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新型隐球菌变种格特变种MATalpha位点23个新基因的基因组组织与表达

Genomic organization and expression of 23 new genes from MATalpha locus of Cryptococcus neoformans var. gattii.

作者信息

Ren Ping, Roncaglia Paola, Springer Deborah J, Fan Jinjiang, Chaturvedi Vishnu

机构信息

Mycology Laboratory, Wadsworth Center, New York State Department of Health, Albany, NY, USA.

出版信息

Biochem Biophys Res Commun. 2005 Jan 7;326(1):233-41. doi: 10.1016/j.bbrc.2004.11.017.

Abstract

The pathogenic yeast Cryptococcus neoformans (Cn) causes cryptococcosis, a life-threatening disease of the brain. Molecular studies of Cn variety gattii have lagged behind other two varieties (var. grubii and var. neoformans) although they have distinct biology and disease patterns. We focused on gene discovery in MATalpha locus because it predominates in clinical strains. A var. gattii cosmid library was screened with DNA probes from other two varieties. Two positive clones were sequenced to identify ORFs based on similarities to known proteins, and to ESTs using bioinformatics, and manually by a curator. Approximately 76kb sequenced DNA revealed 23 genes and ORFs. The existence of predicted genes was verified by RT-PCR analyses designed to amplify spliced sequences. The results confirmed that the transcripts were expressed both at 30 and 37 degrees C. The var. gattii MATalpha locus genes showed rearrangements in order and orientation vis-a-vis other two varieties. Mating-specific genes showed higher nonsynonymous mutation rates, and gene trees showed var. gattii strains in a distinct clade. The identification of the largest number, thus far, of var. gattii structural genes should set the stage for future molecular pathogenesis studies.

摘要

致病性酵母新型隐球菌(Cn)可引发隐球菌病,这是一种威胁生命的脑部疾病。尽管新型隐球菌格特变种(var. gattii)具有独特的生物学特性和疾病模式,但其分子研究仍落后于其他两个变种(格鲁比变种和新生变种)。我们聚焦于MATalpha基因座中的基因发现,因为它在临床菌株中占主导地位。用来自其他两个变种的DNA探针筛选了一个格特变种黏粒文库。对两个阳性克隆进行测序,通过与已知蛋白质的相似性以及利用生物信息学并由一名管理员手动鉴定开放阅读框(ORF)。大约76kb的测序DNA揭示了23个基因和开放阅读框。通过旨在扩增剪接序列的逆转录聚合酶链反应(RT-PCR)分析验证了预测基因的存在。结果证实这些转录本在30℃和37℃时均有表达。与其他两个变种相比,格特变种MATalpha基因座基因在顺序和方向上存在重排。交配特异性基因显示出更高的非同义突变率,并且基因树显示格特变种菌株处于一个独特的进化枝中。迄今为止,格特变种结构基因数量的鉴定应为未来的分子发病机制研究奠定基础。

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