- Home
- Publications
- Publication Search
- Publication Details
Title
Complete chemical structures of human mitochondrial tRNAs
Authors
Keywords
-
Journal
Nature Communications
Volume 11, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2020-08-28
DOI
10.1038/s41467-020-18068-6
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- TRMT2B is responsible for both tRNA and rRNA m5U-methylation in human mitochondria
- (2020) Christopher A. Powell et al. RNA Biology
- Queuine Micronutrient Deficiency Promotes Warburg Metabolism and Reversal of the Mitochondrial ATP Synthase in Hela Cells
- (2020) Patti Hayes et al. Nutrients
- NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs
- (2019) Lindsey Van Haute et al. NUCLEIC ACIDS RESEARCH
- Mammalian NSUN2 introduces 5-methylcytidines into mitochondrial tRNAs
- (2019) Saori Shinoda et al. NUCLEIC ACIDS RESEARCH
- Dual pathways of tRNA hydroxylation ensure efficient translation by expanding decoding capability
- (2019) Yusuke Sakai et al. Nature Communications
- Mouse Trmt2B protein is a dual specific mitochondrial metyltransferase responsible for m5U formation in both tRNA and rRNA
- (2019) Ivan Laptev et al. RNA Biology
- Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease
- (2018) Kana Asano et al. NUCLEIC ACIDS RESEARCH
- Defective Mitochondrial tRNA Taurine Modification Activates Global Proteostress and Leads to Mitochondrial Disease
- (2018) Md Fakruddin et al. Cell Reports
- Queuosine‐modified tRNAs confer nutritional control of protein translation
- (2018) Francesca Tuorto et al. EMBO JOURNAL
- Mitochondrial translation requires folate-dependent tRNA methylation
- (2018) Raphael J. Morscher et al. NATURE
- Acetate-dependent tRNA acetylation required for decoding fidelity in protein synthesis
- (2018) Takaaki Taniguchi et al. Nature Chemical Biology
- Cap-specific terminal N6-methylation of RNA by an RNA polymerase II–associated methyltransferase
- (2018) Shinichiro Akichika et al. SCIENCE
- Three distinct 3-methylcytidine (m 3 C) methyltransferases modify tRNA and mRNA in mice and humans
- (2017) Luang Xu et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Transcriptome-wide measurement of translation by ribosome profiling
- (2017) Nicholas J. McGlincy et al. METHODS
- Epitranscriptome sequencing technologies: decoding RNA modifications
- (2017) Xiaoyu Li et al. NATURE METHODS
- ALKBH1 is an RNA dioxygenase responsible for cytoplasmic and mitochondrial tRNA modifications
- (2017) Layla Kawarada et al. NUCLEIC ACIDS RESEARCH
- NSUN3 and ABH1 modify the wobble position of mt‐tRNAMetto expand codon recognition in mitochondrial translation
- (2016) Sara Haag et al. EMBO JOURNAL
- Precursors of tRNAs are stabilized by methylguanosine cap structures
- (2016) Takayuki Ohira et al. Nature Chemical Biology
- NSUN3 methylase initiates 5-formylcytidine biogenesis in human mitochondrial tRNAMet
- (2016) Saori Nakano et al. Nature Chemical Biology
- A mutation in the THG1L gene in a family with cerebellar ataxia and developmental delay
- (2016) Simon Edvardson et al. NEUROGENETICS
- tRNA base methylation identification and quantification via high-throughput sequencing
- (2016) Wesley C. Clark et al. RNA
- Deficient methylation and formylation of mt-tRNAMet wobble cytosine in a patient carrying mutations in NSUN3
- (2016) Lindsey Van Haute et al. Nature Communications
- Mitochondrial 16S rRNA Is Methylated by tRNA Methyltransferase TRMT61B in All Vertebrates
- (2016) Dan Bar-Yaacov et al. PLOS BIOLOGY
- Mtu1-Mediated Thiouridine Formation of Mitochondrial tRNAs Is Required for Mitochondrial Translation and Is Involved in Reversible Infantile Liver Injury
- (2016) Yong Wu et al. PLoS Genetics
- A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies
- (2016) Masakazu Kohda et al. PLoS Genetics
- Cdk5rap1-Mediated 2-Methylthio Modification of Mitochondrial tRNAs Governs Protein Translation and Contributes to Myopathy in Mice and Humans
- (2015) Fan-Yan Wei et al. Cell Metabolism
- Chemical pulldown reveals dynamic pseudouridylation of the mammalian transcriptome
- (2015) Xiaoyu Li et al. Nature Chemical Biology
- Efficient and quantitative high-throughput tRNA sequencing
- (2015) Guanqun Zheng et al. NATURE METHODS
- Transcriptome-wide dynamics of RNA pseudouridylation
- (2015) John Karijolich et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- NSUN6 is a human RNA methyltransferase that catalyzes formation of m5C72 in specific tRNAs
- (2015) Sara Haag et al. RNA
- The complete structure of the 55S mammalian mitochondrial ribosome
- (2015) B. J. Greber et al. SCIENCE
- The structure of the human mitochondrial ribosome
- (2015) A. Amunts et al. SCIENCE
- MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention
- (2015) Christin Tischner et al. HUMAN MOLECULAR GENETICS
- Pseudouridine: Still mysterious, but never a fake (uridine)!
