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转座子挽救法对转座子突变菌株中插入位点的定位分析 被引量:4

Analysis on Integration Sites of Transposon-insertion Mutant by Transposon Rescue
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摘要 为寻找谷氨酸棒杆菌转座子插入突变菌株中的转座子插入位点 ,采用了转座子挽救法对转座子及其插入位点附近的序列进行分离 ,并测定插入位点相邻DNA序列 ,获得了三个转座子插入位点DNA序列 ,其中一个是柠檬酸合成酶基因 ,另两个为目前未知基因 ,暂命名为orfA和orfB。该方法简便易行 。 In order to define the chromosomal locus of the transposon integration in a mutant of Corynebacterium glutamicum, transposon rescue experiments were performed. By isolating parts of the transposon together with adjacent parts of the bacterial chromosome and subsequent sequencing of the adjacent parts,the mutant was found to have three transposon integrations, one just in front of the citrate synthase gene gltA, the other two in hitherto unknown open reading frames designated orfA and orfB. The transposon rescue experiments are proven to be a easy, practical and ideal way in analyzing the transposon integration sites.
出处 《微生物学报》 CAS CSCD 北大核心 2002年第3期326-330,共5页 Acta Microbiologica Sinica
基金 德国政府DAAD奖学金 国家教育部联合资助
关键词 转座子挽救法 转座子突变菌株 插入位点 定位分析 插入突变 谷氨酸棒杆菌 Transposon rescue, Insertion mutagenesis, Corynebacterium glutamicum
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  • 1[1]Singer M, Berg P. Genes and genomes. Mill Valley, California:Blackwell scientific publications,1991.
  • 2[2]Kim Y, Harker A R. Mol Cells ,1997 , 7 :620 ~ 629.
  • 3[3]Ogura M, Hirao S, OhshiroY, et al. FEBSLett,1999,457:112~116.
  • 4[4]Vermeij P, Wietek C, Kahnert A, et al. Mol Microbiol,1999,32:913 ~ 926.
  • 5[5]Mcnamara P J, Milligan-Monroe K C, Khalili S, et al. J Bacteriol, 2000,182: 3197 ~ 3203.
  • 6[6]Hanahan D. Techniques for transformation of E. coli. Oxford, Wshington DC:IRL-Press, 1985.109 ~ 135.
  • 7[7]Kinoshita S. Glutamic acid bacteria. London: The Benjamin/Cummings Publishing Company, 1985.115 ~ 142.
  • 8[8]VieriaJ, MessingJ. Gene,1982,19:259~268.
  • 9[9]Ankri S, Serebrijski I, Reyes O, et al. J Bacteriol, 1996,178:4412 ~ 4419.
  • 10[10]Sambrook J, Fritsch E F, Maniatis J. Molecular cloning. 2nd. New York:Cold Spring Harbor Laboratory Press, 1989.

同被引文献55

  • 1徐剑宏,洪青,汪婷,张小华,李顺鹏.转座子标签法突变呋喃丹降解菌CFDS-1[J].微生物学通报,2005,32(2):34-38. 被引量:3
  • 2陈永辉,史贤明.利用转座子Tn917构建单核细胞增生李斯特菌菌膜形成突变株[J].微生物学报,2005,45(6):952-954. 被引量:7
  • 3[1]The Arabidopsis Genome Initiative.Analysis of the genome sequence of the flowering plant Arabidopsis thaliana[J].Nature,2000,408:796-815.
  • 4[2]Xun Gu.Evolution of duplicate genes versus genetic robustness against null mutations[J].Trends In Genetics,2003,19 (7):354-356.
  • 5[3]Paul R Muskett,Leah Clissold,Adriano Marocco,et al.A resource of mapped dissociation launch pads for targeted insertional mutsgenesis[J].Plant Physiology,2003,132:506-516.
  • 6[4]Brunaud V,Balzergue S,Dubreucq B,et al.T-DNA integration into the Arabidopsis genome depends on sequences of pre-insertionsites[J].EMBO reports,2002,12:1152-1157.
  • 7[5]AlonsoM,AnnaN,Stepanova I,etal.Genome-wide insertional mutagenesis of Arabidopsis thaliana[J].Science,2003,301:653-657.
  • 8[6]Hiei Y,Ohta S,Komari T,et al.Efficient transformation of rice (Oryza sativa L) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA[J].Plant J,1994,6 (2):271-282.
  • 9[7]Sallaud C,GayC,Larnande P,et al.High throughout T-DNA insertion mutagenesis in rice:a first step towards in silico reverse genetics[J].Plant J,2004,39(3):450-464.
  • 10[8]Mllins E D,Chen P X,Romaine P,et al.Agrobacterium-mediated transformation of Fusarium oxysporum:An efficient tool for insertional mutagenesis and gene transfer[J].Phytopathology,2001,91:173-180.

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