Literature DB >> 34985693

A Platform Technology for Monitoring the Unfolded Protein Response.

Bhagyashree Bachhav1, Carlos A Origel Marmolejo2, Yafet Arefeayne3, Laura Segatori4,5,6.   

Abstract

The unfolded protein response (UPR) is a complex signal transduction pathway that remodels gene expression in response to proteotoxic stress in the endoplasmic reticulum (ER) and is linked to the development of a range of diseases, including Alzheimer's disease, diabetes, and several types of cancer. UPR induction is typically monitored by measuring the expression level of UPR marker genes. Most tools for quantifying gene expression, including DNA microarrays and quantitative PCR with reverse transcription (RT-PCR), produce snapshots of the cell transcriptome, but are not ideal for measurements requiring temporal resolution of gene expression dynamics. Reporter assays for indirect detection of the UPR typically rely on extrachromosomal expression of reporters under the control of minimal or synthetic regulatory sequences that do not recapitulate the native chromosomal context of the UPR target genes. To address the need for tools to monitor chromosomal gene expression that recapitulate gene expression dynamics from the native chromosomal context and generate a readily detectable signal output, we developed a gene signal amplifier platform that links transcriptional and post-translational regulation of a fluorescent output to the expression of a chromosomal gene marker of the UPR. The platform is based on a genetic circuit that amplifies the output signal with high sensitivity and dynamic resolution and is implemented through chromosomal integration of the gene encoding the main control element of the genetic circuit to link its expression to that of the target gene, thereby generating a platform that can be easily adapted to monitor any UPR target through integration of the main control element at the appropriate chromosomal locus. By recapitulating the transcriptional and translational control mechanisms underlying the expression of UPR targets with high sensitivity, this platform provides a novel technology for monitoring the UPR with superior sensitivity and dynamic resolution.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  CRISPR-Cas9; ER stress; Gene signal amplifier; NanoDeg; Unfolded protein response (UPR)

Mesh:

Year:  2022        PMID: 34985693     DOI: 10.1007/978-1-0716-1732-8_4

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  38 in total

1.  XBP1 controls diverse cell type- and condition-specific transcriptional regulatory networks.

Authors:  Diego Acosta-Alvear; Yiming Zhou; Alexandre Blais; Mary Tsikitis; Nathan H Lents; Carolina Arias; Christen J Lennon; Yuval Kluger; Brian David Dynlacht
Journal:  Mol Cell       Date:  2007-07-06       Impact factor: 17.970

Review 2.  A review of the mammalian unfolded protein response.

Authors:  Anirikh Chakrabarti; Aaron W Chen; Jeffrey D Varner
Journal:  Biotechnol Bioeng       Date:  2011-08-09       Impact factor: 4.530

3.  Imaging of single cell responses to ER stress indicates that the relative dynamics of IRE1/XBP1 and PERK/ATF4 signalling rather than a switch between signalling branches determine cell survival.

Authors:  F Walter; J Schmid; H Düssmann; C G Concannon; J H M Prehn
Journal:  Cell Death Differ       Date:  2015-01-30       Impact factor: 15.828

4.  XBP1 activates the transcription of its target genes via an ACGT core sequence under ER stress.

Authors:  Soshi Kanemoto; Shinichi Kondo; Maiko Ogata; Tomohiko Murakami; Fumihiko Urano; Kazunori Imaizumi
Journal:  Biochem Biophys Res Commun       Date:  2005-06-17       Impact factor: 3.575

5.  Transcriptional activation of ATF6 by endoplasmic reticulum stressors.

Authors:  Takushi Namba; Tomoaki Ishihara; Ken-ichiro Tanaka; Tatsuya Hoshino; Tohru Mizushima
Journal:  Biochem Biophys Res Commun       Date:  2007-02-08       Impact factor: 3.575

Review 6.  The unfolded protein response: controlling cell fate decisions under ER stress and beyond.

Authors:  Claudio Hetz
Journal:  Nat Rev Mol Cell Biol       Date:  2012-01-18       Impact factor: 94.444

7.  Stress-independent activation of XBP1s and/or ATF6 reveals three functionally diverse ER proteostasis environments.

Authors:  Matthew D Shoulders; Lisa M Ryno; Joseph C Genereux; James J Moresco; Patricia G Tu; Chunlei Wu; John R Yates; Andrew I Su; Jeffery W Kelly; R Luke Wiseman
Journal:  Cell Rep       Date:  2013-04-11       Impact factor: 9.423

Review 8.  The X-box binding protein-1 transcription factor is required for plasma cell differentiation and the unfolded protein response.

Authors:  Neal N Iwakoshi; Ann-Hwee Lee; Laurie H Glimcher
Journal:  Immunol Rev       Date:  2003-08       Impact factor: 12.988

9.  Dependence of site-2 protease cleavage of ATF6 on prior site-1 protease digestion is determined by the size of the luminal domain of ATF6.

Authors:  Jingshi Shen; Ron Prywes
Journal:  J Biol Chem       Date:  2004-08-06       Impact factor: 5.157

10.  XBP1: a link between the unfolded protein response, lipid biosynthesis, and biogenesis of the endoplasmic reticulum.

Authors:  Rungtawan Sriburi; Suzanne Jackowski; Kazutoshi Mori; Joseph W Brewer
Journal:  J Cell Biol       Date:  2004-10-04       Impact factor: 10.539

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