Mtu1-Mediated Thiouridine Formation of Mitochondrial tRNAs Is Required for Mitochondrial Translation and Is Involved in Reversible Infantile Liver Injury
出版年份 2016 全文链接
标题
Mtu1-Mediated Thiouridine Formation of Mitochondrial tRNAs Is Required for Mitochondrial Translation and Is Involved in Reversible Infantile Liver Injury
作者
关键词
Mitochondria, Mouse models, Hepatocytes, Oxidative stress, Transfer RNA, Embryos, Biosynthesis, Protein translation
出版物
PLoS Genetics
Volume 12, Issue 9, Pages e1006355
出版商
Public Library of Science (PLoS)
发表日期
2016-10-01
DOI
10.1371/journal.pgen.1006355
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Understanding the Physiology of FGF21
- (2016) Ffolliott Martin Fisher et al. Annual Review of Physiology
- Severe respiratory complex III defect prevents liver adaptation to prolonged fasting
- (2016) Laura S. Kremer et al. JOURNAL OF HEPATOLOGY
- Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterations
- (2016) Joshua E. Mangum et al. Scientific Reports
- Optic neuropathy, cardiomyopathy, cognitive disability in patients with a homozygous mutation in the nuclearMTO1and a mitochondrialMT-TFvariant
- (2015) Majida Charif et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- 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
- A Liver-Bone Endocrine Relay by IGFBP1 Promotes Osteoclastogenesis and Mediates FGF21-Induced Bone Resorption
- (2015) Xunde Wang et al. Cell Metabolism
- Opa1 Overexpression Ameliorates the Phenotype of Two Mitochondrial Disease Mouse Models
- (2015) Gabriele Civiletto et al. Cell Metabolism
- 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
- Tissue-Specific Loss of DARS2 Activates Stress Responses Independently of Respiratory Chain Deficiency in the Heart
- (2014) Sukru Anil Dogan et al. Cell Metabolism
- Reversible infantile mitochondrial diseases
- (2014) Veronika Boczonadi et al. JOURNAL OF INHERITED METABOLIC DISEASE
- A complete landscape of post-transcriptional modifications in mammalian mitochondrial tRNAs
- (2014) T. Suzuki et al. NUCLEIC ACIDS RESEARCH
- Hepatic mTORC1 controls locomotor activity, body temperature, and lipid metabolism through FGF21
- (2014) M. Cornu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Biosynthesis and functions of sulfur modifications in tRNA
- (2014) Naoki Shigi Frontiers in Genetics
- The Hallmarks of Aging
- (2013) Carlos López-Otín et al. CELL
- Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency
- (2013) Veronika Boczonadi et al. HUMAN MOLECULAR GENETICS
- Mitonuclear protein imbalance as a conserved longevity mechanism
- (2013) Riekelt H. Houtkooper et al. NATURE
- MODOMICS: a database of RNA modification pathways—2013 update
- (2012) Magdalena A. Machnicka et al. NUCLEIC ACIDS RESEARCH
- Human Mitochondrial tRNAs: Biogenesis, Function, Structural Aspects, and Diseases
- (2011) Tsutomu Suzuki et al. Annual Review of Genetics
- The 2-thiouridylase function of the human MTU1 (TRMU) enzyme is dispensable for mitochondrial translation
- (2011) F. Sasarman et al. HUMAN MOLECULAR GENETICS
- Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease
- (2011) J. Uusimaa et al. JOURNAL OF MEDICAL GENETICS
- Reversible infantile respiratory chain deficiency: A clinical and molecular study
- (2010) Masakazu Mimaki et al. ANNALS OF NEUROLOGY
- Acute liver failure with subsequent cirrhosis as the primary manifestation of TRMU mutations
- (2010) Ulrike Schara et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Acute Infantile Liver Failure Due to Mutations in the TRMU Gene
- (2009) Avraham Zeharia et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy
- (2009) R. Horvath et al. BRAIN
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