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S-adenosylmethionine tRNA modification: unexpected/unsuspected implications of former/new players

S-adenosylmethionine supplies methyl groups to many acceptors, including lipids, proteins, RNA, DNA, and a wide range of small molecules. It acts as the precursor in the biosynthesis of metal ion chelating compounds, such as nicotianamine and phytosiderophores, of the polyamines spermidine and sperm...

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Detalles Bibliográficos
Autores principales: Adami, Raffaella, Bottai, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545696/
https://www.ncbi.nlm.nih.gov/pubmed/33061813
http://dx.doi.org/10.7150/ijbs.49302
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author Adami, Raffaella
Bottai, Daniele
author_facet Adami, Raffaella
Bottai, Daniele
author_sort Adami, Raffaella
collection PubMed
description S-adenosylmethionine supplies methyl groups to many acceptors, including lipids, proteins, RNA, DNA, and a wide range of small molecules. It acts as the precursor in the biosynthesis of metal ion chelating compounds, such as nicotianamine and phytosiderophores, of the polyamines spermidine and spermine and of some plant hormones. Finally, it is the source of catalytic 5′-deoxyadenosyl radicals. Radical S-adenosylmethionine (SAM) enzymes (RS) represent one of the most abundant groups (more than 100,000) of enzymes, exerting a plethora of biological functions, some of which are still unknown. In this work, we will focus on two RS: CDK5RAP1 and CDKAL1, both of which are involved in tRNA modifications that result in important tRNA folding and stability and in maintaining high translational fidelity. Based on this crucial role, their impairment can be important in the development of different human diseases.
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spelling pubmed-75456962020-10-13 S-adenosylmethionine tRNA modification: unexpected/unsuspected implications of former/new players Adami, Raffaella Bottai, Daniele Int J Biol Sci Review S-adenosylmethionine supplies methyl groups to many acceptors, including lipids, proteins, RNA, DNA, and a wide range of small molecules. It acts as the precursor in the biosynthesis of metal ion chelating compounds, such as nicotianamine and phytosiderophores, of the polyamines spermidine and spermine and of some plant hormones. Finally, it is the source of catalytic 5′-deoxyadenosyl radicals. Radical S-adenosylmethionine (SAM) enzymes (RS) represent one of the most abundant groups (more than 100,000) of enzymes, exerting a plethora of biological functions, some of which are still unknown. In this work, we will focus on two RS: CDK5RAP1 and CDKAL1, both of which are involved in tRNA modifications that result in important tRNA folding and stability and in maintaining high translational fidelity. Based on this crucial role, their impairment can be important in the development of different human diseases. Ivyspring International Publisher 2020-09-30 /pmc/articles/PMC7545696/ /pubmed/33061813 http://dx.doi.org/10.7150/ijbs.49302 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Adami, Raffaella
Bottai, Daniele
S-adenosylmethionine tRNA modification: unexpected/unsuspected implications of former/new players
title S-adenosylmethionine tRNA modification: unexpected/unsuspected implications of former/new players
title_full S-adenosylmethionine tRNA modification: unexpected/unsuspected implications of former/new players
title_fullStr S-adenosylmethionine tRNA modification: unexpected/unsuspected implications of former/new players
title_full_unstemmed S-adenosylmethionine tRNA modification: unexpected/unsuspected implications of former/new players
title_short S-adenosylmethionine tRNA modification: unexpected/unsuspected implications of former/new players
title_sort s-adenosylmethionine trna modification: unexpected/unsuspected implications of former/new players
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545696/
https://www.ncbi.nlm.nih.gov/pubmed/33061813
http://dx.doi.org/10.7150/ijbs.49302
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