Caulobase

Bibliography

Key papers

90 papers that shaped what is known about Caulobacter, 25 of them marked as landmarks. Titles, journals and years were copied from PubMed and Crossref records, not from memory, and each note says only what the abstract supports.

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  1. 1962

    Stove JL, Stanier RY Cellular Differentiation in Stalked Bacteria Nature 196:1189-1192

    Early study of cellular differentiation in stalked bacteria, cited by Shapiro et al. (1971) as one of the foundations of the Caulobacter model.

    landmarkOrigins of the modelPolar developmentdoi:10.1038/1961189a0

  2. 1964

    Poindexter JS Biological properties and classification of the Caulobacter group Bacteriol Rev 28:231-295

    Classic review describing the biological properties and classification of the caulobacter group of stalked bacteria.

    landmarkOrigins of the modelPolar developmentdoi:10.1128/br.28.3.231-295.1964PMID 14220656

  3. 1971

    Shapiro L, Agabian-Keshishian N, Bendis I Bacterial differentiation Science 173:884-892

    Proposed Caulobacter as a model for prokaryotic differentiation, defining in synchronous cultures a life cycle of sequential, polar morphological changes.

    landmarkOrigins of the modeldoi:10.1126/science.173.4000.884PMID 5572165

  4. 1977

    Evinger M, Agabian N Envelope-associated nucleoid from Caulobacter crescentus stalked and swarmer cells J Bacteriol 132:294-301

    Isolated envelope-associated nucleoids from stalked and swarmer cells and introduced a Ludox density-gradient method for preparing large quantities of synchronous cells.

    Origins of the modeldoi:10.1128/jb.132.1.294-301.1977PMID 334726

  5. 1977

    Osley MA, Newton A Mutational analysis of developmental control in Caulobacter crescentus Proc Natl Acad Sci U S A 74:124-128

    Conditional division mutants showed cell-cycle events form dependent pathways, with flagellin synthesis and stalk formation coupled to specific cell-cycle steps.

    Origins of the modelCell-cycle controldoi:10.1073/pnas.74.1.124PMID 264665

  6. 1981

    Poindexter JS The caulobacters: ubiquitous unusual bacteria Microbiol Rev 45:123-179

    Broad review of caulobacter biology, framing the group as ubiquitous yet unusual bacteria.

    Origins of the modelReviewsdoi:10.1128/mr.45.1.123-179.1981PMID 7012570

  7. 1982

    Purucker M, Bryan R, Amemiya K, Ely B, Shapiro L Isolation of a Caulobacter gene cluster specifying flagellum production by using nonmotile Tn5 insertion mutants Proc Natl Acad Sci U S A 79:6797-6801

    Used nonmotile Tn5 insertion mutants to clone the flaY/E/F/G flagellar gene cluster and showed it contains at least three promoters.

    Origins of the modelPolar developmentdoi:10.1073/pnas.79.22.6797PMID 16593248

  8. 1987

    Champer R, Dingwall A, Shapiro L Cascade regulation of Caulobacter flagellar and chemotaxis genes J Mol Biol 194:71-80

    Used the transposon promoter probe Tn5-VB32 to follow flagellar gene transcription, showing flagellar promoters are temporally regulated in the cell cycle.

    Polar developmentdoi:10.1016/0022-2836(87)90716-9PMID 3039148

  9. 1990

    Ramakrishnan G, Newton A FlbD of Caulobacter crescentus is a homologue of the NtrC (NRI) protein and activates sigma 54-dependent flagellar gene promoters Proc Natl Acad Sci U S A 87:2369-2373

    Showed FlbD is an NtrC-like activator that stimulates sigma 54-dependent promoters of late genes in the flagellar regulatory hierarchy.

    Polar developmentdoi:10.1073/pnas.87.6.2369PMID 2315326

  10. 1992

    Brun YV, Shapiro L A temporally controlled sigma-factor is required for polar morphogenesis and normal cell division in Caulobacter Genes Dev 6:2395-2408

    Showed sigma 54 (rpoN) is cell cycle-regulated and required for both stalk and flagellum biogenesis and for normal cell division.

    Polar developmentDivision & shapedoi:10.1101/gad.6.12a.2395PMID 1459461

  11. 1992

    Marczynski GT, Shapiro L Cell-cycle control of a cloned chromosomal origin of replication from Caulobacter crescentus J Mol Biol 226:959-977

    Isolated the chromosomal replication origin and showed an origin-based plasmid replicates with temporal control resembling the chromosome.

