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SEG1元件:一个促进接合菌灰绿犁头霉中质粒稳定有丝分裂分离的新DNA区域。

The SEG1 element: a new DNA region promoting stable mitotic segregation of plasmids in the zygomycete Absidia glauca.

作者信息

Burmester A, Wöstemeyer A, Arnau J, Wöstemeyer J

机构信息

Institut für Genbiologische Forschung Berlin GmbH, FRG.

出版信息

Mol Gen Genet. 1992 Nov;235(2-3):166-72. doi: 10.1007/BF00279357.

Abstract

A series of new vectors for the model zygomycete Absidia glauca was constructed on the basis of the structural neomycin resistance (Neor) gene controlled by the promoter of the gene for elongation factor 1 (TEF). In order to select for transformed colonies with a stable Neor phenotype, spores from primary transformants were pooled and grown for two sporulation cycles under non-selective conditions. Southern blot analysis of DNA from single spore isolates originating from independent transformant pools allowed the identification of two autonomously replicating plasmids. Retransformation of Escherichia coli and restriction analysis of the two plasmids provided evidence for spontaneous in vivo insertion of a new DNA element (SEG1) from the A. glauca genome. The inserted regions in both plasmids are essentially identical and do not represent repetitive DNA. Compared with other autonomously replicating vectors, these SEG1-containing plasmids are mitotically extremely stable and are passed on to the vegetative spore progeny of a retransformed A. glauca strain. We assume that SEG1 contains structural elements involved in partitioning and stable segregation of plasmids. For the construction of stable transformants of A. glauca, the SEG1 element may be regarded as a major breakthrough, because stabilization of transformed genetic traits by integration is difficult to achieve in all mucoraceous fungi and all known replicating plasmids are mitotically unstable.

摘要

基于由延伸因子1(TEF)基因启动子控制的结构新霉素抗性(Neor)基因,构建了一系列用于模式接合菌灰绿犁头霉的新型载体。为了选择具有稳定Neor表型的转化菌落,将初级转化体的孢子汇集起来,并在非选择性条件下培养两个孢子形成周期。对来自独立转化体库的单孢子分离物的DNA进行Southern印迹分析,从而鉴定出两种自主复制质粒。大肠杆菌的再转化以及对这两种质粒的限制性分析为来自灰绿犁头霉基因组的一种新DNA元件(SEG1)在体内的自发插入提供了证据。两种质粒中的插入区域基本相同,且不代表重复DNA。与其他自主复制载体相比,这些含有SEG1的质粒在有丝分裂过程中极其稳定,并传递给再转化的灰绿犁头霉菌株的营养孢子后代。我们假设SEG1包含参与质粒分配和稳定分离的结构元件。对于构建灰绿犁头霉的稳定转化体而言,SEG1元件可被视为一项重大突破,因为在所有毛霉科真菌中通过整合来稳定转化遗传性状很难实现,而且所有已知的复制质粒在有丝分裂过程中都不稳定。

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