and molecular mechanisms. Molecular Plant, 8, 983-997.
Woodhouse, M.R., Cheng, F., Pires, J.C., Lisch, D., Freeling, M. & Wang, X. (2014) Origin, inheritance, and gene regulatory consequences of genome dominance in polyploids. Proceedings of the National Academy of Sciences of the United States of America, 111, 5283-5288.
Woodhouse, M.R., Schnable, J.C., Pedersen, B.S., Lyons, E., Lisch, D., Subramaniam, S. et al. (2010) Following tetraploidy in maize, a short deletion mechanism removed genes preferentially from one of the two homeologs. PLoS Biology, 8, e1000409.
Xu, W., Zhang, Q., Yuan, W., Xu, F., Muhammad Aslam, M., Miao, R. et al. (2020) The genome evolution and low-phosphorus adaptation in white lupin. Nature Communications, 11, 1-13.
Yang, L. & Gaut, B.S. (2011) Factors that contribute to variation in evolutionary rate among arabidopsis genes. Molecular Biology and Evolution, 28, 2359-2369.
Yim, W.C., Lee, B.M. & Jang, C.S. (2009) Expression diversity and evolutionary dynamics of rice duplicate genes. Molecular Genetics and Genomics, 281, 483-493.
Zhang, J., Liu, Y., Xia, E.H., Yao, Q.Y., Liu, X.D. & Gao, L.Z. (2015) Autotetraploid rice methylome analysis reveals methylation variation of transposable elements and their effects on gene expression. Proceedings of the National Academy of Sciences of the United States of America, 112, E7022-E7029.
Zhang, Q., Guan, P., Zhao, L., Ma, M., Xie, L., Li, Y. et al. (2021) Asymmetric epigenome maps of subgenomes reveal imbalanced transcription and distinct evolutionary trends in Brassica napus. Molecular Plant, 14, 604-619.
Zhang, X., Shiu, S., Cal, A. & Borevitz, J.O. (2008) Global analysis of genetic, epigenetic and transcriptional polymorphisms in Arabidopsis thaliana using whole genome tiling arrays. PLoS Genetics, 4, e1000032.
Zhao, C., Zayed, O., Zeng, F., Liu, C., Zhang, L., Zhu, P. et al. (2019) Arabinose biosynthesis is critical for salt stress tolerance in Arabidopsis. The New Phytologist, 224, 274-290.
Zhao, M., Zhang, B., Lisch, D. & Ma, J. (2017) Patterns and consequences of subgenome differentiation provide insights into the nature of paleopolyploidy in plants. Plant Cell, 29, 2974-2994.
Zhou, X., Liao, Y., Kim, S.U., Chen, Z., Nie, G., Cheng, S. et al. (2020) Genome-wide identification and characterization of bHLH family genes from Ginkgo biloba. Scientific Reports, 10, 1-15.
Zou, C., Lehti-Shiu, M.D., Thibaud-Nissen, F., Prakash, T., Buell, C.R. & Shiu, S.H. (2009) Evolutionary and expression signatures of pseudogenes in Arabidopsis and rice. Plant Physiology, 151, 3-15.

Auteurs

Arnaud Bellec (A)

INRAE/CNRGV US 1258, 24 Chemin de Borde Rouge, 31320, Auzeville-Tolosane, France.

Mamadou Dia Sow (MD)

UCA, INRAE, GDEC, 5 Chemin de Beaulieu, 63000, Clermont-Ferrand, France.

Caroline Pont (C)

UCA, INRAE, GDEC, 5 Chemin de Beaulieu, 63000, Clermont-Ferrand, France.

Peter Civan (P)

UCA, INRAE, GDEC, 5 Chemin de Beaulieu, 63000, Clermont-Ferrand, France.

Emile Mardoc (E)

UCA, INRAE, GDEC, 5 Chemin de Beaulieu, 63000, Clermont-Ferrand, France.

Wandrille Duchemin (W)

UCA, INRAE, GDEC, 5 Chemin de Beaulieu, 63000, Clermont-Ferrand, France.

David Armisen (D)

UCA, INRAE, GDEC, 5 Chemin de Beaulieu, 63000, Clermont-Ferrand, France.

Cécile Huneau (C)

UCA, INRAE, GDEC, 5 Chemin de Beaulieu, 63000, Clermont-Ferrand, France.

Johanne Thévenin (J)

INRAE/AgroParisTech-UMR 1318. Bat 2. Centre INRA de Versailles, route de Saint Cyr, 78026, Versailles CEDEX, France.

Vanessa Vernoud (V)

INRAE/CNRS/ENS/Univ. Lyon-UMR 879, 46 allée d'Italie, 69364, Lyon Cedex 07, France.

Nathalie Depège-Fargeix (N)

INRAE/CNRS/ENS/Univ. Lyon-UMR 879, 46 allée d'Italie, 69364, Lyon Cedex 07, France.

Laurent Maunas (L)

Arvalis-Institut du végétal, 21 chemin de Pau, 64121 Montardon, France.

Brigitte Escale (B)

Arvalis-Institut du végétal, 21 chemin de Pau, 64121 Montardon, France.
Direction de l'agriculture de Polynésie française, Route de l'Hippodrome, 98713, Papeete, France.

Bertrand Dubreucq (B)

INRAE/AgroParisTech-UMR 1318. Bat 2. Centre INRA de Versailles, route de Saint Cyr, 78026, Versailles CEDEX, France.

Peter Rogowsky (P)

INRAE/CNRS/ENS/Univ. Lyon-UMR 879, 46 allée d'Italie, 69364, Lyon Cedex 07, France.

Hélène Bergès (H)

INRAE/CNRGV US 1258, 24 Chemin de Borde Rouge, 31320, Auzeville-Tolosane, France.

Jerome Salse (J)

UCA, INRAE, GDEC, 5 Chemin de Beaulieu, 63000, Clermont-Ferrand, France.

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