Evidence map›Paper›PMID 25758823›Full record

ArticleG3 (Bethesda, Md.)2015

Condensin II Regulates Interphase Chromatin Organization Through the Mrg-Binding Motif of Cap-H2.

Heather A Wallace, Joseph E Klebba, Thomas Kusch, Gregory C Rogers, Giovanni Bosco

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Condensin action and compaction.Current genetics · 2019
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Condensin I and II behaviour in interphase nuclei and cells undergoing premature chromosome condensation.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2016
    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

5 authors at 3 institutions in 1 country.

Heather A WallaceDepartment of Genetics, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire 03755.
Joseph E KlebbaDepartment of Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, Arizona 85721.
Thomas KuschSomerset, New Jersey 08873.
Gregory C RogersDepartment of Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, Arizona 85721.
Giovanni BoscoDepartment of Genetics, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire 03755 Giovanni.Bosco@Dartmouth.edu.
Dartmouth College · USUniversity of Arizona Cancer CenterSomerset Medical Center · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Fred W Kolling IV · 1985 to 2026
$91.3M
Developmental control of replication by Drosophila RBR01GM069462 · NIGMS · UNIVERSITY OF ARIZONA · PI BOSCO, GIOVANNI · 2004 to 2012
$2.5M
NCI NIH HHS P30 CA023108NIGMS NIH HHS GM069462NIGMS NIH HHS R01 GM069462
6 · The paper itself

Abstract

The spatial organization of the genome within the eukaryotic nucleus is a dynamic process that plays a central role in cellular processes such as gene expression, DNA replication, and chromosome segregation. Condensins are conserved multi-subunit protein complexes that contribute to chromosome organization by regulating chromosome compaction and homolog pairing. Previous work in our laboratory has shown that the Cap-H2 subunit of condensin II physically and genetically interacts with the Drosophila homolog of human MORF4-related gene on chromosome 15 (MRG15). Like Cap-H2, Mrg15 is required for interphase chromosome compaction and homolog pairing. However, the mechanism by which Mrg15 and Cap-H2 cooperate to maintain interphase chromatin organization remains unclear. Here, we show that Cap-H2 localizes to interband regions on polytene chromosomes and co-localizes with Mrg15 at regions of active transcription across the genome. We show that co-localization of Cap-H2 on polytene chromosomes is partially dependent on Mrg15. We have identified a binding motif within Cap-H2 that is essential for its interaction with Mrg15, and have found that mutation of this motif results in loss of localization of Cap-H2 on polytene chromosomes and results in partial suppression of Cap-H2-mediated compaction and homolog unpairing. Our data are consistent with a model in which Mrg15 acts as a loading factor to facilitate Cap-H2 binding to chromatin and mediate changes in chromatin organization.

Indexed as

Protein Interaction Domains and MotifsAdenosine TriphosphatasesAmino Acid MotifsAnimalsCell LineCells, CulturedChromatinChromosomal Proteins, Non-HistoneDNA-Binding ProteinsDrosophilaDrosophila ProteinsGene ExpressionGenes, ReporterGenomeInterphaseMultiprotein ComplexesAdenosine TriphosphatasesCap-H2 protein, DrosophilaChromatinChromosomal Proteins, Non-Histonecondensin complexesDNA-Binding ProteinsDrosophila ProteinsMRG15 protein, DrosophilaMultiprotein Complexeschromatin organizationchromosome structurecondensinhomolog pairingMrg15

Identifiers

PMID25758823
PMCPMC4426367
OpenAlexW2124652267

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.