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FraG对于鱼腥藻Anabaena sp. PCC 7120菌株中的丝状体完整性和异形胞成熟是必需的。

FraG is necessary for filament integrity and heterocyst maturation in the cyanobacterium Anabaena sp. strain PCC 7120.

作者信息

Nayar Asha S, Yamaura Hiroshi, Rajagopalan Ramya, Risser Douglas D, Callahan Sean M

机构信息

Department of Microbiology, University of Hawaii, Honolulu, HI 96822, USA.

出版信息

Microbiology (Reading). 2007 Feb;153(Pt 2):601-607. doi: 10.1099/mic.0.2006/002535-0.

Abstract

Anabaena sp. strain PCC 7120 is a filamentous cyanobacterium that differentiates nitrogen-fixing heterocysts when fixed nitrogen becomes growth limiting in the medium. The gene alr2338 (designated fraG herein), located immediately upstream of the master regulator of differentiation hetR, was identified in a genetic screen for mutants unable to grow diazotrophically. Filaments with a mutation in fraG were unable to fix nitrogen or synthesize heterocyst-specific glycolipids, and they fragmented initially to approximately nine cells in length at 24 h after induction of heterocyst development and eventually became unicellular. The fragmentation phenotype could be duplicated in the presence of fixed nitrogen when differentiation of heterocysts was elicited by overexpression of hetR, suggesting that a defect in differentiation, and not a lack of fixed nitrogen in the medium, was the more direct cause of fragmentation. An intact fraG gene was necessary for differentiation of mature heterocysts, but was not required for proper pattern formation, as indicated by a normal pattern of expression of hetR in a fraG mutant. A transcriptional GFP reporter fusion indicated that the level of expression of fraG was low in vegetative cells in both nitrogen-replete and nitrogen-free media, and was induced in heterocysts. fraG appears to play a role in filament integrity and differentiation of proheterocysts into mature heterocysts.

摘要

鱼腥藻属PCC 7120菌株是一种丝状蓝细菌,当培养基中固定氮成为生长限制因素时,它会分化出固氮异形胞。alr2338基因(本文中命名为fraG)位于分化主调节因子hetR的紧邻上游,是在对无法进行固氮生长的突变体进行遗传筛选时发现的。fraG发生突变的藻丝无法固氮或合成异形胞特异性糖脂,在诱导异形胞发育24小时后,它们最初会断裂成大约九个细胞长,最终变成单细胞。当通过hetR的过表达引发异形胞分化时,在存在固定氮的情况下也会出现断裂表型,这表明分化缺陷而非培养基中缺乏固定氮是断裂的更直接原因。完整的fraG基因对于成熟异形胞的分化是必需的,但对于正确的模式形成不是必需的,如fraG突变体中hetR的正常表达模式所示。转录型绿色荧光蛋白报告基因融合表明,在氮充足和无氮培养基中,营养细胞中fraG的表达水平都很低,而在异形胞中被诱导表达。fraG似乎在藻丝完整性以及前异形胞分化为成熟异形胞的过程中发挥作用。

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