MreB is important for cell shape but not for chromosome segregation of the filamentous cyanobacterium Anabaena sp. PCC 7120
Open accessAbstract
Summary: MreB is a bacterial actin that plays important roles in determination of cell shape and chromosome partitioning in Escherichia coli and Caulobacter crescentus. In this study, the mreB from the filamentous cyanobacterium Anabaena sp. PCC 7120 was inactivated. Although the mreB null mutant showed a drastic change in cell shape, its growth rate, cell division and the filament length were unaltered. Thus, MreB in Anabaena maintains cell shape but is not required for chromosome partitioning. The wild type and the mutant had eight and 10 copies of chromosomes per cell respectively. We demonstrated that DNA content in two daughter cells after cell division in both strains was not always identical. The ratios of DNA content in two daughter cells had a Gaussian distribution with a standard deviation much larger than a value expected if the DNA content in two daughter cells were identical, suggesting that chromosome partitioning is a random process. The multiple copies of chromosomes in cyanobacteria are likely required for chromosome random partitioning in cell division.
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
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.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Polyploidy delays complete chromosomal segregation of engineered constructs.
“polyploidy delays complete chromosomal segregation of engineered constructs”
From Cyanobacteria as a Photosynthetic Chassis for Metabolic Pathway Engineering with Heterologous Gene Expression (2026) · cites this paper as [31]
The chromosome-copy-number results report multiple chromosomes per Anabaena cell, and the Inactivation of mreB section confirms complete segregation of an engineered mutant. Neither passage says that polyploidy delayed that segregation or measures how long it took. (LLM, conf=0.84)
Experimental — accuracy not yet measuredThe polyploid genomic configuration of cyanobacteria complicates genetic manipulation and often delays the segregation of engineered mutations or inserted genetic constructs after genome editing.
“This genomic configuration complicates genetic manipulation and often delays the segregation of engineered mutations or inserted genetic constructs after genome editing.”
From Cyanobacteria as a Photosynthetic Chassis for Metabolic Pathway Engineering with Heterologous Gene Expression (2026) · cites this paper as [31]
The Discussion (page unavailable) states that cyanobacterial cells have many chromosome copies. Gene inactivation and complementation (page unavailable) describes an engineered mreB mutant whose segregation was confirmed, but the paper does not say that multiple copies complicate genetic manipulation or often delay segregation of mutations or inserted constructs. (LLM, conf=0.84)
Experimental — accuracy not yet measuredAnabaena sp. PCC 7120 has approximately eight chromosome copies per wild-type cell, and its complete genome comprises a 6,413,771 bp chromosome together with six plasmids.
“the filamentous cyanobacterium Anabaena sp. PCC 7120 has been reported to contain approximately eight chromosome copies per wild-type cell, and its complete genome comprises a 6,413,771 bp chromosome together with six plasmids [31].”
From Cyanobacteria as a Photosynthetic Chassis for Metabolic Pathway Engineering with Heterologous Gene Expression (2026) · cites this paper as [31]
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measuredMany cyanobacterial species have polyploid genomes, meaning that multiple copies of the chromosome are present within a single cell.
“many cyanobacterial species have polyploid genomes, meaning that multiple copies of the chromosome are present within a single cell.”
