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.
Main Authors: | , , , , , , , , , , |
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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- |
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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 |
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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- |
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