ISCA1 is essential for mitochondrial Fe<sub>4</sub>S<sub>4</sub> biogenesis in vivo.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 28492233.
- Also identified by DOI 10.1038/ncomms15124 and PMC identifier 5437272.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
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 Fe<sub>4</sub>S<sub>4</sub> proteins. Here we report that mouse ISCA1 and ISCA2 are Fe<sub>2</sub>S<sub>2</sub>-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 Fe<sub>4</sub>S<sub>4</sub> proteins biogenesis. Collectively, our data suggest that cellular processes with different requirements for ISCA1, ISCA2 and ISCA1-ISCA2 complex seem to exist.
Medical subject headings
- Aconitate Hydratase
- Iron-Sulfur Proteins
- Mitochondrial Proteins
- Muscle, Skeletal
- Sensory Receptor Cells