Literature DB >> 21686257

The compartmentalized vessel: The bacterial cell as a model for subcellular organization (a tale of two studies).

Orna Amster-Choder1.   

Abstract

The traditional view of bacterial cells as non-compartmentalized, which is based on the lack of membrane-engulfed organelles, is currently being reassessed. Many studies in recent years led to the realization that bacteria have an intricate internal organization that is vital for various cellular processes. Specifically, various machineries were shown to localize to the poles of rod-shaped bacteria. We have recently shown that the control center of the PTS system, which governs carbon uptake and metabolism, localizes to the poles of E. coli cells. Notably, the machinery that controls bacterial taxis along chemical gradients (chemotaxis) has a similar localization pattern. The fact that the two systems need to communicate in order to generate an optimal metabolic response suggests that their similar spatial organization is not a coincidence. Rather, due to their special characteristics, the poles may function as hubs for signaling systems to allow for efficient crosstalk between different pathways in order to improve coordination of their actions.The regulatory mechanisms that underlie the spatial and temporal organization of microbial cells are largely unknown. Thus far, these mechanisms were believed to rely on embedded features of the localized proteins. In another study, we have recently shown that mRNAs are capable of migrating to particular domains in the bacterial cell where their protein products are required. In contrast to the view that transcription and translation are coupled in bacteria, localization of bacterial transcripts may occur in a translation-independent manner. Hence, it seems that the mechanistic basis for separating transcription and translation is more primitive than assumed up until now. We propose that bacteria synthesize proteins either by a transcription-translation coupled mechanism or by transporting mRNAs away from the transcription apparatus. Obviously, eukaryotic cells rely on the latter mechanism. Hence, the capacity of prokaryotic cells to adopt the division between transcription and translation was a crucial step in the evolution of nucleus-containing cells from the prokaryotic origin. Summarily, the line that separates cells with nucleus and cells without is fading, leading to the realization that bacteria are suitable model organisms for studying universal mechanisms that underlie spatial regulation of cellular processes.

Entities:  

Year:  2011        PMID: 21686257      PMCID: PMC3116588          DOI: 10.4161/cl.1.2.16152

Source DB:  PubMed          Journal:  Cell Logist        ISSN: 2159-2780


  31 in total

Review 1.  Protein subcellular localization in bacteria.

Authors:  David Z Rudner; Richard Losick
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-03-03       Impact factor: 10.005

Review 2.  The bacterial cytoskeleton.

Authors:  Matthew T Cabeen; Christine Jacobs-Wagner
Journal:  Annu Rev Genet       Date:  2010       Impact factor: 16.830

Review 3.  Signal transduction in bacterial chemotaxis.

Authors:  Melinda D Baker; Peter M Wolanin; Jeffry B Stock
Journal:  Bioessays       Date:  2006-01       Impact factor: 4.345

Review 4.  Exploration into the spatial and temporal mechanisms of bacterial polarity.

Authors:  Gitte Ebersbach; Christine Jacobs-Wagner
Journal:  Trends Microbiol       Date:  2007-02-01       Impact factor: 17.079

Review 5.  Why cells move messages: the biological functions of mRNA localization.

Authors:  Tung-Gia Du; Maria Schmid; Ralf-Peter Jansen
Journal:  Semin Cell Dev Biol       Date:  2007-02-06       Impact factor: 7.727

Review 6.  Bacterial chromosome organization and segregation.

Authors:  Esteban Toro; Lucy Shapiro
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-02       Impact factor: 10.005

7.  Translation-independent localization of mRNA in E. coli.

Authors:  Keren Nevo-Dinur; Anat Nussbaum-Shochat; Sigal Ben-Yehuda; Orna Amster-Choder
Journal:  Science       Date:  2011-02-25       Impact factor: 47.728

Review 8.  Why and how bacteria localize proteins.

Authors:  L Shapiro; H H McAdams; R Losick
Journal:  Science       Date:  2009-11-27       Impact factor: 47.728

9.  The BglF sensor recruits the BglG transcription regulator to the membrane and releases it on stimulation.

Authors:  Livnat Lopian; Anat Nussbaum-Shochat; Kathryn O'Day-Kerstein; Andrew Wright; Orna Amster-Choder
Journal:  Proc Natl Acad Sci U S A       Date:  2003-05-27       Impact factor: 11.205

Review 10.  How does an mRNA find its way? Intracellular localisation of transcripts.

Authors:  Isabel M Palacios
Journal:  Semin Cell Dev Biol       Date:  2007-01-26       Impact factor: 7.727

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  8 in total

Review 1.  RNA localization in bacteria.

Authors:  Avi-ad Avraam Buskila; Shanmugapriya Kannaiah; Orna Amster-Choder
Journal:  RNA Biol       Date:  2014-10-31       Impact factor: 4.652

2.  Tyrosine phosphorylation-dependent localization of TmaR that controls activity of a major bacterial sugar regulator by polar sequestration.

Authors:  Tamar Szoke; Nitsan Albocher; Sutharsan Govindarajan; Anat Nussbaum-Shochat; Orna Amster-Choder
Journal:  Proc Natl Acad Sci U S A       Date:  2021-01-12       Impact factor: 11.205

Review 3.  Multiple chaperonins in bacteria--novel functions and non-canonical behaviors.

Authors:  C M Santosh Kumar; Shekhar C Mande; Gaurang Mahajan
Journal:  Cell Stress Chaperones       Date:  2015-05-20       Impact factor: 3.667

4.  Microenvironments created by liquid-liquid phase transition control the dynamic distribution of bacterial division FtsZ protein.

Authors:  Begoña Monterroso; Silvia Zorrilla; Marta Sobrinos-Sanguino; Christine D Keating; Germán Rivas
Journal:  Sci Rep       Date:  2016-10-11       Impact factor: 4.379

Review 5.  Illuminating Messengers: An Update and Outlook on RNA Visualization in Bacteria.

Authors:  Lieke A van Gijtenbeek; Jan Kok
Journal:  Front Microbiol       Date:  2017-06-22       Impact factor: 5.640

Review 6.  Getting Closer to Decrypting the Phase Transitions of Bacterial Biomolecules.

Authors:  Katarzyna Sołtys; Aneta Tarczewska; Dominika Bystranowska; Nikola Sozańska
Journal:  Biomolecules       Date:  2022-06-28

7.  RNA-Seq analysis of the multipartite genome of Rhizobium etli CE3 shows different replicon contributions under heat and saline shock.

Authors:  Gamaliel López-Leal; Maria Luisa Tabche; Santiago Castillo-Ramírez; Alfredo Mendoza-Vargas; Miguel A Ramírez-Romero; Guillermo Dávila
Journal:  BMC Genomics       Date:  2014-09-08       Impact factor: 3.969

8.  Phenotypic Heterogeneity in Sugar Utilization by E. coli Is Generated by Stochastic Dispersal of the General PTS Protein EI from Polar Clusters.

Authors:  Sutharsan Govindarajan; Nitsan Albocher; Tamar Szoke; Anat Nussbaum-Shochat; Orna Amster-Choder
Journal:  Front Microbiol       Date:  2018-01-17       Impact factor: 5.640

  8 in total

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