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利用SDS-PAGE和AS-PCR标记鉴定簇毛麦HMW-GS基因
引用本文:刘守斌,梁荣奇.利用SDS-PAGE和AS-PCR标记鉴定簇毛麦HMW-GS基因[J].中国农学通报,2010,26(15):38-43.
作者姓名:刘守斌  梁荣奇
作者单位:中国农业大学农学与生物技术学院植物遗传育种系,农业生物技术国家重点实验室,北京市作物遗传改良重点实验室,农业部作物基因组与遗传改良重点实验室,北京,100193
基金项目:国家自然科学基金项目,北京市自然科学基金项目 
摘    要:通过SDS-PAGE和AS-PCR标记对簇毛麦HMW-GS进行鉴定,对于快速鉴别导入到普通小麦中的簇毛麦HMW-GS和改良普通小麦品质具有重要意义。利用SDS-PAGE对中国春、钱尼、簇毛麦、6个中国春-簇毛麦二体附加系、普通小麦-簇毛麦3V异代换系进行HMW-GS组成分析,进一步确定簇毛麦HMW-GS基因位于1V染色体。根据已发表的普通小麦HMW-GS基因序列同源性比较结果,设计了3对分别扩增普通小麦x-型亚基基因、y-型亚基基因以及所有HMW-GS基因的特异引物。经过对簇毛麦HMW-GS基因进行扩增发现,这3个AS-PCR标记都能很好地鉴别簇毛麦HMW-GS编码基因,并从分子水平上把簇毛麦HMW-GS基因定位于簇毛麦1V染色体上。

关 键 词:抗旱复合肥    抗旱复合肥    玉米    水分利用率    氮素利用率
收稿时间:2010/2/20 0:00:00
修稿时间:2010/3/26 0:00:00

Analysis on HMW-GS genes in Dasypyum villosum by SDS-PAGE and Allelic Specific (AS) -PCR Markers
Liu Shoubin,Liang Rongqi,You Mingshan,Li Baoyun,Liu Guangtian.Analysis on HMW-GS genes in Dasypyum villosum by SDS-PAGE and Allelic Specific (AS) -PCR Markers[J].Chinese Agricultural Science Bulletin,2010,26(15):38-43.
Authors:Liu Shoubin  Liang Rongqi  You Mingshan  Li Baoyun  Liu Guangtian
Institution:( State Key Laboratory for Agrobiotechnology ; Beijing Key Laboratory of Crop Genetic Improvement ; Key Laboratory of Crop Genomics and Genetic Improvement , Ministry of Agriculture ; College of Agronomy and Biotechnology , China Agricultural University , Beijing 100193)
Abstract:Sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) and three allelic specific PCR (AS-PCR) markers were used in this paper to screen and confirm the High-molecular-weight glutenin subunits (HMW-GS) of D. villosum. The results of analysis on HMW-GS of CS, Cheyenny, D. villosum, six addition lines of D. villosum chromosome in CS and substitution line 3V of D. villosum chromosome in T. aestivum by SDS-PAGE indicated that genes encoding for HMW-GS were located in D. villosum chromosome 1V. Three AS-PCR markers, which could amplify x-type HMW glutenin genes, y-type HMW glutenin genes and all HMW glutenin genes of T. aestivum respectively, were synthesized on the basis of all published sequences of HMW-GS genes from T. aestivum. The results of amplification in D. villosum and other materials above showed that all of three markers could be used for characterization of HMW glutenin genes in D. villosum. Therefore, the gene encoding for HMW-GS of D. villosum was located in chromosome 1V in molecular level.
Keywords:Dasypyum villosum  high molecular weight glutenin subunit  allelic specific PCR marker  diversity
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