From Cyanobacteria as a Photosynthetic Chassis for Metabolic Pathway Engineering with Heterologous Gene Expression (2026) · cites this paper as [31]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Generic Assignments, Strain Histories and Properties of Pure Cultures of Cyanobacteria
Rippka, R., Stanier, R. Y., Deruelles, J., Herdman, M., & Waterbury, J. B. (1979) · Microbiology · doi:10.1099/00221287-111-1-1 · Cited by 7,606 · see citing works
Control of Cell Shape in Bacteria
Jones, L. J. F., Carballido‐López, R., & Errington, J. (2001) · Cell · doi:10.1016/s0092-8674(01)00287-2 · Cited by 943 · see citing works
Prokaryotic origin of the actin cytoskeleton
van den Ent, F., Amos, L. A., & Löwe, J. (2001) · Nature · doi:10.1038/35092500 · Cited by 821 · see citing works
Control of Cell Morphogenesis in Bacteria
Daniel, R. A., & Errington, J. (2003) · Cell · doi:10.1016/s0092-8674(03)00421-5 · Cited by 740 · see citing works
Kaneko, T. (2001) · DNA Research · doi:10.1093/dnares/8.5.205 · Cited by 696 · see citing works
[83] Conjugal transfer of DNA to cyanobacteria
Elhai, J., & Wölk, C. P. (1988) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(88)67086-8 · Cited by 568 · see citing works
Heterocyst Metabolism and Development
Wölk, C. P., Ernst, A., & Elhai, J. (1994) · Springer eBooks · doi:10.1007/978-94-011-0227-8_27 · Cited by 526 · see citing works
MipZ, a Spatial Regulator Coordinating Chromosome Segregation with Cell Division in Caulobacter
Thanbichler, M. R., & Shapiro, L. (2006) · Cell · doi:10.1016/j.cell.2006.05.038 · Cited by 517 · see citing works
Heterocyst differentiation and pattern formation in cyanobacteria: a chorus of signals
Zhang, C., Laurent, S., Sakr, S., Peng, L., & Bédu, S. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04979.x · Cited by 429 · see citing works
Figge, R. M., Divakaruni, A. V., & Gober, J. W. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2003.03936.x · Cited by 425 · see citing works
MreB Actin-Mediated Segregation of a Specific Region of a Bacterial Chromosome
Gitai, Z., Dye, N. A., Reisenauer, A., et al. (2005) · Cell · doi:10.1016/j.cell.2005.01.007 · Cited by 393 · see citing works
Heterocyst Pattern Formation Controlled by a Diffusible Peptide
Yoon, H., & Golden, J. W. (1998) · Science · doi:10.1126/science.282.5390.935 · Cited by 387 · see citing works
Rothfield, L. I., Justice, S. S., & Garcı́a-Lara, J. (1999) · Annual Review of Genetics · doi:10.1146/annurev.genet.33.1.423 · Cited by 384 · see citing works
The morphogenetic MreBCD proteins of Escherichia coli form an essential membrane‐bound complex
Kruse, T., Bork‐Jensen, J., & Gerdes, K. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04367.x · Cited by 380 · see citing works
Haselkorn, R. (1978) · Annual Review of Plant Physiology · doi:10.1146/annurev.pp.29.060178.001535 · Cited by 326 · see citing works
Buikema, W. J., & Haselkorn, R. (1991) · Genes & Development · doi:10.1101/gad.5.2.321 · Cited by 314 · see citing works
Spatial control of bacterial division-site placement
Rothfield, L. I., Taghbalout, A., & Shih, Y. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1290 · Cited by 307 · see citing works
An actin-like gene can determine cell polarity in bacteria
Gitai, Z., Dye, N. A., & Shapiro, L. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402638101 · Cited by 306 · see citing works
Dysfunctional MreB inhibits chromosome segregation in Escherichia coli
Kruse, T., Møller‐Jensen, J., Løbner‐Olesen, A., & Gerdes, K. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg504 · Cited by 276 · see citing works
Cryo-Electron Tomography Reveals the Cytoskeletal Structure of Spiroplasma melliferum
Kürner, J., Frangakis, A. S., & Baumeister, W. P. (2005) · Science · doi:10.1126/science.1104031 · Cited by 235 · see citing works
Buikema, W. J., & Haselkorn, R. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.051624898 · Cited by 221 · see citing works
Møller‐Jensen, J., Borch, J., Dam, M., et al. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00451-9 · Cited by 203 · see citing works
Herdman, M., Janvier, M., Rippka, R., & Stanier, R. Y. (1979) · Journal of General Microbiology · doi:10.1099/00221287-111-1-73 · Cited by 200 · see citing works
THE DIVERSE AND DYNAMIC STRUCTURE OF BACTERIAL GENOMES
Casjens, S. (1998) · Annual Review of Genetics · doi:10.1146/annurev.genet.32.1.339 · Cited by 188 · see citing works
A magnesium‐dependent mreB null mutant: implications for the role of mreB in Bacillus subtilis
Formstone, A., & Errington, J. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04506.x · Cited by 185 · see citing works
