(Q38624841)

4 September 2017

Integrating mitochondrial translation into the cellular context (English)

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4 September 2017

3

Peter Rehling

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author name string

Ricarda Richter-Dennerlein

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1

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4 September 2017

Sven Dennerlein

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2

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4 September 2017

Peter Rehling

series ordinal

3

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4 September 2017

1 October 2015

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Nature Reviews Molecular Cell Biology

4 September 2017

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4 September 2017

16

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4 September 2017

10

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4 September 2017

586-592

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https://scigraph.springernature.com/pub.10.1038/nrm4051

4 September 2017

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Making proteins in the powerhouse

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Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia

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Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation

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Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation

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Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy

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MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities.

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Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy

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Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiency

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Small RNA sorting: matchmaking for Argonautes.

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MicroRNA directly enhances mitochondrial translation during muscle differentiation

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Inhibition of human peptide deformylase disrupts mitochondrial function

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NOA1 is an essential GTPase required for mitochondrial protein synthesis

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A functional peptidyl-tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosome

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A mitochondrial ribosomal and RNA decay pathway blocks cell proliferation.

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Inhibition of mitochondrial translation as a therapeutic strategy for human acute myeloid leukemia

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Why translation counts for mitochondria - retrograde signalling links mitochondrial protein synthesis to mitochondrial biogenesis and cell proliferation

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Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology

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Regulation of mitochondrial morphology through proteolytic cleavage of OPA1

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Control of protein synthesis in yeast mitochondria: the concept of translational activators

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Mss51p promotes mitochondrial Cox1p synthesis and interacts with newly synthesized Cox1p.

31 March 2020

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Mss51p and Cox14p jointly regulate mitochondrial Cox1p expression in Saccharomyces cerevisiae

31 March 2020

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Dual functions of Mss51 couple synthesis of Cox1 to assembly of cytochrome c oxidase in Saccharomyces cerevisiae mitochondria

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Inventory control: cytochrome c oxidase assembly regulates mitochondrial translation

31 March 2020

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A heme-sensing mechanism in the translational regulation of mitochondrial cytochrome c oxidase biogenesis

31 March 2020

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Assembly factors monitor sequential hemylation of cytochrome b to regulate mitochondrial translation.

31 March 2020

1 reference

31 March 2020

Identifiers

DOI

10.1038/NRM4051

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Dimensions Publication ID

4 September 2017

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