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Enhancing circuit stability under growth feedback with supplementary repressive regulation.
Stone, Austin; Rijal, Sadikshya; Zhang, Rong; Tian, Xiao-Jun.
Afiliação
  • Stone A; School of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ 85281, USA.
  • Rijal S; School of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ 85281, USA.
  • Zhang R; School of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ 85281, USA.
  • Tian XJ; School of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ 85281, USA.
Nucleic Acids Res ; 52(3): 1512-1521, 2024 Feb 09.
Article em En | MEDLINE | ID: mdl-38164993
ABSTRACT
The field of synthetic biology and biosystems engineering increasingly acknowledges the need for a holistic design approach that incorporates circuit-host interactions into the design process. Engineered circuits are not isolated entities but inherently entwined with the dynamic host environment. One such circuit-host interaction, 'growth feedback', results when modifications in host growth patterns influence the operation of gene circuits. The growth-mediated effects can range from growth-dependent elevation in protein/mRNA dilution rate to changes in resource reallocation within the cell, which can lead to complete functional collapse in complex circuits. To achieve robust circuit performance, synthetic biologists employ a variety of control mechanisms to stabilize and insulate circuit behavior against growth changes. Here we propose a simple strategy by incorporating one repressive edge in a growth-sensitive bistable circuit. Through both simulation and in vitro experimentation, we demonstrate how this additional repressive node stabilizes protein levels and increases the robustness of a bistable circuit in response to growth feedback. We propose the incorporation of repressive links in gene circuits as a control strategy for desensitizing gene circuits against growth fluctuations.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Redes Reguladoras de Genes / Biologia Sintética Idioma: En Revista: Nucleic Acids Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Redes Reguladoras de Genes / Biologia Sintética Idioma: En Revista: Nucleic Acids Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos