Literature DB >> 18369985

Analysis of mRNA partitioning between the cytosol and endoplasmic reticulum compartments of mammalian cells.

Samuel B Stephens1, Rebecca D Dodd, Rachel S Lerner, Brook M Pyhtila, Christopher V Nicchitta.   

Abstract

All eukaryotic cells display a dramatic partitioning of mRNAs between the cytosol and endoplasmic reticulum (ER) compartments-mRNAs encoding secretory and integral membrane proteins are highly enriched on ER-bound ribosomes and mRNAs encoding cytoplasmic/nucleoplasmic proteins are enriched on cytosolic ribosomes. In current views, this partitioning phenomenon occurs through positive selection-mRNAs encoding signal sequence-bearing proteins are directed into the signal recognition particle pathway early in translation and trafficked as mRNA/ribosome/nascent polypeptide chain complexes to the ER. In the absence of an encoded signal sequence, mRNAs undergo continued translation on cytosolic ribosomes. Recent genome-wide analyses of mRNA partitioning between the cytosol and the ER compartments have identified subsets of mRNAs that are non-canonically partitioned to the ER-although lacking an encoded signal sequence, they are translated on ER-bound ribosomes. These findings suggest that multiple, and as yet unidentified, pathways exist for directing mRNA partitioning in the cell. In this contribution, we briefly review the literature describing the subcellular partitioning patterns of mRNAs and present a detailed methodology for studying this fundamental, yet poorly understood process.

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Year:  2008        PMID: 18369985     DOI: 10.1007/978-1-59745-033-1_14

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


  30 in total

1.  Primary role for endoplasmic reticulum-bound ribosomes in cellular translation identified by ribosome profiling.

Authors:  David W Reid; Christopher V Nicchitta
Journal:  J Biol Chem       Date:  2011-12-23       Impact factor: 5.157

Review 2.  DRiPs solidify: progress in understanding endogenous MHC class I antigen processing.

Authors:  Jonathan W Yewdell
Journal:  Trends Immunol       Date:  2011-09-29       Impact factor: 16.687

3.  Signal sequence- and translation-independent mRNA localization to the endoplasmic reticulum.

Authors:  Brook Pyhtila; Tianli Zheng; Patrick J Lager; Jack D Keene; Mary C Reedy; Christopher V Nicchitta
Journal:  RNA       Date:  2008-01-11       Impact factor: 4.942

4.  Chloroplast protein targeting involves localized translation in Chlamydomonas.

Authors:  James Uniacke; William Zerges
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-21       Impact factor: 11.205

5.  Multifunctional roles for the protein translocation machinery in RNA anchoring to the endoplasmic reticulum.

Authors:  Sujatha Jagannathan; Jack C-C Hsu; David W Reid; Qiang Chen; Will J Thompson; Arthur M Moseley; Christopher V Nicchitta
Journal:  J Biol Chem       Date:  2014-07-25       Impact factor: 5.157

6.  Dengue Virus Selectively Annexes Endoplasmic Reticulum-Associated Translation Machinery as a Strategy for Co-opting Host Cell Protein Synthesis.

Authors:  David W Reid; Rafael K Campos; Jessica R Child; Tianli Zheng; Kitti Wing Ki Chan; Shelton S Bradrick; Subhash G Vasudevan; Mariano A Garcia-Blanco; Christopher V Nicchitta
Journal:  J Virol       Date:  2018-03-14       Impact factor: 5.103

7.  Feature Article: mTOR complex 2-Akt signaling at mitochondria-associated endoplasmic reticulum membranes (MAM) regulates mitochondrial physiology.

Authors:  Charles Betz; Daniele Stracka; Cristina Prescianotto-Baschong; Maud Frieden; Nicolas Demaurex; Michael N Hall
Journal:  Proc Natl Acad Sci U S A       Date:  2013-07-12       Impact factor: 11.205

Review 8.  Diversity and selectivity in mRNA translation on the endoplasmic reticulum.

Authors:  David W Reid; Christopher V Nicchitta
Journal:  Nat Rev Mol Cell Biol       Date:  2015-03-04       Impact factor: 94.444

9.  OS-9 and GRP94 deliver mutant alpha1-antitrypsin to the Hrd1-SEL1L ubiquitin ligase complex for ERAD.

Authors:  John C Christianson; Thomas A Shaler; Ryan E Tyler; Ron R Kopito
Journal:  Nat Cell Biol       Date:  2008-02-10       Impact factor: 28.824

10.  Cytosolic N-GlcNAc proteins are formed by the action of endo-β-N-acetylglucosaminidase.

Authors:  Jason C Maynard; Haruhiko Fujihira; Gabby E Dolgonos; Tadashi Suzuki; Alma L Burlingame
Journal:  Biochem Biophys Res Commun       Date:  2020-08-08       Impact factor: 3.575

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