Literature DB >> 18636526

Engineering mRNA stability in E. coli by the addition of synthetic hairpins using a 5' cassette system.

T A Carrier1, J D Keasling.   

Abstract

An expression system has been developed for the introduction of DNA cassettes into the region between the transcription and translation start sites of a gene of interest. This cassette system was used to engineer mRNA stability through the introduction of hairpins at the 5' end. A synthetic DNA cassette was designed so that the resulting mRNA hairpin would be positioned one nucleotide from the 5' mRNA end. The hairpin-containing mRNA exhibited a half-life 3 times that of the mRNA with no hairpin, resulting in increases in both mRNA and protein levels. These results indicate that it is possible to engineer mRNA stability as an additional means of controlling gene expression.

Entities:  

Year:  1997        PMID: 18636526     DOI: 10.1002/(SICI)1097-0290(19970805)55:3<577::AID-BIT16>3.0.CO;2-D

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  12 in total

1.  Coordinated, differential expression of two genes through directed mRNA cleavage and stabilization by secondary structures.

Authors:  C D Smolke; T A Carrier; J D Keasling
Journal:  Appl Environ Microbiol       Date:  2000-12       Impact factor: 4.792

Review 2.  Strategies for enhancing gene expression in Escherichia coli.

Authors:  Tomo Kondo; Shigehiko Yumura
Journal:  Appl Microbiol Biotechnol       Date:  2020-03-03       Impact factor: 4.813

3.  Efficiency of the synthetic self-splicing RiboJ ribozyme is robust to cis- and trans-changes in genetic background.

Authors:  Markéta Vlková; Bhargava Reddy Morampalli; Olin K Silander
Journal:  Microbiologyopen       Date:  2021-08       Impact factor: 3.139

4.  Ribozyme-based insulator parts buffer synthetic circuits from genetic context.

Authors:  Chunbo Lou; Brynne Stanton; Ying-Ja Chen; Brian Munsky; Christopher A Voigt
Journal:  Nat Biotechnol       Date:  2012-10-03       Impact factor: 54.908

5.  Tuning promoter strength through RNA polymerase binding site design in Escherichia coli.

Authors:  Robert C Brewster; Daniel L Jones; Rob Phillips
Journal:  PLoS Comput Biol       Date:  2012-12-13       Impact factor: 4.475

6.  Tunable genetic devices through simultaneous control of transcription and translation.

Authors:  Vittorio Bartoli; Grace A Meaker; Mario di Bernardo; Thomas E Gorochowski
Journal:  Nat Commun       Date:  2020-04-29       Impact factor: 14.919

7.  Non-Invasive Analysis of Recombinant mRNA Stability in Escherichia coli by a Combination of Transcriptional Inducer Wash-Out and qRT-PCR.

Authors:  Veronika Kucharova; Trine Aakvik Strand; Eivind Almaas; Adrian E Naas; Trygve Brautaset; Svein Valla
Journal:  PLoS One       Date:  2013-06-19       Impact factor: 3.240

8.  Antisense transcription as a tool to tune gene expression.

Authors:  Jennifer A N Brophy; Christopher A Voigt
Journal:  Mol Syst Biol       Date:  2016-01-14       Impact factor: 11.429

9.  Distinct and redundant functions of three homologs of RNase III in the cyanobacterium Synechococcus sp. strain PCC 7002.

Authors:  Gina C Gordon; Jeffrey C Cameron; Brian F Pfleger
Journal:  Nucleic Acids Res       Date:  2018-02-28       Impact factor: 16.971

10.  The genetic insulator RiboJ increases expression of insulated genes.

Authors:  Kalen P Clifton; Ethan M Jones; Sudip Paudel; John P Marken; Callan E Monette; Andrew D Halleran; Lidia Epp; Margaret S Saha
Journal:  J Biol Eng       Date:  2018-10-29       Impact factor: 4.355

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