Počet záznamů: 1
Knockout of Tmem70 alters biogenesis of ATP synthase and leads to embryonal lethality in mice
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SYSNO ASEP 0471806 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Knockout of Tmem70 alters biogenesis of ATP synthase and leads to embryonal lethality in mice Tvůrce(i) Vrbacký, Marek (FGU-C) RID, ORCID
Kovalčíková, Jana (FGU-C)
Chawengsaksophak, Kallayanee (UMG-J)
Beck, Inken (UMG-J) RID
Mráček, Tomáš (FGU-C) RID, ORCID
Nůsková, Hana (FGU-C) RID, ORCID
Sedmera, David (FGU-C) RID, ORCID, SAI
Papoušek, František (FGU-C)
Kolář, František (FGU-C) RID, ORCID, SAI
Sobol, Margaryta (UMG-J) RID
Hozák, Pavel (UMG-J) RID, ORCID
Sedláček, Radislav (UMG-J) RID
Houštěk, Josef (FGU-C) RID, ORCIDZdroj.dok. Human Molecular Genetics. - : Oxford University Press - ISSN 0964-6906
Roč. 25, č. 21 (2016), s. 4674-4685Poč.str. 12 s. Jazyk dok. eng - angličtina Země vyd. GB - Velká Británie Klíč. slova mouse knockout ; mitochondria ; ATP synthase ; TMEM70 ; biogenesis ; mitochondrial diseases Vědní obor RIV EB - Genetika a molekulární biologie Obor OECD Human genetics CEP GB14-36804G GA ČR - Grantová agentura ČR LL1204 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy ED1.1.00/02.0109 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy TE01020118 GA TA ČR - Technologická agentura ČR LM2015062 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy NV16-33018A GA MZd - Ministerstvo zdravotnictví LM2015040 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy Institucionální podpora FGU-C - RVO:67985823 ; UMG-J - RVO:68378050 UT WOS 000397061300006 EID SCOPUS 85014822460 DOI 10.1093/hmg/ddw295 Anotace TMEM70, a 21 kDa protein localized in the inner mitochondrial membrane, has been shown to facilitate the biogenesis of mammalian F1Fo ATP synthase. Mutations of the TMEM70 gene represent the most frequent cause of isolated ATP synthase deficiency resulting in a severe mitochondrial disease presenting as neonatal encephalo-cardiomyopathy (OMIM 604273). To better understand the biological role of this factor, we generated Tmem70 deficient mice and found that the homozygous Tmem70 -/- knockouts exhibited profound growth retardation and embryonic lethality at approximately 9.5 days post coitum. Blue-Native electrophoresis demonstrated an isolated deficiency in fully assembled ATP synthase in the Tmem70 -/- embryos (80% decrease) and a marked accumulation of F1 complexes indicative of impairment in ATP synthase biogenesis that was stalled at the early stage, following the formation of F1 oligomer. Consequently, a decrease in ADP-stimulated State 3 respiration, respiratory control ratio and ATP/ADP ratios, indicated compromised mitochondrial ATP production. In Tmem70 -/- embryos development of the cardiovascular system was delayed and heart mitochondrial ultrastructure disturbed, with concentric or irregular cristae structures. Tmem70 +/- heterozygous mice were fully viable and displayed normal postnatal growth and development of the mitochondrial oxidative phosphorylation system. Nevertheless, they presented with mild deterioration of heart function. Our results demonstrated that Tmem70 knockout in the mouse results in embryonic lethality due to the lack of ATP synthase and impairment of mitochondrial energy provision. This is analogous to TMEM70 dysfunction in humans and verifies the crucial role of this factor in the biosynthesis and assembly of mammalian ATP synthase. Pracoviště Fyziologický ústav Kontakt Lucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400 Rok sběru 2017
Počet záznamů: 1