ArticleCellular logistics2011
The compartmentalized vessel: The bacterial cell as a model for subcellular organization (a tale of two studies).
Article in Cellular logistics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
11 citing papers in PubMed, 26 citations in OpenAlex.
- Uncovering the mechanism for polar sequestration of the major bacterial sugar regulator by high-throughput screens and 3D interaction modeling.Cell reports · 2025Article
- Functional diversity and molecular interactions of small membrane proteins in bacteria.microLife · 2025Review
- Review
- Wisdom of the crowds: A suggested polygenic plan for small-RNA-mediated regulation in bacteria.iScience · 2021Article
- Tyrosine phosphorylation-dependent localization of TmaR that controls activity of a major bacterial sugar regulator by polar sequestration.Proceedings of the National Academy of Sciences of the United States of America · 2021Article
- Phenotypic Heterogeneity in Sugar Utilization byFrontiers in microbiology · 2017Article
- Illuminating Messengers: An Update and Outlook on RNA Visualization in Bacteria.Frontiers in microbiology · 2017Review
- Microenvironments created by liquid-liquid phase transition control the dynamic distribution of bacterial division FtsZ protein.Scientific reports · 2016Article
- Multiple chaperonins in bacteria--novel functions and non-canonical behaviors.Cell stress & chaperones · 2015Review
- RNA-Seq analysis of the multipartite genome of Rhizobium etli CE3 shows different replicon contributions under heat and saline shock.BMC genomics · 2014Article
- RNA localization in bacteria.RNA biology · 2014Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
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.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.