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主題 : 2009年全國優秀博士論文:水稻白葉枯病隱性
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樓主  發表于: 2009-12-07   

2009年全國優秀博士論文:水稻白葉枯病隱性

作者姓名:儲昭暉 [S0wwWU |0  
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  論文題目:水稻白葉枯病隱性抗病基因xa13的分離與鑒定的研究 -}RGz_LO/  
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  作者簡介:儲昭暉,男,1977年01月出生,1998年09月師從于華中農業大學王石平教授,于2006年01月獲博士學位。 ED>P>Gg  
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  植物抗病基因的研究一直以來是植物分子生物學研究領域的熱點之一,迄今已經從不同的宿主中分離了50多個抗病基因,其中僅有6個是隱性基因,這些隱性抗病基因的作用機理目前尚不能用廣為接受的顯性基因的作用機理來進行解釋。水稻中已經鑒定32個主效抗白葉枯病基因,其中9個為隱性抗病基因。位于第8染色體長臂末端的xa13基因就是其中的一個典型,它完全隱性抗性、特異性的抗白葉枯病菌菲律賓菌系生理小種6(PXO99)、和其它顯性或隱性抗白葉枯病基因存在抗性互作,說明xa13基因抗病機理的特異性。 27MwZz  
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  為克隆xa13基因,采用基因組飽和雜交的原理,在9個發育時期取材構建了水稻品種明恢63全生育期均一化cDNA文庫。以分子標記E6a和另一端標記S14003為起始,構建了xa13基因區段的物理圖譜,并結合3個F2群體和Shotgun測序結果將該基因定位于一個9.2 kb的DNA片段上。同時通過精細物理定位xa13基因,開發了數個與該基因緊密連鎖的基于PCR技術的分子標記,為采用分子標記輔助選擇xa13育種提供了經濟、方便的分子標記。 t(}g;O-  
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  在優化了一套適合于水稻品種IRBB13的轉基因組培體系的基礎上,通過農桿菌介導的遺傳轉化方法,將攜帶顯性候選基因的片段轉入到攜帶隱性抗病基因的水稻品種IRBB13中,在45株轉基因植株后代中,有全長基因導入的30株的表型變為感病,并且4個單拷貝轉基因的T1代家系也符合共分離檢測,從而驗證了候選基因是xa13基因的顯性基因Xa13,標志用圖位克隆法成功克隆了隱性基因xa13和顯性基因Xa13。同時,通過RNA干擾(RNAi)技術,分別抑制水稻品種明恢63和中花11中顯性基因Xa13的表達,以及水稻品系IRBB13中隱性基因的表達。通過接種白葉枯病菌PXO99和定量RT-PCR分析發現,明恢63和中花11中Xa13基因表達受到抑制的植株表型由感病變為抗病,IRBB13中xa13基因表達受到抑制的植株抗性進一步加強。 ^b 3nEcQn  
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  有趣的是,顯性基因Xa13和隱性基因xa13在花藥中的表達量高于在葉片中的表達量。RNAi轉基因植株中Xa13或xa13的表達受到抑制會導致植株不育或半不育,組織學觀察發現這些不育單株的多數花粉的發育停留在單核花粉期或二核花粉期。原位雜交的實驗證明, Xa13基因在花藥中表達的時期與異常花粉發生的時期非常一致,Xa13在花粉發育的早期不表達,在單核花粉期開始高水平表達。從而說明Xa13基因在花粉的發育中也起著重要的作用。 *DvQnj  
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  進一步通過大量實驗表明,顯性基因Xa13是一個受病原調控表達的基因,由顯性基因Xa13突變成隱性基因xa13的關鍵不是編碼區內的變化,而是在啟動子區的一個約18 bp的區間內的突變使基因表達受病原調控的能力喪失,且這種突變不影響其在花粉中的表達。XA13蛋白是一個未知具體生化功能的細胞膜蛋白,屬于MtN3家族的成員之一。但其在白葉枯病菌PXO99侵染以及在花粉的發育中發揮著重要的功能,且可能介導新的抗病途徑。因此,本研究通過克隆隱性基因xa13以及它的顯性基因Xa13,不僅揭示了一種新的植物抗病機制:即抑制抗病基因的表達是高效抗病的基礎,而且為研究植物抗病和花粉發育的關系提供了一個新的起點。 J|([(  
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  關鍵詞:  水稻;白葉枯病;黃單胞桿菌;抗病基因;cDNA文庫;圖位克隆 _/YM@%d  
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板凳  發表于: 2011-08-12   
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沙發  發表于: 2009-12-07   
 Isolation and Characterization of a Recessive Resistance Gene, xa13, for Bacterial Blight in Rice +e#(p<  
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  Zhaohui Chu D0L s~qr  
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  Studies on plant resistant genes are one of the hotspots in the field of plant molecular biology. Until now, among the over 50 separated resistant genes, only 6 are recessive genes. The mechanisms of recessive genes can not be explained by those of dominant resistant genes, which have been universally accepted. Bacterial blight, caused by Xanthomonas oryzae pv. oryzae (Xoo), is one of the most serious diseases of rice worldwide. Thirty-two bacterial blight resistance genes (23 dominant genes and 9 recessive genes) in rice have been identified. However the xa13, which located on the distal end of the long arm of the chromosome 8, was a typical recessive R gene in rice, that is fully recessive and specifically confers resistance to the Philippine Xoo race 6 (PXO99). The xa13 gene also interacts with other dominant or recessive R genes which indicated the specialty of disease resistant mechanism of xa13. ob/HO (h3  
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  To clone xa13 gene, a normalized whole-life-cycle cDNA library was firstly constructed with different tissues from 9 develomental stages using rice cultivar Minghui 63, based on the strategy of saturation hybridization with genomic DNA. Then a physical map that covers the region flanked by markers E6a and S14003 was constructed by chromosome walking using Minghui 63 BAC clones. And finally we have fine-mapped xa13 to a DNA fragment of 9.2 kb using a series of sequence-based molecular markers. Sequence analysis indicated that this region contain only one candidate gene, which was annotated by full length EST sequence that isolated from the constructed cDNA library. waG &3m  
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  Transformation of IRBB13 with the DNA fragment encompassing the Xa13 candidate that based on the optimised tissue cultural system, including the promoter region isolated from IR64, produced 45 independent transformants. Thirty of the 45 T0 transgenic plants were susceptible upon infection by PXO99. PCR analysis demonstrated that all of the susceptible transgenic plants had the band derived from the Xa13-candidate fragment, while none of the resistant plants amplified this band. T1 families derived from four of the single-copy T0 transgenic plants were further investigated. And the susceptibility cosegregated perfectly with the transgene in all four families, indicated that the clone of xa13 gene by map based cloning strategy was succeed, and the candidate gene in this fragment was indeed Xa13, and the allelic gene in recessive parent was xa13. At the same time, we have suppresssed the expression of Xa13 or xa13 in different rice lines using the RNA interference (RNAi) strategy. We found that suppression of Xa13 expression in rice line Zhonghua 11 and MH63 significantly increased the resistance to PXO99, and the level of increased resistance was associated with the reduced accumulation of Xa13 transcripts. Suppression the expression of xa13 in rice line IRBB13 further enhanced xa13-mediated resistance. W k亚洲国产精品va在线观看麻豆