Phylogeographical studies of Glycine soja: implicating the refugium during the Quaternary glacial period and large-scale expansion after the Last Glacial Maximum

Phylogeographical studies of Glycine soja: implicating the refugium during the Quaternary glacial period and large-scale expansion after the Last Glacial Maximum

Wild soybean (Glycine soja Sieb. & Zucc.), the progenitor of cultivated soybean (Glycine max (L.) Merr.), is widely distributed in the Sino-Japanese Floristic Region (SJFR). Therefore, it is an excellent model organism to study the effect of Quaternary climatic changes on the distribution and migration of plant taxa in the SJFR. To investigate the phylogeography of G. soja, a total of 632 individuals representing 52 populations throughout the species distribution range were genotyped by using the sequencing data of a nuclear locus, AF105221, and a chloroplast locus, trnQ-rps16. We detected a total of 23 haplotypes from two loci, including five common and 18 rare haplotypes. Among them, 17 rare haplotypes were limited to Northeast Asia (Northeast China (NEC) and Korea) and the Yangzi River basin (middle and downstream of the Yangzi River (MDYR) and the eastern end of Southwest China (SWC)). Moreover, two common haplotypes were detected throughout the species distribution wide range. All the haplotypes from Japan and the Korean peninsula were also found in China. The haplotype distribution patterns of the two loci suggested that Northeast Asia (NEC and Korea) and the Yangzi River basin (MDYR and the eastern end of SWC) might have been the refugia for G. soja during the Quaternary glacial period, and G. soja expanded rapidly after the end of the Last Glacial Maximum. There was a land bridge between East China, the Korean peninsula, and Japan that permitted gene flow among populations of these regions in the ice age during the Quaternary.

___

  • Aizawa M, Yoshimaru H, Saito H, Katsuki T, Kawahara T, Kitamura K, Shi F, Kaji M (2007). Phylogeography of a northeast Asian spruce, Picea jezoensis, inferred from genetic variation observed in organelle DNA markers. Mol Ecol 16: 3393-3405.
  • An Z (2000). The history and variability of the East Asian paleomonsoon climate. Quaternary Sci Rev 19: 171-187.
  • Avise JC (1994). Molecular Markers, Natural History and Evolution. New York, NY, USA: Chapman and Hall.
  • Bai WN, Liao WJ, Zhang DY (2010). Nuclear and chloroplast DNA phylogeography reveal two refuge areas with asymmetrical gene flow in a temperate walnut tree from East Asia. New Phytol 188: 892-901.
  • Baloch FS, Alsaleh A, Andeden EE, Hatipoğlu R, Nachit M, Özkan H (2016). High levels of segregation distortion in the molecular linkage map of bread wheat representing the West Asia and North Africa region. Turk J Agric For 40: 352-364.
  • Baloch FS, Kurt C, Arioğlu H, Özkan H (2010). Assaying of diversity among soybean (Glycine max (L.) Merr.) and peanut (Arachis hypogaea L.) genotypes at DNA level. Turk J Agric For 34: 285- 301.
  • Bandelt HJ, Forster P, Röhl A (1999). Median-joining networks for inferring intraspecific phylogenies. Mol Biol Evol 16: 37-48.
  • Burban C, Petit RJ, Carcreff E, Jactel H (1999). Rangewide variation of the maritime pine bast scale Matsucoccus feytaudi Duc. (Homoptera: Matsucoccidae) in relation to the genetic structure of its host. Mol Ecol 8: 1593-1602.
  • Choi IY, Kang JH, Song HS, Kim NS (1999). Genetic diversity measured by simple sequence repeat variations among the wild soybean, Glycine soja, collected along the riverside of five major rivers in Korea. Genes Genet Syst 74: 169-177.
  • Chung CH (2007). Vegetation response to climate change on Jeju Island, South Korea, during the last deglaciation based on pollen record. Geosci J 11:147-155.
  • Dobson M, Kawamura Y (1998). Origin of the Japanese land mammal fauna: Allocation of extant species to historicallybased categories. Quaternary Res 37: 385-395.
  • Doyle JJ, Doyle JL (1987). A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem Bull 19: 11-15. Frankel OH, Soulé ME (1981). Conservation and Evolution. Cambridge, UK: Cambridge University Press.
  • Fujita R, Ohara M, Okazaki K, Shimamoto Y (1997). The extent of natural cross-pollination in wild soybean (Glycine soja). J Hered 88: 124-128.
  • Gao LM, Möller M, Zhang XM, Hollingsworth ML, Liu J, Mill RR, Gibby M, Li DZ (2007). High variation and strong phylogeographic pattern among cpDNA haplotypes in Taxus wallichiana (Taxaceae) in China and North Vietnam. Mol Ecol 16: 4684-4698.
  • Gong W, Chen C, Dobe C, Fu CX, Koch MA (2008). Phylogeography of a living fossil: Pleistocene glaciations forced Ginkgo biloba L. (Ginkgoaceae) into two refuge areas in China with limited subsequent postglacial expansion. Mol Phylogenet Evol 48: 1094-1105.
  • Guan BC, Fu CX, Qiu YX, Zhou SL, Comes HP (2010). Genetic structure and breeding system of a rare understory herb, Dysosma versipellis (Berberidaceae), from temperate deciduous forests in China. Am J Bot 97: 111-122.
  • Hall TA (1999). BIOEDIT: A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser 41: 95-98.
  • Harpending H (1994). Signature of ancient population growth in a low-resolution mitochondrial DNA mismatch distribution. Hum Biol 66: 591e600.
  • Harrison SP, Yu G, Takahara H, Prentice IC (2001). Diversity of temperate plants in East Asia. Nature 413: 129-130.
  • Hewitt GM (1996). Some genetic consequences of ice ages and their role in divergence and speciation. Biol J Linn Soc 58: 247-276.
  • Hewitt GM (2000). The genetic legacy of the Quaternary ice ages. Nature 405: 907-913.
  • Hufford KM, Mazer SJ (2003). Plant ecotypes: genetic differentiation in the age of ecological restoration. Trends Ecol Evol 18: 147-155.
  • Kiang YT, Chiang YC, Kaizuma N (1992). Genetic diversity in natural populations of wild soybean in Iwate prefecture. Japan J Hered 83: 325-329.
  • Kuroda Y, Kaga A, Tomooka N, Vaughan DA (2006). Population genetic structure of Japanese wild soybean (Glycine soja) based on microsatellite variation. Mol Ecol 15: 959-974.
  • Li EY, Yi S, Qiu YX, Guo JT, Comes HP, Fu CX (2008). Phylogeography of two East Asian species in Croomia (Stemonaceae) inferred from chloroplast DNA and ISSR fingerprinting variation. Mol Phylogenet Evol 49: 702-714.
  • Li X, Wang K, Li F, Yan M (2005). Research progress of wild soybean (Glycine soja) and suggestions for improving its effective utilization and protection. Soybean Sci 24: 305-309 (in Chinese with English abstract).
  • Liu KB (1988). Quaternary history of the temperate forests of China. Quaternary Sci Rev 7: 1-20.
  • Liu Y, Wang Y, Huang H (2009). Species-level phylogeographical history of Myricaria plants in the mountain ranges of western China and the origin of M. laxiflora in the Three Gorges mountain region. Mol Ecol 18: 2700-2712.
  • Lomolino MV, Riddle BR, Brown JH (2006). Biogeography. 3rd ed. Sunderland, MA, USA: Sinauer Associates.
  • Lu BR (2004). Conserving biodiversity of soybean gene pool in the biotechnology era. Plant Spec Biol 19: 115-125.
  • Lu HY, Yi SW, Xu ZW, Zhou YL, Zeng L, Zhu FY, Feng H, Dong LN, Zhuo H, Yu KF et al (2013). Chinese deserts and sand fields in Last Glacial Maximum and Holocene Optimum. Chin Sci Bull 58: 2775-2783.
  • Millien-Parra V, Jaeger JJ (1999). Island biogeography of the Japanese terrestrial mammal assemblages: an example of a relict fauna. J Biogeography 26: 959-972.
  • Petit RJ, Duminil J, Fineschi S, Hampe A, Salvini D, Vendramin GG (2005). Comparative organization of chloroplast, mitochondrial and nuclear diversity in plant populations. Mol Ecol 14: 689-701.
  • Qian H, Ricklefs RE (2001). Palaeovegetation - Diversity of temperate plants in East Asia - Reply. Nature 413: 130.
  • Qiu YX, Fu CX, Comes HP (2011). Plant molecular phylogeography in China and adjacent regions: tracing the genetic imprints of Quaternary climate and environmental change in the world’s most diverse temperate flora. Mol Phylogenet Evol 59: 225-244.
  • Qiu YX, Guan BC, Fu CX (2009c). Did glacials and/or interglacials promote allopatric incipient speciation in East Asian temperate plants? Phylogeographic and coalescent analyses on refugial isolation and divergence in Dysosma versipellis. Mol Phylogenet Evol 51: 281-293.
  • Qiu YX, Sun Y, Zhang XP (2009a). Molecular phylogeography of East Asian Kirengeshoma (Hydrangeaceae) in relation to Quaternary climate change and land bridge configurations. New Phytol 183: 480-495.
  • Qiu YX, Qi XS, Jin XF (2009b). Population genetic structure, phylogeography, and demographic history of Platycrater arguta (Hydrangeaceae) endemic to East China and South Japan, inferred from chloroplast DNA sequence variation. Taxon 58: 1226-1241.
  • Rauch EM, Bar-Yam Y (2005). Estimating the total genetic diversity of a spatial field population from a sample and implications of its dependence on habitat area. P Natl Acad Sci USA 102: 9826-9829.
  • Schmitt T (2007). Molecular biogeography of Europe: Pleistocene cycles and postglacial trends. Front Zool 4: 11.
  • Schrimpf A, Theissinger K, Dahlem J (2014). Phylogeography of noble crayfish (Astacus astacus) reveals multiple refugia. Freshwater Biol 59: 761-776.
  • Shahid MQ, Saleem MF, Khan HZ, Anjum SA (2009). Performance of soybean (Glycine max L.) under different phosphorus levels and inoculation. Pak J Agri Sci 46: 1-5.
  • Shaw J, Lickey EB, Schilling EE, Small RL (2007). Comparison of whole chloroplast genome sequences to choose noncoding regions for phylogenetic studies in angiosperms: The tortoise and the hare III. Am J Bot 94: 275-288.
  • Shi Y (1989). Discussion on the reconstruction of paleosnowline during glacial period. In: Shi Y, Cui ZJ, Li JJ, editors. Problems on Quaternary Glaciation and Environments in Eastern China. Beijing, China: Science Press, pp. 363-374 (in Chinese with English abstract).
  • Shi Y (2002). Characteristics of late Quaternary monsoonal glaciation on the Tibetan Plateau and in East Asia. Quatern Int 97-98: 79-91. Simpson GG (1940). Mammals and land bridges. J Washington Acad Sci 30: 137-163.
  • Smil V (2000). Magic beans. Nature 407: 467.
  • Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997). The ClustalX windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 24: 4876-4882.
  • Tian B, Liu R, Wang L, Qui Q, Chen K, Liu J (2009). Phylogeographic analyses suggest that a deciduous species (Ostryopsis davidiana Decne., Betulaceae) survived in northern China during the last Glacial Maximum. J Biogeogr 36: 2148-2155.
  • Van K, Hwang EY, Kim MY (2004). Discovery of single nucleotide polymorphisms in soybean using primers designed from ESTs. Euphytica 139: 147-157.
  • Wang J, Gao P, Kang M (2009). Refugia within refugia: the case study of a canopy tree (Eurycorymbus cavaleriei) in subtropical China. J Biogeogr 36: 2156-2164.
  • Wang KJ, Li XH, Li FS (2008). Phenotypic diversity of the big seed type subcollection of wild soybean (Glycine soja Sieb. et Zucc.) in China. Genet Resour Crop Ev 55: 1335-1346.
  • Wang YS, Shahid MQ, Ghouri F, Baloch FS, Wang Y, Huang H (2015a). Evaluation of the geographical pattern of genetic diversity of Glycine soja and Glycine max based on four single copy nuclear gene loci: for conservation of soybean germplasm. Biochem Syst Ecol 62: 229-235.
  • Wang YS, Shahid MQ, Huang H, Wang Y (2015b). Nucleotide diversity patterns of three divergent soybean populations: evidences for population-dependent linkage disequilibrium and taxonomic status of Glycine gracilis. Ecol Evol 5: 3969-3978.
  • Wu ZY, Wu SG (1998). A proposal for a new floristic kingdom (realm) the Asiatic kingdom, its delineation and characteristics. In: Zhang AL, Wu SG, editors. Floristic Characteristics and Diversity of East Asian Plants. Beijing, China: China Higher Education Press & Springer-Verlag, pp. 3-42.
  • Xia X, Xie Z (2001). DAMBE: Software package for data analysis in molecular biology and evolution. J Hered 92: 371-373.
  • Yu G, Chen X, Ni J Cheddadi R, Guiot J, Han H, Harrison SP, Huang C, Ke M, Kong Z et al (2000). Palaeovegetation of China: a pollen data-based synthesis for the mid-Holocene and last glacial maximum. J Biogeogr 27: 635-664.
  • Zheng Z, Yuan B, Petit-Maire N (1998). Paleoenvironments in China during the Last Glacial Maximum and the Holocene Optimum. Episodes 21: 152-158.
Turkish Journal of Agriculture and Forestry-Cover
  • ISSN: 1300-011X
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK