利用東鄉普通野生稻染色體片段置換係鑒定抗穗發芽QTL

    Identification of QTL for Pre-harvest Sprouting Resistance by Using Chromosome Segment Substitution Lines of Dongxiang Common Wild Rice

    • 摘要:
      目的 高溫陰雨天氣導致水稻生產田出現穗發芽(Pre-harvest Sprouting, PHS), 種子活力降低, 嚴重影響水稻產量與品質性狀。鑒定篩選抗穗發芽種質及基因資源是培育抗穗發芽水稻新品種、消除稻穀穗發芽產生危害的根本途徑。
      方法 以強休眠、不易穗發芽的東鄉野生稻‘C35’為供體親本、較易穗發芽的‘日本晴’(NIP)為受體親本構建的染色體片段置換係(CSSLs)群體為試驗材料, 於2021—2023年進行抗穗發芽特性鑒定評價, 篩選抗穗發芽種質和鑒定主效QTL。
      結果 不同環境下東鄉野生稻‘C35’休眠性較強、穗發芽率均為0.00%, ‘日本晴’存在明顯穗發芽現象、穗發芽率均值為31.95%;CSSLs穗發芽率變幅較大, 不同年份穗發芽率表型重複性較好, 篩選到10份強休眠、抗穗發芽的種質; 共檢測到14個控製穗發芽率QTL, 4個QTL在不同環境下被重複檢測到, 相關QTL在染色體上形成qPHSRC1qPHSRC2qPHSRC8qPHSRC9等4個QTL簇, 其中主效QTL簇qPHSRC2qPHSRC9的LOD值、表型貢獻率和加性效應值較大, qPHSRC2為新發現的主效QTL簇。
      結論 鑒定篩選出一批抗穗發芽的種質材料, 定位到14個抗穗發芽QTL, 篩選出4個重複性較好的QTL簇, 發現1個調控穗發芽率的新主效QTL簇qPHSRC2

       

      Abstract:
      Objective High-temperature and rainy weather lead to pre-harvest sprouting (PHS), severely impacting yield and quality traits of rice. Identification and screening of germplasm or genetic resources is a fundamental pathway for developing new varieties resistant to PHS and eliminating PHS damage.
      Method In the study, a set of chromosome segment substitution lines (CSSLs) derived from Dongxiang wild rice ('C35') as the donor parent and 'Nipponbare' ('NIP') as the recipient parent were used as the experimental materials, and then PHS resistance were evaluated and QTLs were mapped in 2021-2023, with an aim to screen PHS germplasm and identify major QTLs.
      Result Dongxiang wild rice 'C35' exhibited strong dormancy under different environments with a pre-harvest sprouting rate (PHSR) of 0.00%; 'Nipponbare' showed significant PHS with an average PHSR of 31.95%. The PHSR varied widely among CSSL populations, the phenotypic repeatability of PHSR was relatively high in different years, and ten lines from the CSSL populations with strong dormancy and resistance to PHS were screened. A total of 14 QTLs controlling the PHSR were detected, and four QTLs were repeatedly detected under different environments. These QTLs formed four QTL clusters (qPHSRC1, qPHSRC2, qPHSRC8 and qPHSRC9), among which qPHSRC2 and qPHSRC9 had higher LOD values, phenotypic contribution rate (%) and additive effect, and qPHSRC2 was a newly discovered major QTL cluster.
      Conclusion A batch of PHS resistant germplasms were screened and 14 QTLs were mapped, four QTL clusters were repeatedly identified, and a new major QTL cluster qPHSRC2 controlling the PHSR was discovered.

       

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