利用SSR標記分析普通野生稻遺傳多樣性

    Genetic Diversity Analysis of Common Wild Rice By Using SSR Markers

    • 摘要:
      目的  揭示中國雲南景洪、雲南元江、江西東鄉、緬甸普通野生稻(Oryza rufipogen Griff.)遺傳多樣性,以及雲南景洪和元江普通野生稻原、異位保存下變異情況。
      方法  利用36對SSR標記對來自雲南景洪異位保護與原位保護區、雲南元江異位保護與原位保護區、江西東鄉及緬甸共102份普通野生稻進行檢測,開展不同地理來源及不同保存方式下普通野生稻居群遺傳多樣性比較與聚類分析。
      結果  供試普通野生稻檢測出等位變異(Na) 110個,平均3.056個,變幅為1~5個;Nei's基因多樣性指數(Ⅰ)平均為0.448。不同地理來源Nei’s基因多樣性指數大小為:緬甸(0.561)>雲南景洪(0.437)>雲南元江(0.236)>江西東鄉(0.230),雲南景洪和元江的普通野生稻Nei’s基因多樣性指數均表現為異位保護區大於原位保護區(雲南景洪:0.498>0.131,雲南元江:0.264>0.035)。聚類與遺傳分化分析顯示,供試材料平均遺傳相似係數為0.772,變幅0.260~1.000;在遺傳相似係數0.635處可將供試材料劃分為雲南景洪、雲南元江、江西東鄉及緬甸居群。雲南景洪原位保護區與緬甸的普通野生稻遺傳距離較近(0.560),雲南元江原位保護區與江西東鄉的普通野生稻遺傳距離較近(0.552);而雲南元江原位保護區與景洪原位保護區的普通野生稻遺傳距離為0.748,表明雲南元江和景洪普通野生稻有明顯的遺傳分化。
      結論  不同地區的普通野生稻遺傳分化有明顯的地域性,雲南景洪和元江普通野生稻遺傳多樣性因原生境居群減少而下降。

       

      Abstract:
      Objective  The study was conducted to reveal the genetic diversity of common wild rice (Oryza rufipogen Griff.) in Jinghong, Yuanjiang of Yunnan, Dongxiang of Jiangxi, and Myanmar, and the genetic variations of wild rice in Jinghong and Yuanjiang under in-situ and ex-situ conservation.
      Methods  We detected the genetic diversities of 102 O. rufipogen samples from Yunnan Jinghong ex-situ and in-situ conservation zone, Yunnan Yuanjiang ex-situ and in-situ conservation zone, Jiangxi Dongxiang and Myanmar with 36 pairs of SSR markers. A comparison and cluster analysis of genetic diversities of O. rufipogen from different geographical sources and under different conservation methods was conducted.
      Results  A total of 110 allele variations were detected, with an average of 3.056, and a range from 1 to 5. The average of Nei's gene diversity indexes (Ⅰ) was 0.448. The I of different geographical sources ranked as follows: Myanmar (0.561) > Yunnan Jinghong (0.437) > Yunnan Yuanjiang (0.236) > Jiangxi Dongxiang (0.230). The I of O. rufipogen under ex-situ conservation was higher than that under in-situ conservation in Jinghong (0.498 > 0.131) and Yuanjiang (0.264 > 0.035). Clustering and genetic differentiation analysis showed that the average genetic similarity coefficient (GS) of the tested materials was 0.772, with a range of 0.260-1.000. They were were divided into Yunnan Jinghong, Yunnan Yuanjiang, Jiangxi Dongxiang, and Myanmar populations at GS=0.635. The genetic distance of O. rufipogene between Yunnan Jinghong in-situ conservation and Myanmar was close (0.560), and that between Yunnan Yuanjiang in-situ conservation and Jiangxi Dongxiang was close (0.552). And the genetic difference of O. rufipogene between in-situ conservation of Yuanjiang and Jinghong was 0.748, indicating that there was obvious genetic differentiation between Yuanjiang and Jinghong.
      Conclusion  The genetic differentiation of O. rufipogene has obvious regionalism. The genetic diversity of O. rufipogene decreased due to the decrease of in-situ conservation populations in Jinghong and Yuanjiang of Yunnan.

       

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