Subcellular localization of mammalian type II membrane proteins

Aturaliya,Rajith N., Fink, J. Lynn, Davis, Melissa J., Hanson, Kelly A., Miranda,Kevin C., Forrest,Alistair R. R., Grimmond, Sean M., Suzuki,Harukazu, Kanamori,Mutsumi, Kai,Chikatoshi, Kawai,Jun, Carninci,Piero, Hayashizaki,Yoshihide and Teasdale,Rohan D. (2006) Subcellular localization of mammalian type II membrane proteins. Traffic, 7 5: 613-625. doi:10.1111/j.1600-0854.2006.00407.x


Author Aturaliya,Rajith N.
Fink, J. Lynn
Davis, Melissa J.
Hanson, Kelly A.
Miranda,Kevin C.
Forrest,Alistair R. R.
Grimmond, Sean M.
Suzuki,Harukazu
Kanamori,Mutsumi
Kai,Chikatoshi
Kawai,Jun
Carninci,Piero
Hayashizaki,Yoshihide
Teasdale,Rohan D.
Title Subcellular localization of mammalian type II membrane proteins
Journal name Traffic   Check publisher's open access policy
ISSN 1398-9219
Publication date 2006-01-01
Sub-type Article (original research)
DOI 10.1111/j.1600-0854.2006.00407.x
Volume 7
Issue 5
Start page 613
End page 625
Total pages 13
Editor Gillian M. Griffiths
Mark C. P. Marsh
Trina A. Schroer
Tom H. Stevens
Place of publication Denmark
Publisher Blackwell Publishing
Language eng
Subject C1
270103 Protein Targeting and Signal Transduction
780105 Biological sciences
Abstract Application of a computational membrane organization prediction pipeline, MemO, identified putative type II membrane proteins as proteins predicted to encode a single alpha-helical transmembrane domain (TMD) and no signal peptides. MemO was applied to RIKEN's mouse isoform protein set to identify 1436 non-overlapping genomic regions or transcriptional units (TUs), which encode exclusively type II membrane proteins. Proteins with overlapping predicted InterPro and TMDs were reviewed to discard false positive predictions resulting in a dataset comprised of 1831 transcripts in 1408 TUs. This dataset was used to develop a systematic protocol to document subcellular localization of type II membrane proteins. This approach combines mining of published literature to identify subcellular localization data and a high-throughput, polymerase chain reaction (PCR)-based approach to experimentally characterize subcellular localization. These approaches have provided localization data for 244 and 169 proteins. Type II membrane proteins are localized to all major organelle compartments; however, some biases were observed towards the early secretory pathway and punctate structures. Collectively, this study reports the subcellular localization of 26% of the defined dataset. All reported localization data are presented in the LOCATE database (http://www.locate.imb.uq.edu.au).
Keyword membrane proteins
subcellular localization
transmembrane
Green Fluorescent Protein
Dopamine-beta-hydroxylase
Large-scale Analysis
Endoplasmic-reticulum
Gene Ontology
Golgi-localization
Er Stress
Expression
Cells
Receptor
Q-Index Code C1

 
Versions
Version Filter Type
Citation counts: TR Web of Science Citation Count  Cited 16 times in Thomson Reuters Web of Science Article | Citations
Scopus Citation Count Cited 18 times in Scopus Article | Citations
Google Scholar Search Google Scholar
Created: Wed, 15 Aug 2007, 19:16:41 EST