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Redox-Dependent Condensation Of the Mycobacterial Nucleoid By WhiB4

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s00203-014-0953-7openalex-snapshot

Asymmetric cell division in Mycobacterium tuberculosis and its unique features

inferredcites →https://doi.org/10.1016/j.celrep.2015.12.056openalex-snapshot

Ergothioneine Maintains Redox and Bioenergetic Homeostasis Essential for Drug Susceptibility and Virulence of Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1016/j.celrep.2016.07.080openalex-snapshot

Mycobacterial WhiB6 Differentially Regulates ESX-1 and the Dos Regulon to Modulate Granuloma Formation and Virulence in Zebrafish

inferredcites →https://doi.org/10.1016/j.chom.2010.12.004openalex-snapshot

Virulence of Mycobacterium tuberculosis Depends on Lipoamide Dehydrogenase, a Member of Three Multienzyme Complexes

inferredcites →https://doi.org/10.1016/j.chom.2015.05.008openalex-snapshot

The Oxidative Stress Network of Mycobacterium tuberculosis Reveals Coordination between Radical Detoxification Systems

inferredcites →https://doi.org/10.1016/j.febslet.2006.04.026openalex-snapshot

Mycothiol‐dependent mycobacterial response to oxidative stress

inferredcites →https://doi.org/10.1016/j.jmb.2005.04.043openalex-snapshot

AFM Studies on the Role of the Protein RdgC in Bacterial DNA Recombination

inferredcites →https://doi.org/10.1016/j.mimet.2013.12.009openalex-snapshot

A new microarray platform for whole-genome expression profiling of Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1016/j.molcel.2012.04.027openalex-snapshot

Antibiotic-Induced Bacterial Cell Death Exhibits Physiological and Biochemical Hallmarks of Apoptosis

inferredcites →https://doi.org/10.1016/j.tube.2010.09.008openalex-snapshot

TubercuList – 10 years after

inferredcites →https://doi.org/10.1016/s0014-5793(02)03363-xopenalex-snapshot

HU: promoting or counteracting DNA compaction?

inferredcites →https://doi.org/10.1017/s1462399411002079openalex-snapshot

Redox homeostasis in mycobacteria: the key to tuberculosis control?

inferredcites →https://doi.org/10.1038/31159openalex-snapshot

Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence

inferredcites →https://doi.org/10.1038/nature12337openalex-snapshot

The Mycobacterium tuberculosis regulatory network and hypoxia

inferredcites →https://doi.org/10.1038/ncomms5124openalex-snapshot

Targeting Mycobacterium tuberculosis nucleoid-associated protein HU with structure-based inhibitors

inferredcites →https://doi.org/10.1038/ncomms5306openalex-snapshot

Isocitrate lyase mediates broad antibiotic tolerance in Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1038/nrmicro2261openalex-snapshot

Bacterial nucleoid-associated proteins, nucleoid structure and gene expression

inferredcites →https://doi.org/10.1038/s41598-017-03020-4openalex-snapshot

WhiB4 Regulates the PE/PPE Gene Family and is Essential for Virulence of Mycobacterium marinum

inferredcites →https://doi.org/10.1038/sj.emboj.7601414openalex-snapshot

Dynamic state of DNA topology is essential for genome condensation in bacteria

inferredcites →https://doi.org/10.1038/srep10333openalex-snapshot

The cytochrome bd-type quinol oxidase is important for survival of Mycobacterium smegmatis under peroxide and antibiotic-induced stress

inferredcites →https://doi.org/10.1038/srep27631openalex-snapshot

Cytochrome bd Displays Significant Quinol Peroxidase Activity

inferredcites →https://doi.org/10.1042/bj20101440openalex-snapshot

Mycobacterium tuberculosis WhiB1 is an essential DNA-binding protein with a nitric oxide-sensitive iron–sulfur cluster

inferredcites →https://doi.org/10.1046/j.1365-2249.1998.00554.xopenalex-snapshot

Differential potentiation of anti-mycobacterial activity and reactive nitrogen intermediate-producing ability of murine peritoneal macrophages activated by interferon-gamma (IFN-γ) and tumour necrosis factor-alpha (TNF-α)

inferredcites →https://doi.org/10.1046/j.1365-2958.1999.01656.xopenalex-snapshot

A DNA architectural protein couples cellular physiology and DNA topology in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01805.xopenalex-snapshot

Escherichia coli response to hydrogen peroxide: a role for DNA supercoiling, Topoisomerase I and Fis

inferredcites →https://doi.org/10.1046/j.1365-2958.2002.03095.xopenalex-snapshot

Nitric oxide scavenging and detoxification by the Mycobacterium tuberculosis haemoglobin, HbN in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03416.xopenalex-snapshot