    Replication & segregationdoi:10.1016/0022-2836(92)91045-qPMID 1518064

  12. 1994

    Zweiger G, Marczynski G, Shapiro L A Caulobacter DNA methyltransferase that functions only in the predivisional cell J Mol Biol 235:472-485

    Identified CcrM, a GANTC adenine methyltransferase expressed only in predivisional cells; constitutive expression caused aberrant cells and extra initiation.

    landmarkDNA methylationdoi:10.1006/jmbi.1994.1007PMID 8289276

  13. 1995

    Hecht GB, Lane T, Ohta N, Sommer JM, Newton A An essential single domain response regulator required for normal cell division and differentiation in Caulobacter crescentus EMBO J 14:3915-3924

    Identified DivK, an essential single-domain response regulator phosphorylated by the PleC and DivJ kinases, required for normal division and differentiation.

    Phosphosignalling & proteolysisdoi:10.1002/j.1460-2075.1995.tb00063.xPMID 7664732

  14. 1995

    McAdams HH, Shapiro L Circuit simulation of genetic networks Science 269:650-656

    Proposed modeling genetic networks as circuits, illustrated with the phage lambda lysis-lysogeny decision, treating operons as logic elements with time delays.

    landmarkSystems & modellingdoi:10.1126/science.7624793PMID 7624793

  15. 1996

    Quardokus E, Din N, Brun YV Cell cycle regulation and cell type-specific localization of the FtsZ division initiation protein in Caulobacter Proc Natl Acad Sci U S A 93:6314-6319

    Showed FtsZ levels vary dramatically over the cell cycle and that after division only the stalked cell contains FtsZ.

    Division & shapedoi:10.1073/pnas.93.13.6314PMID 8692812

  16. 1996

    Quon KC, Marczynski GT, Shapiro L Cell cycle control by an essential bacterial two-component signal transduction protein Cell 84:83-93

    Identified CtrA, an essential response regulator that binds target promoters and controls cell division, stalk synthesis and cell cycle-regulated transcription.

    landmarkCell-cycle controlPhosphosignalling & proteolysisdoi:10.1016/s0092-8674(00)80995-2PMID 8548829

  17. 1997

    Bingle WH, Nomellini JF, Smit J Cell-surface display of a Pseudomonas aeruginosa strain K pilin peptide within the paracrystalline S-layer of Caulobacter crescentus Mol Microbiol 26:277-288

    Inserted a Pseudomonas pilin peptide at many sites in the S-layer protein RsaA, showing the S-layer can display epitope-size heterologous peptides.

    Applicationsdoi:10.1046/j.1365-2958.1997.5711932.xPMID 9383153

  18. 1997

    Domian IJ, Quon KC, Shapiro L Cell type-specific phosphorylation and proteolysis of a transcriptional regulator controls the G1-to-S transition in a bacterial cell cycle Cell 90:415-424

    Showed CtrA is controlled by cell type-specific phosphorylation and proteolysis, and that a stable, constitutively active CtrA blocks the G1-to-S transition.

    landmarkCell-cycle controlPhosphosignalling & proteolysisdoi:10.1016/s0092-8674(00)80502-4PMID 9267022

  19. 1997

    McAdams HH, Arkin A Stochastic mechanisms in gene expression Proc Natl Acad Sci U S A 94:814-819

    Simulations showed proteins are produced in random bursts from activated promoters, which can partition a cell population into different phenotypes.

    Systems & modellingdoi:10.1073/pnas.94.3.814PMID 9023339

  20. 1997

    Mohl DA, Gober JW Cell cycle-dependent polar localization of chromosome partitioning proteins in Caulobacter crescentus Cell 88:675-684

    Showed ParA and ParB localize to both poles of the predivisional cell after replication, with ParB binding DNA near the origin.

    landmarkReplication & segregationdoi:10.1016/s0092-8674(00)81910-8PMID 9054507

  21. 1997

    Shapiro L, Losick R Protein localization and cell fate in bacteria Science 276:712-718

    Review of how protein localization governs replication, segregation, cytokinesis and cell fate, using Caulobacter and Bacillus subtilis as paradigms.

    Reviewsdoi:10.1126/science.276.5313.712PMID 9115191

  22. 1998

    Jenal U, Fuchs T An essential protease involved in bacterial cell-cycle control EMBO J 17:5658-5669

    Showed the ClpXP protease is essential for viability and required for cell cycle-dependent CtrA degradation and the G1-to-S transition.

    Phosphosignalling & proteolysisCell-cycle controldoi:10.1093/emboj/17.19.5658PMID 9755166

  23. 1998

    McAdams HH, Arkin A Simulation of prokaryotic genetic circuits Annu Rev Biophys Biomol Struct 27:199-224

    Review arguing for molecular-level simulation of bacterial genetic circuits and signaling networks to identify their design principles.

    Systems & modellingReviewsdoi:10.1146/annurev.biophys.27.1.199PMID 9646867

  24. 1998

    Quon KC, Yang B, Domian IJ, Shapiro L, Marczynski GT Negative control of bacterial DNA replication by a cell cycle regulatory protein that binds at the chromosome origin Proc Natl Acad Sci U S A 95:120-125

    Showed CtrA binds five sites in the chromosome replication origin and represses replication in vivo, restricting initiation to the stalked cell.

