首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Mapping point mutations in the Drosophila rosy locus using denaturing gradient gel blots.
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Mapping point mutations in the Drosophila rosy locus using denaturing gradient gel blots.

机译:使用变性梯度凝胶印迹法在果蝇玫​​瑰色基因座中定位点突变。

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Mutations within the rosy locus of Drosophila were mapped using blots of genomic DNA fragments separated on denaturing gradient gels. DNA sequence differences between otherwise identical small rosy DNA fragments were detected among the mutants as mobility shifts on the blots. Mutations were mapped to within a few hundred base pairs of rosy sequence in 100 of 130 mutants tested--a 77% detection rate. The sequence changes in 43 rosy mutations are presented; all but six of these were single base changes. Thirty-four of 36 sequenced mutations induced by the alkylating agents N-ethyl-N-nitrosourea and ethyl methanesulfonate were transitions. All of the mutations mapped in the rosy transcription unit. Twenty-three of the 43 sequenced mutations change the predicted rosy gene polypeptide sequence; the remainder would interrupt protein translation (17), or disrupt mRNA processing (3).
机译:使用在变性梯度凝胶上分离的基因组DNA片段的印迹,对果蝇玫瑰色基因座内的突变进行定位。随着印迹上迁移率的变化,在突变体之间检测到了其他相同的小玫瑰色DNA片段之间的DNA序列差异。在测试的130个突变体中的100个中,突变被映射到玫瑰色序列的几百个碱基对内,检出率为77%。呈现了43个玫瑰色突变的序列变化;除了六个以外,所有这些都是单一基础更改。由烷基化剂N-乙基-N-亚硝基脲和甲磺酸乙酯诱导的36个序列突变中的34个为过渡。所有的突变都位于玫瑰色转录单位中。 43个测序突变中有23个改变了预测的玫瑰色基因多肽序列;其余的将中断蛋白质翻译(17)或破坏mRNA的加工(3)。

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