Uncovering Mechanisms of Bistability and Ultrasensitivity in Bacterial Stress Response

dc.contributor.advisorIgoshin, Oleg A.en_US
dc.contributor.committeeMemberNakhleh, Luay K.en_US
dc.contributor.committeeMemberQutub, Amina A.en_US
dc.contributor.committeeMemberBalazsi, Gaboren_US
dc.creatorTiwari, Abhinaven_US
dc.date.accessioned2014-10-14T14:59:37Zen_US
dc.date.available2014-10-14T14:59:37Zen_US
dc.date.created2013-12en_US
dc.date.issued2013-11-26en_US
dc.date.submittedDecember 2013en_US
dc.date.updated2014-10-14T14:59:38Zen_US
dc.description.abstractBacteria have evolved optimized biochemical and genetic networks to sense diverse stimuli and implement appropriate dynamic responses. Despite the remarkable progress in experimental approaches and the increasingly common use of mathematical modeling, very few examples exist of general design principles that relate a network’s structure to its response. To improve this understanding we develop biochemically accurate models of networks that contain well-conserved regulatory modules, which allows us to make both specific and biologically-relevant predictions. First, we analyze the mycobacterial stress-response network which consists of the MprA/MprB two-component system and the alternative sigma factor Sig E. This network contains multiple positive feedback loops which may give rise to bistability, thereby making it a good candidate for controlling the mycobacterial persistence switch. We find that neither the positive autoregulation in the two-component system nor the Sig E-mediated feedback is sufficient to induce bistability. Nonetheless, including the post-translational regulation of SigE by RseA increases system’s effective cooperativity resulting in bistability. We predict that overexpression or deletion of RseA, the key element controlling the ultrasensitive response, can eliminate bistability. Second, we investigate how dynamical properties of a network with positive autoregulation are affected by additive or multiplicative coupling with another positive or negative feedback. We find that a network’s bistability range is positively correlated with its maximum open-loop gain and that both the quantities depend on the sign of feedback loops and the type of feedback coupling. Moreover, we show that addition of a positive feedback can decrease, whereas addition of a negative feedback can increase the bistability range. Third, we examine the mechanism of pulsing in Bacillus subtilis stress-response sigma factor Sig B. We determine that the concentration of anti-sigma factor RsbW must lie in an optimal range for pulsing. We also observe that pulsing occurs only above a phosphatase threshold, beyond which the amount of RsbW is insufficient to fully sequester its binding partners Sig B and anti-anti-sigma factor RsbV. Furthermore, we compare our simulation results with experimental data to show that the network encodes phosphatase burst size into Sig B pulses. We predict that genetic perturbations which disrupt the fine-tuning of RsbW concentration will curb pulsing.en_US
dc.format.mimetypeapplication/pdfen_US
dc.identifier.citationTiwari, Abhinav. "Uncovering Mechanisms of Bistability and Ultrasensitivity in Bacterial Stress Response." (2013) Diss., Rice University. <a href="https://hdl.handle.net/1911/77560">https://hdl.handle.net/1911/77560</a>.en_US
dc.identifier.urihttps://hdl.handle.net/1911/77560en_US
dc.language.isoengen_US
dc.rightsCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.en_US
dc.subjectMultiplicativeen_US
dc.subjectBimodalityen_US
dc.subjectLogarithmic gainen_US
dc.subjectOpen-loop gainen_US
dc.subjectDecoupling approximationen_US
dc.subjectRobustnessen_US
dc.subjectPulsingen_US
dc.subjectThresholden_US
dc.subjectTwo-component systemen_US
dc.subjectSigma factoren_US
dc.subjectFeedback loopsen_US
dc.subjectBistabilityen_US
dc.subjectUltrasensitivityen_US
dc.subjectStress-responseen_US
dc.subjectMolecular titrationen_US
dc.subjectProtein sequestrationen_US
dc.subjectCouplingen_US
dc.subjectAdditiveen_US
dc.titleUncovering Mechanisms of Bistability and Ultrasensitivity in Bacterial Stress Responseen_US
dc.typeThesisen_US
dc.type.materialTexten_US
thesis.degree.departmentBioengineeringen_US
thesis.degree.disciplineEngineeringen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophyen_US
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