doktorska disertacija
Maja Meško (Author), Mojca Benčina (Mentor), Igor Križaj (Thesis defence commission member)

Abstract

Umetno načrtovani transkripcijski dejavniki so pomembno orodje za specifično uravnavanje tarčnih genov v sintezni biologiji. Privlačen pristop za načrtovanje celičnih orodij za nadzor izražanja genov predstavljajo signalne poti na osnovi Ca2+, saj lahko vdor Ca2+ v celice sprožijo različni dražljaji. V okviru dela smo na osnovi signalne poti Ca2+-kalmodulin-kalcinevrin-NFAT razvili umetne transkripcijske dejavnike. Pri načrtovanju sintetičnih celičnih vezij je zelo pomembno, da z ustreznim načrtovanjem dosežemo nadzor nad aktivnostjo pripravljenih transkripcijskih dejavnikov, za katere želimo, da niso aktivni v odsotnosti stimulacijskega signala. Neželeno konstitutivno aktivnost NFAT v odsotnosti stimulacije smo znižali preko vpliva na lokalizacijo NFAT v celici. Pokazali smo, da z dodatkom signala za transport iz jedra NES ali preko fuzije s sidrnim peptidom KR? zmanjšamo prehajanje NFAT v jedro v odsotnosti stimulacije in tako znižamo neželeno konstitutivno transkripcijsko aktivnost. Večina v literaturi opisanih od Ca2+ odvisnih načrtovanih genskih vezij izkorišča endogeni NFAT, vendar je za optimalno delovanje sintetičnih vezij ključnega pomena, da le-ta delujejo neodvisno od endogenih procesov gostiteljske celice. Naš cilj je bil pripraviti umetne transkripcijske dejavnike, ki omogočajo ciljanje poljubnih tarčnih genov in hkrati ne vplivajo na izražanje endogenih genov v gostiteljski celici. Pripravili smo umetne transkripcijske dejavnike na osnovi regulatorne domene humanega ali mišjega NFAT in načrtovane DNA-vezavne domene efektorjev TAL ter potrdili, da aktivirajo transkripcijo poročevalskih genov v odvisnosti od znotrajcelične koncentracije Ca2+ v več vrstah sesalskih celic. Pomembna lastnost načrtovanih celičnih orodij je njihov odziv na fizikalno-kemijske signale, kar omogoča zunanji nadzor celičnih procesov. Ultrazvok omogoča natančno fokusiranje signala in je bil že uporabljen za stimulacijo mehansko občutljivih ionskih kanalov. V okviru dela smo razvili metodo za stimulacijo sesalskih celic z ultrazvokom in pokazali, da lahko z ultrazvokom aktiviramo pripravljene transkripcijske dejavnike v sesalskih celičnih linijah in poskusnih živalih, v katere smo vnesli predhodno pripravljene celice. Razvita metoda stimulacije sesalskih celic z ultrazvokom zaradi neinvazivnosti in sposobnosti prodiranja globoko v tkiva predstavlja inovativen način stimulacije s potencialom za terapevtsko uporabo.

Keywords

molekularna biologija;

Data

Language: Slovenian
Year of publishing:
Typology: 2.08 - Doctoral Dissertation
Organization: UL MF - Faculty of Medicine
Publisher: [M. Meško]
UDC: 577
COBISS: 37244931 Link will open in a new window
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Downloads: 207
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Other data

Secondary language: English
Secondary title: Transcriptional regulation by designed calcium-dependent transcription factors
Secondary abstract: Calcium signaling represents an attractive regulatory mechanism for use in engineered biological circuits, as the influx of calcium ions into cells can be triggered by a plethora of chemical and physical signals. Engineered calcium-dependent transcription factors, presented in this work, are based on the family of transcription factors NFAT. Their activity is regulated by the calcium/calmodulin-dependent phosphatase calcineurin which controls the translocation of NFAT proteins from the cytoplasm to the nucleus. Since tight regulation of each component of a synthetic cellular circuit is crucial for robust functioning of such systems, we prepared engineered NFAT variants with modified and controlled subcellular localization properties. This enabled potent NFAT activity while maintaining robust activation control. Undesired NFAT activity in the absence of stimulation was shown to be reduced both by insertion of additional nuclear export signal (NES) or via fusion of the synthetic membrane anchor peptide KRɸ to the transcription factor. Most synthetic calcium-dependent gene circuits use the endogenous NFAT signaling pathway for signal transduction. For incorporation of NFAT signaling into a controllable synthetic genetic circuit, it is crucial for the system to function independently of endogenous cell processes. For this reason, we prepared artificial transcription factors in which the native human or murine NFAT DNA-binding domain was replaced with a designed TALE DNA-binding domain, allowing targeting of specific DNA regulatory regions, and the VP16 or VP64 activation domain, allowing transcription upregulation of downstream genes. Replacement of the DNA-binding domain allows targeting of selected target genes while at the same time eliminates off-target activation of NFAT promoter-driven gene expression. This replacement ensured efficient calcium-dependent activation of target transgene expression in several mammalian cell lines. The possibility of external control of cell-signaling pathways through various physicochemical signals is an important feature of synthetic biological circuits, as it allows non-invasive control of cellular processes. Ultrasound represents a signal which can be highly spatio-temporally controlled and has been previously shown to stimulate mechanosensitive ion channels. In the present work, we developed a method for stimulation of mammalian cells with ultrasound and showed that ultrasonic waves can trigger the activation of engineered Ca2+-dependent transcription factors in cell lines as well as in experimental animals. The developed method of ultrasound stimulation represents an innovative approach for control of engineered biologic circuits due to its non-invasive properties and the ability to penetrate deep into tissues. In vivo applicability of the designed synthetic system underlines important potential use in therapeutic applications.
Secondary keywords: Gene expression;Molecular targeted therapy;Calcium signaling;Transcription factors;Regulatory elements, transcriptional;Calcium channels;Cells;Ultrasonics;Animal experimentation;Synthetic biology;Gensko izražanje;Molekularna tarčna terapija;Kalcijevo signaliziranje;Transkripcijski faktorji;Elementi uravnavanja transkripcije;Kalcijevi kanalčki;Celice;Ultrazvok;Poskusi na živalih;Sintezna biologija;
Type (COBISS): Dissertation
Study programme: 0
Embargo end date (OpenAIRE): 1970-01-01
Thesis comment: Univ. v Ljubljani, Medicinska fak.
Pages: XII, 85 f.
ID: 12078838