The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Prophage-encoded small protein YqaH counteracts the activities of the replication initiator DnaA in Bacillus subtilis
Open accessPreprint — published as 10.1099/mic.0.001268 · Paper page
Abstract
Bacterial genomes harbor cryptic prophages that are mostly transcriptionally silent with many unannotated genes. Still, cryptic prophages may contribute to their host fitness and phenotypes. In B. subtilis , the yqaF-yqaN operon belongs to the prophage element skin , and is tightly repressed by the Xre-like repressor sknR . This operon contains several short open reading frames (smORFs) potentially encoding small-sized proteins. The smORF-encoded peptide YqaH was previously reported to bind to the replication initiator DnaA. Here, using a yeast two-hybrid assay, we found that YqaH binds to the DNA binding domain IV of DnaA and interacts with Spo0A, a master regulator of sporulation. We isolated single amino acid substitutions in YqaH that abolished interaction with DnaA but not with Spo0A. Then, we studied in B. subtilis the phenotypes associated with the specific loss-of-interaction with DnaA (DnaA-LOI). We found that expression of yqaH carrying DnaA-LOI mutations abolished the deleterious effects of yqaH WT expression on chromosome segregation, replication initiation and DnaA-regulated transcription. When YqaH was induced after vegetative growth, DnaA-LOI mutations abolished the deleterious effects of YqaH WT on sporulation and biofilm formation. Thus, YqaH inhibits replication, sporulation and biofilm formation mainly by antagonizing DnaA in a manner that is independent of the cell cycle checkpoint Sda.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764
Research works printed but not linked: 96
- 2015, small ORFs: A new class of essential genes for development, Genetics and molecular biology, 38, 278, 10.1590/S1415-475738320150009 · DOI
- 10.1002/mbo3.303 · DOI
- 2019, Synthetic developmental regulator MciZ targets FtsZ across Bacillus species and inhibits bacterial division, Mol Microbiol, 111, 965, 10.1111/mmi.14198 · DOI
- 10.1128/jb.176.2.296-306.1994 · DOI
- 10.1073/pnas.1414242112 · DOI
- 10.1073/pnas.1405336111 · DOI
- 10.1128/JB.00958-12 · DOI
- Bradshaw, N. , Levdikov, V.M. , Zimanyi, C.M. , Gaudet, R. , Wilkinson, A.J. , and Losick, R. (2017). A widespread family of serine/threonine protein phosphatases shares a common regulatory switch with proteasomal proteases. Elife 6. · DOI
- 10.1016/S0092-8674(01)00211-2 · DOI
- 10.1046/j.1365-2958.2003.03580.x · DOI
- 10.1074/jbc.274.51.36679 · DOI
- 2015, Identification and characterization of sORF-encoded polypeptides, Crit Rev Biochem Mol Biol, 50, 134, 10.3109/10409238.2015.1016215 · DOI
- 10.1038/nrm.2017.58 · DOI
- 10.1111/j.1365-2958.2008.06554.x · DOI
- 10.1104/pp.17.01743 · DOI
- 10.1111/mmi.13411 · DOI
- 10.1128/JB.01695-07 · DOI
- 10.1016/j.mib.2017.09.010 · DOI
- 10.1111/j.1365-2958.2012.08052.x · DOI
- 2018, The Long History of the Diverse Roles of Short ORFs: sPEPs in Fungi, Proteomics, 18, e1700219, 10.1002/pmic.201700219 · DOI
- 2017, Cell Cycle Machinery in Bacillus subtilis, Sub-cellular biochemistry, 84, 67, 10.1007/978-3-319-53047-5_3 · DOI
- 10.1093/nar/gkv1318 · DOI
- L., 2016, Tetramerization and interdomain flexibility of the replication initiation controller YabA enables simultaneous binding to multiple partners, 44, 449
- 10.1186/s12864-017-3932-y · DOI
- 10.1093/nar/gkg309 · DOI
- 10.1128/JB.187.4.1357-1368.2005 · DOI
- 10.1073/pnas.0506174102 · DOI
- 2012, Regulation of protein function by interfering protein species, Biomolecular concepts, 3, 71, 10.1515/bmc.2011.053 · DOI
- 10.1111/j.1365-2958.2004.04282.x · DOI
- 10.1111/j.1365-2958.2008.06173.x · DOI
- 10.1021/acs.jproteome.8b00032 · DOI
- 10.1016/j.tplants.2015.11.005 · DOI
- Hood, I.V. , and Berger, J.M. (2016). Viral hijacking of a replicative helicase loader and its implications for helicase loading control and phage replication. Elife 5. · DOI
- 10.1128/JB.00210-10 · DOI
- 1992, Opening of the replication origin of Escherichia coli by DnaA protein with protein HU or IHF, J Biol Chem, 267, 23083, 10.1016/S0021-9258(18)50059-4 · DOI
- 10.1093/genetics/144.4.1425 · DOI
- 10.1111/mmi.12713 · DOI
