Base composition at mtDNA boundaries suggests a DNA triple helix model for human mitochondrial DNA large-scale rearrangements. (Q44041085)

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10 November 2019

title

Base composition at mtDNA boundaries suggests a DNA triple helix model for human mitochondrial DNA large-scale rearrangements (English)

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10 November 2019

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1

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10 November 2019

William C Copeland

series ordinal

3

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10 November 2019

author name string

Thierry Letellier

series ordinal

2

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10 November 2019

Patrick Lestienne

series ordinal

4

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10 November 2019

publication date

1 June 2002

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Molecular Genetics and Metabolism

10 November 2019

published in

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10 November 2019

volume

76

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10 November 2019

issue

2

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10 November 2019

page(s)

123-132

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Replication of animal mitochondrial DNA.

10 November 2019

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Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

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A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.

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Partial triplication of mtDNA in maternally transmitted diabetes mellitus and deafness

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Initiation of DNA replication by DNA polymerases from primers forming a triple helix

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Cloning and characterization of the human mitochondrial DNA polymerase, DNA polymerase gamma

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The mitochondrial p55 accessory subunit of human DNA polymerase gamma enhances DNA binding, promotes processive DNA synthesis, and confers N-ethylmaleimide resistance

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Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

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Sequence and organization of the human mitochondrial genome

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Triplex DNA structures.

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Parallel and antiparallel (G.GC)2 triple helix fragments in a crystal structure

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Telomeric DNA oligonucleotides form novel intramolecular structures containing guanine-guanine base pairs

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Probing the structure of a putative intermediate in homologous recombination: the third strand in the parallel DNA triplex is in contact with the major groove of the duplex

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Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?

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Duplications of mitochondrial DNA in Kearns-Sayre syndrome

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Characterization of the native and recombinant catalytic subunit of human DNA polymerase gamma: identification of residues critical for exonuclease activity and dideoxynucleotide sensitivity

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7 January 2021

The accessory subunit of Xenopus laevis mitochondrial DNA polymerase gamma increases processivity of the catalytic subunit of human DNA polymerase gamma and is related to class II aminoacyl-tRNA synthetases

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7 January 2021

Termination within oligo(dT) tracts in template DNA by DNA polymerase gamma occurs with formation of a DNA triplex structure and is relieved by mitochondrial single-stranded DNA-binding protein

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Formation of a stable triplex from a single DNA strand

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Detection of a specific mitochondrial DNA deletion in tissues of older humans

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Differential regulation of the catalytic and accessory subunit genes of Drosophila mitochondrial DNA polymerase

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The fidelity of human DNA polymerase gamma with and without exonucleolytic proofreading and the p55 accessory subunit

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Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

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Role of adenine nucleotide translocator 1 in mtDNA maintenance

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Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

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Identifiers

DOI

1 reference

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10 November 2019

1 reference