Zhang Cheng-Cai, Laurent Sophie, Sakr Samer, Peng Ling, Bédu Sylvie
Laboratoire de Chimie Bactérienne, UPR9043-CNRS, Institut de Biologie Structurale et Microbiologie, 31, chemin Joseph Aiguier, 13402 Marseille cedex 20, France.
Mol Microbiol. 2006 Jan;59(2):367-75. doi: 10.1111/j.1365-2958.2005.04979.x.
Heterocyst differentiation in filamentous cyanobacteria provides an excellent prokaryotic model for studying multicellular behaviour and pattern formation. In Anabaena sp. strain PCC 7120, for example, 5-10% of the cells along each filament are induced, when deprived of combined nitrogen, to differentiate into heterocysts. Heterocysts are specialized in the fixation of N(2) under oxic conditions and are semi-regularly spaced among vegetative cells. This developmental programme leads to spatial separation of oxygen-sensitive nitrogen fixation (by heterocysts) and oxygen-producing photosynthesis (by vegetative cells). The interdependence between these two cell types ensures filament growth under conditions of combined-nitrogen limitation. Multiple signals have recently been identified as necessary for the initiation of heterocyst differentiation, the formation of the heterocyst pattern and pattern maintenance. The Krebs cycle metabolite 2-oxoglutarate (2-OG) serves as a signal of nitrogen deprivation. Accumulation of a non-metabolizable analogue of 2-OG triggers the complex developmental process of heterocyst differentiation. Once heterocyst development has been initiated, interactions among the various components involved in heterocyst differentiation determine the developmental fate of each cell. The free calcium concentration is crucial to heterocyst differentiation. Lateral diffusion of the PatS peptide or a derivative of it from a developing cell may inhibit the differentiation of neighbouring cells. HetR, a protease showing DNA-binding activity, is crucial to heterocyst differentiation and appears to be the central processor of various early signals involved in the developmental process. How the various signalling pathways are integrated and used to control heterocyst differentiation processes is a challenging question that still remains to be elucidated.
丝状蓝细菌中的异形胞分化为研究多细胞行为和模式形成提供了一个出色的原核模型。例如,在鱼腥藻PCC 7120菌株中,当缺乏化合态氮时,每根藻丝上5%-10%的细胞会被诱导分化为异形胞。异形胞专门在有氧条件下固定N₂,并在营养细胞之间呈半规则间隔排列。这种发育程序导致了对氧敏感的固氮作用(由异形胞进行)和产生氧气的光合作用(由营养细胞进行)在空间上的分离。这两种细胞类型之间的相互依存关系确保了在化合态氮限制条件下藻丝的生长。最近已确定多种信号对于异形胞分化的起始、异形胞模式的形成和模式维持是必需的。三羧酸循环代谢物2-氧代戊二酸(2-OG)作为氮缺乏的信号。2-OG的一种不可代谢类似物的积累触发了异形胞分化这一复杂的发育过程。一旦异形胞发育开始,参与异形胞分化的各种组分之间的相互作用就决定了每个细胞的发育命运。游离钙浓度对异形胞分化至关重要。PatS肽或其衍生物从正在发育的细胞侧向扩散可能会抑制相邻细胞的分化。HetR是一种具有DNA结合活性的蛋白酶,对异形胞分化至关重要,似乎是发育过程中各种早期信号的中央处理器。各种信号通路如何整合并用于控制异形胞分化过程是一个仍有待阐明的具有挑战性的问题。