Evidence map›Paper›PMID 37230964›Full record

ArticleNature communications2023

An Aurora B-RPA signaling axis secures chromosome segregation fidelity.

Poonam Roshan, Sahiti Kuppa, Jenna R Mattice, Vikas Kaushik, Rahul Chadda, Nilisha Pokhrel, Brunda R Tumala, Aparna Biswas, Brian Bothner, Edwin Antony and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Fluorescent human RPA to track assembly dynamics on DNA.bioRxiv : the preprint server for biology · 2023
    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 3 institutions in 1 country.

Poonam Roshan *Department of Biology, St. Louis University, St. Louis, MO, 63103, USA.
Sahiti Kuppa *Department of Biochemistry and Molecular Biology, St. Louis University School of Medicine, St. Louis, MO, 63104, USA.
Jenna R MatticeDepartment of Biochemistry, Montana State University, Bozeman, MT, 59717, USA.
Vikas KaushikDepartment of Biochemistry and Molecular Biology, St. Louis University School of Medicine, St. Louis, MO, 63104, USA.
Rahul ChaddaDepartment of Biochemistry and Molecular Biology, St. Louis University School of Medicine, St. Louis, MO, 63104, USA.
Nilisha PokhrelDepartment of Biological Sciences, Marquette University, Milwaukee, WI, 53217, USA.
Brunda R TumalaDepartment of Biochemistry and Molecular Biology, St. Louis University School of Medicine, St. Louis, MO, 63104, USA.
Aparna BiswasDepartment of Biology, St. Louis University, St. Louis, MO, 63103, USA.
Brian BothnerDepartment of Biochemistry, Montana State University, Bozeman, MT, 59717, USA.ORCID 0000-0003-1295-9609
Edwin AntonyDepartment of Biochemistry and Molecular Biology, St. Louis University School of Medicine, St. Louis, MO, 63104, USA. edwin.antony@health.slu.edu.ORCID 0000-0002-1888-054X
Sofia OrigantiDepartment of Biology, St. Louis University, St. Louis, MO, 63103, USA. sofia.origanti@slu.edu.ORCID 0000-0002-6953-0160
Saint Louis University · USMontana State University · USMarquette University · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
Research Core (Developmental Research Project Program)P20GM103474 · NIGMS · MONTANA STATE UNIVERSITY - BOZEMAN · PI BRIAN P BOTHNER · 2012 to 2026
$60.0M
Coordination of DNA Metabolism by Replication Protein AR35GM149320 · NIGMS · SAINT LOUIS UNIVERSITY · PI Edwin Antony · 2023 to 2026
$2.3M
Mechanism and Regulation of eIF6 in TranslationR01GM143179 · NIGMS · SAINT LOUIS UNIVERSITY · PI Sofia Origanti · 2022 to 2026
$1.8M
Supplement Request for a FluorometerR01GM133967 · NIGMS · SAINT LOUIS UNIVERSITY · PI ANTONY, EDWIN · 2019 to 2023
$1.5M
Mechanisms of DNA hand-off during lesion repair in BER and NER supplementR01GM130746 · NIGMS · SAINT LOUIS UNIVERSITY · PI ANTONY, EDWIN · 2019 to 2022
$1.4M
Ultra Performance Liquid Chromatography Tandem Mass Spectrometer for MetabolomicsS10OD028650 · OD · MONTANA STATE UNIVERSITY - BOZEMAN · PI BOTHNER, BRIAN P · 2020 to 2020
$599k
Acquisition of an Optima Analytical UltracentrifugeS10OD030343 · OD · SAINT LOUIS UNIVERSITY · PI ANTONY, EDWIN · 2021 to 2021
$515k
Role of nuclear chaperones in genomic instability and carcinogenesisK00CA274696 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Sahiti Kuppa · 2023 to 2026
$377k
Role of nuclear chaperones in genomic instability and carcinogenesisF99CA274696 · NCI · SAINT LOUIS UNIVERSITY · PI KUPPA, SAHITI · 2022 to 2022
$34k
NCI NIH HHS F99 CA274696NCI NIH HHS K00 CA274696NCI NIH HHS P30 CA091842NIGMS NIH HHS P20 GM103474NIGMS NIH HHS R01 GM130746NIGMS NIH HHS R01 GM133967NIGMS NIH HHS R01 GM143179NIGMS NIH HHS R35 GM149320NIH HHS S10 OD028650NIH HHS S10 OD030343
6 · The paper itself

Abstract

Errors in chromosome segregation underlie genomic instability associated with cancers. Resolution of replication and recombination intermediates and protection of vulnerable single-stranded DNA (ssDNA) intermediates during mitotic progression requires the ssDNA binding protein Replication Protein A (RPA). However, the mechanisms that regulate RPA specifically during unperturbed mitotic progression are poorly resolved. RPA is a heterotrimer composed of RPA70, RPA32 and RPA14 subunits and is predominantly regulated through hyperphosphorylation of RPA32 in response to DNA damage. Here, we have uncovered a mitosis-specific regulation of RPA by Aurora B kinase. Aurora B phosphorylates Ser-384 in the DNA binding domain B of the large RPA70 subunit and highlights a mode of regulation distinct from RPA32. Disruption of Ser-384 phosphorylation in RPA70 leads to defects in chromosome segregation with loss of viability and a feedback modulation of Aurora B activity. Phosphorylation at Ser-384 remodels the protein interaction domains of RPA. Furthermore, phosphorylation impairs RPA binding to DSS1 that likely suppresses homologous recombination during mitosis by preventing recruitment of DSS1-BRCA2 to exposed ssDNA. We showcase a critical Aurora B-RPA signaling axis in mitosis that is essential for maintaining genomic integrity.

Indexed as

Chromosome SegregationReplication Protein AAurora Kinase BDNA-Binding ProteinsDNA, Single-StrandedPhosphorylationAurora Kinase BDNA-Binding ProteinsDNA, Single-StrandedReplication Protein A

Identifiers

PMID37230964
PMCPMC10212944
OpenAlexW4378220816

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Registered trials

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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.