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Series GSE93133 Query DataSets for GSE93133
Status Public on Jan 05, 2017
Title The novel lysine specific methyltransferase METTL21B affects mRNA translation through inducible and dynamic methylation of Lys-165 in human eukaryotic elongation factor 1 alpha (eEF1A)
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Other
Summary Lysine methylation is abundant on histone proteins, representing a dynamic regulator of chromatin state and gene activity, but is also frequent on many nonhistone proteins, including eukaryotic elongation factor 1 alpha (eEF1A). However, the functional significance of eEF1Amethylation remains obscure and it has remained unclear whether eEF1A methylation is dynamic and subject to active regulation. We here demonstrate, using a wide range of in vitro and in vivo approaches, that the previously uncharacterized human methyltransferase METTL21B specifically targets Lys-165 in eEF1A in an aminoacyl-tRNA- and GTP-dependent manner. Interestingly, METTL21B mediated eEF1A methylation showed strong variation across different tissues and cell lines, and was induced by altering growth conditions or by treatment with certain ER-stress-inducing drugs, concomitant with an increase in METTL21B gene expression. Moreover, genetic ablation of METTL21B function in mammalian cells caused substantial alterations in mRNA translation, as measured by ribosome profiling. A non-canonical function for eEF1A in organization of the cellular cytoskeleton has been reported, and interestingly, METTL21B accumulated in centrosomes, in addition to the expected cytosolic localization. In summary, the present study identifies METTL21B as the enzyme responsible for methylation of eEF1A on Lys-165 and shows that this modification is dynamic, inducible and likely of regulatory importance.
 
Overall design Ribosome profiling libraries from haploid human cells from both wt and METTL21B knockouts.
 
Contributor(s) Matecki J, Aileni VK, Ho AY, Schwarz J, Moen A, Sørensen V, Nilges BS, Jakobsson M, Leidel SA, Falnes P
Citation(s) 28108655
Submission date Jan 04, 2017
Last update date May 15, 2019
Contact name Benedikt Sebastian Nilges
E-mail(s) benedikt.nilges@mpi-muenster.mpg.de
Organization name Max Planck Institute for Molecular Biomedicine
Department RNA Biology Group
Street address Von-Esmarch-Straße 54
City Muenster
ZIP/Postal code 48149
Country Germany
 
Platforms (1)
GPL15456 Illumina HiScanSQ (Homo sapiens)
Samples (4)
GSM2445294 WT-1
GSM2445295 WT-2
GSM2445296 METTL21B-1
Relations
BioProject PRJNA360112
SRA SRP096025

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Supplementary file Size Download File type/resource
GSE93133_counttable.csv.gz 252.6 Kb (ftp)(http) CSV
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Raw data are available in SRA
Processed data are available on Series record

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