    Cell-cycle controlReplication & segregationdoi:10.1073/pnas.95.1.120PMID 9419339

  25. 1999

    Jacobs C, Domian IJ, Maddock JR, Shapiro L Cell cycle-dependent polar localization of an essential bacterial histidine kinase that controls DNA replication and cell division Cell 97:111-120

    Identified CckA, an essential histidine kinase required for CtrA phosphorylation that localizes to a cell pole in S phase and disperses after division.

    landmarkPhosphosignalling & proteolysisCell-cycle controldoi:10.1016/s0092-8674(00)80719-9PMID 10199407

  26. 1999

    Wheeler RT, Shapiro L Differential localization of two histidine kinases controlling bacterial cell differentiation Mol Cell 4:683-694

    Showed the antagonistic kinases DivJ and PleC localize to opposite poles in a cell cycle-dependent manner, with PleC required for DivJ localization.

    Phosphosignalling & proteolysisdoi:10.1016/s1097-2765(00)80379-2PMID 10619016

  27. 2000

    Laub MT, McAdams HH, Feldblyum T, Fraser CM, Shapiro L Global analysis of the genetic network controlling a bacterial cell cycle Science 290:2144-2148

    Microarrays of synchronized cells identified 553 cell cycle-regulated genes (19% of the genome), about a quarter under direct or indirect CtrA control.

    landmarkCell-cycle controlGenome-wide studiesdoi:10.1126/science.290.5499.2144PMID 11118148

  28. 2000

    Skerker JM, Shapiro L Identification and cell cycle control of a novel pilus system in Caulobacter crescentus EMBO J 19:3223-3234

    Identified a pilus gene cluster including pilA and showed late, CtrA-regulated pilA transcription helps time pilus assembly.

    Polar developmentdoi:10.1093/emboj/19.13.3223PMID 10880436

  29. 2001

    Nierman WC, Feldblyum TV, Laub MT, Paulsen IT, Nelson KE, Eisen JA, et al. Complete genome sequence of Caulobacter crescentus Proc Natl Acad Sci U S A 98:4136-4141

    Reported the complete 4,016,942-bp single-chromosome genome (3,767 genes), noting an unusually large set of 105 two-component signaling proteins.

    landmarkGenomedoi:10.1073/pnas.061029298PMID 11259647

  30. 2002

    Laub MT, Chen SL, Shapiro L, McAdams HH Genes directly controlled by CtrA, a master regulator of the Caulobacter cell cycle Proc Natl Acad Sci U S A 99:4632-4637

    In vivo genomic binding analysis combined with expression data showed CtrA directly regulates at least 95 genes, including 14 regulatory genes.

    Cell-cycle controlGenome-wide studiesdoi:10.1073/pnas.062065699PMID 11930012

  31. 2002

    Shapiro L, McAdams HH, Losick R Generating and exploiting polarity in bacteria Science 298:1942-1946

    Review of how dynamic localization of signaling proteins, cytoskeletal proteins and chromosome regions generates and exploits bacterial polarity.

    Reviewsdoi:10.1126/science.1072163PMID 12471245

  32. 2003

    Ausmees N, Kuhn JR, Jacobs-Wagner C The bacterial cytoskeleton: an intermediate filament-like function in cell shape Cell 115:705-713

    Identified crescentin, an intermediate filament-like cytoskeletal protein required for the curved cell shape; without it cells grow as straight rods.

    landmarkDivision & shapedoi:10.1016/s0092-8674(03)00935-8PMID 14675535

  33. 2003

    McAdams HH, Shapiro L A bacterial cell-cycle regulatory network operating in time and space Science 301:1874-1877

    Perspective arguing that Caulobacter cell-cycle control combines transcriptional circuits with localized, nontranscriptional pathways under a few master regulators.

    landmarkCell-cycle controlSystems & modellingReviewsdoi:10.1126/science.1087694PMID 14512618

  34. 2004

    Holtzendorff J, Hung D, Brende P, Reisenauer A, Viollier PH, McAdams HH, et al. Oscillating global regulators control the genetic circuit driving a bacterial cell cycle Science 304:983-987

    Identified GcrA, a master regulator oscillating out of phase with CtrA, forming a circuit that drives cell-cycle progression and polar morphogenesis.

    landmarkCell-cycle controldoi:10.1126/science.1095191PMID 15087506

  35. 2004

    Paul R, Weiser S, Amiot NC, Chan C, Schirmer T, Giese B, et al. Cell cycle-dependent dynamic localization of a bacterial response regulator with a novel di-guanylate cyclase output domain Genes Dev 18:715-727

    Showed the response regulator PleD has a diguanylate cyclase output domain and is sequestered to the cell pole when activated by phosphorylation.

    Phosphosignalling & proteolysisdoi:10.1101/gad.289504PMID 15075296

  36. 2004

    Skerker JM, Laub MT Cell-cycle progression and the generation of asymmetry in Caulobacter crescentus Nat Rev Microbiol 2:325-337

    Review of cell-cycle progression and the generation of asymmetry in Caulobacter crescentus.

