A novel allele of ASY3 is associated with greater meiotic stability in autotetraploid Arabidopsis lyrata

. 2020 Jul ; 16 (7) : e1008900. [epub] 20200715

Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid32667955

Grantová podpora
BB/M01973X/1 Biotechnology and Biological Sciences Research Council - United Kingdom
BB/P013511/1 Biotechnology and Biological Sciences Research Council - United Kingdom

Odkazy

PubMed 32667955
PubMed Central PMC7392332
DOI 10.1371/journal.pgen.1008900
PII: PGENETICS-D-19-01978
Knihovny.cz E-zdroje

In this study we performed a genotype-phenotype association analysis of meiotic stability in 10 autotetraploid Arabidopsis lyrata and A. lyrata/A. arenosa hybrid populations collected from the Wachau region and East Austrian Forealps. The aim was to determine the effect of eight meiosis genes under extreme selection upon adaptation to whole genome duplication. Individual plants were genotyped by high-throughput sequencing of the eight meiosis genes (ASY1, ASY3, PDS5b, PRD3, REC8, SMC3, ZYP1a/b) implicated in synaptonemal complex formation and phenotyped by assessing meiotic metaphase I chromosome configurations. Our results reveal that meiotic stability varied greatly (20-100%) between individual tetraploid plants and associated with segregation of a novel ASYNAPSIS3 (ASY3) allele derived from A. lyrata. The ASY3 allele that associates with meiotic stability possesses a putative in-frame tandem duplication (TD) of a serine-rich region upstream of the coiled-coil domain that appears to have arisen at sites of DNA microhomology. The frequency of multivalents observed in plants homozygous for the ASY3 TD haplotype was significantly lower than in plants heterozygous for ASY3 TD/ND (non-duplicated) haplotypes. The chiasma distribution was significantly altered in the stable plants compared to the unstable plants with a shift from proximal and interstitial to predominantly distal locations. The number of HEI10 foci at pachytene that mark class I crossovers was significantly reduced in a plant homozygous for ASY3 TD compared to a plant heterozygous for ASY3 ND/TD. Fifty-eight alleles of the 8 meiosis genes were identified from the 10 populations analysed, demonstrating dynamic population variability at these loci. Widespread chimerism between alleles originating from A. lyrata/A. arenosa and diploid/tetraploids indicates that this group of rapidly evolving genes may provide precise adaptive control over meiotic recombination in the tetraploids, the very process that gave rise to them.

Zobrazit více v PubMed

Alix K, Gerard PR, Schwarzacher T, Heslop-Harrison JSP. Polyploidy and interspecific hybridization: partners for adaptation, speciation and evolution in plants. Ann Bot. 2017;120(2):183–94. 10.1093/aob/mcx079 . PubMed DOI PMC

Selmecki AM, Maruvka YE, Richmond PA, Guillet M, Shoresh N, Sorenson AL, et al. Polyploidy can drive rapid adaptation in yeast. Nature. 2015;519(7543):349–52. 10.1038/nature14187 . PubMed DOI PMC

Baduel P, Bray S, Vallejo-Marin M, Kolar F, Yant L. The "Polyploid Hop": Shifting Challenges and Opportunities Over the Evolutionary Lifespan of Genome Duplications. Front Ecol Evol. 2018;6 ARTN 117 10.3389/fevo.2018.00117 DOI

Rey MD, Martin AC, Higgins J, Swarbreck D, Uauy C, Shaw P, et al. Exploiting the ZIP4 homologue within the wheat Ph1 locus has identified two lines exhibiting homoeologous crossover in wheat-wild relative hybrids. Mol Breed. 2017;37(8):95 10.1007/s11032-017-0700-2 . PubMed DOI PMC

Gonzalo A, Lucas MO, Charpentier C, Sandmann G, Lloyd A, Jenczewski E. Reducing MSH4 copy number prevents meiotic crossovers between non-homologous chromosomes in Brassica napus. Nat Commun. 2019;10(1):2354 10.1038/s41467-019-10010-9 . PubMed DOI PMC

Jenczewski E, Eber F, Grimaud A, Huet S, Lucas MO, Monod H, et al. PrBn, a major gene controlling homeologous pairing in oilseed rape (Brassica napus) haploids. Genetics. 2003;164(2):645–53. . PubMed PMC

Henry IM, Dilkes BP, Tyagi A, Gao J, Christensen B, Comai L. The BOY NAMED SUE quantitative trait locus confers increased meiotic stability to an adapted natural allopolyploid of Arabidopsis. Plant Cell. 2014;26(1):181–94. 10.1105/tpc.113.120626 . PubMed DOI PMC

Yant L, Hollister JD, Wright KM, Arnold BJ, Higgins JD, Franklin FCH, et al. Meiotic adaptation to genome duplication in Arabidopsis arenosa. Curr Biol. 2013;23(21):2151–6. Epub 2013/10/22. 10.1016/j.cub.2013.08.059 . PubMed DOI PMC

