Journals / Turkish Journal of Agriculture and Forestry / 2016 / Cilt: 40 - Sayı: 6

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

Pages
825–838
Publication Date
2022-10-19
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

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.

📌 3 Key Takeaways

🎯
Objective & Hypothesis: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).
📊
Key Findings & Data: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.
💡
Conclusion & Impact: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.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

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.

🔖

Cite This Article

SHAHID, M. Q., WANG, Y., BALOCH, F. S. (2022). Phylogeographical studies of Glycine soja: implicating the refugium during the Quaternary glacial period and large-scale expansion after the Last Glacial Maximum. Turkish Journal of Agriculture and Forestry, Cilt: 40 - Sayı: 6, 825–838. https://ajindex.com/articles/599386

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. 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.
  2. An Z (2000). The history and variability of the East Asian paleomonsoon climate. Quaternary Sci Rev 19: 171-187.
  3. Avise JC (1994).
  4. 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.
  5. 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.
  6. 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.
  7. 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.
  8. 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.
  9. 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.
  10. Dobson M, Kawamura Y (1998). Origin of the Japanese land mammal fauna: Allocation of extant species to historicallybased categories. Quaternary Res 37: 385-395.
  11. Doyle JJ, Doyle JL (1987). A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem Bull 19: 11-15.
  12. Frankel OH, Soulé ME (1981). Conservation and Evolution. Cambridge, UK: Cambridge University Press.
  13. 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.
  14. Gao LM, Möller M, Zhang XM, Hollingsworth ML, Liu J, Mill RR, Gibby M, Li DZ (2007). High variation and strong phylogeographic patter