Evidence map›Paper›PMID 23384289›Full record

ArticleBMC microbiology2013

Transcriptional analysis of ftsZ within the dcw cluster in Bacillus mycoides.

Tiziana Santini, Luana Turchi, Giulia Ceccarelli, Carmen Di Franco, Elena Beccari

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Article in BMC microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Molecular Characterization of theAntibiotics (Basel, Switzerland) · 2020
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Tiziana SantiniDipartimento di Biologia e Biotecnologie “C. Darwin”, Rome 00185, Italy.
Luana Turchi
Giulia Ceccarelli
Carmen Di Franco
Elena Beccari

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn Bacillus mycoides, as well as in other members of the B. cereus group, the tubulin-like protein of the division septum FtsZ is encoded by the distal gene of the cluster division and cell wall (dcw). Along the cluster the genes coding for structural proteins of the division apparatus are intermingled with those coding for enzymes of peptidoglycan biosynthesis, raising the possibility that genes with this different function might be coexpressed. Transcription of ftsZ in two model bacteria had been reported to differ: in B. subtilis, the ftsZ gene was found transcribed as a bigenic mRNA in the AZ operon; in E. coli, the transcripts of ftsZ were monogenic, expressed by specific promoters. Here we analyzed the size and the initiation sites of RNAs transcribed from ftsZ and from other cluster genes in two B. mycoides strains, DX and SIN, characterized by colonies of different chirality and density, to explore the correlation of the different morphotypes with transcription of the dcw genes.

resultsIn both strains, during vegetative growth, the ftsZ-specific RNAs were composed mainly of ftsZ, ftsA-ftsZ and ftsQ-ftsA-ftsZ transcripts. A low number of RNA molecules included the sequences of the upstream murG and murB genes, which are involved in peptidoglycan synthesis. No cotranscription was detected between ftsZ and the downstream genes of the SpoIIG cluster. The monogenic ftsZ RNA was found in both strains, with the main initiation site located inside the ftsA coding sequence. To confirm the promoter property of the site, a B. mycoides construct carrying the ftsA region in front of the shortened ftsZ gene was inserted into the AmyE locus of B. subtilis 168. The promoter site in the ftsA region was recognized in the heterologous cellular context and expressed as in B. mycoides.

conclusionsThe DX and SIN strains of B. mycoides display very similar RNA transcription specificity. The ftsZ messenger RNA can be found either as an independent transcript or expressed together with ftsA and ftsQ and, in low amounts, with genes that are specific to peptidoglycan biosynthesis.

Indexed as

Gene Expression ProfilingGene Expression Regulation, BacterialBacillusBacterial ProteinsCytoskeletal ProteinsDNA, BacterialMolecular Sequence DataRNA, MessengerSequence Analysis, DNATranscription, GeneticTranscription Initiation SiteBacterial ProteinsCytoskeletal ProteinsDNA, BacterialFtsZ protein, BacteriaRNA, Messenger

Identifiers

PMID23384289
PMCPMC3762067

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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.