RESUMO
Human translational methyltransferase (methylase) HEMK2, whose orthologues are found in many prokaryotes and eukaryotes, methylates such diverse substrates as glutamine and lysine residues in proteins, deoxyadenosine in DNA, and arsenicals. One of the important substrate of HEMK2 methylase is a glutamine residue in the GGQ ultra-conservative motif of the eukaryotic release factor 1 (eRF1). Release factor methylation by HEMK2 orthologs is conserved among eukaryotes, archaea, and bacteria, although bacterial release factors differ in sequence and structure from eukaryotic ones. In this review, we consider the features of human HEMK2 methylase and its orthologs as multifunctional enzymes that regulate cellular processes, in particular, protein biosynthesis.
Assuntos
Glutamina , Metiltransferases , Sequência de Aminoácidos , Glutamina/química , Glutamina/genética , Glutamina/metabolismo , Humanos , Metilação , Metiltransferases/genética , Metiltransferases/metabolismo , Processamento de Proteína Pós-TraducionalRESUMO
Currently, there is no single concept of the optimal spatial structure of mRNA during translation. It is known that many proteins, associated with the 5' end of mRNA, interact with proteins associated with the 3' end. Moreover, this interaction often affects the activity of these proteins. It is possible within the same mRNA molecule only when the mRNA forms a circular structure in which its ends are spatially close. Discovery of such proteins, in the 90s of the 20th century, made it possible to formulate the closed-loop mRNA structure hypothesis, in which it is assumed that the ends of translationally active mRNA are fixed next to each other due to the interaction of proteins and (or) RNA. However, later it was shown that a closed-loop structure is not always necessary for translation. Moreover, some authors have proposed a model according to which the translating mRNA, on the contrary, should be unfolded into a linear structure. Thus, the spatial structure of the translating mRNA does not have to be universal for all mRNA and can change dynamically, which affects its functional activity. In this review, we have summarized a variety of experimental data and concepts on the relationship between the spatial structure of mRNA and its translational activity.