Evidence map›Paper›PMID 27129233›Full record

ArticleThe Journal of biological chemistry2016

The C-terminal 20 Amino Acids of Drosophila Topoisomerase 2 Are Required for Binding to a BRCA1 C Terminus (BRCT) Domain-containing Protein, Mus101, and Fidelity of DNA Segregation.

Yu-Tsung Shane Chen, Jianhong Wu, Paul Modrich, Tao-Shih Hsieh

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. The Role of Topoisomerase II in DNA Repair and Recombination inInternational journal of molecular sciences · 2021
    Article
  3. 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

4 authors at 3 institutions in 2 countries.

Yu-Tsung Shane ChenFrom the Department of Biochemistry and.
Jianhong WuFrom the Department of Biochemistry and.
Paul ModrichFrom the Department of Biochemistry and.
Tao-Shih HsiehFrom the Department of Biochemistry and the Institute of Cellular and Organismic Biology, Academia Sinica, Taipei 115, Taiwan Howard Hughes Medical Institute, Duke University Medical Center, Durham, North Carolina 27710 and hsieh002@gate.sinica.edu.tw.
Duke University Hospital · USDuke Medical Center · USInstitute of Cellular and Organismic Biology, Academia Sinica · TW

Funding

Enzymology Of Eukaryotic Mismatch RepairR01GM045190 · NIGMS · DUKE UNIVERSITY · PI MODRICH, PAUL LAWRENCE · 1991 to 2018
$6.8M
FUNCTION AND MECHANISM OF DNA TOPOISOMERASER01GM029006 · NIGMS · DUKE UNIVERSITY · PI HSIEH, TAO-SHIH · 1985 to 2010
$5.5M
NIGMS NIH HHS R01 GM029006NIGMS NIH HHS R01 GM045190
6 · The paper itself

Abstract

Eukaryotic topoisomerase 2 (Top2) and one of its interacting partners, topoisomerase IIβ binding protein 1 (TopBP1) are two proteins performing essential cellular functions. We mapped the interacting domains of these two proteins using co-immunoprecipitation and pulldown experiments with truncated or mutant Drosophila Top2 with various Ser-to-Ala substitutions. We discovered that the last 20 amino acids of Top2 represent the key region for binding with Mus101 (the Drosophila homolog of TopBP1) and that phosphorylation of Ser-1428 and Ser-1443 is important for Top2 to interact with the N terminus of Mus101, which contains the BRCT1/2 domains. The interaction between Mus101 and the Top2 C-terminal regulatory domain is phosphorylation-dependent because treatment with phosphatase abolishes their association in pulldown assays. The binding affinity of N-terminal Mus101 with a synthetic phosphorylated peptide spanning the last 25 amino acids of Top2 (with Ser(P)-1428 and Ser(P)-1443) was determined by surface plasmon resonance with a Kd of 0.57 μm In an in vitro decatenation assay, Mus101 can specifically reduce the decatenation activity of Top2, and dephosphorylation of Top2 attenuates this response. Next, we endeavored to establish a cellular system for testing the biological function of Top2-Mus101 interaction. Top2-silenced S2 cells rescued by Top2Δ20, Top2 with 20 amino acids truncated from the C terminus, developed abnormally high chromosome numbers, which implies that Top2-Mus101 interaction is important for maintaining the fidelity of chromosome segregation during mitosis.

Indexed as

Chromosome SegregationAmino Acid SequenceAnimalsBinding SitesCell CycleCell Cycle ProteinsCell LineChromosomes, InsectDNA, KinetoplastDNA Topoisomerases, Type IIDrosophila melanogasterDrosophila ProteinsMolecular Sequence DataProtein BindingProtein Interaction Domains and MotifsCell Cycle ProteinsDNA, KinetoplastDNA Topoisomerases, Type IIDrosophila Proteinsmus101 protein, Drosophilachromosome missegregationDNA replicationDNA topoisomeraseDrosophilaprotein phosphorylationRNA interference (RNAi)

Identifiers

PMID27129233
PMCPMC4933235
OpenAlexW2342983482

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.