Krista G Freeman, Michael J Lauer, Danny Jiang, Jennifer Roscher, Sterling Sandler, Nicholas Mercado, Robert Fryberger, Julia Kovalski, Abigail R Lutz, Lee E Hughes, Andrew P VanDemark, Graham F Hatfull
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引用次数: 0
摘要
分枝杆菌噬菌体 Adephagia 是一种 K 群噬菌体,可感染烟曲霉分枝杆菌和一些分枝杆菌病原体菌株。Adephagia 具有虹吸病毒病毒形态,性情温和。其基因组长 59,646 bp,编码一个 tRNA 基因和 94 个预测的蛋白质编码基因;大多数与病毒结构和组装无关的基因功能不明确。在这里,我们确定了阿德法吉亚基因在裂解和溶解性生长过程中的表达模式,并利用结构预测确定了其他基因的功能。我们对 66 个非结构基因在 M. smegmatis 中表达时的毒性表型进行了鉴定,结果表明其中 25 个基因(38%)具有毒性或强烈抑制生长,导致存活率降低或菌落体积变小。我们预测其中一些基因参与了 DNA 代谢或调控,但其他基因的功能尚不清楚。我们还描述了阿德菲格编码的类似 HicAB 的毒素-抗毒素系统(分别为 gp91 和 gp90)的特征,结果表明 gp90 抗毒素具有溶解性表达,可减弱 gp91 的毒性,并且是正常溶解和溶解性生长所必需的。
Characterization of mycobacteriophage Adephagia cytotoxic proteins.
Mycobacterium phage Adephagia is a cluster K phage that infects Mycobacterium smegmatis and some strains of Mycobacterium pathogens. Adephagia has a siphoviral virion morphology and is temperate. Its genome is 59,646 bp long and codes for one tRNA gene and 94 predicted protein-coding genes; most genes not associated with virion structure and assembly are functionally ill-defined. Here, we determined the Adephagia gene expression patterns in lytic and lysogenic growth and used structural predictions to assign additional gene functions. We characterized 66 nonstructural genes for their toxic phenotypes when expressed in M. smegmatis, and we show that 25 of these (38%) are either toxic or strongly inhibit growth, resulting in either reduced viability or small colony sizes. Some of these genes are predicted to be involved in DNA metabolism or regulation, but others are of unknown function. We also characterize the HicAB-like toxin-antitoxin (TA) system encoded by Adephagia (gp91 and gp90, respectively) and show that the gp90 antitoxin is lysogenically expressed, abrogates gp91 toxicity, and is required for normal lytic and lysogenic growth.
期刊介绍:
G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights.
G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.