    Reviewsdoi:10.1038/nrmicro864PMID 15031731

  37. 2004

    Viollier PH, Thanbichler M, McGrath PT, West L, Meewan M, McAdams HH, et al. Rapid and sequential movement of individual chromosomal loci to specific subcellular locations during bacterial DNA replication Proc Natl Acad Sci U S A 101:9257-9262

    Imaged 112 chromosomal loci, showing each has a specific subcellular address in linear order and loci move sequentially there as they are replicated.

    Replication & segregationdoi:10.1073/pnas.0402606101PMID 15178755

  38. 2005

    Hottes AK, Shapiro L, McAdams HH DnaA coordinates replication initiation and cell cycle transcription in Caulobacter crescentus Mol Microbiol 58:1340-1353

    Showed DnaA acts as a global transcription factor, activating genes such as gcrA, ftsZ and podJ and coupling replication initiation to cell-cycle transcription.

    Cell-cycle controlReplication & segregationdoi:10.1111/j.1365-2958.2005.04912.xPMID 16313620

  39. 2005

    Hu P, Brodie EL, Suzuki Y, McAdams HH, Andersen GL Whole-genome transcriptional analysis of heavy metal stresses in Caulobacter crescentus J Bacteriol 187:8437-8449

    Transcriptional profiling of chromium, cadmium, selenium and uranium exposure found high uranium tolerance and oxidative-stress protection as the main response.

    ApplicationsStress responsesdoi:10.1128/jb.187.24.8437-8449.2005PMID 16321948

  40. 2005

    Skerker JM, Prasol MS, Perchuk BS, Biondi EG, Laub MT Two-component signal transduction pathways regulating growth and cell cycle progression in a bacterium: a system-level analysis PLoS Biol 3:e334

    Deletion of 106 two-component genes found 39 required for growth, cell cycle or morphogenesis; phosphotransfer profiling revealed the essential CenK-CenR pathway.

    Phosphosignalling & proteolysisdoi:10.1371/journal.pbio.0030334PMID 16176121

  41. 2006

    Biondi EG, Reisinger SJ, Skerker JM, Arif M, Perchuk BS, Ryan KR, et al. Regulation of the bacterial cell cycle by an integrated genetic circuit Nature 444:899-904

    Identified ChpT, an essential phosphotransferase in two CckA-initiated phosphorelays that phosphorylate and stabilize CtrA, closing a feedback loop through DivK.

    landmarkPhosphosignalling & proteolysisCell-cycle controldoi:10.1038/nature05321PMID 17136100

  42. 2006

    Collier J, Murray SR, Shapiro L DnaA couples DNA replication and the expression of two cell cycle master regulators EMBO J 25:346-356

    Showed DnaA activates gcrA transcription, linking replication initiation to the DnaA/GcrA/CtrA regulatory cascade that drives cell-cycle progression.

    landmarkCell-cycle controlDNA methylationdoi:10.1038/sj.emboj.7600927PMID 16395331

  43. 2006

    Iniesta AA, McGrath PT, Reisenauer A, McAdams HH, Shapiro L A phospho-signaling pathway controls the localization and activity of a protease complex critical for bacterial cell cycle progression Proc Natl Acad Sci U S A 103:10935-10940

    Showed unphosphorylated CpdR localizes ClpXP to the cell pole for CtrA degradation, while CckA-dependent CpdR phosphorylation prevents it.

    Phosphosignalling & proteolysisdoi:10.1073/pnas.0604554103PMID 16829582

  44. 2006

    Lam H, Schofield WB, Jacobs-Wagner C A landmark protein essential for establishing and perpetuating the polarity of a bacterial cell Cell 124:1011-1023

    Identified TipN, a new-pole landmark protein whose relocation at division orients polarity in the progeny; its loss causes pleiotropic polarity defects.

    Polar developmentdoi:10.1016/j.cell.2005.12.040PMID 16530047

  45. 2006

    McGrath PT, Iniesta AA, Ryan KR, Shapiro L, McAdams HH A dynamically localized protease complex and a polar specificity factor control a cell cycle master regulator Cell 124:535-547

    Showed ClpXP is dynamically localized and degrades CtrA at the cell pole, and identified RcdA, required for CtrA polar localization and degradation.

    landmarkPhosphosignalling & proteolysisCell-cycle controldoi:10.1016/j.cell.2005.12.033PMID 16469700

  46. 2006

    Thanbichler M, Shapiro L MipZ, a spatial regulator coordinating chromosome segregation with cell division in Caulobacter Cell 126:147-162

    Identified MipZ, a ParB-associated FtsZ inhibitor whose polar localization restricts Z-ring formation to midcell, coupling segregation to division.

    landmarkDivision & shapeReplication & segregationdoi:10.1016/j.cell.2006.05.038PMID 16839883

  47. 2006

    Tsang PH, Li G, Brun YV, Freund LB, Tang JX Adhesion of single bacterial cells in the micronewton range Proc Natl Acad Sci U S A 103:5764-5768

    Micromanipulation measured holdfast-mediated adhesion of single cells at 0.11-2.26 micronewtons, reported as the strongest biological adhesive measured.

