Literature DB >> 27543838

Protease regulation and capacity during Caulobacter growth.

Robert H Vass1, Rilee D Zeinert1, Peter Chien2.   

Abstract

Cell growth requires the removal of proteins that are unwanted or toxic. In bacteria, AAA+ proteases like the Clp family and Lon selectively destroy proteins defined by intrinsic specificity or adaptors. Caulobacter crescentus is a gram-negative bacterium that undergoes an obligate developmental transition every cell division cycle. Here we highlight recent work that reveals how a hierarchy of adaptors targets the degradation of key proteins at specific times during this cell cycle, integrating protein destruction with other cues. We describe recent insight into how Caulobacter manages DNA replication and repair through Lon and Clp proteases. Because proteases must manage a broad substrate repertoire there must be methods to compensate for protease saturation and we discuss these scenarios.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27543838      PMCID: PMC5164839          DOI: 10.1016/j.mib.2016.07.017

Source DB:  PubMed          Journal:  Curr Opin Microbiol        ISSN: 1369-5274            Impact factor:   7.934


  49 in total

1.  PHOTOREVERSIBILITY OF INDUCED MUTATIONS IN A NONPHOTOREACTIVABLE STRAIN OF ESCHERICHIA COLI.

Authors:  E M WITKIN; N A SICURELLA; G M BENNETT
Journal:  Proc Natl Acad Sci U S A       Date:  1963-12       Impact factor: 11.205

2.  A dynamically localized protease complex and a polar specificity factor control a cell cycle master regulator.

Authors:  Patrick T McGrath; Antonio A Iniesta; Kathleen R Ryan; Lucy Shapiro; Harley H McAdams
Journal:  Cell       Date:  2006-02-10       Impact factor: 41.582

3.  Versatile modes of peptide recognition by the ClpX N domain mediate alternative adaptor-binding specificities in different bacterial species.

Authors:  Tahmeena Chowdhury; Peter Chien; Shamsah Ebrahim; Robert T Sauer; Tania A Baker
Journal:  Protein Sci       Date:  2010-02       Impact factor: 6.725

Review 4.  AAA+ proteases: ATP-fueled machines of protein destruction.

Authors:  Robert T Sauer; Tania A Baker
Journal:  Annu Rev Biochem       Date:  2011       Impact factor: 23.643

5.  A cell-type-specific protein-protein interaction modulates transcriptional activity of a master regulator in Caulobacter crescentus.

Authors:  Kasia G Gora; Christos G Tsokos; Y Erin Chen; Balaji S Srinivasan; Barrett S Perchuk; Michael T Laub
Journal:  Mol Cell       Date:  2010-07-01       Impact factor: 17.970

6.  A phospho-signaling pathway controls the localization and activity of a protease complex critical for bacterial cell cycle progression.

Authors:  Antonio A Iniesta; Patrick T McGrath; Ann Reisenauer; Harley H McAdams; Lucy Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  2006-07-07       Impact factor: 11.205

7.  A Quality-Control Mechanism Removes Unfit Cells from a Population of Sporulating Bacteria.

Authors:  Irene S Tan; Cordelia A Weiss; David L Popham; Kumaran S Ramamurthi
Journal:  Dev Cell       Date:  2015-09-17       Impact factor: 12.270

8.  Proteotoxic stress induces a cell-cycle arrest by stimulating Lon to degrade the replication initiator DnaA.

Authors:  Kristina Jonas; Jing Liu; Peter Chien; Michael T Laub
Journal:  Cell       Date:  2013-08-01       Impact factor: 41.582

9.  Identification of ClpP substrates in Caulobacter crescentus reveals a role for regulated proteolysis in bacterial development.

Authors:  Nowsheen H Bhat; Robert H Vass; Patrick R Stoddard; Dong K Shin; Peter Chien
Journal:  Mol Microbiol       Date:  2013-05-07       Impact factor: 3.501

10.  The DNA polymerase III holoenzyme contains γ and is not a trimeric polymerase.

Authors:  Paul R Dohrmann; Raul Correa; Ryan L Frisch; Susan M Rosenberg; Charles S McHenry
Journal:  Nucleic Acids Res       Date:  2016-01-18       Impact factor: 16.971

View more
  8 in total

1.  Regulation of Bacterial Cell Cycle Progression by Redundant Phosphatases.

Authors:  Jérôme Coppine; Andreas Kaczmarczyk; Kenny Petit; Thomas Brochier; Urs Jenal; Régis Hallez
Journal:  J Bacteriol       Date:  2020-08-10       Impact factor: 3.490

Review 2.  Hit the right spots: cell cycle control by phosphorylated guanosines in alphaproteobacteria.

Authors:  Régis Hallez; Marie Delaby; Stefano Sanselicio; Patrick H Viollier
Journal:  Nat Rev Microbiol       Date:  2017-01-31       Impact factor: 60.633

3.  Rv0004 is a new essential member of the mycobacterial DNA replication machinery.

Authors:  Katherine M Mann; Deborah L Huang; Anna J Hooppaw; Michelle M Logsdon; Kirill Richardson; Hark Joon Lee; Jacqueline M Kimmey; Bree B Aldridge; Christina L Stallings
Journal:  PLoS Genet       Date:  2017-11-27       Impact factor: 5.917

4.  The Essential Role of ClpXP in Caulobacter crescentus Requires Species Constrained Substrate Specificity.

Authors:  Robert H Vass; Jacob Nascembeni; Peter Chien
Journal:  Front Mol Biosci       Date:  2017-05-09

5.  Environmental Conditions Modulate the Transcriptomic Response of Both Caulobacter crescentus Morphotypes to Cu Stress.

Authors:  Laurens Maertens; Pauline Cherry; Françoise Tilquin; Rob Van Houdt; Jean-Yves Matroule
Journal:  Microorganisms       Date:  2021-05-21

6.  Iron-regulated small RNA expression as Neisseria gonorrhoeae FA 1090 transitions into stationary phase growth.

Authors:  Lydgia A Jackson; Michael Day; Jennie Allen; Edgar Scott; David W Dyer
Journal:  BMC Genomics       Date:  2017-04-21       Impact factor: 3.969

7.  Proteolysis of histidine kinase VgrS inhibits its autophosphorylation and promotes osmostress resistance in Xanthomonas campestris.

Authors:  Chao-Ying Deng; Huan Zhang; Yao Wu; Li-Li Ding; Yue Pan; Shu-Tao Sun; Ya-Jun Li; Li Wang; Wei Qian
Journal:  Nat Commun       Date:  2018-11-15       Impact factor: 14.919

8.  Feedback Control of a Two-Component Signaling System by an Fe-S-Binding Receiver Domain.

Authors:  Benjamin J Stein; Aretha Fiebig; Sean Crosson
Journal:  mBio       Date:  2020-03-17       Impact factor: 7.867

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.