作物学报
作物學報
작물학보
ACTA AGRONOMICA SINICA
2009年
11期
1967-1972
,共6页
罗远章%赵芳明%桑贤春%凌英华%杨正林%何光华
囉遠章%趙芳明%桑賢春%凌英華%楊正林%何光華
라원장%조방명%상현춘%릉영화%양정림%하광화
水稻%显性卷叶基因%遗传分析%基因定位
水稻%顯性捲葉基因%遺傳分析%基因定位
수도%현성권협기인%유전분석%기인정위
Oryza sativa%Dominant rolled leaf gene%Genetic analysis%Gene mapping
叶片是水稻光合作用的重要器官,适度卷曲有利于改善群体光照、提高光能利用率,卷叶基因是培育理想株型的重要资源.本研究利用EMS诱变优良恢复系缙恢10号,获得了一个水稻新型卷叶突变体,该性状受一对显性基因控制,表现为新叶不卷,老叶全卷,而成熟叶片叶上部约1/3卷曲、中下部正常,叶绿素含量极显著高于对照,暂被命名为rl12(t).利用SSR标记将该基因定位于第10染色体SWU-1和SWU-2之间,遗传距离分别是1.5 cM和0.2cM.目前,类似于rl12(t)卷叶突变体表型未见报道,RL12(t)是唯一一个在第10染色体被分子定位的显性卷叶主基因.研究结果为该卷叶基因的克隆和功能分析奠定了基础,对于揭示卷叶机理及应用于株型改良具有重要的意义.
葉片是水稻光閤作用的重要器官,適度捲麯有利于改善群體光照、提高光能利用率,捲葉基因是培育理想株型的重要資源.本研究利用EMS誘變優良恢複繫縉恢10號,穫得瞭一箇水稻新型捲葉突變體,該性狀受一對顯性基因控製,錶現為新葉不捲,老葉全捲,而成熟葉片葉上部約1/3捲麯、中下部正常,葉綠素含量極顯著高于對照,暫被命名為rl12(t).利用SSR標記將該基因定位于第10染色體SWU-1和SWU-2之間,遺傳距離分彆是1.5 cM和0.2cM.目前,類似于rl12(t)捲葉突變體錶型未見報道,RL12(t)是唯一一箇在第10染色體被分子定位的顯性捲葉主基因.研究結果為該捲葉基因的剋隆和功能分析奠定瞭基礎,對于揭示捲葉機理及應用于株型改良具有重要的意義.
협편시수도광합작용적중요기관,괄도권곡유리우개선군체광조、제고광능이용솔,권협기인시배육이상주형적중요자원.본연구이용EMS유변우량회복계진회10호,획득료일개수도신형권협돌변체,해성상수일대현성기인공제,표현위신협불권,로협전권,이성숙협편협상부약1/3권곡、중하부정상,협록소함량겁현저고우대조,잠피명명위rl12(t).이용SSR표기장해기인정위우제10염색체SWU-1화SWU-2지간,유전거리분별시1.5 cM화0.2cM.목전,유사우rl12(t)권협돌변체표형미견보도,RL12(t)시유일일개재제10염색체피분자정위적현성권협주기인.연구결과위해권협기인적극륭화공능분석전정료기출,대우게시권협궤리급응용우주형개량구유중요적의의.
Leaf is an important organ in photosynthesis, its moderate rolling could facilitate the improvement of plant population's structure and enhance light-use efficiency, which is significant in ideotype breeding. Recently, more attention has been paid to the identification of rice rolled leaf mutants and related gene cloning by breeders and geneticists. This paper reported a rolled leaf mutant, temporarily named rl12(t), from the restorer line Jinhui10 treated by EMS. In the mutant, the initializing leaves did not roll, the mature leaves curled the upper 1/3 section of them and the older mature leaves rolled completely, the pigment contents increased significantly. To date, such phenotype has never been reported. One CMS line Xinong 1A with normal leaves was crossed with the rl12(t) mutant, the F1/F2 populations were used for genetic analysis, suggesting that the mutant trait were controlled completely by one single dominant nuclear gene. rl12(t) was finally located on the chromosome 10 between SWU-1 and SWU-2 with genetic distances of 1.5 and 0.2 cM, respectively. There has been no rolled leaf gene reported on this chromosome. Therefore, the RL12(t) should be novel, and also the unique dominant rolled leaf gene mapped by molecular markers up to now. The results provide a basis for RL12(t) gene cloning and functional analysis, as well as mechanism studies of rolled leaf and the application in plant-type breeding.