Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly

Ecsit is a cytosolic adaptor protein essential for inflammatory response and embryonic development via the Toll-like and BMP (bone morphogenetic protein) signal transduction pathways, respectively. Here, we demonstrate a mitochondrial function for Ecsit (an evolutionary conserved signaling intermediate in Toll pathways) in the assembly of mitochondrial complex I (NADH:ubiquinone oxidoreductase). An N-terminal targeting signal directs Ecsit to mitochondria, where it interacts with assembly chaperone NDUFAF1 in 500- to 850-kDa complexes as demonstrated by affinity purification and vice versa RNA interference (RNAi) knockdowns. In addition, Ecsit knockdown results in severely impaired complex I assembly and disturbed mitochondrial function. These findings support a function for Ecsit in the assembly or stability of mitochondrial complex I, possibly linking assembly of oxidative phosphorylation complexes to inflammatory response and embryonic development.

Saved in:
Bibliographic Details
Main Authors: Vogel, Rutger O., Janssen, Rolf J.R.J., Van Den Brand, Mariël A.M., Dieteren, Cindy E.J., Verkaart, Sjoerd, Koopman, Werner J.H., Willems, Peter H.G.M., Pluk, Wendy, Van Den Heuvel, Lambert P.W.J., Smeitink, Jan A.M., Nijtmans, Leo G.J.
Format: Article/Letter to editor biblioteca
Language:English
Subjects:Complex I, Ecsit, Mitochondria, NADH:ubiquinone oxidoreductase, NDUFAF1, Oxidative phosphorylation,
Online Access:https://research.wur.nl/en/publications/cytosolic-signaling-protein-ecsit-also-localizes-to-mitochondria-
Tags: Add Tag
No Tags, Be the first to tag this record!
id dig-wur-nl-wurpubs-624414
record_format koha
spelling dig-wur-nl-wurpubs-6244142024-12-04 Vogel, Rutger O. Janssen, Rolf J.R.J. Van Den Brand, Mariël A.M. Dieteren, Cindy E.J. Verkaart, Sjoerd Koopman, Werner J.H. Willems, Peter H.G.M. Pluk, Wendy Van Den Heuvel, Lambert P.W.J. Smeitink, Jan A.M. Nijtmans, Leo G.J. Article/Letter to editor Genes and Development 21 (2007) 5 ISSN: 0890-9369 Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly 2007 Ecsit is a cytosolic adaptor protein essential for inflammatory response and embryonic development via the Toll-like and BMP (bone morphogenetic protein) signal transduction pathways, respectively. Here, we demonstrate a mitochondrial function for Ecsit (an evolutionary conserved signaling intermediate in Toll pathways) in the assembly of mitochondrial complex I (NADH:ubiquinone oxidoreductase). An N-terminal targeting signal directs Ecsit to mitochondria, where it interacts with assembly chaperone NDUFAF1 in 500- to 850-kDa complexes as demonstrated by affinity purification and vice versa RNA interference (RNAi) knockdowns. In addition, Ecsit knockdown results in severely impaired complex I assembly and disturbed mitochondrial function. These findings support a function for Ecsit in the assembly or stability of mitochondrial complex I, possibly linking assembly of oxidative phosphorylation complexes to inflammatory response and embryonic development. en text/html https://research.wur.nl/en/publications/cytosolic-signaling-protein-ecsit-also-localizes-to-mitochondria- 10.1101/gad.408407 https://edepot.wur.nl/646174 Complex I Ecsit Mitochondria NADH:ubiquinone oxidoreductase NDUFAF1 Oxidative phosphorylation (c) publisher Wageningen University & Research
institution WUR NL
collection DSpace
country Países bajos
countrycode NL
component Bibliográfico
access En linea
databasecode dig-wur-nl
tag biblioteca
region Europa del Oeste
libraryname WUR Library Netherlands
language English
topic Complex I
Ecsit
Mitochondria
NADH:ubiquinone oxidoreductase
NDUFAF1
Oxidative phosphorylation
Complex I
Ecsit
Mitochondria
NADH:ubiquinone oxidoreductase
NDUFAF1
Oxidative phosphorylation
spellingShingle Complex I
Ecsit
Mitochondria
NADH:ubiquinone oxidoreductase
NDUFAF1
Oxidative phosphorylation
Complex I
Ecsit
Mitochondria
NADH:ubiquinone oxidoreductase
NDUFAF1
Oxidative phosphorylation
Vogel, Rutger O.
Janssen, Rolf J.R.J.
Van Den Brand, Mariël A.M.
Dieteren, Cindy E.J.
