Evidence map›Paper›PMID 40791357›Full record

ArticlebioRxiv : the preprint server for biology2025

An activator of a two-component system controls cell separation and intrinsic drug resistance in

Liam D McDonough, Shuqi Li, Vanisha Munsamy-Govender, Celena M Gwin, Jeremy M Rock, E Hesper Rego

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

5 · Who and what money

Authors and funding

6 authors.

Liam D McDonoughDepartment of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT.ORCID 0000-0002-1251-7678
Shuqi LiLaboratory of Host-Pathogen Biology, The Rockefeller University, New York, NY.
Vanisha Munsamy-GovenderLaboratory of Host-Pathogen Biology, The Rockefeller University, New York, NY.
Celena M GwinDepartment of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT.
Jeremy M RockLaboratory of Host-Pathogen Biology, The Rockefeller University, New York, NY.
E Hesper RegoDepartment of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT.ORCID 0000-0002-2973-8354

Funding

Towards a molecular understanding of persistent tuberculosis infectionDP2AI144850 · NIAID · ROCKEFELLER UNIVERSITY · PI ROCK, JEREMY MICHAEL · 2018 to 2018
$2.5M
"The molecular mechanisms of asymmetric cell division in mycobacteria."R01AI148255 · NIAID · YALE UNIVERSITY · PI REGO, ELIZABETH HESPER · 2020 to 2024
$2.1M
NIAID NIH HHS DP2 AI144850NIAID NIH HHS R01 AI148255
6 · The paper itself

Abstract

Unlike commonly studied rod-shaped bacteria, mycobacteria grow from their poles, requiring precise coordination between division and initiation of new pole growth. The mechanisms that mediate this transition are largely unknown, but likely represent a rich source of drug targets for the treatment of mycobacterial infections, including tuberculosis. Here, we identify TapA (MSMEG_3748/Rv1697) as a key regulator of this transition. TapA interacts with the sensor kinase MtrB at the septum to initiate a signaling cascade that ultimately results in the expression of the essential peptidoglycan hydrolases RipAB, amongst others, at the end of division. Loss of TapA disrupts division, dysregulates pole formation, and sensitizes

Identifiers

PMID40791357
PMCPMC12338722

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.