{"id":22398,"date":"2016-11-01T11:04:04","date_gmt":"2016-11-01T10:04:04","guid":{"rendered":"https:\/\/fgu.antstudio.dev\/?p=22398"},"modified":"2024-08-08T11:06:54","modified_gmt":"2024-08-08T09:06:54","slug":"tmem70-disease","status":"publish","type":"post","link":"https:\/\/fgu.cas.cz\/en\/2016\/11\/tmem70-disease\/","title":{"rendered":"TMEM70 disease"},"content":{"rendered":"

Animal models of human mitochondrial diseases enable detailed insight into pathogenic mechanisms, from molecular to organismal levels.<\/strong><\/p>\n

According to previous studies performed at the Institute Physiology CAS, the mitochondrial ATP synthase, the key producer of cellular ATP, uniquely depends on a TMEM70, a 21-kDa protein that facilitates the biogenesis of mammalian enzyme. TMEM70 gene mutations turned out to represent the most frequent cause of ATP synthase deficiency resulting in a severe mitochondrial disease, neonatal encephalo-cardiomyopathy in humans (OMIM 604273). To further study this ancillary factor in vivo, Tmem70-deficient mice was generated. Tmem70 ablation resulted in profound growth retardation and embryonic lethality at 9.5 days of fetal development. Affected embryos displayed 80% decrease of ATP synthase and impaired biogenesis of ATP synthase, stalled at the early stage, following the formation of the F1 catalytic part of enzyme. Consequently, a decrease in ADP-stimulated respiration, respiratory control and ATP\/ADP ratios, demonstrated compromised mitochondrial ATP production. Tmem70-\/- embryos exhibited delayed development of the cardiovascular system and disturbed heart mitochondrial ultrastructure. These results thus showed that Tmem70 knockout in the mouse leads to embryonic lethality due to the lack of ATP synthase and impairment of mitochondrial energy provision and fully confirmed the expected mechanism of human TMEM70 disease.<\/p>\n

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ATP synthase deficiency and accumulation of F1 subcomplex in Tmem70-\/- embryos.<\/strong><\/p>\n

Blue-Native electrophoresis of ATP synthase (F1Fo) and respiratory chain complexes of wt (+\/+) null (-\/-) and heterozygous (+\/-) Tmem70 knockout E9 embryos. ATPase in gel activity and WB detection with antibodies to ATP synthase (F1-\u03b1) and respiratory complexes II-IV (CII – SDHA subunit; CIII – Core 1 subunit; CIV – Cox4 subunit).<\/p>\n

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Impaired morphology of Tmem70-\/- embryos.<\/strong><\/p>\n

(A) Confocal microscopy of retarded heart in null (-\/-) embryo in comparison with wt (+\/+) and heterozygous (+\/-) E9.5 embryos. OT \u2013 outer tract, LV \u2013 left ventricle, LA \u2013 left atrium, NA \u2013 neuroporus anterior. Immunohistochemistry: SMA (alpha smooth muscle actin), red \u2013 myocardium; CD31, green \u2013 endocardium; Hoechst 33342, blue \u2013 nuclei; arrows \u2013 emerging ventricular trabeculation, scale bar 100 \u00b5m. (B) Electron microscopy of disturbed cristae morphology in null (-\/-) compared to wt (+\/+) heart mitochondria of E9.5 embryos. M \u2013 mitochondria, MF \u2013 myofibrils, LM \u2013 lysed mitochondria, N \u2013 nucleus, scale bar 1 \u00b5m.<\/p>\n

Vrback\u00fd, Marek \u2013 Koval\u010d\u00edkov\u00e1, Jana \u2013 Chawengsaksophak, Kallayanee \u2013 Beck, Inken \u2013 Mr\u00e1\u010dek, Tom\u00e1\u0161 \u2013 N\u016fskov\u00e1, Hana \u2013 Sedmera, David \u2013 Papou\u0161ek, Franti\u0161ek \u2013 Kol\u00e1\u0159, Franti\u0161ek \u2013 Sobol, Margarita \u2013 Hoz\u00e1k, Pavel \u2013 Sedlacek, Radislav \u2013 Hou\u0161t\u011bk, Josef. Knockout of Tmem70 alters biogenesis of ATP synthase and leads to embryonal lethality in mice. Human Molecular Genetics, Vol. 25, No 21 (2016), p. 4674-4685. IF=5.985<\/p>\n","protected":false},"excerpt":{"rendered":"

Animal models of human mitochondrial diseases enable detailed insight into pathogenic mechanisms, from molecular to organismal levels. According to previous studies performed at the Institute Physiology CAS, the mitochondrial ATP synthase, the key producer of cellular ATP, uniquely depends on a TMEM70, a 21-kDa protein that facilitates the biogenesis of mammalian enzyme. TMEM70 gene mutations […]<\/p>\n","protected":false},"author":1,"featured_media":22391,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"categories":[113],"tags":[],"class_list":["post-22398","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-important-success"],"acf":[],"_links":{"self":[{"href":"https:\/\/fgu.cas.cz\/en\/wp-json\/wp\/v2\/posts\/22398","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/fgu.cas.cz\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/fgu.cas.cz\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/fgu.cas.cz\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/fgu.cas.cz\/en\/wp-json\/wp\/v2\/comments?post=22398"}],"version-history":[{"count":0,"href":"https:\/\/fgu.cas.cz\/en\/wp-json\/wp\/v2\/posts\/22398\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/fgu.cas.cz\/en\/wp-json\/wp\/v2\/media\/22391"}],"wp:attachment":[{"href":"https:\/\/fgu.cas.cz\/en\/wp-json\/wp\/v2\/media?parent=22398"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/fgu.cas.cz\/en\/wp-json\/wp\/v2\/categories?post=22398"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/fgu.cas.cz\/en\/wp-json\/wp\/v2\/tags?post=22398"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}