<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-29T02:49:03Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/6362" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/6362</identifier><datestamp>2023-08-06T01:19:48Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Low abundance of NDUFV2 and NDUFS4 subunits of the hydrophilic complex I domain and VDAC1 predicts mammalian longevity</dc:title>
   <dc:creator>Mota-Martorell, Natalia</dc:creator>
   <dc:creator>Jové, Mariona</dc:creator>
   <dc:creator>Pradas, Irene</dc:creator>
   <dc:creator>Sánchez, Isabel</dc:creator>
   <dc:creator>Gómez, José</dc:creator>
   <dc:creator>Naudí, Alba</dc:creator>
   <dc:creator>Barja de Quiroga, Gustavo</dc:creator>
   <dc:creator>Pamplona, Reinald</dc:creator>
   <dc:subject>591.1</dc:subject>
   <dc:subject>577.112</dc:subject>
   <dc:subject>599</dc:subject>
   <dc:subject>Complex I</dc:subject>
   <dc:subject>Droplet digital PCR</dc:subject>
   <dc:subject>Longevity</dc:subject>
   <dc:subject>Mammals</dc:subject>
   <dc:subject>Mitochondria</dc:subject>
   <dc:subject>NDUFV2 subunit</dc:subject>
   <dc:subject>NDUFS4 subunit</dc:subject>
   <dc:subject>VDAC</dc:subject>
   <dc:subject>Western blot</dc:subject>
   <dc:subject>Bioquímica (Biología)</dc:subject>
   <dc:subject>Fisiología animal (Biología)</dc:subject>
   <dc:subject>Mamíferos</dc:subject>
   <dc:subject>2302 Bioquímica</dc:subject>
   <dc:subject>2401.13 Fisiología Animal</dc:subject>
   <dc:subject>2401.18 Mamíferos</dc:subject>
   <dc:description>Mitochondrial reactive oxygen species (ROS) production, specifically at complex I (Cx I), has been widely suggested to be one of the determinants of species longevity. The present study follows a comparative approach to analyse complex I in heart tissue from 8 mammalian species with a longevity ranging from 3.5 to 46 years. Gene expression and protein content of selected Cx I subunits were analysed using droplet digital PCR (ddPCR) and western blot, respectively. Our results demonstrate: 1) the existence of species-specific differences in gene expression and protein content of Cx I in relation to longevity; 2) the achievement of a longevity phenotype is associated with low protein abundance of subunits NDUFV2 and NDUFS4 from the matrix hydrophilic domain of Cx I; and 3) long-lived mammals show also lower levels of VDAC (voltage-dependent anion channel) amount. These differences could be associated with the lower mitochondrial ROS production and slower aging rate of long-lived animals and, unexpectedly, with a low content of the mitochondrial permeability transition pore in these species.</dc:description>
   <dc:description>Ministerio de Economía y Competitividad (MINECO). Instituto de Salud Carlos III</dc:description>
   <dc:description>Ministerio de Ciencia, Innovación y Universidades (MICIU)</dc:description>
   <dc:description>Generalitat de Cataluña</dc:description>
   <dc:description>Fondo Europeo de Desarrollo Regional(FEDER)</dc:description>
   <dc:description>Depto. de Genética, Fisiología y Microbiología</dc:description>
   <dc:description>Fac. de Ciencias Biológicas</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2023-06-16T15:19:39Z</dc:date>
   <dc:date>2023-06-16T15:19:39Z</dc:date>
   <dc:date>2020-04-20</dc:date>
   <dc:type>journal article</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/6362</dc:identifier>
   <dc:identifier>2213-2317, ESSN: 2213-2317</dc:identifier>
   <dc:identifier>10.1016/j.redox.2020.101539</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>(PI14/00328)</dc:relation>
   <dc:relation>(RTI2018-099200-B-I00)</dc:relation>
   <dc:relation>(2017SGR696), SLT002/16/00250, PR [19] BIO MET 0155,AGAUR, ref 2018FI_B2_00104)</dc:relation>
   <dc:rights>Atribución-NoComercial-SinDerivadas 3.0 España</dc:rights>
   <dc:rights>https://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Elsevier</dc:publisher>
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