    Polar developmentdoi:10.1073/pnas.0601705103PMID 16585522

  48. 2006

    Wagner JK, Setayeshgar S, Sharon LA, Reilly JP, Brun YV A nutrient uptake role for bacterial cell envelope extensions Proc Natl Acad Sci U S A 103:11772-11777

    Showed stalks take up and hydrolyze organic phosphate and contain PstS, arguing their long thin shape aids nutrient uptake in dilute environments.

    Polar developmentGrowth & physiologydoi:10.1073/pnas.0602047103PMID 16861302

  49. 2007

    Alvarez-Martinez CE, Lourenço RF, Baldini RL, Laub MT, Gomes SL The ECF sigma factor sigma(T) is involved in osmotic and oxidative stress responses in Caulobacter crescentus Mol Microbiol 66:1240-1255

    Showed the ECF sigma factor sigma T is needed to survive osmotic and oxidative stress and identified about 40 putative sigma T regulon members.

    Stress responsesdoi:10.1111/j.1365-2958.2007.06005.xPMID 17986185

  50. 2007

    Collier J, McAdams HH, Shapiro L A DNA methylation ratchet governs progression through a bacterial cell cycle Proc Natl Acad Sci U S A 104:17111-17116

    Showed promoter methylation state times dnaA and ctrA transcription, so replication-fork passage and late CcrM synthesis act as a ratchet on the cell cycle.

    DNA methylationCell-cycle controldoi:10.1073/pnas.0708112104PMID 17942674

  51. 2007

    Hillson NJ, Hu P, Andersen GL, Shapiro L Caulobacter crescentus as a whole-cell uranium biosensor Appl Environ Microbiol 73:7615-7621

    Engineered a urcA promoter-GFP reporter strain that detects micromolar uranium and distinguished contaminated from uncontaminated groundwater samples.

    Applicationsdoi:10.1128/aem.01566-07PMID 17905881

  52. 2007

    Laub MT, Shapiro L, McAdams HH Systems biology of Caulobacter Annu Rev Genet 41:429-441

    Review of the genetic network and the phosphosignaling, proteolysis and epigenetic mechanisms that control the Caulobacter cell cycle.

    ReviewsSystems & modellingdoi:10.1146/annurev.genet.41.110306.130346PMID 18076330

  53. 2007

    McGrath PT, Lee H, Zhang L, Iniesta AA, Hottes AK, Tan MH, et al. High-throughput identification of transcription start sites, conserved promoter motifs and predicted regulons Nat Biotechnol 25:584-592

    Tiled microarrays identified transcription start sites of 769 genes and 27 promoter motifs, used to predict regulons including stress responses.

    landmarkGenome-wide studiesdoi:10.1038/nbt1294PMID 17401361

  54. 2007

    Thanbichler M, Iniesta AA, Shapiro L A comprehensive set of plasmids for vanillate- and xylose-inducible gene expression in Caulobacter crescentus Nucleic Acids Res 35:e137

    Characterized a vanillate-inducible promoter and built a set of integrating and replicating vectors for gene expression and protein tagging.

    Applicationsdoi:10.1093/nar/gkm818PMID 17959646

  55. 2008

    Bowman GR, Comolli LR, Zhu J, Eckart M, Koenig M, Downing KH, et al. A polymeric protein anchors the chromosomal origin/ParB complex at a bacterial cell pole Cell 134:945-955

    Identified PopZ, a polymeric polar protein that binds ParB and anchors the segregated chromosome origins at the cell poles.

    landmarkReplication & segregationdoi:10.1016/j.cell.2008.07.015PMID 18805088

  56. 2008

    da Rocha RP, Paquola AC, Marques Mdo V, Menck CF, Galhardo RS Characterization of the SOS regulon of Caulobacter crescentus J Bacteriol 190:1209-1218

    Identified 37 LexA-dependent genes forming the SOS regulon and confirmed GTTCN7GTTC as the SOS operator.

    Stress responsesdoi:10.1128/jb.01419-07PMID 18083815

  57. 2008

    Ebersbach G, Briegel A, Jensen GJ, Jacobs-Wagner C A self-associating protein critical for chromosome attachment, division, and polar organization in caulobacter Cell 134:956-968

    Showed PopZ is a self-associating polar hub that captures ParB-ori complexes and mediates polar localization of CckA and DivJ.

    landmarkReplication & segregationDivision & shapedoi:10.1016/j.cell.2008.07.016PMID 18805089

  58. 2008

    Lesley JA, Shapiro L SpoT regulates DnaA stability and initiation of DNA replication in carbon-starved Caulobacter crescentus J Bacteriol 190:6867-6880

    Showed carbon starvation raises (p)ppGpp via SpoT, which is required for DnaA proteolysis and for blocking replication initiation in starved swarmer cells.

