Evidence map›Paper›PMID 33536448›Full record

ArticleScientific reports2021

Lsr2, a nucleoid-associated protein influencing mycobacterial cell cycle.

Marta Kołodziej, Damian Trojanowski, Katarzyna Bury, Joanna Hołówka, Weronika Matysik, Hanna Kąkolewska, Helge Feddersen, Giacomo Giacomelli, Igor Konieczny, Marc Bramkamp and 1 more

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.8field-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

23 citing papers in PubMed, 31 citations in OpenAlex.

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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

11 authors at 3 institutions in 2 countries.

Marta KołodziejDepartment of Molecular Microbiology, Faculty of Biotechnology, University of Wrocław, Wrocław, Poland.
Damian TrojanowskiDepartment of Molecular Microbiology, Faculty of Biotechnology, University of Wrocław, Wrocław, Poland.
Katarzyna BuryIntercollegiate Faculty of Biotechnology of University of Gdansk and Medical University of Gdansk, University of Gdansk, Gdansk, Poland.
Joanna HołówkaDepartment of Molecular Microbiology, Faculty of Biotechnology, University of Wrocław, Wrocław, Poland.
Weronika MatysikDepartment of Molecular Microbiology, Faculty of Biotechnology, University of Wrocław, Wrocław, Poland.
Hanna KąkolewskaDepartment of Molecular Microbiology, Faculty of Biotechnology, University of Wrocław, Wrocław, Poland.
Helge FeddersenInstitut Für Allgemeine Mikrobiologie, Christian-Albrechts-Universität Zu Kiel, 24118, Kiel, Germany.
Giacomo GiacomelliInstitut Für Allgemeine Mikrobiologie, Christian-Albrechts-Universität Zu Kiel, 24118, Kiel, Germany.
Igor KoniecznyIntercollegiate Faculty of Biotechnology of University of Gdansk and Medical University of Gdansk, University of Gdansk, Gdansk, Poland.
Marc BramkampInstitut Für Allgemeine Mikrobiologie, Christian-Albrechts-Universität Zu Kiel, 24118, Kiel, Germany.
Jolanta Zakrzewska-CzerwińskaDepartment of Molecular Microbiology, Faculty of Biotechnology, University of Wrocław, Wrocław, Poland. jolanta.zakrzewska-czerwinska@uwr.edu.pl.
University of Wrocław · PLKiel University · DEGdańsk Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleoid-associated proteins (NAPs) are responsible for maintaining highly organized and yet dynamic chromosome structure in bacteria. The genus Mycobacterium possesses a unique set of NAPs, including Lsr2, which is a DNA-bridging protein. Importantly, Lsr2 is essential for the M. tuberculosis during infection exhibiting pleiotropic activities including regulation of gene expression (mainly as a repressor). Here, we report that deletion of lsr2 gene profoundly impacts the cell morphology of M. smegmatis, which is a model organism for studying the cell biology of M. tuberculosis and other mycobacterial pathogens. Cells lacking Lsr2 are shorter, wider, and more rigid than the wild-type cells. Using time-lapse fluorescent microscopy, we showed that fluorescently tagged Lsr2 forms large and dynamic nucleoprotein complexes, and that the N-terminal oligomerization domain of Lsr2 is indispensable for the formation of nucleoprotein complexes in vivo. Moreover, lsr2 deletion exerts a significant effect on the replication time and replisome dynamics. Thus, we propose that the Lsr2 nucleoprotein complexes may contribute to maintaining the proper organization of the newly synthesized DNA and therefore influencing mycobacterial cell cycle.

Indexed as

Cell CycleDNA ReplicationAntigens, BacterialBacterial ProteinsDNA, BacterialIntravital MicroscopyMycobacterium smegmatisProtein DomainsProtein MultimerizationTime-Lapse ImagingAntigens, BacterialBacterial ProteinsDNA, BacterialLsr2 protein, Mycobacterium smegmatis

Identifiers

PMID33536448
PMCPMC7858621
OpenAlexW3128937571

What OpenQuestion holds

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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.