Počet záznamů: 1  

The Distinct Function and Localization of METTL3/METTL14 and METTL16 Enzymes in Cardiomyocytes

  1. 1.
    SYSNO ASEP0537440
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevThe Distinct Function and Localization of METTL3/METTL14 and METTL16 Enzymes in Cardiomyocytes
    Tvůrce(i) Arcidiacono, Orazio Angelo (BFU-R) ORCID
    Krejčí, Jana (BFU-R) RID, ORCID
    Bártová, Eva (BFU-R) ORCID
    Celkový počet autorů3
    Číslo článku8139
    Zdroj.dok.International Journal of Molecular Sciences. - : MDPI
    Roč. 21, č. 21 (2020)
    Poč.str.19 s.
    Forma vydáníOnline - E
    Jazyk dok.eng - angličtina
    Země vyd.CH - Švýcarsko
    Klíč. slovamessenger-rna methylation ; embryonic stem-cells ; cardiac-hypertrophy ; gene-expression ; m(6)a methyltransferase ; histone deacetylase-1 ; hdac inhibitors ; tet proteins
    Vědní obor RIVCE - Biochemie
    Obor OECDBiochemistry and molecular biology
    CEPGA18-07384S GA ČR - Grantová agentura ČR
    Způsob publikováníOpen access
    Institucionální podporaBFU-R - RVO:68081707
    UT WOS000588866000001
    EID SCOPUS85095575320
    DOI10.3390/ijms21218139
    AnotaceIt has become evident that epitranscriptome events, mediated by specific enzymes, regulate gene expression and, subsequently, cell differentiation processes. We show that methyltransferase-like proteins METTL3/METTL14 and N-6-adenosine methylation (m6A) in RNAs are homogeneously distributed in embryonic hearts, and histone deacetylase (HDAC) inhibitors valproic acid and Trichostatin A (TSA) up-regulate METTL3/METTL14 proteins. The levels of METTL3 in mouse adult hearts, isolated from male and female animals, were lower in the aorta and pulmonary trunks when compared with atria, but METT14 was up-regulated in the aorta and pulmonary trunk, in comparison with ventriculi. Aging caused METTL3 down-regulation in aorta and atria in male animals. Western blot analysis in differentiated mouse embryonic stem cells (mESCs), containing 10-30 percent of cardiomyocytes, showed METTL3/METTL14 down-regulation, while the differentiation-induced increased level of METTL16 was observed in both wild type (wt) and HDAC1 depleted (dn) cells. In parallel, experimental differentiation in especially HDAC1 wild type cells was accompanied by depletion of m6A in RNA. Immunofluorescence analysis of individual cells revealed the highest density of METTL3/METTL14 in alpha-actinin positive cardiomyocytes when compared with the other cells in the culture undergoing differentiation. In both wt and HDAC1 dn cells, the amount of METTL16 was also up-regulated in cardiomyocytes when compared to co-cultivated cells. Together, we showed that distinct anatomical regions of the mouse adult hearts are characterized by different levels of METTL3 and METTL14 proteins, which are changed during aging. Experimental cell differentiation was also accompanied by changes in METTL-like proteins and m6A in RNA, in particular, levels and distribution patterns of METTL3/METTL14 proteins were different from the same parameters studied in the case of the METTL16 protein.
    PracovištěBiofyzikální ústav
    KontaktJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Rok sběru2021
    Elektronická adresahttp://apps.webofknowledge.com/InboundService.do?customersID=Alerting&mode=FullRecord&IsProductCode=Yes&product=WOS&Init=Yes&Func=Frame&DestFail=http%3A%2F%2Fwww.webofknowledge.com&action=retrieve&SrcApp=Alerting&SrcAuth=Alerting&SID=F5ecl7TTnxXPl2FJDDH&UT=WOS%3A000588866000001
Počet záznamů: 1  

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