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RAM/Fam103a1 Is Required for mRNA Cap Methylation

The 7-methylguanosine cap added to the 5′ end of mRNA is required for efficient gene expression in eukaryotes. In mammals, methylation of the guanosine cap is catalyzed by RNMT (RNA guanine-7 methyltransferase), an enzyme previously thought to function as a monomer. We have identified an obligate co...

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Detalles Bibliográficos
Autores principales: Gonatopoulos-Pournatzis, Thomas, Dunn, Sianadh, Bounds, Rebecca, Cowling, Victoria H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235549/
https://www.ncbi.nlm.nih.gov/pubmed/22099306
http://dx.doi.org/10.1016/j.molcel.2011.08.041
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author Gonatopoulos-Pournatzis, Thomas
Dunn, Sianadh
Bounds, Rebecca
Cowling, Victoria H.
author_facet Gonatopoulos-Pournatzis, Thomas
Dunn, Sianadh
Bounds, Rebecca
Cowling, Victoria H.
author_sort Gonatopoulos-Pournatzis, Thomas
collection PubMed
description The 7-methylguanosine cap added to the 5′ end of mRNA is required for efficient gene expression in eukaryotes. In mammals, methylation of the guanosine cap is catalyzed by RNMT (RNA guanine-7 methyltransferase), an enzyme previously thought to function as a monomer. We have identified an obligate component of the mammalian cap methyltransferase, RAM (RNMT-Activating Mini protein)/Fam103a1, a previously uncharacterized protein. RAM consists of an N-terminal RNMT-activating domain and a C-terminal RNA-binding domain. As monomers RNMT and RAM have a relatively weak affinity for RNA; however, together their RNA affinity is significantly increased. RAM is required for efficient cap methylation in vitro and in vivo, and is indirectly required to maintain mRNA expression levels, for mRNA translation and for cell viability. Our findings demonstrate that RAM is an essential component of the core gene expression machinery.
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spelling pubmed-32355492011-12-28 RAM/Fam103a1 Is Required for mRNA Cap Methylation Gonatopoulos-Pournatzis, Thomas Dunn, Sianadh Bounds, Rebecca Cowling, Victoria H. Mol Cell Article The 7-methylguanosine cap added to the 5′ end of mRNA is required for efficient gene expression in eukaryotes. In mammals, methylation of the guanosine cap is catalyzed by RNMT (RNA guanine-7 methyltransferase), an enzyme previously thought to function as a monomer. We have identified an obligate component of the mammalian cap methyltransferase, RAM (RNMT-Activating Mini protein)/Fam103a1, a previously uncharacterized protein. RAM consists of an N-terminal RNMT-activating domain and a C-terminal RNA-binding domain. As monomers RNMT and RAM have a relatively weak affinity for RNA; however, together their RNA affinity is significantly increased. RAM is required for efficient cap methylation in vitro and in vivo, and is indirectly required to maintain mRNA expression levels, for mRNA translation and for cell viability. Our findings demonstrate that RAM is an essential component of the core gene expression machinery. Cell Press 2011-11-18 /pmc/articles/PMC3235549/ /pubmed/22099306 http://dx.doi.org/10.1016/j.molcel.2011.08.041 Text en © 2011 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Gonatopoulos-Pournatzis, Thomas
Dunn, Sianadh
Bounds, Rebecca
Cowling, Victoria H.
RAM/Fam103a1 Is Required for mRNA Cap Methylation
title RAM/Fam103a1 Is Required for mRNA Cap Methylation
title_full RAM/Fam103a1 Is Required for mRNA Cap Methylation
title_fullStr RAM/Fam103a1 Is Required for mRNA Cap Methylation
title_full_unstemmed RAM/Fam103a1 Is Required for mRNA Cap Methylation
title_short RAM/Fam103a1 Is Required for mRNA Cap Methylation
title_sort ram/fam103a1 is required for mrna cap methylation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235549/
https://www.ncbi.nlm.nih.gov/pubmed/22099306
http://dx.doi.org/10.1016/j.molcel.2011.08.041
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