Page SL, Hawley RS. The genetics and molecular biology of the synaptonemal complex. Annu Rev Cell Dev Biol. 2004;20:525–58. 10.1146/annurev.cellbio.19.111301.155141 . PubMed DOI

Lam WS, Yang X, Makaroff CA. Characterization of Arabidopsis thaliana SMC1 and SMC3: evidence that AtSMC3 may function beyond chromosome cohesion. J Cell Sci. 2005;118(Pt 14):3037–48. 10.1242/jcs.02443 . PubMed DOI

Pradillo M, Knoll A, Oliver C, Varas J, Corredor E, Puchta H, et al. Involvement of the Cohesin Cofactor PDS5 (SPO76) During Meiosis and DNA Repair in Arabidopsis thaliana. Front Plant Sci. 2015;6:1034 10.3389/fpls.2015.01034 . PubMed DOI PMC

Bhatt AM, Lister C, Page T, Fransz P, Findlay K, Jones GH, et al. The DIF1 gene of Arabidopsis is required for meiotic chromosome segregation and belongs to the REC8/RAD21 cohesin gene family. Plant J. 1999;19(4):463–72. 10.1046/j.1365-313x.1999.00548.x PubMed DOI

Cai X, Dong F, Edelmann RE, Makaroff CA. The Arabidopsis SYN1 cohesin protein is required for sister chromatid arm cohesion and homologous chromosome pairing. J Cell Sci. 2003;116(Pt 14):2999–3007. 10.1242/jcs.00601 . PubMed DOI

Chelysheva L, Diallo S, Vezon D, Gendrot G, Vrielynck N, Belcram K, et al. AtREC8 and AtSCC3 are essential to the monopolar orientation of the kinetochores during meiosis. J Cell Sci. 2005;118(Pt 20):4621–32. 10.1242/jcs.02583 . PubMed DOI

Lambing C, Tock AJ, Topp SD, Choi K, Kuo PC, Zhao X, et al. Interacting genomic landscapes of REC8-cohesin, chromatin and meiotic recombination in Arabidopsis thaliana. Plant Cell. 2020. Epub 2020/02/07. 10.1105/tpc.19.00866 . PubMed DOI PMC

Tesse S, Bourbon HM, Debuchy R, Budin K, Dubois E, Liangran Z, et al. Asy2/Mer2: an evolutionarily conserved mediator of meiotic recombination, pairing, and global chromosome compaction. Genes Dev. 2017;31(18):1880–93. Epub 2017/10/13. 10.1101/gad.304543.117 . PubMed DOI PMC

De Muyt A, Pereira L, Vezon D, Chelysheva L, Gendrot G, Chambon A, et al. A high throughput genetic screen identifies new early meiotic recombination functions in Arabidopsis thaliana. Plos Genet. 2009;5(9):e1000654 10.1371/journal.pgen.1000654 . PubMed DOI PMC

Armstrong SJ, Caryl AP, Jones GH, Franklin FC. Asy1, a protein required for meiotic chromosome synapsis, localizes to axis-associated chromatin in Arabidopsis and Brassica. J Cell Sci. 2002;115(Pt 18):3645–55. 10.1242/jcs.00048 . PubMed DOI

Ferdous M, Higgins JD, Osman K, Lambing C, Roitinger E, Mechtler K, et al. Inter-homolog crossing-over and synapsis in Arabidopsis meiosis are dependent on the chromosome axis protein AtASY3. Plos Genet. 2012;8(2):e1002507 10.1371/journal.pgen.1002507 . PubMed DOI PMC

Chambon A, West A, Vezon D, Horlow C, De Muyt A, Chelysheva L, et al. Identification of ASYNAPTIC4, a Component of the Meiotic Chromosome Axis. Plant Physiol. 2018;178(1):233–46. 10.1104/pp.17.01725 . PubMed DOI PMC

Caryl AP, Armstrong SJ, Jones GH, Franklin FC. A homologue of the yeast HOP1 gene is inactivated in the Arabidopsis meiotic mutant asy1. Chromosoma. 2000;109(1–2):62–71. Epub 2000/06/16. 10.1007/s004120050413 . PubMed DOI

West AMV, Rosenbereg SC, Ur SN, Lehmern MK, Ye QZ, Hagemann G, et al. A conserved filamentous assembly underlies the structure of the meiotic chromosome axis. Elife. 2019;8 ARTN e40372 10.7554/eLife.40372 PubMed DOI PMC

Higgins JD, Sanchez-Moran E, Armstrong SJ, Jones GH, Franklin FC. The Arabidopsis synaptonemal complex protein ZYP1 is required for chromosome synapsis and normal fidelity of crossing over. Genes Dev. 2005;19(20):2488–500. 10.1101/gad.354705 . PubMed DOI PMC