- Jameson, K.H. , and Wilkinson, A.J. (2017). Control of Initiation of DNA Replication in Bacillus subtilis and Escherichia coli. Genes 8. · DOI
- 2006, Functional genomics of genes with small open reading frames (sORFs) in S, cerevisiae. Genome research, 16, 365, 10.1101/gr.4355406 · DOI
- 10.3389/fmicb.2017.02496 · DOI
- 10.1038/nrmicro2314 · DOI
- 10.1128/JB.00625-10 · DOI
- 10.1101/gad.4.4.525 · DOI
- 10.1016/j.molcel.2008.08.018 · DOI
- 10.1146/annurev-micro-090110-102934 · DOI
- 10.1093/nar/gku080 · DOI
- 10.4161/bact.28520 · DOI
- 10.1038/nbt932 · DOI
- Lloyd, C.R. , Park, S. , Fei, J. , and Vanderpool, C.K. (2017). The Small Protein SgrT Controls Transport Activity of the Glucose-Specific Phosphotransferase System. J Bacteriol 199. · DOI
- 10.1016/j.tcb.2017.04.006 · DOI
- 10.1002/pmic.201000791 · DOI
- 2019, DNA replication initiation in Bacillus subtilis: structural and functional characterization of the essential DnaA-DnaD interaction, Nucleic Acids Res, 47, 2101, 10.1093/nar/gky1220 · DOI
- 10.1111/j.1365-2958.2011.07821.x · DOI
- 2002, The bacterial replication initiator DnaA, DnaA and oriC, the bacterial mode to initiate DNA replication. FEMS microbiology reviews, 26, 355
- 10.1016/S0076-6879(03)70030-5 · DOI
- 10.15252/msb.20188290 · DOI
- 10.1371/journal.pgen.1002048 · DOI
- 10.1128/JB.01644-07 · DOI
- 10.1046/j.1365-2958.2003.03818.x · DOI
- 10.1038/nrmicro1640 · DOI
- 10.1016/j.cell.2008.07.044 · DOI
- 10.1371/journal.pgen.1004731 · DOI
- 10.1073/pnas.0908966106 · DOI
- 2003, Purification and characterization of bacteriophage-encoded inhibitors of host RNA polymerase: T-odd phage gp2-like proteins, Methods in enzymology, 370, 212, 10.1016/S0076-6879(03)70019-6 · DOI
- 10.1126/science.1206848 · DOI · Paper page
- 10.1073/pnas.122040799 · DOI
- 10.1073/pnas.0506914103 · DOI
- 10.1016/j.plasmid.2009.06.003 · DOI
- 10.1073/pnas.1205638109 · DOI
- 2016, Multiple DNA Binding Proteins Contribute to Timing of Chromosome Replication in E, coli. Frontiers in molecular biosciences, 3, 29
- 10.1016/S1097-2765(04)00084-X · DOI
- 10.1038/nchembio.1964 · DOI · Paper page
- 10.1093/bioinformatics/btr275 · DOI
- 10.1016/j.jmb.2010.07.012 · DOI
- 10.1128/JB.00534-10 · DOI
- 10.1111/mmi.12353 · DOI
- 10.1016/j.tcb.2010.10.006 · DOI
- 10.1016/j.tim.2007.02.004 · DOI
- 10.1101/cshperspect.a012922 · DOI
- 10.1074/jbc.C113.533968 · DOI
- 10.1038/nchembio.1120 · DOI
- 10.1016/j.devcel.2008.09.010 · DOI
- 10.1038/embor.2010.196 · DOI
- 10.1042/bj1130029 · DOI
- 10.1146/annurev-biochem-070611-102400 · DOI · Paper page
- 10.1016/0092-8674(88)90407-2 · DOI
- 10.1093/gbe/evx041 · DOI
- 10.1002/pmic.201700064 · DOI
- 10.1101/gad.528209 · DOI
- 2017, Genetic networks controlled by the bacterial replication initiator and transcription factor DnaA in Bacillus subtilis, Mol Microbiol, 106, 109, 10.1111/mmi.13755 · DOI
- 2014, PCR mutagenesis and gap repair in yeast, Methods in molecular biology, 1205, 29, 10.1007/978-1-4939-1363-3_3 · DOI
- 10.1038/nrmicro2671 · DOI
- 10.1128/JB.187.17.6058-6068.2005 · DOI
- 2016, Identification and validation of novel small proteins in Pseudomonas putida, Environmental microbiology reports, 8, 966, 10.1111/1758-2229.12473 · DOI
- 10.1126/science.aac5677 · DOI
- 10.1016/S0196-9781(01)00492-2 · DOI
Metadata
- Authors
- Ventroux, M., & Noirot-Gros, M.-F.
- Affiliations
- AgroParisTech (FR)
- ORCID
- Ventroux, Magali
- Venue
- Microbiology
- Publisher
- openRxiv
- Published
- 2020-11-18
- Volume
- 168
- Issue
- 11
- Pages
- 001268
- ISSN
- 1350-0872 (ISSN-L)
- OpenAlex
- W4310359231
- Cited by
- 1
- References
- 1
- Citations by year
- 2024: 1
- FWCI
- 0.15
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Microbiology (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- HAL (submittedVersion, other-oa)
- Funders
- Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Life Sciences › Immunology and Microbiology › Virology › Bacteriophages and microbial interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- cryptic prophage, DnaA, Bacillus subtilis, Spo0A, sporulation, biofilm formation, chromosome segregation, DNA replication initiation, protein-protein interaction, transcriptional repression
- MeSH terms
- Bacillus subtilis, Bacterial Proteins, DNA Replication, DNA-Binding Proteins, Transcription Factors, Prophages
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review