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Design and Evaluation of Synthetic Terminators for Regulating Mammalian Cell Transgene Expression.
Cheng, Joseph K; Morse, Nicholas J; Wagner, James M; Tucker, Scott K; Alper, Hal S.
Afiliação
  • Cheng JK; McKetta Department of Chemical Engineering , The University of Texas at Austin , 200 E Dean Keeton Street, Stop C0400 , Austin , Texas 78712 , United States.
  • Morse NJ; McKetta Department of Chemical Engineering , The University of Texas at Austin , 200 E Dean Keeton Street, Stop C0400 , Austin , Texas 78712 , United States.
  • Wagner JM; McKetta Department of Chemical Engineering , The University of Texas at Austin , 200 E Dean Keeton Street, Stop C0400 , Austin , Texas 78712 , United States.
  • Tucker SK; Institute for Cellular and Molecular Biology , The University of Texas at Austin , 2500 Speedway Avenue , Austin , Texas 78712 , United States.
  • Alper HS; McKetta Department of Chemical Engineering , The University of Texas at Austin , 200 E Dean Keeton Street, Stop C0400 , Austin , Texas 78712 , United States.
ACS Synth Biol ; 8(6): 1263-1275, 2019 06 21.
Article em En | MEDLINE | ID: mdl-31091408
ABSTRACT
Tuning heterologous gene expression in mammalian production hosts has predominantly relied upon engineering the promoter elements driving the transcription of the transgene. Moreover, most regulatory elements have borrowed genetic sequences from viral elements. Here, we generate a set of 10 rational and 30 synthetic terminators derived from nonviral elements and evaluate them in the HT1080 and HEK293 cell lines to demonstrate that they are comparable in terms of tuning gene expression/protein output to the viral SV40 element and often require less sequence footprint. The mode of action of these terminators is determined to be an increase in mRNA half-life. Furthermore, we demonstrate that constructs comprising completely nonviral regulatory elements ( i.e., promoters and terminators) can outperform commonly used, strong viral based elements by nearly 2-fold. Ultimately, this novel set of terminators expanded our genetic toolkit for engineering mammalian host cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Engenharia Genética / Regiões Promotoras Genéticas / Regiões Terminadoras Genéticas / Transgenes / Biologia Sintética Limite: Humans Idioma: En Revista: ACS Synth Biol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Engenharia Genética / Regiões Promotoras Genéticas / Regiões Terminadoras Genéticas / Transgenes / Biologia Sintética Limite: Humans Idioma: En Revista: ACS Synth Biol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos