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Cohesin acetyltransferase Esco2 is a cell viability factor and is required for cohesion in pericentric heterochromatin
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scholarly article
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PubMed
PubMed ID
22101327
retrieved
25 January 2017
title
Cohesin acetyltransferase Esco2 is a cell viability factor and is required for cohesion in pericentric heterochromatin
(English)
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PubMed
PubMed ID
22101327
retrieved
25 January 2017
main subject
Chromobox 5
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GOA release 2020-03-11
Establishment of sister chromatid cohesion N-acetyltransferase 2
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GOA release 2020-03-11
author
Jan-Michael Peters
series ordinal
5
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Gordana Wutz
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3
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Gabriela Whelan
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1
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author name string
Emanuel Kreidl
series ordinal
2
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PubMed
PubMed ID
22101327
retrieved
25 January 2017
Alexander Egner
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
22101327
retrieved
25 January 2017
Gregor Eichele
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
22101327
retrieved
25 January 2017
language of work or name
English
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publication date
4 January 2012
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PubMed
PubMed ID
22101327
retrieved
25 January 2017
published in
The EMBO Journal
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stated in
PubMed
PubMed ID
22101327
retrieved
25 January 2017
volume
31
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stated in
PubMed
PubMed ID
22101327
retrieved
25 January 2017
issue
1
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stated in
PubMed
PubMed ID
22101327
retrieved
25 January 2017
page(s)
71–82
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stated in
PubMed
PubMed ID
22101327
retrieved
25 January 2017
cites work
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Mediator and cohesin connect gene expression and chromatin architecture
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Phosphorylation of H2A by Bub1 prevents chromosomal instability through localizing shugoshin
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The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2
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Eco1-dependent cohesin acetylation during establishment of sister chromatid cohesion
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PubMed Central
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19 March 2017
Acetylation of Smc3 by Eco1 is required for S phase sister chromatid cohesion in both human and yeast
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PubMed Central
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19 March 2017
Sororin is required for stable binding of cohesin to chromatin and for sister chromatid cohesion in interphase
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PubMed Central
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19 March 2017
Wapl controls the dynamic association of cohesin with chromatin
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PubMed Central
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19 March 2017
Human Wapl is a cohesin-binding protein that promotes sister-chromatid resolution in mitotic prophase
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PubMed Central
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19 March 2017
Establishment of sister chromatid cohesion at the S. cerevisiae replication fork
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PCNA controls establishment of sister chromatid cohesion during S phase
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Separase: a universal trigger for sister chromatid disjunction but not chromosome cycle progression
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19 March 2017
Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation
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19 March 2017
Two human orthologues of Eco1/Ctf7 acetyltransferases are both required for proper sister-chromatid cohesion
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PubMed Central
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19 March 2017
Shugoshin prevents dissociation of cohesin from centromeres during mitosis in vertebrate cells
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PubMed Central
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Mitotic regulation of the human anaphase-promoting complex by phosphorylation
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19 March 2017
Cohesin cleavage by separase required for anaphase and cytokinesis in human cells
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PubMed Central
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19 March 2017
Yeast cohesin complex requires a conserved protein, Eco1p(Ctf7), to establish cohesion between sister chromatids during DNA replication
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PubMed Central
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19 March 2017
Ctf7p is essential for sister chromatid cohesion and links mitotic chromosome structure to the DNA replication machinery
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PubMed Central
reference URL
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Efficient in vivo manipulation of mouse genomic sequences at the zygote stage
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PubMed Central
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7 April 2017
Cohesin: its roles and mechanisms
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PubMed Central
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High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP
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PubMed Central
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Efficient recombination in diverse tissues by a tamoxifen-inducible form of Cre: a tool for temporally regulated gene activation/inactivation in the mouse
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7 April 2017
A zebrafish model of Roberts syndrome reveals that Esco2 depletion interferes with development by disrupting the cell cycle
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PubMed Central
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29 September 2017
A conserved motif at the C terminus of sororin is required for sister chromatid cohesion
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PubMed Central
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29 September 2017
Sororin cooperates with the acetyltransferase Eco2 to ensure DNA replication-dependent sister chromatid cohesion
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PubMed Central
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The expanding universe of cohesin functions: a new genome stability caretaker involved in human disease and cancer.
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29 September 2017
Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
Studies of meiosis disclose distinct roles of cohesion in the core centromere and pericentromeric regions
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
Sister chromatid cohesion: a simple concept with a complex reality
1 reference
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PubMed Central
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29 September 2017
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
BAC TransgeneOmics: a high-throughput method for exploration of protein function in mammals
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
The complete removal of cohesin from chromosome arms depends on separase
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
Regulatory pathway analysis by high-throughput in situ hybridization
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PubMed Central
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29 September 2017
Roles of the sister chromatid cohesion apparatus in gene expression, development, and human syndromes
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in Nmd efficiency.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
The temporal program of DNA replication: new insights into old questions
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PubMed Central
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29 September 2017
The selective continued linkage of centromeres from mitosis to interphase in the absence of mammalian separase
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
A CAF-1 dependent pool of HP1 during heterochromatin duplication
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
Roberts syndrome: a review of 100 cases and a new rating system for severity
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
Abnormalities in the cell-division cycle in Roberts syndrome fibroblasts: a cellular basis for the phenotypic characteristics?
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
Cytogenetic findings in Roberts-SC phocomelia syndrome(s)
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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29 September 2017
Distinct targets of the Eco1 acetyltransferase modulate cohesion in S phase and in response to DNA damage
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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2 June 2018
Cortical excitatory neurons and glia, but not GABAergic neurons, are produced in the Emx1-expressing lineage.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3252581
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2 June 2018
Existence of two populations of cyclin/proliferating cell nuclear antigen during the cell cycle: association with DNA replication sites
1 reference
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PubMed Central
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2 June 2018
Studies of mitotic and centromeric abnormalities in Roberts syndrome: Implications for a defect in the mitotic mechanism
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Crossref
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https://api.crossref.org/works/10.1038%2FEMBOJ.2011.381
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21 January 2018
Building sister chromatid cohesion: smc3 acetylation counteracts an antiestablishment activity.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEMBOJ.2011.381
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21 January 2018
Budding yeast Wpl1(Rad61)-Pds5 complex counteracts sister chromatid cohesion-establishing reaction.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEMBOJ.2011.381
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21 January 2018
Cohesion between sister chromatids must be established during DNA replication
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FEMBOJ.2011.381
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21 January 2018
A molecular determinant for the establishment of sister chromatid cohesion
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEMBOJ.2011.381
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21 January 2018
Two histone marks establish the inner centromere and chromosome bi-orientation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEMBOJ.2011.381
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21 January 2018
Premature centromere splitting in a presumptive mild form of Roberts syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEMBOJ.2011.381
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21 January 2018
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22101327
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1038/EMBOJ.2011.381
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PMC publication ID
3252581
0 references
PubMed ID
22101327
1 reference
stated in
PubMed
PubMed ID
22101327
retrieved
25 January 2017
ResearchGate publication ID
51815561
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