Evidence map›Paper›PMID 23721164›Full record

ArticleMolecular microbiology2013

Transcriptional regulation of fatty acid biosynthesis in mycobacteria.

S Mondino, G Gago, H Gramajo

Open access · greenAbstract read
In one paragraph

Article in Molecular microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 49 citations in OpenAlex.

  1. Genome-wide transcriptional landscape ofFrontiers in immunology · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. MadR mediates acyl CoA-dependent regulation of mycolic acid desaturation in mycobacteria.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. Mycobacterial fatty acid catabolism is repressed by FdmR to sustain lipogenesis and virulence.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Analysis of coenzyme A activated compounds in actinomycetes.Applied microbiology and biotechnology · 2016
    Article
  18. Article
  19. Article
  20. 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 2 institutions in 1 country.

S MondinoMicrobiology Division, IBR-Instituto de Biología Molecular y Celular de Rosario, Universidad Nacional de Rosario, Ocampo y Esmeralda (2000), Rosario, Argentina.
G Gago
H Gramajo
Consejo Nacional de Investigaciones Científicas y Técnicas · ARNational University of Rosario · AR

Funding

Transcriptional regulation of lipid homeostasis in mycobacteriaR01AI095183 · NIAID · INSTITUTE OF MOLECULAR /CELLULAR BIOLOGY · PI GRAMAJO, HUGO · 2011 to 2014
$373k
NIAID NIH HHS 1R01AI095183-01NIAID NIH HHS R01 AI095183
6 · The paper itself

Abstract

The main purpose of our study is to understand how mycobacteria exert control over the biosynthesis of their membrane lipids and find out the key components of the regulatory network that control fatty acid biosynthesis at the transcriptional level. In this article we describe the identification and purification of FasR, a transcriptional regulator from Mycobacterium sp. that controls the expression of the fatty acid synthase (fas) and the 4-phosphopantetheinyl transferase (acpS) encoding genes, whose products are involved in the fatty acid and mycolic acid biosynthesis pathways. In vitro studies demonstrated that fas and acpS genes are part of the same transcriptional unit and that FasR specifically binds to three conserved operator sequences present in the fas-acpS promoter region (Pfas). The construction and further characterization of a fasR conditional mutant confirmed that FasR is a transcriptional activator of the fas-acpS operon and that this protein is essential for mycobacteria viability. Furthermore, the combined used of Pfas-lacZ fusions in different fasR backgrounds and electrophoretic mobility shift assays experiments, strongly suggested that long-chain acyl-CoAs are the effector molecules that modulate the affinity of FasR for its DNA binding sequences and therefore the expression of the essential fas-acpS operon.

Indexed as

Gene Expression Regulation, BacterialBacterial ProteinsBinding SitesFatty AcidsFatty Acid SynthasesGenes, RegulatorLipid MetabolismMycobacterium smegmatisMycobacterium tuberculosisOperonPromoter Regions, GeneticTranscription FactorsTransferases (Other Substituted Phosphate Groups)Bacterial ProteinsFatty AcidsFatty Acid Synthasesphosphopantetheinyl transferaseTranscription FactorsTransferases (Other Substituted Phosphate Groups)

Identifiers

PMID23721164
PMCPMC3752660
OpenAlexW1938282636

What OpenQuestion holds

Textmetadata
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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.