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细菌化学感应途径中信号精度与放大的进化及设计原理

Evolution and Design Governing Signal Precision and Amplification in a Bacterial Chemosensory Pathway.

作者信息

Guzzo Mathilde, Agrebi Rym, Espinosa Leon, Baronian Grégory, Molle Virginie, Mauriello Emilia M F, Brochier-Armanet Céline, Mignot Tâm

机构信息

Laboratoire de Chimie Bactérienne, Institut de Microbiologie de la Méditerranée, CNRS Aix-Marseille University UMR 7283, Marseille, France.

Laboratoire de Dynamique des Interactions Membranaires Normales et Pathologiques, CNRS Universités de Montpellier II et I, UMR 5235, case 107, Montpellier, France.

出版信息

PLoS Genet. 2015 Aug 20;11(8):e1005460. doi: 10.1371/journal.pgen.1005460. eCollection 2015 Aug.

DOI:10.1371/journal.pgen.1005460
PMID:26291327
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4546325/
Abstract

Understanding the principles underlying the plasticity of signal transduction networks is fundamental to decipher the functioning of living cells. In Myxococcus xanthus, a particular chemosensory system (Frz) coordinates the activity of two separate motility systems (the A- and S-motility systems), promoting multicellular development. This unusual structure asks how signal is transduced in a branched signal transduction pathway. Using combined evolution-guided and single cell approaches, we successfully uncoupled the regulations and showed that the A-motility regulation system branched-off an existing signaling system that initially only controlled S-motility. Pathway branching emerged in part following a gene duplication event and changes in the circuit structure increasing the signaling efficiency. In the evolved pathway, the Frz histidine kinase generates a steep biphasic response to increasing external stimulations, which is essential for signal partitioning to the motility systems. We further show that this behavior results from the action of two accessory response regulator proteins that act independently to filter and amplify signals from the upstream kinase. Thus, signal amplification loops may underlie the emergence of new connectivity in signal transduction pathways.

摘要

理解信号转导网络可塑性背后的原理是解读活细胞功能的基础。在黄色粘球菌中,一种特殊的化学感应系统(Frz)协调两个独立运动系统(A运动系统和S运动系统)的活动,促进多细胞发育。这种不同寻常的结构引发了一个问题:信号在分支信号转导途径中是如何转导的。通过结合进化引导和单细胞方法,我们成功地解开了调控机制,并表明A运动调控系统从一个最初仅控制S运动的现有信号系统分支出来。通路分支部分是在基因复制事件和电路结构变化之后出现的,这些变化提高了信号传导效率。在进化后的通路中,Frz组氨酸激酶对不断增加的外部刺激产生陡峭的双相反应,这对于将信号分配到运动系统至关重要。我们进一步表明,这种行为是由两种辅助反应调节蛋白的作用导致的,它们独立作用以过滤和放大来自上游激酶的信号。因此,信号放大环可能是信号转导途径中新连接出现的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/d7544067617d/pgen.1005460.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/a7d48cc2a618/pgen.1005460.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/41bfebcfbaf3/pgen.1005460.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/30027eec879e/pgen.1005460.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/b445e7b5deec/pgen.1005460.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/358486c0096f/pgen.1005460.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/90f5293910d7/pgen.1005460.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/5c9c2030e811/pgen.1005460.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/d7544067617d/pgen.1005460.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/a7d48cc2a618/pgen.1005460.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/41bfebcfbaf3/pgen.1005460.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/30027eec879e/pgen.1005460.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/b445e7b5deec/pgen.1005460.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/358486c0096f/pgen.1005460.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/90f5293910d7/pgen.1005460.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/5c9c2030e811/pgen.1005460.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f4c/4546325/d7544067617d/pgen.1005460.g008.jpg

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