Literature DB >> 9506517

TRAM regulates the exposure of nascent secretory proteins to the cytosol during translocation into the endoplasmic reticulum.

R S Hegde1, S Voigt, T A Rapoport, V R Lingappa.   

Abstract

Translocational pausing is a mechanism used by certain specialized secretory proteins whereby discrete domains of a nascent chain destined for the endoplasmic reticulum lumen are transiently exposed to the cytosol. Proteoliposomes reconstituted from total endoplasmic reticulum proteins properly assemble translocationally paused intermediates. The capacity of the translocon to correctly pause the nascent chain is dependent on a glycoprotein fraction whose active component is TRAM. In the absence of TRAM, the normally sealed ribosome-membrane junction still opens in response to a pause transfer sequence. However, nascent chain domains that are not exposed to the cytosol in the presence of TRAM are so exposed in its absence. Thus, TRAM regulates which domains of the nascent chain are visible to the cytosol during a translocational pause.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9506517     DOI: 10.1016/s0092-8674(00)81130-7

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  22 in total

1.  Substrate-specific regulation of the ribosome- translocon junction by N-terminal signal sequences.

Authors:  D T Rutkowski; V R Lingappa; R S Hegde
Journal:  Proc Natl Acad Sci U S A       Date:  2001-06-19       Impact factor: 11.205

2.  TRAM2 protein interacts with endoplasmic reticulum Ca2+ pump Serca2b and is necessary for collagen type I synthesis.

Authors:  Branko Stefanovic; Lela Stefanovic; Bernd Schnabl; Ramon Bataller; David A Brenner
Journal:  Mol Cell Biol       Date:  2004-02       Impact factor: 4.272

3.  Substrate-specific translocational attenuation during ER stress defines a pre-emptive quality control pathway.

Authors:  Sang-Wook Kang; Neena S Rane; Soo Jung Kim; Jennifer L Garrison; Jack Taunton; Ramanujan S Hegde
Journal:  Cell       Date:  2006-12-01       Impact factor: 41.582

Review 4.  Marginally hydrophobic transmembrane α-helices shaping membrane protein folding.

Authors:  Minttu T De Marothy; Arne Elofsson
Journal:  Protein Sci       Date:  2015-05-30       Impact factor: 6.725

Review 5.  Protein translocation across the rough endoplasmic reticulum.

Authors:  Elisabet C Mandon; Steven F Trueman; Reid Gilmore
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-02-01       Impact factor: 10.005

Review 6.  Components and Mechanisms of Import, Modification, Folding, and Assembly of Immunoglobulins in the Endoplasmic Reticulum.

Authors:  Richard Zimmermann
Journal:  J Clin Immunol       Date:  2016-02-29       Impact factor: 8.317

7.  Mutation in the Trapalpha/Ssr1 gene, encoding translocon-associated protein alpha, results in outflow tract morphogenetic defects.

Authors:  K Mesbah; A Camus; C Babinet; J Barra
Journal:  Mol Cell Biol       Date:  2006-10       Impact factor: 4.272

Review 8.  Biogenesis of CFTR and other polytopic membrane proteins: new roles for the ribosome-translocon complex.

Authors:  H Sadlish; W R Skach
Journal:  J Membr Biol       Date:  2004-12       Impact factor: 1.843

9.  Two endoplasmic reticulum (ER) membrane proteins that facilitate ER-to-Golgi transport of glycosylphosphatidylinositol-anchored proteins.

Authors:  W P Barz; P Walter
Journal:  Mol Biol Cell       Date:  1999-04       Impact factor: 4.138

10.  Apoprotein B100 has a prolonged interaction with the translocon during which its lipidation and translocation change from dependence on the microsomal triglyceride transfer protein to independence.

Authors:  D M Mitchell; M Zhou; R Pariyarath; H Wang; J D Aitchison; H N Ginsberg; E A Fisher
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-08       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.