Literature DB >> 17979529

Unconventional splicing of XBP-1 mRNA in the unfolded protein response.

Hiderou Yoshida1.   

Abstract

Cytoplasmic splicing is one of the major regulatory mechanisms of the unfolded protein response (UPR). The molecular mechanism of cytoplasmic splicing is unique and completely different from that of conventional nuclear splicing. The mammalian substrate of cytoplasmic splicing is XBP1 pre-mRNA, which is converted to spliced mRNA in response to UPR, leading to the production of an active transcription factor [pXBP1(S)] responsible for UPR. Interestingly, XBP1 pre-mRNA is also translated into a functional protein [pXBP1(U)] that negatively regulates the UPR. Thus, mammalian cells can quickly adapt to a change in conditions in the endoplasmic reticulum by switching proteins encoded in the mRNA from a negative regulator to an activator. This elaborate system contributes to various cellular functions, including plasma cell differentiation, viral infections, and carcinogenesis. In this short review, I briefly summarize research on cytoplasmic splicing and focus on current hot topics.

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Year:  2007        PMID: 17979529     DOI: 10.1089/ars.2007.1800

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  46 in total

1.  The RtcB RNA ligase is an essential component of the metazoan unfolded protein response.

Authors:  Sara Guckian Kosmaczewski; Tyson James Edwards; Sung Min Han; Matthew J Eckwahl; Benjamin Isaiah Meyer; Sally Peach; Jay R Hesselberth; Sandra L Wolin; Marc Hammarlund
Journal:  EMBO Rep       Date:  2014-11-03       Impact factor: 8.807

2.  The alternative TrkAIII splice variant targets the centrosome and promotes genetic instability.

Authors:  Antonietta Rosella Farina; Antonella Tacconelli; Lucia Cappabianca; Gesilia Cea; Sonia Panella; Antonella Chioda; Alessandra Romanelli; Carlo Pedone; Alberto Gulino; Andrew Reay Mackay
Journal:  Mol Cell Biol       Date:  2009-06-29       Impact factor: 4.272

3.  Sustained production of spliced X-box binding protein 1 (XBP1) induces pancreatic beta cell dysfunction and apoptosis.

Authors:  F Allagnat; F Christulia; F Ortis; P Pirot; S Lortz; S Lenzen; D L Eizirik; A K Cardozo
Journal:  Diabetologia       Date:  2010-03-29       Impact factor: 10.122

4.  Expression of XBP1s in bone marrow stromal cells is critical for myeloma cell growth and osteoclast formation.

Authors:  Guoshuang Xu; Kai Liu; Judy Anderson; Kenneth Patrene; Suzanne Lentzsch; G David Roodman; Hongjiao Ouyang
Journal:  Blood       Date:  2012-03-16       Impact factor: 22.113

Review 5.  Endoplasmic reticulum stress, the unfolded protein response, autophagy, and the integrated regulation of breast cancer cell fate.

Authors:  Robert Clarke; Katherine L Cook; Rong Hu; Caroline O B Facey; Iman Tavassoly; Jessica L Schwartz; William T Baumann; John J Tyson; Jianhua Xuan; Yue Wang; Anni Wärri; Ayesha N Shajahan
Journal:  Cancer Res       Date:  2012-03-15       Impact factor: 12.701

Review 6.  The promiscuous life of plant NUCLEAR FACTOR Y transcription factors.

Authors:  Katia Petroni; Roderick W Kumimoto; Nerina Gnesutta; Valentina Calvenzani; Monica Fornari; Chiara Tonelli; Ben F Holt; Roberto Mantovani
Journal:  Plant Cell       Date:  2012-12-28       Impact factor: 11.277

Review 7.  The role of X-box binding protein-1 in tumorigenicity.

Authors:  Ayesha N Shajahan; Rebecca B Riggins; Robert Clarke
Journal:  Drug News Perspect       Date:  2009-06

8.  Functional relationship between protein disulfide isomerase family members during the oxidative folding of human secretory proteins.

Authors:  Lori A Rutkevich; Myrna F Cohen-Doyle; Ulf Brockmeier; David B Williams
Journal:  Mol Biol Cell       Date:  2010-07-21       Impact factor: 4.138

9.  Ischemia activates the ATF6 branch of the endoplasmic reticulum stress response.

Authors:  Shirin Doroudgar; Donna J Thuerauf; Marie C Marcinko; Peter J Belmont; Christopher C Glembotski
Journal:  J Biol Chem       Date:  2009-07-21       Impact factor: 5.157

10.  Analysis of the heat shock response in mouse liver reveals transcriptional dependence on the nuclear receptor peroxisome proliferator-activated receptor alpha (PPARalpha).

Authors:  Beena Vallanat; Steven P Anderson; Holly M Brown-Borg; Hongzu Ren; Sander Kersten; Sudhakar Jonnalagadda; Rajagopalan Srinivasan; J Christopher Corton
Journal:  BMC Genomics       Date:  2010-01-07       Impact factor: 3.969

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