Supercomplex assembly determines electron flux in the mitochondrial electron transport chain

…, R Acín-Pérez, A Latorre-Pellicer… - Science, 2013 - science.org
The textbook description of mitochondrial respiratory complexes (RCs) views them as free-moving
entities linked by the mobile carriers coenzyme Q (CoQ) and cytochrome c (cyt c). This …

Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing

A Latorre-Pellicer, R Moreno-Loshuertos… - Nature, 2016 - nature.com
Human mitochondrial DNA (mtDNA) shows extensive within-population sequence variability
1 . Many studies suggest that mtDNA variants may be associated with ageing or diseases 2 …

[HTML][HTML] Priming of dendritic cells by DNA-containing extracellular vesicles from activated T cells through antigen-driven contacts

…, I Fernández-Delgado, A Latorre-Pellicer… - Nature …, 2018 - nature.com
Interaction of T cell with antigen-bearing dendritic cells (DC) results in T cell activation, but
whether this interaction has physiological consequences on DC function is largely unexplored…

[HTML][HTML] ROS-triggered phosphorylation of complex II by Fgr kinase regulates cellular adaptation to fuel use

…, F Baixauli, M Roche-Molina, A Latorre-Pellicer… - Cell metabolism, 2014 - cell.com
Electron flux in the mitochondrial electron transport chain is determined by the superassembly
of mitochondrial respiratory complexes. Different superassemblies are dedicated to …

[PDF][PDF] Regulation of mother-to-offspring transmission of mtDNA heteroplasmy

A Latorre-Pellicer, AV Lechuga-Vieco, IG Johnston… - Cell metabolism, 2019 - cell.com
mtDNA is present in multiple copies in each cell derived from the expansions of those in the
oocyte. Heteroplasmy, more than one mtDNA variant, may be generated by mutagenesis, …

[HTML][HTML] Disruption of NIPBL/Scc2 in Cornelia de Lange Syndrome provokes cohesin genome-wide redistribution with an impact in the transcriptome

…, A Gomez, M Maqueda, A Latorre-Pellicer… - Nature …, 2021 - nature.com
Cornelia de Lange syndrome (CdLS) is a rare disease affecting multiple organs and systems
during development. Mutations in the cohesin loader, NIPBL/Scc2, were first described and …

Cell identity and nucleo-mitochondrial genetic context modulate OXPHOS performance and determine somatic heteroplasmy dynamics

AV Lechuga-Vieco, A Latorre-Pellicer, IG Johnston… - Science …, 2020 - science.org
Heteroplasmy, multiple variants of mitochondrial DNA (mtDNA) in the same cytoplasm, may
be naturally generated by mutations but is counteracted by a genetic mtDNA bottleneck …

[HTML][HTML] Evaluating Face2Gene as a tool to identify Cornelia de Lange syndrome by facial phenotypes

A Latorre-Pellicer, Á Ascaso, L Trujillano… - International journal of …, 2020 - mdpi.com
Characteristic or classic phenotype of Cornelia de Lange syndrome (CdLS) is associated
with a recognisable facial pattern. However, the heterogeneity in causal genes and the …

[PDF][PDF] Comprehensive quantification of the modified proteome reveals oxidative heart damage in mitochondrial heteroplasmy

…, I Ezkurdia, JM Rodríguez, R Magni, A Latorre-Pellicer… - Cell Reports, 2018 - cell.com
Post-translational modifications hugely increase the functional diversity of proteomes.
Recent algorithms based on ultratolerant database searching are forging a path to unbiased …

[HTML][HTML] Remission of obesity and insulin resistance is not sufficient to restore mitochondrial homeostasis in visceral adipose tissue

…, N Dahdah, S Moreno-Gomez, A Latorre-Pellicer… - Redox Biology, 2022 - Elsevier
Metabolic plasticity is the ability of a biological system to adapt its metabolic phenotype to
different environmental stressors. We used a whole-body and tissue-specific phenotypic, …