Evidence map›Paper›PMID 42344150›Full record

ArticleFrontiers in molecular biosciences2026

Transcriptional regulatory network analysis identifies conserved cis-antisense ncRNAs in the vancomycin and ceftriaxone stress response of

Javiera Pino-Gaete, Jorge Torres, Maximiliano Véliz-González, Jaime Ortega, Gladis Serrano, Gabriel Gálvez, Alex Di Genova, Álvaro Glavic, Diana Panesso-Botero, Raúl Mera-Adasme and 3 more

Abstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Javiera Pino-Gaete *Laboratorio de Bioingeniería; Instituto de Ciencias de La Ingeniería; Universidad de O'Higgins, Rancagua, Chile.
Jorge Torres *Laboratorio de Bioingeniería; Instituto de Ciencias de La Ingeniería; Universidad de O'Higgins, Rancagua, Chile.
Maximiliano Véliz-GonzálezLaboratorio de Genética Del Desarrollo, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Jaime OrtegaLaboratorio de Bioingeniería; Instituto de Ciencias de La Ingeniería; Universidad de O'Higgins, Rancagua, Chile.
Gladis SerranoLaboratorio de Bioingeniería; Instituto de Ciencias de La Ingeniería; Universidad de O'Higgins, Rancagua, Chile.
Gabriel GálvezLaboratorio de Bioingeniería; Instituto de Ciencias de La Ingeniería; Universidad de O'Higgins, Rancagua, Chile.
Alex Di GenovaCentro de Biología de Sistemas para el Estudio de Comunidades Extremófilas de Relaves Mineros (SYSTEMIX), Universidad de O'Higgins, Rancagua, Chile.
Álvaro GlavicLaboratorio de Genética Del Desarrollo, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Diana Panesso-BoteroDivision of Infectious Diseases, Department of Medicine, Houston Methodist Hospital, Houston, TX, United States.
Raúl Mera-AdasmeDepartamento de Química, Facultad de Ciencias, Universidad de Tarapacá, Arica, Chile.
Valentina ParraCentro de Biología de Sistemas para el Estudio de Comunidades Extremófilas de Relaves Mineros (SYSTEMIX), Universidad de O'Higgins, Rancagua, Chile.
Víctor Aliaga-TobarCentro de Biología de Sistemas para el Estudio de Comunidades Extremófilas de Relaves Mineros (SYSTEMIX), Universidad de O'Higgins, Rancagua, Chile.
Mauricio LatorreLaboratorio de Bioingeniería; Instituto de Ciencias de La Ingeniería; Universidad de O'Higgins, Rancagua, Chile.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Methods: Here, we analyzed RNA-seq profiles of Results: Both antibiotics activated a substantial shared response dominated by envelope remodeling/proteostasis and bioenergetic-nucleotide economy, while vancomycin recruited a broader condition-specific program. Despite differing scale (Van-TRN: 533 nodes/587 edges; Cef-TRN: 375 nodes/431 edges), both networks displayed sparse, hub-centered hierarchies and strong nesting, with ∼90% of ceftriaxone regulation contained within the vancomycin scaffold. From the shared ncRNA layer, we prioritized two inducible Conclusion: Together, these results provide an integrated TRN framework that connects network rewiring to conserved ncRNA-centered candidate control during vancomycin and ceftriaxone stress responses, prioritizing testable ncRNA regulons for downstream functional validation.

Indexed as

antibiotic stress responseceftriaxoneEnterococcus faecalisnon-coding RNAtranscriptional regulatory networkvancomycin

Identifiers

PMID42344150
PMCPMC13286765

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Registered trials

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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.