Literature DB >> 23654277

A genome-wide activity assessment of terminator regions in Saccharomyces cerevisiae provides a ″terminatome″ toolbox.

Mamoru Yamanishi1, Yoichiro Ito, Reiko Kintaka, Chie Imamura, Satoshi Katahira, Akinori Ikeuchi, Hisao Moriya, Takashi Matsuyama.   

Abstract

The terminator regions of eukaryotes encode functional elements in the 3' untranslated region (3'-UTR) that influence the 3'-end processing of mRNA, mRNA stability, and translational efficiency, which can modulate protein production. However, the contribution of these terminator regions to gene expression remains unclear, and therefore their utilization in metabolic engineering or synthetic genetic circuits has been limited. Here, we comprehensively evaluated the activity of 5302 terminator regions from a total of 5880 genes in the budding yeast Saccharomyces cerevisiae by inserting each terminator region downstream of the P TDH3 - green fluorescent protein (GFP) reporter gene and measuring the fluorescent intensity of GFP. Terminator region activities relative to that of the PGK1 standard terminator ranged from 0.036 to 2.52, with a mean of 0.87. We thus could isolate the most and least active terminator regions. The activities of the terminator regions showed a positive correlation with mRNA abundance, indicating that the terminator region is a determinant of mRNA abundance. The least active terminator regions tended to encode longer 3'-UTRs, suggesting the existence of active degradation mechanisms for those mRNAs. The terminator regions of ribosomal protein genes tended to be the most active, suggesting the existence of a common regulator of those genes. The ″terminatome″ (the genome-wide set of terminator regions) thus not only provides valuable information to understand the modulatory roles of terminator regions on gene expression but also serves as a useful toolbox for the development of metabolically and genetically engineered yeast.

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Year:  2013        PMID: 23654277     DOI: 10.1021/sb300116y

Source DB:  PubMed          Journal:  ACS Synth Biol        ISSN: 2161-5063            Impact factor:   5.110


  27 in total

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Journal:  World J Microbiol Biotechnol       Date:  2016-11-30       Impact factor: 3.312

3.  Use of expression-enhancing terminators in Saccharomyces cerevisiae to increase mRNA half-life and improve gene expression control for metabolic engineering applications.

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4.  The Mitotic Exit Network Regulates Spindle Pole Body Selection During Sporulation of Saccharomyces cerevisiae.

Authors:  Christian Renicke; Ann-Katrin Allmann; Anne Pia Lutz; Thomas Heimerl; Christof Taxis
Journal:  Genetics       Date:  2017-04-26       Impact factor: 4.562

5.  High-Titer Production of the Fungal Anhydrotetracycline, TAN-1612, in Engineered Yeasts.

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Review 7.  Technology development for natural product biosynthesis in Saccharomyces cerevisiae.

Authors:  John M Billingsley; Anthony B DeNicola; Yi Tang
Journal:  Curr Opin Biotechnol       Date:  2016-03-16       Impact factor: 9.740

8.  Challenges and advances in the heterologous expression of cellulolytic enzymes: a review.

Authors:  Camilla Lambertz; Megan Garvey; Johannes Klinger; Dirk Heesel; Holger Klose; Rainer Fischer; Ulrich Commandeur
Journal:  Biotechnol Biofuels       Date:  2014-10-18       Impact factor: 6.040

9.  Genetic circuit design automation for yeast.

Authors:  Ye Chen; Shuyi Zhang; Eric M Young; Timothy S Jones; Douglas Densmore; Christopher A Voigt
Journal:  Nat Microbiol       Date:  2020-08-03       Impact factor: 17.745

10.  Transcription interference and ORF nature strongly affect promoter strength in a reconstituted metabolic pathway.

Authors:  Marie Carquet; Denis Pompon; Gilles Truan
Journal:  Front Bioeng Biotechnol       Date:  2015-02-26
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