Suppr超能文献

新型隐球菌ADE2基因的分子分析,一种用于转化和基因破坏的选择标记。

Molecular analysis of the Cryptococcus neoformans ADE2 gene, a selectable marker for transformation and gene disruption.

作者信息

Sudarshan S, Davidson R C, Heitman J, Alspaugh J A

机构信息

Department of Pharmacology and Cancer Biology, Howard Hughes Medical Institute, Durham, North Carolina 27710, USA.

出版信息

Fungal Genet Biol. 1999 Jun;27(1):36-48. doi: 10.1006/fgbi.1999.1126.

Abstract

Cryptococcus neoformans is an important fungal pathogen of man. The incidence of cryptococcal disease has increased dramatically in patients immunocompromised because of HIV infection, organ transplantation, or treatment with cytotoxic chemotherapy or corticosteroids. This organism is an excellent model for molecular dissection of fungal pathogenesis and virulence factors. Here we report the nucleotide sequence of the C. neoformans serotype D genomic ADE2 gene, which encodes a phosphoribosylaminoimidazole carboxylase required for purine biosynthesis. Importantly, this version of the ADE2 gene has been used as the selectable marker for virtually all gene disruptions by transformation and homologous recombination in C. neoformans. We compare the nucleotide and amino acid sequences of the ADE2 gene and product to other highly related adenine biosynthetic genes and enzymes from other yeasts and fungi. We also describe a series of convenient ADE2 cassettes for gene disruption construct preparation. Finally, we have identified the ade2 mutations in strains M001 and M049, adenine auxotrophic mutants derived from the serotype A strain H99. These mutant strains have served as recipients for targeted gene disruptions using the ADE2 gene. These studies should facilitate transformation and gene disruption approaches using the ADE2 selectable marker in this important human fungal pathogen.

摘要

新型隐球菌是人类重要的真菌病原体。由于感染HIV、进行器官移植或接受细胞毒性化疗或皮质类固醇治疗而免疫受损的患者中,隐球菌病的发病率急剧上升。这种生物体是用于分子剖析真菌发病机制和毒力因子的极佳模型。在此,我们报告新型隐球菌D血清型基因组ADE2基因的核苷酸序列,该基因编码嘌呤生物合成所需的磷酸核糖氨基咪唑羧化酶。重要的是,ADE2基因的这个版本几乎已被用作通过转化和同源重组在新型隐球菌中进行所有基因破坏的选择标记。我们将ADE2基因和产物的核苷酸及氨基酸序列与来自其他酵母和真菌的其他高度相关的腺嘌呤生物合成基因及酶进行比较。我们还描述了一系列用于制备基因破坏构建体的便捷ADE2盒。最后,我们在源自A血清型菌株H99的腺嘌呤营养缺陷型突变体M001和M049菌株中鉴定出ade2突变。这些突变菌株已用作使用ADE2基因进行靶向基因破坏的受体。这些研究应有助于在这种重要的人类真菌病原体中使用ADE2选择标记进行转化和基因破坏方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验