Schmickl R, Koch MA. Arabidopsis hybrid speciation processes. Proc Natl Acad Sci U S A. 2011;108(34):14192–7. Epub 2011/08/10. 10.1073/pnas.1104212108 . PubMed DOI PMC

Marburger S, Monnahan P, Seear PJ, Martin SH, Koch J, Paajanen P, et al. Interspecific introgression mediates adaptation to whole genome duplication. Nat Commun. 2019;10(1):5218 Epub 2019/11/20. 10.1038/s41467-019-13159-5 . PubMed DOI PMC

Hohmann N, Koch MA. An Arabidopsis introgression zone studied at high spatio-temporal resolution: interglacial and multiple genetic contact exemplified using whole nuclear and plastid genomes. BMC Genomics. 2017;18(1):810 Epub 2017/10/24. 10.1186/s12864-017-4220-6 . PubMed DOI PMC

Arnold B, Kim ST, Bomblies K. Single Geographic Origin of a Widespread Autotetraploid Arabidopsis arenosa Lineage Followed by Interploidy Admixture. Mol Biol Evol. 2015;32(6):1382–95. Epub 2015/04/12. 10.1093/molbev/msv089 . PubMed DOI

Lafon-Placette C, Köhler C. Endosperm-based postzygotic hybridization barriers: developmental mechanisms and evolutionary drivers. Molecular Ecology. 2016;25(11):2620–9. 10.1111/mec.13552 PubMed DOI

Morgan C, Zhang H, Henry CE, Franklin FCH, Bomblies K. Derived alleles of two axis proteins affect meiotic traits in autotetraploid Arabidopsis arenosa. Proceedings of the National Academy of Sciences. 2020;117(16):8980–8. 10.1073/pnas.1919459117 PubMed DOI PMC

Chelysheva L, Vezon D, Chambon A, Gendrot G, Pereira L, Lemhemdi A, et al. The Arabidopsis HEI10 is a new ZMM protein related to Zip3. Plos Genet. 2012;8(7):e1002799 Epub 2012/07/31. 10.1371/journal.pgen.1002799 . PubMed DOI PMC

Wright KM, Arnold B, Xue K, Surinova M, O'Connell J, Bomblies K. Selection on meiosis genes in diploid and tetraploid Arabidopsis arenosa. Mol Biol Evol. 2015;32(4):944–55. 10.1093/molbev/msu398 . PubMed DOI PMC

Grishaeva TM, Bogdanov YF. Conservation and variability of synaptonemal complex proteins in phylogenesis of eukaryotes. Int J Evol Biol. 2014;2014:856230 Epub 2014/08/26. 10.1155/2014/856230 . PubMed DOI PMC

Yang C, Sofroni K, Wijnker E, Hamamura Y, Carstens L, Harashima H, et al. The Arabidopsis Cdk1/Cdk2 homolog CDKA;1 controls chromosome axis assembly during plant meiosis. The EMBO Journal. 2020;39(3):e101625 10.15252/embj.2019101625 PubMed DOI PMC

Osman K, Yang J, Roitinger E, Lambing C, Heckmann S, Howell E, et al. Affinity proteomics reveals extensive phosphorylation of the Brassica chromosome axis protein ASY1 and a network of associated proteins at prophase I of meiosis. Plant J. 2018;93(1):17–33. 10.1111/tpj.13752 . PubMed DOI PMC

Brakenhoff RH, Schoenmakers JG, Lubsen NH. Chimeric cDNA clones: a novel PCR artifact. Nucleic Acids Res. 1991;19(8):1949 Epub 1991/04/25. 10.1093/nar/19.8.1949 . PubMed DOI PMC

Chen JM, Cooper DN, Chuzhanova N, Ferec C, Patrinos GP. Gene conversion: mechanisms, evolution and human disease. Nat Rev Genet. 2007;8(10):762–75. Epub 2007/09/12. 10.1038/nrg2193 . PubMed DOI

Hazarika MH, Rees H. Genotypic control of chromosome behaviour in rye X. Chromosome pairing and fertility in autotetraploids. Heredity. 1967;22(3):317–32. 10.1038/hdy.1967.44 DOI

He W, Rao H, Tang S, Bhagwat N, Kulkarni DS, Ma Y, et al. Regulated Proteolysis of MutSgamma Controls Meiotic Crossing Over. Mol Cell. 2020. Epub 2020/03/05. 10.1016/j.molcel.2020.02.001 . PubMed DOI PMC

Mergner J, Frejno M, List M, Papacek M, Chen X, Chaudhary A, et al. Mass-spectrometry-based draft of the Arabidopsis proteome. Nature. 2020. 10.1038/s41586-020-2094-2 PubMed DOI

