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A Novel Pathway of Cytochrome c Biogenesis Is Involved in the Assembly of the Cytochrome b6f Complex in Arabidopsis Chloroplasts

Authors :
Geneviève Ephritikhine
Lina Lezhneva
Richard Kuras
Catherine de Vitry
Physiologie membranaire et moléculaire du chloroplaste (PMMC)
Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)
Institut des sciences du végétal (ISV)
Centre National de la Recherche Scientifique (CNRS)
Université Paris Diderot - Paris 7 (UPD7)
Source :
Journal of Biological Chemistry, Journal of Biological Chemistry, 2008, 283 (36), pp.24608-16. ⟨10.1074/jbc.M803869200⟩, Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2008, 283 (36), pp.24608-16. ⟨10.1074/jbc.M803869200⟩
Publication Year :
2008
Publisher :
Elsevier BV, 2008.

Abstract

International audience; We recently characterized a novel heme biogenesis pathway required for heme c(i)' covalent binding to cytochrome b6 in Chlamydomonas named system IV or CCB (cofactor assembly, complex C (b6f), subunit B (PetB)). To find out whether this CCB pathway also operates in higher plants and extend the knowledge of the c-type cytochrome biogenesis, we studied Arabidopsis insertion mutants in the orthologs of the CCB genes. The ccb1, ccb2, and ccb4 mutants show a phenotype characterized by a deficiency in the accumulation of the subunits of the cytochrome b6f complex and lack covalent heme binding to cytochrome b6. These mutants were functionally complemented with the corresponding wild type cDNAs. Using fluorescent protein reporters, we demonstrated that the CCB1, CCB2, CCB3, and CCB4 proteins are targeted to the chloroplast compartment of Arabidopsis. We have extended our study to the YGGT family, to which CCB3 belongs, by studying insertion mutants of two additional members of this family for which no mutants were previously characterized, and we showed that they are not functionally involved in the CCB system. Thus, we demonstrate the ubiquity of the CCB proteins in chloroplast heme c(i)' binding.

Details

ISSN :
00219258 and 1083351X
Volume :
283
Database :
OpenAIRE
Journal :
Journal of Biological Chemistry
Accession number :
edsair.doi.dedup.....10f4c6ce825e38279b98e2b5e5180331
Full Text :
https://doi.org/10.1074/jbc.m803869200