Evidence map›Paper›PMID 22092065›Full record

ReviewFEMS microbiology reviews2012

A growing family: the expanding universe of the bacterial cytoskeleton.

Michael Ingerson-Mahar, Zemer Gitai

Open access · bronzeAbstract readReview
In one paragraph

Review in FEMS microbiology reviews, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
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  10. Morphology ofPrzeglad gastroenterologiczny · 2018
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Michael Ingerson-MaharDepartment of Molecular Biology, Princeton University, Princeton, NJ, USA.
Zemer Gitai
Princeton University · US

Funding

Discovering Antibiotic Drugs & Targets via High-Throughput Bacterial Cell BiologyDP2OD004389 · OD · PRINCETON UNIVERSITY · PI GITAI, ZEMER · 2008 to 2008
$2.4M
Caulobacter cell shape and cytoskeletal regulationR01GM107384 · NIGMS · PRINCETON UNIVERSITY · PI GITAI, ZEMER · 2013 to 2016
$1.5M
NIGMS NIH HHS R01 GM107384NIH HHS DP2 OD004389
6 · The paper itself

Abstract

Cytoskeletal proteins are important mediators of cellular organization in both eukaryotes and bacteria. In the past, cytoskeletal studies have largely focused on three major cytoskeletal families, namely the eukaryotic actin, tubulin, and intermediate filament (IF) proteins and their bacterial homologs MreB, FtsZ, and crescentin. However, mounting evidence suggests that these proteins represent only the tip of the iceberg, as the cellular cytoskeletal network is far more complex. In bacteria, each of MreB, FtsZ, and crescentin represents only one member of large families of diverse homologs. There are also newly identified bacterial cytoskeletal proteins with no eukaryotic homologs, such as WACA proteins and bactofilins. Furthermore, there are universally conserved proteins, such as the metabolic enzyme CtpS, that assemble into filamentous structures that can be repurposed for structural cytoskeletal functions. Recent studies have also identified an increasing number of eukaryotic cytoskeletal proteins that are unrelated to actin, tubulin, and IFs, such that expanding our understanding of cytoskeletal proteins is advancing the understanding of the cell biology of all organisms. Here, we summarize the recent explosion in the identification of new members of the bacterial cytoskeleton and describe a hypothesis for the evolution of the cytoskeleton from self-assembling enzymes.

Indexed as

Protein MultimerizationBacteriaBacterial ProteinsCytoskeletal ProteinsCytoskeletonBacterial ProteinsCytoskeletal Proteins

Identifiers

PMID22092065
PMCPMC4114309
OpenAlexW2053125816

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.