Association of mycothiol with protection of Mycobacterium tuberculosis from toxic oxidants and antibiotics

inferredcites →https://doi.org/10.1073/pnas.0308230101openalex-snapshot

Dual architectural roles of HU: Formation of flexible hinges and rigid filaments

inferredcites →https://doi.org/10.1073/pnas.0505446102openalex-snapshot

Ancestral antibiotic resistance in Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1073/pnas.0506687102openalex-snapshot

Studies of the distribution of Escherichia coli cAMP-receptor protein and RNA polymerase along the E. coli chromosome

inferredcites →https://doi.org/10.1073/pnas.0700490104openalex-snapshot

Mycobacterium tuberculosis WhiB3 responds to O 2 and nitric oxide via its [4Fe-4S] cluster and is essential for nutrient starvation survival

inferredcites →https://doi.org/10.1073/pnas.0810126106openalex-snapshot

The multifunctional histone-like protein Lsr2 protects mycobacteria against reactive oxygen intermediates

inferredcites →https://doi.org/10.1073/pnas.1510932112openalex-snapshot

E1 of α-ketoglutarate dehydrogenase defends Mycobacterium tuberculosis against glutamate anaplerosis and nitroxidative stress

inferredcites →https://doi.org/10.1074/jbc.m115.684597openalex-snapshot

Mycobacterium tuberculosis WhiB3 Responds to Vacuolar pH-induced Changes in Mycothiol Redox Potential to Modulate Phagosomal Maturation and Virulence

inferredcites →https://doi.org/10.1074/jbc.m117.797563openalex-snapshot

Protein kinase G confers survival advantage to Mycobacterium tuberculosis during latency-like conditions

inferredcites →https://doi.org/10.1093/nar/gkq934openalex-snapshot

Direct and indirect effects of H-NS and Fis on global gene expression control in Escherichia coli

inferredcites →https://doi.org/10.1093/nar/gkr1236openalex-snapshot

Genomic analysis of DNA binding and gene regulation by homologous nucleoid-associated proteins IHF and HU in Escherichia coli K12

inferredcites →https://doi.org/10.1093/nar/gks014openalex-snapshot

The nucleoid-associated proteins H-NS and FIS modulate the DNA supercoiling response of the pel genes, the major virulence factors in the plant pathogen bacterium Dickeya dadantii

inferredcites →https://doi.org/10.1093/nar/gku548openalex-snapshot

Genomic mapping of cAMP receptor protein (CRPMt) inMycobacterium tuberculosis: relation to transcriptional start sites and the role of CRPMtas a transcription factor

inferredcites →https://doi.org/10.1097/inf.0b013e31815b494copenalex-snapshot

Susceptibility to Mycobacterial Infections in Children With X-Linked Chronic Granulomatous Disease

inferredcites →https://doi.org/10.1099/00221287-129-7-2315openalex-snapshot

Electron Microscopic Observations of Cell Division in Mycobacterium vaccae V1

inferredcites →https://doi.org/10.1099/00221287-148-10-3139openalex-snapshot

Oxidative stress response genes in Mycobacterium tuberculosis: role of ahpC in resistance to peroxynitrite and stage-specific survival in macrophages

inferredcites →https://doi.org/10.1099/mic.0.053702-0openalex-snapshot

Genetic and biochemical characteristics of the histone-like protein DR0199 in Deinococcus radiodurans

inferredcites →https://doi.org/10.1099/mic.0.28911-0openalex-snapshot

Mycobacterium smegmatis whmD and its homologue Mycobacterium tuberculosis whiB2 are functionally equivalent

inferredcites →https://doi.org/10.1101/gr.070276.107openalex-snapshot

Genome-wide analysis of Fis binding in Escherichia coli indicates a causative role for A-/AT-tracts

inferredcites →https://doi.org/10.1111/1574-6968.12598openalex-snapshot

Nucleoid compaction by MrgAAsp56Ala/Glu60Aladoes not contribute to staphylococcal cell survival against oxidative stress and phagocytic killing by macrophages

inferredcites →https://doi.org/10.1111/j.1365-2443.2006.00949.xopenalex-snapshot

Bacterial nucleoid dynamics: oxidative stress response in Staphylococcus aureus

inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06365.xopenalex-snapshot

Mycothiol biosynthesis is essential for ethionamide susceptibility in Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1111/j.1365-2958.2009.06848.xopenalex-snapshot

Streptomyces coelicolor Dps‐like proteins: differential dual roles in response to stress during vegetative growth and in nucleoid condensation during reproductive cell division

inferredcites →https://doi.org/10.1111/j.1365-2958.2012.08165.xopenalex-snapshot

Mycobacterium tuberculosis WhiB4 regulates oxidative stress response to modulate survival and dissemination in vivo

inferredcites →https://doi.org/10.1111/j.1462-5822.2009.01335.xopenalex-snapshot

Mycobacterial survival strategies in the phagosome: defence against host stresses

inferredcites →https://doi.org/10.1111/j.1742-4658.2012.08662.xopenalex-snapshot

WhiB2/Rv3260c, a cell division‐associated protein of Mycobacterium tuberculosis H37Rv, has properties of a chaperone

inferredcites →https://doi.org/10.1111/mmi.12981openalex-snapshot

Phylogeny to function: PE / PPE protein evolution and impact on M ycobacterium tuberculosis pathogenicity

inferredcites →https://doi.org/10.1128/aac.05874-11openalex-snapshot

Mechanisms of Action of Escapin, a Bactericidal Agent in the Ink Secretion of the Sea Hare Aplysia californica: Rapid and Long-Lasting DNA Condensation and Involvement of the OxyR-Regulated Oxidative Stress Pathway

inferredcites →https://doi.org/10.1128/br.41.1.217-372.1977openalex-snapshot

Mycobacterium

inferredcites →https://doi.org/10.1128/iai.06328-11openalex-snapshot

WhiB5, a Transcriptional Regulator That Contributes to Mycobacterium tuberculosis Virulence and Reactivation

inferredcites →https://doi.org/10.1128/iai.68.3.1231-1234.2000openalex-snapshot

Transient Loss of Resistance to Pulmonary Tuberculosis in p47phox−/−Mice

inferredcites →https://doi.org/10.1128/jb.00393-06openalex-snapshot

A Mycothiol Synthase Mutant of Mycobacterium tuberculosis Has an Altered Thiol-Disulfide Content and Limited Tolerance to Stress

inferredcites →https://doi.org/10.1128/jb.06184-11openalex-snapshot

Unveiling Unusual Features of Formation of Septal Partition and Constriction in Mycobacteria—an Ultrastructural Study

inferredcites →https://doi.org/10.1128/jb.179.16.5188-5194.1997openalex-snapshot

Protection of DNA during oxidative stress by the nonspecific DNA-binding protein Dps

inferredcites →https://doi.org/10.1128/mbio.01106-14openalex-snapshot

Mycobacterium tuberculosis Lsr2 Is a Global Transcriptional Regulator Required for Adaptation to Changing Oxygen Levels and Virulence

inferredcites →https://doi.org/10.1186/s12864-016-3190-4openalex-snapshot

Developmental transcriptome of resting cell formation in Mycobacterium smegmatis

inferredcites →https://doi.org/10.1371/journal.pcbi.1000216openalex-snapshot

Distinct Modes of Regulation by Chromatin Encoded through Nucleosome Positioning Signals

inferredcites →https://doi.org/10.1371/journal.pone.0001502openalex-snapshot

The Enduring Hypoxic Response of Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1371/journal.pone.0005150openalex-snapshot

Acute and Persistent Mycobacterium tuberculosis Infections Depend on the Thiol Peroxidase TPX

inferredcites →https://doi.org/10.1371/journal.ppat.1000545openalex-snapshot

Mycobacterium tuberculosis WhiB3 Maintains Redox Homeostasis by Regulating Virulence Lipid Anabolism to Modulate Macrophage Response

inferredcites →https://doi.org/10.1371/journal.ppat.1003902openalex-snapshot

Reengineering Redox Sensitive GFP to Measure Mycothiol Redox Potential of Mycobacterium tuberculosis during Infection

inferredcites →https://doi.org/10.1371/journal.ppat.1004839openalex-snapshot

A Redox Regulatory System Critical for Mycobacterial Survival in Macrophages and Biofilm Development

inferredcites →https://doi.org/10.1586/eri.12.90openalex-snapshot

WhiB7, a transcriptional activator that coordinates physiology with intrinsic drug resistance inMycobacterium tuberculosis

inferredcites →https://doi.org/10.3109/10520299509108199openalex-snapshot

DAPI: a DNA-Specific Fluorescent Probe

inferredcites →https://doi.org/10.3389/fmicb.2016.00947openalex-snapshot

Mild Nutrient Starvation Triggers the Development of a Small-Cell Survival Morphotype in Mycobacteria

inferredcites →https://doi.org/10.7554/elife.25624openalex-snapshot

Efficacy of β-lactam/β-lactamase inhibitor combination is linked to WhiB4-mediated changes in redox physiology of Mycobacterium tuberculosis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1093/femspd/fty036openalex-snapshot

Host-pathogen redox dynamics modulate Mycobacterium tuberculosis pathogenesis

inferred← citeshttps://doi.org/10.7554/elife.25624openalex-snapshot

Efficacy of β-lactam/β-lactamase inhibitor combination is linked to WhiB4-mediated changes in redox physiology of Mycobacterium tuberculosis

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