The comprehensive interactomes of human adenosine RNA methyltransferases and demethylases reveal distinct functional and regulatory features

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Publikace nespadá pod Filozofickou fakultu, ale pod Středoevropský technologický institut. Oficiální stránka publikace je na webu muni.cz.
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COVELO MOLARES Helena OBRDLÍK Aleš POSTULKOVA I. DOHNÁLKOVÁ Michaela GREGOROVÁ Pavlína GANJI Sri Ranjani POTĚŠIL David GAWRIYSKI L. VARJOSALO M. VAŇÁČOVÁ Štěpánka

Rok publikování 2021
Druh Článek v odborném periodiku
Časopis / Zdroj Nucleic acids research
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
www https://watermark.silverchair.com/gkab900.pdf?token=AQECAHi208BE49Ooan9kkhW_Ercy7Dm3ZL_9Cf3qfKAc485ysgAAAtowggLWBgkqhkiG9w0BBwagggLHMIICwwIBADCCArwGCSqGSIb3DQEHATAeBglghkgBZQMEAS4wEQQMYI0atmVmxuSJtvGtAgEQgIICjTOr8naIxPbW6AIOXEA-BqaQ4jGkEwiuhTJ9NCzQmkhQdI
Doi http://dx.doi.org/10.1093/nar/gkab900
Klíčová slova PRE-MESSENGER-RNA; SINGLE-STRANDED-DNA; POLYMERASE-II; NUCLEAR-RNA; M(6)A METHYLTRANSFERASE; GENE-EXPRESSION; 7SK SNRNP; P-TEFB; METHYLATION; PROTEIN
Přiložené soubory
Popis N6-methyladenosine (m(6)A) and N6,2 '-O-dimethyladenosine (m(6)Am) are two abundant modifications found in mRNAs and ncRNAs that can regulate multiple aspects of RNA biology. They function mainly by regulating interactions with specific RNA-binding proteins. Both modifications are linked to development, disease and stress response. To date, three methyltransferases and two demethylases have been identified that modify adenosines in mammalian mRNAs. Here, we present a comprehensive analysis of the interactomes of these enzymes. PCIF1 protein network comprises mostly factors involved in nascent RNA synthesis by RNA polymerase II, whereas ALKBH5 is closely linked with most aspects of pre-mRNA processing and mRNA export to the cytoplasm. METTL16 resides in subcellular compartments co-inhabited by several other RNA modifiers and processing factors. FTO interactome positions this demethylase at a crossroad between RNA transcription, RNA processing and DNA replication and repair. Altogether, these enzymes share limited spatial interactomes, pointing to specific molecular mechanisms of their regulation.
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