Verkaart, Sjoerd
Koopman, Werner J.H.
Willems, Peter H.G.M.
Pluk, Wendy
Van Den Heuvel, Lambert P.W.J.
Smeitink, Jan A.M.
Nijtmans, Leo G.J.
Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly
description Ecsit is a cytosolic adaptor protein essential for inflammatory response and embryonic development via the Toll-like and BMP (bone morphogenetic protein) signal transduction pathways, respectively. Here, we demonstrate a mitochondrial function for Ecsit (an evolutionary conserved signaling intermediate in Toll pathways) in the assembly of mitochondrial complex I (NADH:ubiquinone oxidoreductase). An N-terminal targeting signal directs Ecsit to mitochondria, where it interacts with assembly chaperone NDUFAF1 in 500- to 850-kDa complexes as demonstrated by affinity purification and vice versa RNA interference (RNAi) knockdowns. In addition, Ecsit knockdown results in severely impaired complex I assembly and disturbed mitochondrial function. These findings support a function for Ecsit in the assembly or stability of mitochondrial complex I, possibly linking assembly of oxidative phosphorylation complexes to inflammatory response and embryonic development.
format Article/Letter to editor
topic_facet Complex I
Ecsit
Mitochondria
NADH:ubiquinone oxidoreductase
NDUFAF1
Oxidative phosphorylation
author Vogel, Rutger O.
Janssen, Rolf J.R.J.
Van Den Brand, Mariël A.M.
Dieteren, Cindy E.J.
Verkaart, Sjoerd
Koopman, Werner J.H.
Willems, Peter H.G.M.
Pluk, Wendy
Van Den Heuvel, Lambert P.W.J.
Smeitink, Jan A.M.
Nijtmans, Leo G.J.
author_facet Vogel, Rutger O.
Janssen, Rolf J.R.J.
Van Den Brand, Mariël A.M.
Dieteren, Cindy E.J.
Verkaart, Sjoerd
Koopman, Werner J.H.
Willems, Peter H.G.M.
Pluk, Wendy
Van Den Heuvel, Lambert P.W.J.
Smeitink, Jan A.M.
Nijtmans, Leo G.J.
author_sort Vogel, Rutger O.
title Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly
title_short Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly
title_full Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly
title_fullStr Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly
title_full_unstemmed Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly
title_sort cytosolic signaling protein ecsit also localizes to mitochondria where it interacts with chaperone ndufaf1 and functions in complex i assembly
url https://research.wur.nl/en/publications/cytosolic-signaling-protein-ecsit-also-localizes-to-mitochondria-
work_keys_str_mv AT vogelrutgero cytosolicsignalingproteinecsitalsolocalizestomitochondriawhereitinteractswithchaperonendufaf1andfunctionsincomplexiassembly
AT janssenrolfjrj cytosolicsignalingproteinecsitalsolocalizestomitochondriawhereitinteractswithchaperonendufaf1andfunctionsincomplexiassembly
AT vandenbrandmarielam cytosolicsignalingproteinecsitalsolocalizestomitochondriawhereitinteractswithchaperonendufaf1andfunctionsincomplexiassembly
AT dieterencindyej cytosolicsignalingproteinecsitalsolocalizestomitochondriawhereitinteractswithchaperonendufaf1andfunctionsincomplexiassembly
AT verkaartsjoerd cytosolicsignalingproteinecsitalsolocalizestomitochondriawhereitinteractswithchaperonendufaf1andfunctionsincomplexiassembly
AT koopmanwernerjh cytosolicsignalingproteinecsitalsolocalizestomitochondriawhereitinteractswithchaperonendufaf1andfunctionsincomplexiassembly
AT willemspeterhgm cytosolicsignalingproteinecsitalsolocalizestomitochondriawhereitinteractswithchaperonendufaf1andfunctionsincomplexiassembly
AT plukwendy cytosolicsignalingproteinecsitalsolocalizestomitochondriawhereitinteractswithchaperonendufaf1andfunctionsincomplexiassembly
AT vandenheuvellambertpwj cytosolicsignalingproteinecsitalsolocalizestomitochondriawhereitinteractswithchaperonendufaf1andfunctionsincomplexiassembly
AT smeitinkjanam cytosolicsignalingproteinecsitalsolocalizestomitochondriawhereitinteractswithchaperonendufaf1andfunctionsincomplexiassembly
AT nijtmansleogj cytosolicsignalingproteinecsitalsolocalizestomitochondriawhereitinteractswithchaperonendufaf1andfunctionsincomplexiassembly
_version_ 1819150633307996160