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Two zinc finger proteins with functions in m(6)A writing interact with HAKAI

The methyltransferase complex (m(6)A writer), which catalyzes the deposition of N(6)-methyladenosine (m(6)A) in mRNAs, is highly conserved across most eukaryotic organisms, but its components and interactions between them are still far from fully understood. Here, using in vivo interaction proteomic...

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Detalles Bibliográficos
Autores principales: Zhang, Mi, Bodi, Zsuzsanna, Mackinnon, Katarzyna, Zhong, Silin, Archer, Nathan, Mongan, Nigel P., Simpson, Gordon G., Fray, Rupert G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891334/
https://www.ncbi.nlm.nih.gov/pubmed/35236848
http://dx.doi.org/10.1038/s41467-022-28753-3
Descripción
Sumario:The methyltransferase complex (m(6)A writer), which catalyzes the deposition of N(6)-methyladenosine (m(6)A) in mRNAs, is highly conserved across most eukaryotic organisms, but its components and interactions between them are still far from fully understood. Here, using in vivo interaction proteomics, two HAKAI-interacting zinc finger proteins, HIZ1 and HIZ2, are discovered as components of the Arabidopsis m(6)A writer complex. HAKAI is required for the interaction between HIZ1 and MTA (mRNA adenosine methylase A). Whilst HIZ1 knockout plants have normal levels of m(6)A, plants in which it is overexpressed show reduced methylation and decreased lateral root formation. Mutant plants lacking HIZ2 are viable but have an 85% reduction in m(6)A abundance and show severe developmental defects. Our findings suggest that HIZ2 is likely the plant equivalent of ZC3H13 (Flacc) of the metazoan m(6)A-METTL Associated Complex.