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利用反向聚合酶链反应分析番茄中携带转座子的T-DNA的染色体分布。

Analysis of the chromosomal distribution of transposon-carrying T-DNAs in tomato using the inverse polymerase chain reaction.

作者信息

Thomas C M, Jones D A, English J J, Carroll B J, Bennetzen J L, Harrison K, Burbidge A, Bishop G J, Jones J D

机构信息

Sainsbury Laboratory, John Innes Centre, Norwich, UK.

出版信息

Mol Gen Genet. 1994 Mar;242(5):573-85. doi: 10.1007/BF00285281.

Abstract

We are developing a system for isolating tomato genes by transposon mutagenesis. In maize and tobacco, the transposon Activator (Ac) transposes preferentially to genetically linked sites. To identify transposons linked to various target genes, we have determined the RFLP map locations of Ac- and Dissociation (Ds)-carrying T-DNAs in a number of transformants. T-DNA flanking sequences were isolated using the inverse polymerase chain reaction (IPCR) and located on the RFLP map of tomato. The authenticity of IPCR reaction products was tested by several criteria including nested primer amplification, DNA sequence analysis and PCR amplification of the corresponding insertion target sequences. We report the RFLP map locations of 37 transposon-carrying T-DNAs. We also report the map locations of nine transposed Ds elements. T-DNAs were identified on all chromosomes except chromosome 6. Our data revealed no apparent chromosomal preference for T-DNA integration events. Lines carrying transposons at known map locations have been established which should prove a useful resource for isolating tomato genes by transposon mutagenesis.

摘要

我们正在开发一种通过转座子诱变分离番茄基因的系统。在玉米和烟草中,转座子激活子(Ac)优先转座到遗传连锁位点。为了鉴定与各种靶基因连锁的转座子,我们已经确定了许多转化体中携带Ac和解离(Ds)的T-DNA的RFLP图谱位置。使用反向聚合酶链反应(IPCR)分离T-DNA侧翼序列,并将其定位在番茄的RFLP图谱上。通过包括巢式引物扩增、DNA序列分析和相应插入靶序列的PCR扩增等多个标准来测试IPCR反应产物的真实性。我们报告了37个携带转座子的T-DNA的RFLP图谱位置。我们还报告了9个转座的Ds元件的图谱位置。除了6号染色体外,在所有染色体上都鉴定到了T-DNA。我们的数据显示T-DNA整合事件没有明显的染色体偏好性。已经建立了在已知图谱位置携带转座子的株系,这将为通过转座子诱变分离番茄基因提供有用的资源。

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