Huang, X., Dong, Y., & Zhao, J. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400429101 · Cited by 178 · see citing works
Self-citationMultiplicity of genome equivalents in the radiation-resistant bacterium Micrococcus radiodurans
Hansen, M. T. (1978) · Journal of Bacteriology · doi:10.1128/jb.134.1.71-75.1978 · Cited by 177 · see citing works
Labarre, J.-S., Chauvat, F., & Thuriaux, P. (1989) · Journal of Bacteriology · doi:10.1128/jb.171.6.3449-3457.1989 · Cited by 176 · see citing works
Roles for MreC and MreD proteins in helical growth of the cylindrical cell wall in Bacillus subtilis
Leaver, M., & Errington, J. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04736.x · Cited by 161 · see citing works
Soufo, H. J. D., & Graumann, P. L. (2003) · Current Biology · doi:10.1016/j.cub.2003.10.024 · Cited by 155 · see citing works
Dynamic movement of actin‐like proteins within bacterial cells
Soufo, H. J. D., & Graumann, P. L. (2004) · EMBO Reports · doi:10.1038/sj.embor.7400209 · Cited by 154 · see citing works
Identification of Bacillus subtilis genes for septum placement and shape determination
Levin, P. A., Margolis, P. S., Setlow, P., et al. (1992) · Journal of Bacteriology · doi:10.1128/jb.174.21.6717-6728.1992 · Cited by 144 · see citing works
Two independent spiral structures control cell shape in Caulobacter
Dye, N. A., Pincus, Z., Theriot, J. A., Shapiro, L., & Gitai, Z. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507708102 · Cited by 128 · see citing works
New mre genes mreC and mreD, responsible for formation of the rod shape of Escherichia coli cells
Wachi, M., Doi, M., Okada, Y., et al. (1989) · Journal of Bacteriology · doi:10.1128/jb.171.12.6511-6516.1989 · Cited by 122 · see citing works
Gerdes, K., Møller‐Jensen, J., Ebersbach, G., et al. (2004) · Cell · doi:10.1016/s0092-8674(04)00116-3 · Cited by 121 · see citing works
Kruse, T., Blagoev, B., Løbner‐Olesen, A., et al. (2006) · Genes & Development · doi:10.1101/gad.366606 · Cited by 121 · see citing works
Bacterial ancestry of actin and tubulin
van den Ent, F. (2001) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(01)00262-4 · Cited by 113 · see citing works
Kitten, T. O., & Barbour, A. G. (1992) · Genetics · doi:10.1093/genetics/132.2.311 · Cited by 112 · see citing works
Mazza, P., Noens, E. E. E., Schirner, K., et al. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05134.x · Cited by 105 · see citing works
Changes of ploidy during the Azotobacter vinelandii growth cycle
Maldonado, R., Jiménez, J., & Casadesús, J. (1994) · Journal of Bacteriology · doi:10.1128/jb.176.13.3911-3919.1994 · Cited by 93 · see citing works
Supramolecular Membrane Organization
Gantt, E. (1994) · Springer eBooks · doi:10.1007/978-94-011-0227-8_6 · Cited by 91 · see citing works
Slovak, P. M., Wadhams, G. H., & Armitage, J. P. (2004) · Journal of Bacteriology · doi:10.1128/jb.187.1.54-64.2005 · Cited by 81 · see citing works
Zhao, Y., Shi, Y., Zhao, W., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501782102 · Cited by 76 · see citing works
Self-citationStructural/functional homology between the bacterial and eukaryotic cytoskeletons
Amos, L., van den Ent, F., & Löwe, J. (2003) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2003.11.005 · Cited by 75 · see citing works
Li, Y.-F., & Austin, S. J. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.03156.x · Cited by 74 · see citing works
Differentiation of Hormogonia and Relationships with Other Biological Processes
de Marsac, N. T. (1994) · Springer eBooks · doi:10.1007/978-94-011-0227-8_28 · Cited by 67 · see citing works
Su, Z. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkj496 · Cited by 63 · see citing works
Inhibition of Cell Division Suppresses Heterocyst Development in Anabaena sp. Strain PCC 7120
Sakr, S., Jeanjean, R., Zhang, C.-C., & Arcondéguy, T. (2006) · Journal of Bacteriology · doi:10.1128/jb.188.4.1396-1404.2006 · Cited by 61 · see citing works
Bacterial DNA segregation by the actin-like MreB protein
Kruse, T., & Gerdes, K. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.05.002 · Cited by 55 · see citing works
Taking shape: control of bacterial cell wall biosynthesis
Stewart, G. C. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04760.x · Cited by 52 · see citing works
Kaneko, T. (2001) · DNA Research · doi:10.1093/dnares/8.5.227 · Cited by 49 · see citing works
Bacterial subcellular architecture: recent advances and future prospects
Lewis, P. J. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04343.x · Cited by 47 · see citing works
Clustering versus random segregation of plasmids lacking a partitioning function: a plasmid paradox?
