Literature DB >> 15978082

A chaperone-like HrpG protein acts as a suppressor of HrpV in regulation of the Pseudomonas syringae pv. syringae type III secretion system.

Chia-Fong Wei1, Wen-Ling Deng, Hsiou-Chen Huang.   

Abstract

The cloned hrp/hrc cluster of Pseudomonas syringae pv. syringae 61 (Pss61) contains 28 proteins, and many of those are assembled into a type III secretion system (TTSS) that is responsible for eliciting the hypersensitive response (HR) in non-host plants and causing diseases on host plants (Huang et al., 1995). hrpG, the second gene in the hrpC operon, encodes a 15.4 kDa cytoplasmic protein whose predicted structure is similar to SicP (E-value: 0.19), a TTSS chaperone of Salmonella typhimurium. Two non-polar hrpG mutants, Pss61-N826 and Pss61-N674, were produced to investigate the biological function of hrpG gene. Pss61-N826, generated by replacing the coding sequence of hrpG with an nptII gene lacking both the promoter and the terminator, was found to be capable of eliciting the wild-type HR; whereas Pss61-N674 generated by replacement of a terminatorless nptII gene in the hrpG coding sequence showed the delayed HR phenotype. Northern and Western blotting analyses showed that the expression of hrpZ, hrcJ and hrcQb genes residing on two different operons in Pss61-N674 was reduced due to the nptII promoter-driven constitutive expression of hrpV that codes for a negative regulator. Interestingly, a plasmid-borne hrpG can derepress the hrp expression in Pss61-N674 and in Pss61 overexpressing HrpV without decreasing the hrpV transcript. Moreover, results of yeast two-hybrid assay, pull-down assay and far Western analysis show that HrpG and HrpV interact with each other in vivo and in vitro. Additionally, HrpV interacts with a positive regulator HrpS according to analysis of a yeast two-hybrid system. Based on the results presented in this study, we propose that HrpG acts as a suppressor of the negative regulator HrpV mediated via protein-protein interaction, leading to modulation of hrp/hrc expression subsequently freeing HrpS to promote the activation of other downstream hrp/hrc genes.

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Year:  2005        PMID: 15978082     DOI: 10.1111/j.1365-2958.2005.04704.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  19 in total

Review 1.  Protein export according to schedule: architecture, assembly, and regulation of type III secretion systems from plant- and animal-pathogenic bacteria.

Authors:  Daniela Büttner
Journal:  Microbiol Mol Biol Rev       Date:  2012-06       Impact factor: 11.056

2.  The pathogenicity factor HrpF interacts with HrpA and HrpG to modulate type III secretion system (T3SS) function and t3ss expression in Pseudomonas syringae pv. averrhoi.

Authors:  Yi-Chiao Huang; Yuan-Chuen Lin; Chia-Fong Wei; Wen-Ling Deng; Hsiou-Chen Huang
Journal:  Mol Plant Pathol       Date:  2016-04-03       Impact factor: 5.663

3.  Alternative sigma factor RpoN and its modulation protein YhbH are indispensable for Erwinia amylovora virulence.

Authors:  Veronica Ancona; Wenting Li; Youfu Zhao
Journal:  Mol Plant Pathol       Date:  2013-08-13       Impact factor: 5.663

4.  Identification of Pseudomonas syringae pv. syringae 61 type III secretion system Hrp proteins that can travel the type III pathway and contribute to the translocation of effector proteins into plant cells.

Authors:  Adela R Ramos; Joanne E Morello; Sandeep Ravindran; Wen-Ling Deng; Hsiou-Chen Huang; Alan Collmer
Journal:  J Bacteriol       Date:  2007-05-25       Impact factor: 3.490

5.  Integration of multiple stimuli-sensing systems to regulate HrpS and type III secretion system in Erwinia amylovora.

Authors:  Jae Hoon Lee; Youfu Zhao
Journal:  Mol Genet Genomics       Date:  2017-09-30       Impact factor: 3.291

6.  Pseudomonas syringae senses polyphenols via phosphorelay crosstalk to inhibit virulence.

Authors:  Yingpeng Xie; Yiqing Ding; Xiaolong Shao; Chunyan Yao; Jingwei Li; Jingui Liu; Xin Deng
Journal:  EMBO Rep       Date:  2021-09-28       Impact factor: 8.807

7.  Regulation of the co-evolved HrpR and HrpS AAA+ proteins required for Pseudomonas syringae pathogenicity.

Authors:  Milija Jovanovic; Ellen H James; Patricia C Burrows; Fabiane G M Rego; Martin Buck; Jörg Schumacher
Journal:  Nat Commun       Date:  2011-02-01       Impact factor: 14.919

Review 8.  Type III chaperones & Co in bacterial plant pathogens: a set of specialized bodyguards mediating effector delivery.

Authors:  David Lohou; Fabien Lonjon; Stéphane Genin; Fabienne Vailleau
Journal:  Front Plant Sci       Date:  2013-11-22       Impact factor: 5.753

9.  Plant innate immunity induced by flagellin suppresses the hypersensitive response in non-host plants elicited by Pseudomonas syringae pv. averrhoi.

Authors:  Chia-Fong Wei; Shih-Tien Hsu; Wen-Ling Deng; Yu-Der Wen; Hsiou-Chen Huang
Journal:  PLoS One       Date:  2012-07-23       Impact factor: 3.240

10.  Interplay among Pseudomonas syringae HrpR, HrpS and HrpV proteins for regulation of the type III secretion system.

Authors:  Milija Jovanovic; Edward Lawton; Jörg Schumacher; Martin Buck
Journal:  FEMS Microbiol Lett       Date:  2014-06-19       Impact factor: 2.742

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