(Q28512334)

25 January 2017

title

Covalent modification of the Werner's syndrome gene product with the ubiquitin-related protein, SUMO-1 (English)

1 reference

Ubiquitin-conjugating enzyme E2I

25 January 2017

main subject

1 reference

GOA release 2020-03-11

author name string

Y. Kawabe

1

1 reference

25 January 2017

M. Seki

2

1 reference

25 January 2017

T. Seki

3

1 reference

25 January 2017

W. S. Wang

4

1 reference

25 January 2017

O. Imamura

5

1 reference

25 January 2017

Y. Furuichi

6

1 reference

25 January 2017

H. Saitoh

7

1 reference

25 January 2017

T. Enomoto

8

1 reference

25 January 2017

language of work or name

English

0 references

publication date

14 July 2000

1 reference

Journal of Biological Chemistry

25 January 2017

published in

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25 January 2017

volume

275

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25 January 2017

issue

28

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25 January 2017

page(s)

20963–20966

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A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process

25 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Positional cloning of the Werner's syndrome gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

The recQ gene of Escherichia coli K12: molecular cloning and isolation of insertion mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

The Werner syndrome protein is a DNA helicase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

The premature ageing syndrome protein, WRN, is a 3'-->5' exonuclease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli Rec Q helicase and localization of the gene at chromosome 12p12

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

The Bloom's syndrome gene product is homologous to RecQ helicases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

The Werner syndrome protein is involved in RNA polymerase II transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

p53-mediated apoptosis is attenuated in Werner syndrome cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Replication focus-forming activity 1 and the Werner syndrome gene product

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Functional and physical interaction between WRN helicase and human replication protein A

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

The Werner syndrome gene product co-purifies with the DNA replication complex and interacts with PCNA and topoisomerase I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Physical and functional interaction between p53 and the Werner's syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Role of a ubiquitin-conjugating enzyme in degradation of S- and M-phase cyclins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Ubc9p is the conjugating enzyme for the ubiquitin-like protein Smt3p

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Preferential interaction of sentrin with a ubiquitin-conjugating enzyme, Ubc9.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Ubc9p and the conjugation of SUMO-1 to RanGAP1 and RanBP2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Cloning of a mouse homologue of the human Werner syndrome gene and assignment to 8A4 by fluorescence in situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

cDNA cloning of mouse BLM gene, the homologue to human Bloom's syndrome gene, which is highly expressed in the testis at the mRNA level

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Cloning of two isoforms of mouse DNA helicase Q1/RecQL cDNA; alpha form is expressed ubiquitously and beta form specifically in the testis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Role of Schizosaccharomyces pombe RecQ homolog, recombination, and checkpoint genes in UV damage tolerance

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Evidence for covalent modification of the nuclear dot-associated proteins PML and Sp100 by PIC1/SUMO-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Conjugation with the ubiquitin-related modifier SUMO-1 regulates the partitioning of PML within the nucleus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

SUMO-1 modification of IkappaBalpha inhibits NF-kappaB activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

SUMO-1 modification activates the transcriptional response of p53

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Activation of p53 by conjugation to the ubiquitin-like protein SUMO-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Covalent modification of the homeodomain-interacting protein kinase 2 (HIPK2) by the ubiquitin-like protein SUMO-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Identification of three major sentrinization sites in PML

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

The ubiquitin-like protein Smt3p is activated for conjugation to other proteins by an Aos1p/Uba2p heterodimer

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Characterisation of Schizosaccharomyces pombe rad31, a UBA-related gene required for DNA damage tolerance

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

Characterization of a fission yeast SUMO-1 homologue, pmt3p, required for multiple nuclear events, including the control of telomere length and chromosome segregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

rqh1+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C000273200

21 January 2018

Identifiers

DOI

10.1074/JBC.C000273200

0 references

1 reference