Transcription elongation and tissue-specific somatic CAG instability (Q34499436)

2 August 2017

title

Transcription elongation and tissue-specific somatic CAG instability (English)

1 reference

2 August 2017

author name string

Agathi-Vasiliki Goula

1

1 reference

2 August 2017

Agnieszka Stys

2

1 reference

2 August 2017

Jackson P K Chan

3

1 reference

2 August 2017

Yvon Trottier

4

1 reference

2 August 2017

Richard Festenstein

5

1 reference

2 August 2017

Karine Merienne

6

1 reference

2 August 2017

language of work or name

1 reference

29 November 2012

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2 August 2017

1 reference

2 August 2017

volume

8

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2 August 2017

issue

11

1 reference

2 August 2017

page(s)

e1003051

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Creative Commons Attribution 4.0 International

2 August 2017

copyright license

start time

29 November 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Hyperexpansion of GAA repeats affects post-initiation steps of FXN transcription in Friedreich's ataxia

7 July 2018

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DNA slip-outs cause RNA polymerase II arrest in vitro: potential implications for genetic instability

7 July 2018

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Repeat expansion affects both transcription initiation and elongation in friedreich ataxia cells

7 July 2018

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Bidirectional transcription stimulates expansion and contraction of expanded (CTG)*(CAG) repeats.

7 July 2018

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Pol II waiting in the starting gates: Regulating the transition from transcription initiation into productive elongation.

7 July 2018

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Determinants of R-loop formation at convergent bidirectionally transcribed trinucleotide repeats

7 July 2018

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Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues

7 July 2018

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The distribution of repressive histone modifications on silenced FMR1 alleles provides clues to the mechanism of gene silencing in fragile X syndrome

7 July 2018

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Convergent transcription through a long CAG tract destabilizes repeats and induces apoptosis

7 July 2018

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Mechanisms and implications of transcription blockage by guanine-rich DNA sequences.

7 July 2018

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Long intronic GAA repeats causing Friedreich ataxia impede transcription elongation

7 July 2018

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Effects of transcriptional pausing on gene expression dynamics

7 July 2018

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Repeat instability as the basis for human diseases and as a potential target for therapy

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

R loops stimulate genetic instability of CTG.CAG repeats

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Stoichiometry of base excision repair proteins correlates with increased somatic CAG instability in striatum over cerebellum in Huntington's disease transgenic mice

7 July 2018

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Epigenetic silencing in Friedreich ataxia is associated with depletion of CTCF (CCCTC-binding factor) and antisense transcription

7 July 2018

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Instability and chromatin structure of expanded trinucleotide repeats

7 July 2018

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Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset

7 July 2018

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The DNA-encoded nucleosome organization of a eukaryotic genome

7 July 2018

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Transcription-coupled DNA repair: two decades of progress and surprises

7 July 2018

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Single-RNA counting reveals alternative modes of gene expression in yeast

7 July 2018

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Chromatin remodeling in the noncoding repeat expansion diseases

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes

7 July 2018

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SIRT1 inhibition alleviates gene silencing in Fragile X mental retardation syndrome

7 July 2018

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The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissues

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

RNA polymerase is poised for activation across the genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Small molecules affecting transcription in Friedreich ataxia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

A chromatin landmark and transcription initiation at most promoters in human cells

7 July 2018

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Transcription-induced CAG repeat contraction in human cells is mediated in part by transcription-coupled nucleotide excision repair

7 July 2018

1 reference

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High-resolution profiling of histone methylations in the human genome

7 July 2018

1 reference

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OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells

7 July 2018

1 reference

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Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Chromatin modifications and their function

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Breaking barriers to transcription elongation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Histone deacetylase inhibitors reverse gene silencing in Friedreich's ataxia.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Transcription promotes contraction of CAG repeat tracts in human cells

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Stochasticity in gene expression: from theories to phenotypes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

MSH2-dependent germinal CTG repeat expansions are produced continuously in spermatogonia from DM1 transgenic mice.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacities.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Identification of a long huntingtin mRNA transcript in mouse brain

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Expression of normal and mutant huntingtin in the developing brain

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Trinucleotide repeat length instability and age of onset in Huntington's disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Huntington's disease gene (IT15) is widely expressed in human and rat tissues

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Trinucleotide repeats that expand in human disease form hairpin structures in vitro

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease

7 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

Progressive GAA expansions in dorsal root ganglia of Friedreich's ataxia patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

The GAA triplet-repeat is unstable in the context of the human FXN locus and displays age-dependent expansions in cerebellum and DRG in a transgenic mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

IT15 gene expression in fetal human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

Antisense transcription and heterochromatin at the DM1 CTG repeats are constrained by CTCF.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

Spatial distribution of di- and tri-methyl lysine 36 of histone H3 at active genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

Efficient release from promoter-proximal stall sites requires transcript cleavage factor TFIIS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

P-TEFb-mediated phosphorylation of hSpt5 C-terminal repeats is critical for processive transcription elongation

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

Synthesis and maturation of viral transcripts in herpes simplex virus type 1 infected HeLa cells: the role of interchromatin granules

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Expression of the mutant allele of IT-15 (the HD gene) in striatum and cortex of Huntington's disease patients

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510035

Survival and CTG repeat expansion in adults with myotonic dystrophy type 1

27 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

DNA triplet repeats mediate heterochromatin-protein-1-sensitive variegated gene silencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003051

Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23209427

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23209427

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Slipped (CTG)*(CAG) repeats can be correctly repaired, escape repair or undergo error-prone repair

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23209427

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1003051

1 reference

2 August 2017

1 reference

2 August 2017

1 reference