ISCA1 is essential for mitochondrial Fe4S4 biogenesis in vivo-Reference-Cited by-同舟云学术

ISCA1 is essential for mitochondrial Fe4S4 biogenesis in vivo

Published:2017-05-11 Issue:1 Volume:8 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Beilschmidt Lena Kristina,Ollagnier de Choudens Sandrine,Fournier Marjorie,Sanakis Ioannis,Hograindleur Marc-André,Clémancey Martin,Blondin Geneviève,Schmucker Stéphane,Eisenmann Aurélie,Weiss Amélie,Koebel Pascale,Messaddeq Nadia,Puccio Hélène,Martelli Alain

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms15124.pdf

Reference59 articles.

1. Beilschmidt, L. K. & Puccio, H. M. Mammalian Fe-S cluster biogenesis and its implication in disease. Biochimie 100, 48–60 (2014).

2. Lill, R. Function and biogenesis of iron-sulphur proteins. Nature 460, 831–838 (2009).

3. Colin, F. et al. Mammalian frataxin controls sulfur production and iron entry during de novo Fe4S4 cluster assembly. J. Am. Chem. Soc. 135, 733–740 (2013).

4. Tsai, C. L. & Barondeau, D. P. Human frataxin is an allosteric switch that activates the Fe-S cluster biosynthetic complex. Biochemistry 49, 9132–9139 (2010).

5. Bridwell-Rabb, J., Fox, N. G., Tsai, C. L., Winn, A. M. & Barondeau, D. P. Human frataxin activates Fe-S cluster biosynthesis by facilitating sulfur transfer chemistry. Biochemistry 53, 4904–4913 (2014).

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