The 7472insC mitochondrial DNA mutation impairs the synthesis and extent of aminoacylation of tRNASer(UCN) but not its structure or rate of turnover (Q43937103)

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scientific article published on 27 March 2002

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English	The 7472insC mitochondrial DNA mutation impairs the synthesis and extent of aminoacylation of tRNASer(UCN) but not its structure or rate of turnover	scientific article published on 27 March 2002

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scholarly article

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Europe PubMed Central

PubMed publication ID

28 November 2017

The 7472insC mitochondrial DNA mutation impairs the synthesis and extent of aminoacylation of tRNASer(UCN) but not its structure or rate of turnover (English)

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Europe PubMed Central

PubMed publication ID

28 November 2017

mitochondrial DNA

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28 November 2017

Johannes N Spelbrink

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28 November 2017

author name string

Marina Toompuu

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28 November 2017

Takehiro Yasukawa

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28 November 2017

Terhi Hakkinen

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28 November 2017

Kimitsuna Watanabe

6

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28 November 2017

Howard T Jacobs

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28 November 2017

language of work or name

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publication date

27 March 2002

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28 November 2017

Journal of Biological Chemistry

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28 November 2017

277

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28 November 2017

25

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28 November 2017

22240-22250

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28 November 2017

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: two genotypes produce similar phenotypes.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Search for differences in post-transcriptional modification patterns of mitochondrial DNA-encoded wild-type and mutant human tRNALys and tRNALeu(UUR).

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu)(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Mitochondrial tRNALeu isoforms in lung carcinoma cybrid cells containing the np 3243 mtDNA mutation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Mitochondrial DNA and RNA processing in MELAS.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Molecular phenotype of a human lymphoblastoid cell-line homoplasmic for the np 7445 deafness-associated mitochondrial mutation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Phy M: an RNase activity specific for U and A residues useful in RNA sequence analysis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

In vitro 3'-end endonucleolytic processing defect in a human mitochondrial tRNA(Ser(UCN)) precursor with the U7445C substitution, which causes non-syndromic deafness

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Higher-order structure of bovine mitochondrial tRNA(Phe) lacking the 'conserved' GG and T psi CG sequences as inferred by enzymatic and chemical probing.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

In vivo functional analysis of the human mitochondrial DNA polymerase POLG expressed in cultured human cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

A mitochondrial elongation factor-like protein is over-expressed in tumours and differentially expressed in normal tissues

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Compilation of tRNA sequences and sequences of tRNA genes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

A novel cloverleaf structure found in mammalian mitochondrial tRNA(Ser) (UCN).

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Evidence for aminoacylation-induced conformational changes in human mitochondrial tRNAs.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Mitochondria-associated ribonucleic acid of the HeLa cell. Effect of ethidium bromide on the synthesis of ribosomal and 4S ribonucleic acid

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Synthesis and turnover of mitochondrial ribonucleic acid in HeLa cells: the mature ribosomal and messenger ribonucleic acid species are metabolically unstable

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Additional copies of the mitochondrial Ef-Tu and aspartyl-tRNA synthetase genes can compensate for a mutation affecting the maturation of the mitochondrial tRNA Asp

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Ts mutations in mitochondrial tRNA genes: characterization and effects of two point mutations in the mitochondrial gene for tRNAphe in Saccharomyces cerevisiae.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Human tRNASer gene organization and a tRNASer gene sequence

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Site selection by Xenopus laevis RNAase P.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

The RNase P associated with HeLa cell mitochondria contains an essential RNA component identical in sequence to that of the nuclear RNase P.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Human mitochondrial tRNA processing

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

The long extra arms of human tRNA((Ser)Sec) and tRNA(Ser) function as major identify elements for serylation in an orientation-dependent, but not sequence-specific manner

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Dual mode recognition of two isoacceptor tRNAs by mammalian mitochondrial seryl-tRNA synthetase.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

A novel point mutation in the mitochondrial tRNA(Ser(UCN)) gene detected in a family with MERRF/MELAS overlap syndrome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Functional defects of pathogenic human mitochondrial tRNAs related to structural fragility

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

The effects of matrices of paired substitutions in mid-acceptor stem on Drosophila tRNA(His) structure and end-processing

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tRNA punctuation model of RNA processing in human mitochondria

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https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Inherited palmoplantar keratoderma and sensorineural deafness associated with A7445G point mutation in the mitochondrial genome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness families

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M200338200

21 January 2018

Identifiers

10.1074/JBC.M200338200

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

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