Sanchez-Moran E, Santos JL, Jones GH, Franklin FC. ASY1 mediates AtDMC1-dependent interhomolog recombination during meiosis in Arabidopsis. Genes Dev. 2007;21(17):2220–33. 10.1101/gad.439007 . PubMed DOI PMC

Jorgensen MH, Ehrich D, Schmickl R, Koch MA, Brysting AK. Interspecific and interploidal gene flow in Central European Arabidopsis (Brassicaceae). BMC Evol Biol. 2011;11:346 10.1186/1471-2148-11-346 . PubMed DOI PMC

Bomblies K, Higgins JD, Yant L. Meiosis evolves: adaptation to external and internal environments. The New phytologist. 2015;208(2):306–23. 10.1111/nph.13499 . PubMed DOI

Giraut L, Falque M, Drouaud J, Pereira L, Martin OC, Mezard C. Genome-Wide Crossover Distribution in Arabidopsis thaliana Meiosis Reveals Sex-Specific Patterns along Chromosomes. Plos Genet. 2011;7(11). ARTN e1002354 10.1371/journal.pgen.1002354 PubMed DOI PMC

Otto SP. The evolutionary consequences of polyploidy. Cell. 2007;131(3):452–62. 10.1016/j.cell.2007.10.022 . PubMed DOI

Monnahan P, Kolar F, Baduel P, Sailer C, Koch J, Horvath R, et al. Pervasive population genomic consequences of genome duplication in Arabidopsis arenosa. Nat Ecol Evol. 2019;3(3):457–68. 10.1038/s41559-019-0807-4 . PubMed DOI

Hu TT, Pattyn P, Bakker EG, Cao J, Cheng JF, Clark RM, et al. The Arabidopsis lyrata genome sequence and the basis of rapid genome size change. Nat Genet. 2011;43(5):476–+. 10.1038/ng.807 PubMed DOI PMC

Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 2004;32(5):1792–7. 10.1093/nar/gkh340 . PubMed DOI PMC

Guindon S, Dufayard JF, Lefort V, Anisimova M, Hordijk W, Gascuel O. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol. 2010;59(3):307–21. Epub 2010/06/09. 10.1093/sysbio/syq010 . PubMed DOI

Huelsenbeck JP, Ronquist F. MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics. 2001;17(8):754–5. Epub 2001/08/29. 10.1093/bioinformatics/17.8.754 . PubMed DOI

Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms. Mol Biol Evol. 2018;35(6):1547–9. Epub 2018/05/04. 10.1093/molbev/msy096 . PubMed DOI PMC

Mascher M, Gundlach H, Himmelbach A, Beier S, Twardziok SO, Wicker T, et al. A chromosome conformation capture ordered sequence of the barley genome. Nature. 2017;544(7651):427–33. 10.1038/nature22043 . PubMed DOI

Higgins JD, Wright KM, Bomblies K, Franklin FC. Cytological techniques to analyze meiosis in Arabidopsis arenosa for investigating adaptation to polyploidy. Front Plant Sci. 2014;4:546 10.3389/fpls.2013.00546 . PubMed DOI PMC

Chelysheva L, Grandont L, Vrielynck N, le Guin S, Mercier R, Grelon M. An easy protocol for studying chromatin and recombination protein dynamics during Arabidopsis thaliana meiosis: immunodetection of cohesins, histones and MLH1. Cytogenet Genome Res. 2010;129(1–3):143–53. Epub 2010/07/16. 10.1159/000314096 . PubMed DOI

Lambing C, Osman K, Nuntasoontorn K, West A, Higgins JD, Copenhaver GP, et al. Arabidopsis PCH2 Mediates Meiotic Chromosome Remodeling and Maturation of Crossovers. Plos Genet. 2015;11(7):e1005372 10.1371/journal.pgen.1005372 . PubMed DOI PMC

Wong YH, Lee TY, Liang HK, Huang CM, Wang TY, Yang YH, et al. KinasePhos 2.0: a web server for identifying protein kinase-specific phosphorylation sites based on sequences and coupling patterns. Nucleic Acids Research. 2007;35:W588–W94. 10.1093/nar/gkm322 PubMed DOI PMC

Blom N, Sicheritz-Ponten T, Gupta R, Gammeltoft S, Brunak S. Prediction of post-translational glycosylation and phosphorylation of proteins from the amino acid sequence. Proteomics. 2004;4(6):1633–49. 10.1002/pmic.200300771 . PubMed DOI

Zhao Q, Xie YB, Zheng YY, Jiang S, Liu WZ, Mu WP, et al. GPS-SUMO: a tool for the prediction of sumoylation sites and SUMO-interaction motifs. Nucleic Acids Research. 2014;42(W1):W325–W30. 10.1093/nar/gku383 PubMed DOI PMC

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...