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新型隐球菌致病真菌18S和25S核糖体DNA的克隆

Cloning of 18S and 25S rDNAs from the pathogenic fungus Cryptococcus neoformans.

作者信息

Restrepo B I, Barbour A G

机构信息

Department of Medicine, University of Texas Health Science Center, San Antonio 78284.

出版信息

J Bacteriol. 1989 Oct;171(10):5596-600. doi: 10.1128/jb.171.10.5596-5600.1989.

Abstract

Cryptococcus neoformans is an important pathogenic fungus that has been classified as a basidiomycete. Little is known of the molecular genetics of this fungal pathogen. To begin such studies, we devised a procedure for extraction of DNA from cryptococci; this method involved the use of the cell wall-active enzyme NovoZym 234. Using cloned rDNA of Saccharomyces cerevisiae as a probe, we identified homologous restriction fragments in a Southern blot of digested C. neoformans DNA. An 8.6-kilobase HindIII fragment that hybridized with the yeast rDNA probe was ligated with the vector pBR322 and cloned into Escherichia coli. When the fragment was used as a probe, it hybridized to the 18S and 25S rRNAs of C. neoformans in Northern (RNA) blots of native and denatured RNA. It bound at high stringency only weakly to the rRNAs of the ascomycete S. cerevisiae. The locations of the genes for 5/5.8S, 18S, and 25S subunits in the cloned fragment were identified with labeled rRNA of these different types.

摘要

新型隐球菌是一种重要的致病真菌,已被归类为担子菌。对这种真菌病原体的分子遗传学了解甚少。为了开展此类研究,我们设计了一种从隐球菌中提取DNA的方法;该方法使用了细胞壁活性酶诺维信234。以酿酒酵母的克隆rDNA作为探针,我们在消化后的新型隐球菌DNA的Southern印迹中鉴定出同源限制性片段。将与酵母rDNA探针杂交的一个8.6千碱基的HindIII片段与载体pBR322连接,并克隆到大肠杆菌中。当该片段用作探针时,它在天然和变性RNA的Northern(RNA)印迹中与新型隐球菌的18S和25S rRNA杂交。它在高严谨度下仅与子囊菌酿酒酵母的rRNA弱结合。用这些不同类型的标记rRNA确定了克隆片段中5/5.8S、18S和25S亚基基因的位置。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/beec/210402/73bbb8c401d5/jbacter00176-0372-a.jpg

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