    Stress responsesReplication & segregationdoi:10.1128/jb.00700-08PMID 18723629

  59. 2008

    Li S, Brazhnik P, Sobral B, Tyson JJ A quantitative study of the division cycle of Caulobacter crescentus stalked cells PLoS Comput Biol 4:e9

    Built a quantitative model of the stalked-cell cycle based on CtrA, GcrA and DnaA that reproduces wild-type protein time courses and many mutant phenotypes.

    Systems & modellingCell-cycle controldoi:10.1371/journal.pcbi.0040009PMID 18225942

  60. 2008

    Shen X, Collier J, Dill D, Shapiro L, Horowitz M, McAdams HH Architecture and inherent robustness of a bacterial cell-cycle control system Proc Natl Acad Sci U S A 105:11340-11345

    Built a hybrid simulation of cell-cycle control and used formal model checking to show it is robust to stochastic variation and nutrient starvation.

    Systems & modellingCell-cycle controldoi:10.1073/pnas.0805258105PMID 18685108

  61. 2008

    Toro E, Hong SH, McAdams HH, Shapiro L Caulobacter requires a dedicated mechanism to initiate chromosome segregation Proc Natl Acad Sci U S A 105:15435-15440

    Showed the parS site is where segregation force is exerted via the essential ParABS system, independent of its position on the chromosome.

    Replication & segregationdoi:10.1073/pnas.0807448105PMID 18824683

  62. 2009

    Duerig A, Abel S, Folcher M, Nicollier M, Schwede T, Amiot N, et al. Second messenger-mediated spatiotemporal control of protein degradation regulates bacterial cell cycle progression Genes Dev 23:93-104

    Showed c-di-GMP promotes CtrA degradation through the effector PopA, which localizes to the old pole and recruits CtrA via RcdA.

    Phosphosignalling & proteolysisdoi:10.1101/gad.502409PMID 19136627

  63. 2009

    Shapiro L, McAdams HH, Losick R Why and how bacteria localize proteins Science 326:1225-1228

    Review of how and why bacteria deploy proteins to specific subcellular locations in step with the organized deployment of the chromosome.

    Reviewsdoi:10.1126/science.1175685PMID 19965466

  64. 2009

    Werner JN, Chen EY, Guberman JM, Zippilli AR, Irgon JJ, Gitai Z Quantitative genome-scale analysis of protein localization in an asymmetric bacterium Proc Natl Acad Sci U S A 106:7858-7863

    Built a high-throughput fluorescent-fusion imaging pipeline that identified nearly 300 localized proteins, a genome-scale localization map.

    Systems & modellingGenome-wide studiesdoi:10.1073/pnas.0901781106PMID 19416866

  65. 2010

    Christen B, Fero MJ, Hillson NJ, Bowman G, Hong SH, Shapiro L, et al. High-throughput identification of protein localization dependency networks Proc Natl Acad Sci U S A 107:4681-4686

    Automated imaging of 854 transposon mutants identified genes affecting localization of PleC, DivJ and CpaE, mapping localization dependency networks.

    Systems & modellingGenome-wide studiesdoi:10.1073/pnas.1000846107PMID 20176934

  66. 2010

    Curtis PD, Brun YV Getting in the loop: regulation of development in Caulobacter crescentus Microbiol Mol Biol Rev 74:13-41

    Review of Caulobacter development, emphasizing how multiple processes are integrated and coordinated in space and time.

    ReviewsPolar developmentdoi:10.1128/mmbr.00040-09PMID 20197497

  67. 2010

    Gora KG, Tsokos CG, Chen YE, Srinivasan BS, Perchuk BS, Laub MT A cell-type-specific protein-protein interaction modulates transcriptional activity of a master regulator in Caulobacter crescentus Mol Cell 39:455-467

    Identified SciP, a small protein that accumulates in G1 and binds CtrA to inhibit activation of its target genes without affecting CtrA stability or phosphorylation.

    Cell-cycle controldoi:10.1016/j.molcel.2010.06.024PMID 20598601

  68. 2010

    Herrou J, Foreman R, Fiebig A, Crosson S A structural model of anti-anti-σ inhibition by a two-component receiver domain: the PhyR stress response regulator Mol Microbiol 78:290-304

    Placed PhyR genetically in the sigma T/NepR general stress pathway and solved its crystal structure, proposing a model of anti-anti-sigma regulation.

    Stress responsesdoi:10.1111/j.1365-2958.2010.07323.xPMID 20735776

  69. 2010

    Marks ME, Castro-Rojas CM, Teiling C, Du L, Kapatral V, Walunas TL, et al. The genetic basis of laboratory adaptation in Caulobacter crescentus J Bacteriol 192:3678-3688

    Whole-genome sequencing mapped the polymorphisms at five loci underlying phenotypic differences between strain CB15 and its lab-adapted derivative NA1000.

