Evidence map›Paper›PMID 20065034›Full record

ArticleMolecular and cellular biology2010

The DNA unwinding element binding protein DUE-B interacts with Cdc45 in preinitiation complex formation.

A Chowdhury, G Liu, M Kemp, X Chen, N Katrangi, S Myers, M Ghosh, J Yao, Y Gao, P Bubulya and 1 more

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 54 citations in OpenAlex.

  1. Mammalian Tolerance to Amino Acid Heterochirality.Chembiochem : a European journal of chemical biology · 2025
    Review
  2. Article
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  8. Protein phosphatases in chromatin structure and function.Biochimica et biophysica acta. Molecular cell research · 2019
    Review
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  10. Article
  11. Article
  12. Review
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  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Regulating DNA replication in eukarya.Cold Spring Harbor perspectives in biology · 2013
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

A ChowdhuryDepartment of Biochemistry and Molecular Biology, Boonshoft School of Medicine, Wright State University, Dayton, Ohio 45435, USA.
G Liu
M Kemp
X Chen
N Katrangi
S Myers
M Ghosh
J Yao
Y Gao
P Bubulya
M Leffak
Wright State University · US

Funding

HUMAN C MYC GENE REPLICATION ORIGINR01GM053819 · NIGMS · WRIGHT STATE UNIVERSITY · PI LEFFAK, MICHAEL · 1996 to 2012
$3.3M
Pre-mRNA Processing Factors Maintain Normal MitosisR15GM084407 · NIGMS · WRIGHT STATE UNIVERSITY · PI BUBULYA, PAULA A. · 2009 to 2019
$1.3M
The Role of the DNA Unwinding Element Binding Protein, DUE-B, in DNA ReplicationR01GM082995 · NIGMS · WRIGHT STATE UNIVERSITY · PI LEFFAK, MICHAEL · 2009 to 2010
$592k
NIGMS NIH HHS GM53819NIGMS NIH HHS GM82995NIGMS NIH HHS R01 GM053819NIGMS NIH HHS R01 GM082995NIGMS NIH HHS R15 GM084407
6 · The paper itself

Abstract

Template unwinding during DNA replication initiation requires the loading of the MCM helicase activator Cdc45 at replication origins. We show that Cdc45 interacts with the DNA unwinding element (DUE) binding protein DUE-B and that these proteins localize to the DUEs of active replication origins. DUE-B and Cdc45 are not bound at the inactive c-myc replicator in the absence of a functional DUE or at the recently identified ataxin 10 (ATX10) origin, which is silent before disease-related (ATTCT)(n) repeat length expansion of its DUE sequence, despite the presence of the origin recognition complex (ORC) and MCM proteins at these origins. Addition of a heterologous DUE to the ectopic c-myc origin, or expansion of the ATX10 DUE, leads to origin activation, DUE-B binding, and Cdc45 binding. DUE-B, Cdc45, and topoisomerase IIbeta binding protein 1 (TopBP1) form complexes in cell extracts and when expressed from baculovirus vectors. During replication in Xenopus egg extracts, DUE-B and Cdc45 bind to chromatin with similar kinetics, and DUE-B immunodepletion blocks replication and the loading of Cdc45 and a fraction of TopBP1. The coordinated binding of DUE-B and Cdc45 to origins and the physical interactions of DUE-B, Cdc45, and TopBP1 suggest that complexes of these proteins are necessary for replication initiation.

Indexed as

Replication OriginAmino Acid SequenceAnimalsCarrier ProteinsCell Cycle ProteinsChromatinDNA-Binding ProteinsFluorescent Antibody TechniqueHCT116 CellsHeLa CellsHumansIntracellular SpaceModels, BiologicalMolecular Sequence DataNuclear ProteinsOrigin Recognition ComplexCarrier ProteinsCDC45 protein, humanCell Cycle ProteinsChromatinDNA-Binding ProteinsDTD1 protein, humanNuclear ProteinsORC2 protein, humanOrigin Recognition ComplexSaccharomyces cerevisiae ProteinsSld3 protein, S cerevisiaeTOPBP1 protein, human

Identifiers

PMID20065034
PMCPMC2832489
OpenAlexW2024055173

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.