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在用于产油真菌高山被孢霉的转化载体中分离和使用同源组蛋白H4启动子及核糖体DNA区域。

Isolation and use of a homologous histone H4 promoter and a ribosomal DNA region in a transformation vector for the oil-producing fungus Mortierella alpina.

作者信息

Mackenzie D A, Wongwathanarat P, Carter A T, Archer D B

机构信息

Institute of Food Research, Norwich Research Park, Colney, Norwich, Norfolk, NR4 7UA, United Kingdom.

出版信息

Appl Environ Microbiol. 2000 Nov;66(11):4655-61. doi: 10.1128/AEM.66.11.4655-4661.2000.

Abstract

Mortierella alpina was transformed successfully to hygromycin B resistance by using a homologous histone H4 promoter to drive gene expression and a homologous ribosomal DNA region to promote chromosomal integration. This is the first description of transformation in this commercially important oleaginous organism. Two pairs of histone H3 and H4 genes were isolated from this fungus. Each pair consisted of one histone H3 gene and one histone H4 gene, transcribed divergently from an intergenic promoter region. The pairs of encoded histone H3 or H4 proteins were identical in amino acid sequence. At the DNA level, each histone H3 or H4 open reading frame showed 97 to 99% identity to its counterpart but the noncoding regions had little sequence identity. Unlike the histone genes from other filamentous fungi, all four M. alpina genes lacked introns. During normal vegetative growth, transcripts from the two histone H4 genes were produced at approximately the same level, indicating that either histone H4 promoter could be used in transformation vectors. The generation of stable, hygromycin B-resistant transformants required the incorporation of a homologous ribosomal DNA region into the transformation vector to promote chromosomal integration.

摘要

通过使用同源组蛋白H4启动子驱动基因表达以及同源核糖体DNA区域促进染色体整合,高山被孢霉成功转化为对潮霉素B具有抗性。这是对这种具有重要商业价值的产油生物进行转化的首次描述。从这种真菌中分离出了两对组蛋白H3和H4基因。每对由一个组蛋白H3基因和一个组蛋白H4基因组成,它们从基因间启动子区域向不同方向转录。所编码的组蛋白H3或H4蛋白对在氨基酸序列上是相同的。在DNA水平上,每个组蛋白H3或H4开放阅读框与其对应物显示出97%至99%的同一性,但非编码区域几乎没有序列同一性。与其他丝状真菌的组蛋白基因不同,所有四个高山被孢霉基因都没有内含子。在正常营养生长期间,两个组蛋白H4基因的转录本以大致相同的水平产生,这表明任何一个组蛋白H4启动子都可用于转化载体。产生稳定的、对潮霉素B具有抗性的转化体需要将同源核糖体DNA区域整合到转化载体中以促进染色体整合。

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