Evidence map›Paper›PMID 27977672›Full record

ArticlePLoS genetics2016

Unique Function of the Bacterial Chromosome Segregation Machinery in Apically Growing Streptomyces - Targeting the Chromosome to New Hyphal Tubes and its Anchorage at the Tips.

Agnieszka Kois-Ostrowska, Agnieszka Strzałka, Natalia Lipietta, Emma Tilley, Jolanta Zakrzewska-Czerwińska, Paul Herron, Dagmara Jakimowicz

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 42 citations in OpenAlex.

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  17. Ultrastructure of Exospore Formation inFrontiers in microbiology · 2020
    Article
  18. Review
  19. Journal of bacteriology · 2019
    Article
  20. ¡vIVA la DivIVA!Journal of bacteriology · 2019
    Review
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

7 authors at 2 institutions in 2 countries.

Agnieszka Kois-OstrowskaFaculty of Biotechnology, University of Wroclaw, Poland.
Agnieszka StrzałkaFaculty of Biotechnology, University of Wroclaw, Poland.
Natalia LipiettaFaculty of Biotechnology, University of Wroclaw, Poland.
Emma TilleyInstitute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, United Kingdom.
Jolanta Zakrzewska-CzerwińskaFaculty of Biotechnology, University of Wroclaw, Poland.
Paul HerronInstitute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, United Kingdom.
Dagmara JakimowiczFaculty of Biotechnology, University of Wroclaw, Poland.ORCID http://orcid.org/0000-0002-7857-064X
University of Wrocław · PLUniversity of Strathclyde · GB

Funding

Biotechnology and Biological Sciences Research Council BB/D521657/1
6 · The paper itself

Abstract

The coordination of chromosome segregation with cell growth is fundamental to the proliferation of any organism. In most unicellular bacteria, chromosome segregation is strictly coordinated with cell division and involves ParA that moves the ParB nucleoprotein complexes bi- or unidirectionally toward the cell pole(s). However, the chromosome organization in multiploid, apically extending and branching Streptomyces hyphae challenges the known mechanisms of bacterial chromosome segregation. The complex Streptomyces life cycle involves two stages: vegetative growth and sporulation. In the latter stage, multiple cell divisions accompanied by chromosome compaction and ParAB assisted segregation turn multigenomic hyphal cell into a chain of unigenomic spores. However, the requirement for active chromosome segregation is unclear in the absence of canonical cell division during vegetative growth except in the process of branch formation. The mechanism by which chromosomes are targeted to new hyphae in streptomycete vegetative growth has remained unknown until now. Here, we address the question of whether active chromosome segregation occurs at this stage. Applied for the first time in Streptomyces, labelling of the chromosomal replication initiation region (oriC) and time-lapse microscopy, revealed that in vegetative hyphae every copy of the chromosome is complexed with ParB, whereas ParA, through interaction with the apical protein complex (polarisome), tightly anchors only one chromosome at the hyphal tip. The anchor is maintained during replication, when ParA captures one of the daughter oriCs. During spore germination and branching, ParA targets one of the multiple chromosomal copies to the new hyphal tip, enabling efficient elongation of hyphal tube. Thus, our studies reveal a novel role for ParAB proteins during hyphal tip establishment and extension.

Indexed as

Bacterial ProteinsCell DivisionChromosomes, BacterialChromosome SegregationDNA PrimaseDNA ReplicationGene Expression Regulation, BacterialHyphaeNucleoproteinsOrigin Recognition ComplexSpores, BacterialStreptomycesBacterial ProteinsDNA PrimaseNucleoproteinsOriC chromosomal replication originOrigin Recognition Complex

Identifiers

PMID27977672
PMCPMC5157956
OpenAlexW2563762340

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.