Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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MitoRibo-seq and RNA-seq of parental and MRM2 knockout HEK 293T Flp-In T-REx cells


ABSTRACT: Methyltransferase MRM2 methylates the 2’-hydroxyl group of ribonucleotide U1369 of human 16S mt-rRNA. Mutations in MRM2 have been implicated in human mitochondrial-related disease. This study investigates the role of MRM2 in the biogenesis and function of human mitochondrial ribosomes. Absence of MRM2 leads to a severe defect in mitochondrial translation, with the mtLSU being trapped in immature assembly states.

INSTRUMENT(S): Illumina HiSeq 4000

ORGANISM(S): Homo sapiens

SUBMITTER: Pedro Rebelo-Guiomar 

PROVIDER: E-MTAB-11292 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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