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甘薯栽培种及其近缘野生种的DAPI核型及rDNA FISH分析
引用本文:安婷婷,汤佳立,孙健英,曹清河,马代夫,李宗芸.甘薯栽培种及其近缘野生种的DAPI核型及rDNA FISH分析[J].西北植物学报,2012,32(4):682-687.
作者姓名:安婷婷  汤佳立  孙健英  曹清河  马代夫  李宗芸
作者单位:1. 江苏师范大学 生命科学学院,江苏徐州 221116;江苏师范大学,江苏省药用植物生物技术重点实验室,江苏徐州 221116
2. 江苏师范大学 生命科学学院,江苏徐州 221116;江苏师范大学,江苏省药用植物生物技术重点实验室,江苏徐州 221116;中国药科大学 生命科学与技术学院,南京 210009
3. 中国农业科学院甘薯研究所徐州甘薯研究中心,江苏徐州,221121
基金项目:国家自然科学基金项目(30800698);江苏高校优势学科建设工程资助项目
摘    要:利用DAPI显带和rDNA-FISH技术对栽培种甘薯(‘徐薯18’)(Ipomoea batatas cv.Xushu No.18)及2种不同产地近缘野生种(Ipomoea hederacea Jacq.)进行了细胞遗传学研究。DAPI核型分析表明,‘徐薯18’核型公式为2n=6x=90=72m+18sm(18SAT),随体位于第1、3、6染色体上;美国近缘野生种核型公式为2n=2x=30=30m(4SAT),香港近缘野生种核型公式为2n=2x=30=20m+10sm(4SAT),随体均位于第6、12染色体上。rD-NA-FISH结果显示,栽培种甘薯基因组中含有3对5SrDNA位点,分别位于着丝粒区、亚着丝粒区和染色体端部;美国近缘野生种基因组中含有2对5SrDNA位点,香港近缘野生种基因组中含有1对5SrDNA位点,均位于随体部位;两种不同地域来源的近缘野生种基因组中均含有2对45SrDNA位点,分别位于第6和第12染色体上。

关 键 词:栽培种甘薯  近缘野生种  DAPI显带  rDNA-FISH

rDNA FISH Analysis and DAPI karyotype of Ipomoea batatas cv.and Ipomoea hederacea Jacq.
AN Ting ting,TANG Jia li,SUN Jian ying,CAO Qing he,MA Dai fu,LI Zong yun.rDNA FISH Analysis and DAPI karyotype of Ipomoea batatas cv.and Ipomoea hederacea Jacq.[J].Acta Botanica Boreali-Occidentalia Sinica,2012,32(4):682-687.
Authors:AN Ting ting  TANG Jia li  SUN Jian ying  CAO Qing he  MA Dai fu  LI Zong yun
Institution:1,2* (1 School of Life Science,Jiangsu Normal University,Xuzhou,Jiangsu 221116,China;2 Jiangsu Normal University,The Key Laboratory of Biotechnology for Medicinal Plants of Jiangsu Province,Xuzhou,Jiangsu 221116,China;3 School of Life Science and Technology,China Pharmaceutical University,Nanjing 210009,China;4 Xuzhou Sweet Potato Research Centre,Institute of Sweet Potato,Chinese Academy of Agricultural Sciences,Xuzhou,Jiangsu 221121,China)
Abstract:Ipomoea batatas cv.Xushu 18 and its two wild relatives I.hederacea Jacq.from American and Hong Kong in China were studied by DAPI banding and rDNA-fluorescence in situ hybridization.The DAPI banding showed the karyotype of I.batatas and I.hederacea Jacq.from American and Hong Kong in China are 2n=6x=90=72m+18sm(18SAT) with satellites on chromosome 1,3 and 6;2n=2x=30=30m(4SAT);2n=2x=30=20m+10sm(4SAT),both with satellite on chromosome 6 and 12,respectively.The FISH data indicated that three pairs of 5S rDNA signals,located on centromere,pericentromere and the telomere of chromosome respectively of I.batatas;Two pairs of 45S rDNA signals,located on chromosome 6 and 12 were detected on both I.hederacea Jacq.;While 1 pairs of 5S rDNA signals presented on chromosome 6 of I.hederacea Jacq.from Hong Kong,2 pairs of 5S rDNA signals occurred on the chromosome 6 and 12 of that from American.Taking all the data obtained in the study,both I.hederacea Jacq.were distant from the sweet potato,and there were some differentiations in the chromosomes of the I.hederacea Jacq.from different territories.
Keywords:Ipomoea batatas cv  Xushu No  18  I  hederacea Jacq    DAPI banding  rDNA-fluorescence in situ hybridization
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