    Genomedoi:10.1128/jb.00255-10PMID 20472802

  70. 2010

    Ptacin JL, Lee SF, Garner EC, Toro E, Eckart M, Comolli LR, et al. A spindle-like apparatus guides bacterial chromosome segregation Nat Cell Biol 12:791-798

    Showed ParA forms linear polymers that ParB destabilizes, proposing a burnt-bridge Brownian ratchet for segregation, with TipN keeping it directional.

    landmarkReplication & segregationdoi:10.1038/ncb2083PMID 20657594

  71. 2010

    Tan MH, Kozdon JB, Shen X, Shapiro L, McAdams HH An essential transcription factor, SciP, enhances robustness of Caulobacter cell cycle regulation Proc Natl Acad Sci U S A 107:18985-18990

    Showed SciP is an essential DNA-binding transcription factor forming an incoherent feedforward loop with CtrA that regulates at least 58 genes.

    Cell-cycle controldoi:10.1073/pnas.1014395107PMID 20956288

  72. 2011

    Boutte CC, Crosson S The complex logic of stringent response regulation in Caulobacter crescentus: starvation signalling in an oligotrophic environment Mol Microbiol 80:695-714

    Defined the input logic and transcriptional output of the stringent response; the sole Rsh enzyme SpoT binds the ribosome and needs amino-acid starvation to act.

    Stress responsesdoi:10.1111/j.1365-2958.2011.07602.xPMID 21338423

  73. 2011

    Christen B, Abeliuk E, Collier JM, Kalogeraki VS, Passarelli B, Coller JA, et al. The essential genome of a bacterium Mol Syst Biol 7:528

    Hyper-saturated Tn-seq defined 1,012 essential genome features at 8-bp resolution, including 480 ORFs, 402 regulatory sequences and 130 non-coding elements.

    landmarkGenome-wide studiesdoi:10.1038/msb.2011.58PMID 21878915

  74. 2011

    Goley ED, Yeh YC, Hong SH, Fero MJ, Abeliuk E, McAdams HH, et al. Assembly of the Caulobacter cell division machine Mol Microbiol 80:1680-1698

    Used synchronized cells to determine the order in which divisome components arrive at the division site, with high temporal resolution.

    Division & shapedoi:10.1111/j.1365-2958.2011.07677.xPMID 21542856

  75. 2011

    McAdams HH, Shapiro L The architecture and conservation pattern of whole-cell control circuitry J Mol Biol 409:28-35

    Review arguing that the cell-cycle control circuitry is co-conserved across alphaproteobacteria and optimized for robust whole-cell operation.

    ReviewsSystems & modellingdoi:10.1016/j.jmb.2011.02.041PMID 21371478

  76. 2011

    Modell JW, Hopkins AC, Laub MT A DNA damage checkpoint in Caulobacter crescentus inhibits cell division through a direct interaction with FtsW Genes Dev 25:1328-1343

    Showed DNA damage induces the SOS regulon and inhibits CtrA, and that the SOS-induced protein SidA delays division by binding FtsW.

    Stress responsesDivision & shapedoi:10.1101/gad.2038911PMID 21685367

  77. 2011

    Tsokos CG, Perchuk BS, Laub MT A dynamic complex of signaling proteins uses polar localization to regulate cell-fate asymmetry in Caulobacter crescentus Dev Cell 20:329-341

    Showed the unorthodox kinase DivL promotes CckA activity while phosphorylated DivK inhibits CckA by binding DivL, with polar localization protecting CckA.

    Phosphosignalling & proteolysisdoi:10.1016/j.devcel.2011.01.007PMID 21397844

  78. 2013

    Kozdon JB, Melfi MD, Luong K, Clark TA, Boitano M, Wang S, et al. Global methylation state at base-pair resolution of the Caulobacter genome throughout the cell cycle Proc Natl Acad Sci U S A 110:E4658-E4667

    SMRT sequencing tracked 4,515 GANTC sites through the cell cycle, finding 27 persistently unmethylated sites and 59 candidate epigenetically regulated genes.

    DNA methylationGenome-wide studiesdoi:10.1073/pnas.1319315110PMID 24218615

  79. 2013

    Le TB, Imakaev MV, Mirny LA, Laub MT High-resolution mapping of the spatial organization of a bacterial chromosome Science 342:731-734

    Used Hi-C to show the chromosome is organized into multiple stable spatial domains, with HU and SMC promoting compaction and arm colinearity.

    landmarkReplication & segregationGenome-wide studiesdoi:10.1126/science.1242059PMID 24158908

  80. 2014

    Campos M, Surovtsev IV, Kato S, Paintdakhi A, Beltran B, Ebmeier SE, et al. A constant size extension drives bacterial cell size homeostasis Cell 159:1433-1446

    Showed E. coli and C. crescentus maintain size homeostasis by adding a constant size between divisions rather than dividing at a critical size.