Nordström, K., & Gerdes, K. (2003) · Plasmid · doi:10.1016/s0147-619x(03)00056-8 · Cited by 40 · see citing works
Dong, Y., Huang, X., Wu, X., et al. (2000) · Journal of Bacteriology · doi:10.1128/jb.182.6.1575-1579.2000 · Cited by 37 · see citing works
Transcriptional Analysis and Mutation of a dnaA -Like Gene in Synechocystis sp. Strain PCC 6803
Richter, S., Hagemann, M., & Messer, W. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.18.4946-4949.1998 · Cited by 31 · see citing works
Cloning and sequence of ftsZ and flanking regions from the cyanobacterium Anabaena PCC 7120
Doherty, H. M., & Adams, D. G. (1995) · Gene · doi:10.1016/0378-1119(95)00416-4 · Cited by 28 · see citing works
Coordination of DNA replication and cell division in CyanobacteriaMicrocystis aeruginosa
Yoshida, T., Maki, M., Okamoto, H., et al. (2005) · FEMS Microbiology Letters · doi:10.1016/j.femsle.2005.07.041 · Cited by 24 · see citing works
An intracellular actin motor in bacteria?
Graumann, P. L., & Soufo, H. J. D. (2004) · BioEssays · doi:10.1002/bies.20126 · Cited by 24 · see citing works
Ohki, K., & Fujita, Y. (1992) · Journal of Phycology · doi:10.1111/j.0022-3646.1992.00803.x · Cited by 23 · see citing works
Bacterial Mitosis: Actin in a New Role at the Origin
Margolin, W. (2005) · Current Biology · doi:10.1016/j.cub.2005.03.026 · Cited by 18 · see citing works
vitro及In, I., vivo中HetR為homodimer, hetR hetRC, A., et al. (2005) · Cited by 17 · see citing works
Wachi, M., Osaka, K., KOHAMA, T., et al. (2006) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.60315 · Cited by 16 · see citing works
Herdman, M., & Carr, N. G. (1971) · Journal of Bacteriology · doi:10.1128/jb.107.2.583-584.1971 · Cited by 13 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Griese, M., Lange, C., & Soppa, J. (2011) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2011.02368.x · Cited by 264 · see citing works
Zhang, J.-Y., Lin, G.-M., Xing, W.-Y., & Zhang, C.-C. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00791 · Cited by 34 · see citing works
Genome Engineering by RNA-Guided Transposition for <i>Anabaena</i> sp. PCC 7120
Arévalo, S., Pérez Rico, D., Abarca, D., Dijkhuizen, L. W., Sarasa-Buisan, C., Lindblad, P., Flores, E., Nierzwicki-Bauer, S., & Schluepmann, H. (2024) · ACS Synthetic Biology · doi:10.1021/acssynbio.3c00583 · Cited by 13 · see citing works
Zhang, T., Li, S., Chen, L., Zhang, W., & Sun, T. (2024) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.4c04497 · Cited by 6 · see citing works
Walshe, J., & Saha, S. K. (2026) · Current Issues in Molecular Biology · doi:10.3390/cimb48060638 · Cited by 1 · see citing works
“For example, the filamentous cyanobacterium Anabaena sp. PCC 7120 has been reported to contain approximately eight chromosome copies per wild-type cell, and its complete genome comprises a 6,413,771 bp chromosome together with six plasmids [31].”
- Authors
- Hu, B., Yang, G., Zhao, W., Zhang, Y., & Zhao, J.
- Affiliations
- Peking University (CN)
- Corresponding author
- Zhao, Jindong
- Venue
- Molecular Microbiology
- Publisher
- Wiley
- Published
- 2007-01-22
- Volume
- 63
- Issue
- 6
- Pages
- 1640-1652
- ISSN
- 0950-382X (ISSN-L)
- 1365-2958
- OpenAlex
- W2111871013
- Cited by
- 116
- References
- 63
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 5 · 2023: 4 · 2022: 8 · 2021: 2 · 2020: 8 · 2019: 11 · 2018: 11 · 2017: 3 · 2016: 3 · 2015: 5 · 2014: 8 · 2012: 7
- FWCI
- 5.00
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Molecular Microbiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Natural Science Foundation of China (30230040)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Structural Characterization
- Keywords
- MreB, bacterial actin, cell shape, chromosome segregation, Anabaena sp. PCC 7120, cyanobacteria, DNA content, filament length, cell division, chromosome copy number
- MeSH terms
- Bacterial Proteins, Chromosomes, Bacterial, DNA-Binding Proteins, Anabaena, Chromosome Segregation, Escherichia coli Proteins
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