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C信号:一种与细胞表面相关的形态发生素,可诱导并协调黄色粘球菌中多细胞子实体的形态发生和孢子形成。

C-signal: a cell surface-associated morphogen that induces and co-ordinates multicellular fruiting body morphogenesis and sporulation in Myxococcus xanthus.

作者信息

Kruse T, Lobedanz S, Berthelsen N M, Søgaard-Andersen L

机构信息

Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Campusvej 55, 5230 Odense M, Denmark.

出版信息

Mol Microbiol. 2001 Apr;40(1):156-68. doi: 10.1046/j.1365-2958.2001.02365.x.

Abstract

In Myxococcus xanthus, morphogenesis of multicellular fruiting bodies and sporulation are co-ordinated temporally and spatially. csgA mutants fail to synthesize the cell surface-associated C-signal and are unable to aggregate and sporulate. We report that csgA encodes two proteins, a 25 kDa species corresponding to full-length CsgA protein and a 17 kDa species similar in size to C-factor protein, which has been shown previously to have C-signal activity. By systematically varying the accumulation of the csgA proteins, we show that overproduction of the csgA proteins results in premature aggregation and sporulation, uncoupling of the two events and the formation of small fruiting bodies, whereas reduced synthesis of the csgA proteins causes delayed aggregation, reduced sporulation and the formation of large fruiting bodies. These results show that C-signal induces aggregation as well as sporulation, and that an ordered increase in the level of C-signalling during development is essential for the spatial co-ordination of these events. The results support a quantitative model, in which aggregation and sporulation are induced at distinct threshold levels of C-signalling. In this model, the two events are temporally co-ordinated by the regulated increase in C-signalling levels during development. The contact-dependent C-signal transmission mechanism allows the spatial co-ordination of aggregation and sporulation by coupling cell position and signalling levels.

摘要

在黄色黏球菌中,多细胞子实体的形态发生和孢子形成在时间和空间上是协调的。csgA突变体无法合成与细胞表面相关的C信号,并且不能聚集和形成孢子。我们报告称,csgA编码两种蛋白质,一种是对应全长CsgA蛋白的25 kDa蛋白,另一种是大小与C因子蛋白相似的17 kDa蛋白,先前已证明C因子蛋白具有C信号活性。通过系统地改变csgA蛋白的积累量,我们发现csgA蛋白的过量产生会导致过早聚集和孢子形成,这两个事件解偶联并形成小的子实体,而csgA蛋白合成减少则会导致聚集延迟、孢子形成减少以及形成大的子实体。这些结果表明,C信号既诱导聚集也诱导孢子形成,并且在发育过程中C信号水平的有序增加对于这些事件的空间协调至关重要。这些结果支持一种定量模型,其中聚集和孢子形成是在不同的C信号阈值水平下诱导的。在这个模型中,这两个事件在发育过程中通过C信号水平的调节增加而在时间上协调。接触依赖性C信号传递机制通过耦合细胞位置和信号水平实现聚集和孢子形成的空间协调。

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