Translational Pausing Ensures Membrane Targeting and Cytoplasmic Splicing of XBP1u mRNA-Reference-Cited by-同舟云学术

Translational Pausing Ensures Membrane Targeting and Cytoplasmic Splicing of XBP1u mRNA

Published:2011-02-04 Issue:6017 Volume:331 Page:586-589
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Yanagitani Kota¹,Kimata Yukio¹,Kadokura Hiroshi¹,Kohno Kenji¹

Affiliation:

1. Laboratory of Molecular and Cell Genetics, Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5, Takayama, Ikoma, Nara 630-0192, Japan.

Abstract

A peptide-mediated translational pause facilitates the unconventional splicing of a messenger RNA on the endoplasmic reticulum.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference7 articles.

1. Cotranslational Targeting of XBP1 Protein to the Membrane Promotes Cytoplasmic Splicing of Its Own mRNA

2. XBP1 mRNA Is Induced by ATF6 and Spliced by IRE1 in Response to ER Stress to Produce a Highly Active Transcription Factor

3. IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA

4. Protein Folding during Cotranslational Translocation in the Endoplasmic Reticulum

5. Genetically Encoded but Nonpolypeptide Prolyl-tRNA Functions in the A Site for SecM-Mediated Ribosomal Stall

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