Author
Listed:
- Lena Kristina Beilschmidt
(IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire) Translational Medicine and Neurogenetics Department
Inserm U596
CNRS, UMR7104
Université de Strasbourg)
- Sandrine Ollagnier de Choudens
(CEA/DRF/BIG/CBM/BioCat
CNRS UMR 5249, LCBM
Université Grenoble Alpes, LCBM)
- Marjorie Fournier
(IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire) Translational Medicine and Neurogenetics Department
Inserm U596
CNRS, UMR7104
Université de Strasbourg)
- Ioannis Sanakis
(NCSR, Demokritos, Institut of Materials Science)
- Marc-André Hograindleur
(CEA/DRF/BIG/CBM/BioCat
CNRS UMR 5249, LCBM
Université Grenoble Alpes, LCBM
CEA/DRF/BIG/CBM/pmb)
- Martin Clémancey
(CNRS UMR 5249, LCBM
Université Grenoble Alpes, LCBM
CEA/DRF/BIG/CBM/pmb)
- Geneviève Blondin
(CNRS UMR 5249, LCBM
Université Grenoble Alpes, LCBM
CEA/DRF/BIG/CBM/pmb)
- Stéphane Schmucker
(IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire) Translational Medicine and Neurogenetics Department
Inserm U596
CNRS, UMR7104
Université de Strasbourg)
- Aurélie Eisenmann
(IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire) Translational Medicine and Neurogenetics Department
Inserm U596
CNRS, UMR7104
Université de Strasbourg)
- Amélie Weiss
(IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire) Translational Medicine and Neurogenetics Department
Inserm U596
CNRS, UMR7104
Université de Strasbourg)
- Pascale Koebel
(IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire) Translational Medicine and Neurogenetics Department
Inserm U596
CNRS, UMR7104
Université de Strasbourg)
- Nadia Messaddeq
(IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire) Translational Medicine and Neurogenetics Department
Inserm U596
CNRS, UMR7104
Université de Strasbourg)
- Hélène Puccio
(IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire) Translational Medicine and Neurogenetics Department
Inserm U596
CNRS, UMR7104
Université de Strasbourg)
- Alain Martelli
(IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire) Translational Medicine and Neurogenetics Department
Inserm U596
CNRS, UMR7104
Université de Strasbourg)
Abstract
Mammalian A-type proteins, ISCA1 and ISCA2, are evolutionarily conserved proteins involved in iron–sulfur cluster (Fe–S) biogenesis. Recently, it was shown that ISCA1 and ISCA2 form a heterocomplex that is implicated in the maturation of mitochondrial Fe4S4 proteins. Here we report that mouse ISCA1 and ISCA2 are Fe2S2-containing proteins that combine all features of Fe–S carrier proteins. We use biochemical, spectroscopic and in vivo approaches to demonstrate that despite forming a complex, ISCA1 and ISCA2 establish discrete interactions with components of the late Fe–S machinery. Surprisingly, knockdown experiments in mouse skeletal muscle and in primary cultures of neurons suggest that ISCA1, but not ISCA2, is required for mitochondrial Fe4S4 proteins biogenesis. Collectively, our data suggest that cellular processes with different requirements for ISCA1, ISCA2 and ISCA1–ISCA2 complex seem to exist.
Suggested Citation
Lena Kristina Beilschmidt & Sandrine Ollagnier de Choudens & Marjorie Fournier & Ioannis Sanakis & Marc-André Hograindleur & Martin Clémancey & Geneviève Blondin & Stéphane Schmucker & Aurélie Eisenma, 2017.
"ISCA1 is essential for mitochondrial Fe4S4 biogenesis in vivo,"
Nature Communications, Nature, vol. 8(1), pages 1-12, August.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15124
DOI: 10.1038/ncomms15124
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