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植物再生相关基因的QTL定位及克隆应用研究进展
引用本文:王永芳,刁现民.植物再生相关基因的QTL定位及克隆应用研究进展[J].河北农业科学,2010,14(11):85-88.
作者姓名:王永芳  刁现民
作者单位:[1]河北省农林科学院谷子研究所国家谷子改良中心河北省杂粮研究实验室,河北石家庄050031 [2]中国农业科学院作物科学研究所,北京100081
摘    要:植物转基因育种研究已在世界范围内广泛开展并取得辉煌成就,高效转基因的前提是高效的组织培养再生系统。植物组织培养的再生能力受基因型决定,不同基因型间再生能力差异很大,且多为数量性状。对高效转基因育种的追求使得研究再生相关基因显得很重要,国内外在水稻、小麦、玉米、大麦等多种作物上开展了再生相关基因的定位研究,发现了一些QTL位点。在高效再生QTL克隆方面,仅在水稻上克隆了PSR1基因,并确定PSR1为铁氧还蛋白亚硝酸盐还原酶,将PSR1转化到低再生能力的品种中,提高了该品种的再生能力。对植物再生相关基因的QTL定位及克隆应用的研究进展进行综述,并对再生相关基因作为一种新型选择标记的应用前景进行了讨论。

关 键 词:植株再生  再生相关基因  QTL定位  基因克隆

Advances on QTL Location and Cloning of Genes Related to Regeneration Ability of Plant Tissue Culture
WANG Yong-fang,DIAO Xian-min.Advances on QTL Location and Cloning of Genes Related to Regeneration Ability of Plant Tissue Culture[J].Journal of Hebei Agricultural Sciences,2010,14(11):85-88.
Authors:WANG Yong-fang  DIAO Xian-min
Institution:1.Institute of Millet Crops of Hebei Academy of Agriculture and Forestry Sciences,National Millet Improvement Center of China,Cereal Crops Research Laboratory of Hebei Province,Shijiazhuang 050031,China;2.Institute of Crop Sciences,Chinese Academy of Agricultural Sciences,Beijing 100081,China)
Abstract:The plant transgenic breeding had been widely developed in world scale,and brilliant achievements had been achieved.The high efficient in vitro regeneration system was the premise of high efficient plant transformation system.The regeneration ability of plant tissue culture was determined by genotype.The regeneration ability was controlled by multiple QTLs,and different genotypes of same plant species showed diversified response to tissue culture.QTL analysis had been carried out in rice,maize,wheat and barley,and some QTLs were identified.But so far only PSR1 from rice was cloned.The advances on the genetic mapping and cloning of QTLs for tissue culture response in plants were summarized,and the application prospect of using the genes related to tissue culture response as selectable marker genes was discussed.
Keywords:Plant regeneration  Regeneration gene  QTL location  Gene cloning
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