Evidence map›Paper›PMID 29446505›Full record

ArticleMolecular microbiology2018

ClpC and MecA, components of a proteolytic machine, prevent Spo0A-P-dependent transcription without degradation.

Andrew W Tanner, Valerie J Carabetta, David Dubnau

Open access · bronzeAbstract read
In one paragraph

Article in Molecular microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. MecA inmSphere · 2024
    Article
  4. Article
  5. Article
  6. Deficiency of MecA inFrontiers in microbiology · 2018
    Article
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

3 authors at 1 institution in 1 country.

Andrew W TannerPublic Health Research Institute Center, New Jersey Medical School Rutgers University, Newark, NJ 07103, USA.ORCID 0000-0001-6412-7201
Valerie J CarabettaPublic Health Research Institute Center, New Jersey Medical School Rutgers University, Newark, NJ 07103, USA.
David DubnauPublic Health Research Institute Center, New Jersey Medical School Rutgers University, Newark, NJ 07103, USA.ORCID 0000-0001-9713-6120
Rutgers, The State University of New Jersey · US

Funding

Understanding the mechanism of genetic transformationR01GM057720 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI DAVID A DUBNAU, Matthew B Neiditch · 1998 to 2026
$15.4M
NIGMS NIH HHS R01 GM057720
6 · The paper itself

Abstract

In Bacillus subtilis, a proteolytic machine composed of MecA, ClpC and ClpP degrades the transcription factor ComK, controlling its accumulation during growth. MecA also inhibits sporulation and biofilm formation by down-regulating spoIIG and sinI, genes that are dependent for their transcription on the phosphorylated protein Spo0A-P. Additionally, MecA has been shown to interact in vitro with Spo0A. Although the inhibitory effect on transcription requires MecA's binding partner ClpC, inhibition is not accompanied by the degradation of Spo0A, pointing to a previously unsuspected regulatory mechanism involving these proteins. Here, we further investigate the MecA and ClpC effects on Spo0A-P-dependent transcription. We show that MecA inhibits the transcription of several Spo0A-P activated genes, but fails to de-repress several Spo0A-P repressed promoters. This demonstrates that MecA and ClpC do not act by preventing the binding of Spo0A-P to its target promoters. Consistent with this, MecA by itself has no effect in vitro on the transcription from PspoIIG while the addition of both MecA and ClpC has a strong inhibitory effect. A complex of MecA and ClpC likely binds to Spo0A-P on its target promoters, preventing the activation of transcription. Thus, components of a degradative machine have been harnessed to directly repress transcription.

Indexed as

Gene Expression Regulation, BacterialBacillus subtilisBacterial ProteinsHeat-Shock ProteinsPromoter Regions, GeneticProteolysisTranscription FactorsTranscription, GeneticBacterial ProteinsClpC protein, BacteriaHeat-Shock ProteinsmecA protein, Bacillus subtilisSpo0A protein, Bacillus subtilisTranscription Factors

Identifiers

PMID29446505
PMCPMC5897911
OpenAlexW2922227759

What OpenQuestion holds

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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.