    Growth & physiologydoi:10.1016/j.cell.2014.11.022PMID 25480302

  81. 2014

    Childers WS, Xu Q, Mann TH, Mathews II, Blair JA, Deacon AM, et al. Cell fate regulation governed by a repurposed bacterial histidine kinase PLoS Biol 12:e1001979

    Crystal structure and biochemistry showed the pseudokinase DivL preferentially binds phosphorylated DivK, repurposing kinase domains as a regulator sensor.

    Phosphosignalling & proteolysisdoi:10.1371/journal.pbio.1001979PMID 25349992

  82. 2014

    Fumeaux C, Radhakrishnan SK, Ardissone S, Théraulaz L, Frandi A, Martins D, et al. Cell cycle transition from S-phase to G1 in Caulobacter is mediated by ancestral virulence regulators Nat Commun 5:4081

    Identified MucR1/2, zinc-finger regulators related to alphaproteobacterial virulence regulators, as part of a module directing the S-to-G1 transcriptional switch.

    Cell-cycle controldoi:10.1038/ncomms5081PMID 24939058

  83. 2014

    Iyer-Biswas S, Wright CS, Henry JT, Lo K, Burov S, Lin Y, et al. Scaling laws governing stochastic growth and division of single bacterial cells Proc Natl Acad Sci U S A 111:15912-15917

    Single-cell measurements showed exponential growth and division at a critical size multiple (about 1.8), with distributions collapsing onto universal curves.

    Growth & physiologydoi:10.1073/pnas.1403232111PMID 25349411

  84. 2014

    Schrader JM, Zhou B, Li GW, Lasker K, Childers WS, Williams B, et al. The coding and noncoding architecture of the Caulobacter crescentus genome PLoS Genet 10:e1004463

    Combined RNA-seq, 5'-RACE, ribosome profiling and proteomics to map transcripts and coding regions; most start codons lack Shine-Dalgarno sites.

    Genome-wide studiesdoi:10.1371/journal.pgen.1004463PMID 25078267

  85. 2015

    Lori C, Ozaki S, Steiner S, Böhm R, Abel S, Dubey BN, et al. Cyclic di-GMP acts as a cell cycle oscillator to drive chromosome replication Nature 523:236-239

    Showed c-di-GMP levels oscillate in the cell cycle and that c-di-GMP binds CckA, switching it from kinase to phosphatase to allow replication initiation.

    landmarkCell-cycle controlPhosphosignalling & proteolysisdoi:10.1038/nature14473PMID 25945741

  86. 2015

    Zhou B, Schrader JM, Kalogeraki VS, Abeliuk E, Dinh CB, Pham JQ, et al. The global regulatory architecture of transcription during the Caulobacter cell cycle PLoS Genet 11:e1004831

    Mapped 2,726 transcription start sites through the cell cycle, finding 586 cell cycle-regulated and 529 binding sites for the master regulators.

    Cell-cycle controlGenome-wide studiesdoi:10.1371/journal.pgen.1004831PMID 25569173

  87. 2016

    Collier J Cell cycle control in Alphaproteobacteria Curr Opin Microbiol 30:107-113

    Review of conserved cell-cycle regulators and signals such as c-di-GMP and (p)ppGpp in Alphaproteobacteria, building on Caulobacter work.

    Reviewsdoi:10.1016/j.mib.2016.01.010PMID 26871482

  88. 2016

    Lasker K, Schrader JM, Men Y, Marshik T, Dill DL, McAdams HH, et al. CauloBrowser: A systems biology resource for Caulobacter crescentus Nucleic Acids Res 44:D640-D645

    Introduced CauloBrowser, an online resource integrating expression, essentiality, localization and methylation datasets for Caulobacter.

    Genome-wide studiesdoi:10.1093/nar/gkv1050PMID 26476443

  89. 2017

    Ellison CK, Kan J, Dillard RS, Kysela DT, Ducret A, Berne C, et al. Obstruction of pilus retraction stimulates bacterial surface sensing Science 358:535-538

    Showed pili stop retracting upon surface contact and that obstructing retraction alone triggers holdfast synthesis, revealing a surface-sensing mechanism.

    Polar developmentdoi:10.1126/science.aan5706PMID 29074778

  90. 2020

    Lasker K, von Diezmann L, Zhou X, Ahrens DG, Mann TH, Moerner WE, et al. Selective sequestration of signalling proteins in a membraneless organelle reinforces the spatial regulation of asymmetry in Caulobacter crescentus Nat Microbiol 5:418-429

    Showed the PopZ polar microdomain selectively concentrates CckA, ChpT and CtrA and enhances phosphosignaling, producing a gradient of active CtrA.

    Phosphosignalling & proteolysisdoi:10.1038/s41564-019-0647-7PMID 31959967