- (2015) Felix Spenkuch et al. RNA Biology
- Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
- (2014) Robert Kopajtich et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Making Proteins in the Powerhouse
- (2014) B. Martin Hällberg et al. Cell Metabolism
- Improved Calibration of the Human Mitochondrial Clock Using Ancient Genomes
- (2014) Adrien Rieux et al. MOLECULAR BIOLOGY AND EVOLUTION
- Pseudouridine profiling reveals regulated mRNA pseudouridylation in yeast and human cells
- (2014) Thomas M. Carlile et al. NATURE
- A complete landscape of post-transcriptional modifications in mammalian mitochondrial tRNAs
- (2014) T. Suzuki et al. NUCLEIC ACIDS RESEARCH
- MTO1-Deficient Mouse Model Mirrors the Human Phenotype Showing Complex I Defect and Cardiomyopathy
- (2014) Lore Becker et al. PLoS One
- Defective i6A37 Modification of Mitochondrial and Cytosolic tRNAs Results from Pathogenic Mutations in TRIT1 and Its Substrate tRNA
- (2014) John W. Yarham et al. PLoS Genetics
- MTO1 Mutations are Associated with Hypertrophic Cardiomyopathy and Lactic Acidosis and Cause Respiratory Chain Deficiency in Humans and Yeast
- (2013) Enrico Baruffini et al. HUMAN MUTATION
- Expanded use of sense codons is regulated by modified cytidines in tRNA
- (2013) W. A. Cantara et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Multiplex Genome Engineering Using CRISPR/Cas Systems
- (2013) L. Cong et al. SCIENCE
- Mutations of the Mitochondrial-tRNA Modifier MTO1 Cause Hypertrophic Cardiomyopathy and Lactic Acidosis
- (2012) Daniele Ghezzi et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
- (2012) Lia Abbasi-Moheb et al. AMERICAN JOURNAL OF HUMAN GENETICS
- STAR: ultrafast universal RNA-seq aligner
- (2012) Alexander Dobin et al. BIOINFORMATICS
- A subcomplex of human mitochondrial RNase P is a bifunctional methyltransferase—extensive moonlighting in mitochondrial tRNA biogenesis
- (2012) Elisa Vilardo et al. NUCLEIC ACIDS RESEARCH
- Widespread occurrence of 5-methylcytosine in human coding and non-coding RNA
- (2012) Jeffrey E. Squires et al. NUCLEIC ACIDS RESEARCH
- Trmt61B is a methyltransferase responsible for 1-methyladenosine at position 58 of human mitochondrial tRNAs
- (2012) T. Chujo et al. RNA
- Human Mitochondrial tRNAs: Biogenesis, Function, Structural Aspects, and Diseases
- (2011) Tsutomu Suzuki et al. Annual Review of Genetics
- Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease
- (2011) J. Uusimaa et al. JOURNAL OF MEDICAL GENETICS
- Firefly luciferase mutants as sensors of proteome stress
- (2011) Rajat Gupta et al. NATURE METHODS
- Actin-binding protein ABP140 is a methyltransferase for 3-methylcytidine at position 32 of tRNAs in Saccharomyces cerevisiae
- (2011) A. Noma et al. RNA
- A domain of the actin binding protein Abp140 is the yeast methyltransferase responsible for 3-methylcytidine modification in the tRNA anti-codon loop
- (2011) S. D'Silva et al. RNA
- Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs
- (2011) Suzuki Tsutomu et al. Wiley Interdisciplinary Reviews-RNA
- Human mitochondrial mRNAs—like members of all families, similar but different
- (2010) Richard J. Temperley et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- Acute liver failure with subsequent cirrhosis as the primary manifestation of TRMU mutations
- (2010) Ulrike Schara et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Characterization of the human tRNA-guanine transglycosylase: Confirmation of the heterodimeric subunit structure
- (2010) Y. C. Chen et al. RNA
- Mitochondrial tRNA mutations and disease
- (2010) John W. Yarham et al. Wiley Interdisciplinary Reviews-RNA
- Acute Infantile Liver Failure Due to Mutations in the TRMU Gene
- (2009) Avraham Zeharia et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Tertiary network in mammalian mitochondrial tRNAAsp revealed by solution probing and phylogeny
- (2009) Marie Messmer et al. NUCLEIC ACIDS RESEARCH
- Unconventional decoding of the AUA codon as methionine by mitochondrial tRNA Met with the anticodon f 5 CAU as revealed with a mitochondrial in vitro translation system
- (2009) Chie Takemoto et al. NUCLEIC ACIDS RESEARCH
- A Disease-causing Point Mutation in Human Mitochondrial tRNAMetResults in tRNA Misfolding Leading to Defects in Translational Initiation and Elongation
- (2008) Christie N. Jones et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Modified Uridines with C5-methylene Substituents at the First Position of the tRNA Anticodon Stabilize U·G Wobble Pairing during Decoding
- (2008) Shinya Kurata et al. JOURNAL OF BIOLOGICAL CHEMISTRY
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started