TY - JOUR A1 - Rabl, Regina A1 - Soubannier, Vincent A1 - Scholz, Roland A1 - Vogel, Frank A1 - Mendl, Nadine A1 - Vasiljev-Neumeyer, Andreja A1 - Körner, Christian A1 - Jagasia, Ravi A1 - Keil, Thomas A1 - Baumeister, Wolfgang A1 - Cyrklaff, Marek A1 - Neupert, Walter A1 - Reichert, Andreas T1 - Formation of cristae and crista junctions in mitochondria depends on antagonism between Fcj1 and Su e/g T2 - The Journal of Cell Biology N2 - Crista junctions (CJs) are important for mitochondrial organization and function, but the molecular basis of their formation and architecture is obscure. We have identified and characterized a mitochondrial membrane protein in yeast, Fcj1 (formation of CJ protein 1), which is specifically enriched in CJs. Cells lacking Fcj1 lack CJs, exhibit concentric stacks of inner membrane in the mitochondrial matrix, and show increased levels of F1FO–ATP synthase (F1FO) supercomplexes. Overexpression of Fcj1 leads to increased CJ formation, branching of cristae, enlargement of CJ diameter, and reduced levels of F1FO supercomplexes. Impairment of F1FO oligomer formation by deletion of its subunits e/g (Su e/g) causes CJ diameter enlargement and reduction of cristae tip numbers and promotes cristae branching. Fcj1 and Su e/g genetically interact. We propose a model in which the antagonism between Fcj1 and Su e/g locally modulates the F1FO oligomeric state, thereby controlling membrane curvature of cristae to generate CJs and cristae tips. Y1 - 2009 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/7335 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30-58684 N1 - © 2009 Rabl et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). VL - 185 IS - 6 SP - 1047 EP - 1063 ER -