中国水稻科学
中國水稻科學
중국수도과학
CHINESE JOURNAL OF RICE SCIENCE
2014年
5期
465-472
,共8页
刘林%张迎信%李枝%刘群恩%余宁%孙滨%杨正福%周全%程式华%曹立勇
劉林%張迎信%李枝%劉群恩%餘寧%孫濱%楊正福%週全%程式華%曹立勇
류림%장영신%리지%류군은%여저%손빈%양정복%주전%정식화%조립용
水稻%类病变突变体%基因定位%防卫反应
水稻%類病變突變體%基因定位%防衛反應
수도%류병변돌변체%기인정위%방위반응
rice%lesion mimic mutant%gene mapping%defense response
通过γ射线辐射诱变籼稻9311和中恢8015分别获得了2个类病变突变体 g303和 g342.g303播种4~5周叶片开始出现黄褐色斑点.随着植株的生长发育,至成熟期病斑几乎布满整个植株.与野生型相比,突变体 g303株高、结实率、千粒重显著下降,叶绿素含量、光合速率显著降低.遗传分析表明,g303类病变性状由一对隐性基因控制.利用 g303/日本晴 F2群体进行定位,将突变基因定位于第12染色体标记 InD10和 InD12之间,遗传距离分别为0.19 cM 和0.76 cM.测序分析发现,该基因与 SL 基因等位,其中 g303和 g342分别在编码区第572位和第1206位发生单碱基缺失,导致翻译提前终止.实时 RT-PCR 结果显示抗病相关基因在突变体 g303中表达量显著上升,说明该基因突变很可能激活了防卫反应.
通過γ射線輻射誘變秈稻9311和中恢8015分彆穫得瞭2箇類病變突變體 g303和 g342.g303播種4~5週葉片開始齣現黃褐色斑點.隨著植株的生長髮育,至成熟期病斑幾乎佈滿整箇植株.與野生型相比,突變體 g303株高、結實率、韆粒重顯著下降,葉綠素含量、光閤速率顯著降低.遺傳分析錶明,g303類病變性狀由一對隱性基因控製.利用 g303/日本晴 F2群體進行定位,將突變基因定位于第12染色體標記 InD10和 InD12之間,遺傳距離分彆為0.19 cM 和0.76 cM.測序分析髮現,該基因與 SL 基因等位,其中 g303和 g342分彆在編碼區第572位和第1206位髮生單堿基缺失,導緻翻譯提前終止.實時 RT-PCR 結果顯示抗病相關基因在突變體 g303中錶達量顯著上升,說明該基因突變很可能激活瞭防衛反應.
통과γ사선복사유변선도9311화중회8015분별획득료2개류병변돌변체 g303화 g342.g303파충4~5주협편개시출현황갈색반점.수착식주적생장발육,지성숙기병반궤호포만정개식주.여야생형상비,돌변체 g303주고、결실솔、천립중현저하강,협록소함량、광합속솔현저강저.유전분석표명,g303류병변성상유일대은성기인공제.이용 g303/일본청 F2군체진행정위,장돌변기인정위우제12염색체표기 InD10화 InD12지간,유전거리분별위0.19 cM 화0.76 cM.측서분석발현,해기인여 SL 기인등위,기중 g303화 g342분별재편마구제572위화제1206위발생단감기결실,도치번역제전종지.실시 RT-PCR 결과현시항병상관기인재돌변체 g303중표체량현저상승,설명해기인돌변흔가능격활료방위반응.
The lesion mimic mutant g303 and g342 were isolated by treating the seeds of indica varieties 93 1 1 and R801 5 with γ-ray radiation,respectively.The yellow spots initially appear on g303 leaves at 4-leaf stage.With the growth and development of the plant,the lesions almost occupied the whole plant till the maturity stage.Compared with the wild type,the plant height,seed setting rate and 1000-grain weight of g303 significantly dropped,the chlorophyll and photosynthetic rate obviously decreased.Genetic analysis showed that the mutant phenotype was controlled by a single recessive gene.Using F2 mapping population of g303/ Nipponbare,the g303 mutant gene was mapped between marker InD10 and InD12 on rice chromosome 12,with genetic distances of 0.1 9 cM and 0.76 cM, respectively.Sequence analysis revealed that the mutated gene was allelic to SL ,g303 and g342 mutated gene had a single nucleotide deletion (T572 and G1206,respectively),leading to a premature termination codon.Real-time PCR analysis showed that the expression level of defense-related genes upregulated significantly,these results demonstrated that the mutation may activate the defense response.