Evidence map›Paper›PMID 27093083›Full record

ArticleDevelopmental cell2016

Co-evolving CENP-A and CAL1 Domains Mediate Centromeric CENP-A Deposition across Drosophila Species.

Leah Rosin, Barbara G Mellone

Abstract read
In one paragraph

Article in Developmental cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

  1. Article
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  3. Article
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  12. Centromere drive: model systems and experimental progress.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2022
    Review
  13. Article
  14. Article
  15. Kinetochore assembly throughout the cell cycle.Seminars in cell & developmental biology · 2021
    Article
  16. Article
  17. Article
  18. Histone variants at a glance.Journal of cell science · 2021
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Leah RosinDepartment of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269, USA.
Barbara G MelloneDepartment of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269, USA; Institute for Systems Genomics, University of Connecticut, Storrs, CT 06269, USA. Electronic address: barbara.mellone@uconn.edu.

Funding

A novel animal model approach to investigate neocentromere formation and inactivaR01GM108829 · NIGMS · UNIVERSITY OF CONNECTICUT STORRS · PI MELLONE, BARBARA · 2014 to 2018
$1.5M
NIGMS NIH HHS GM108829NIGMS NIH HHS R01 GM108829
6 · The paper itself

Abstract

Centromeres mediate the conserved process of chromosome segregation, yet centromeric DNA and the centromeric histone, CENP-A, are rapidly evolving. The rapid evolution of Drosophila CENP-A loop 1 (L1) is thought to modulate the DNA-binding preferences of CENP-A to counteract centromere drive, the preferential transmission of chromosomes with expanded centromeric satellites. Consistent with this model, CENP-A from Drosophila bipectinata (bip) cannot localize to Drosophila melanogaster (mel) centromeres. We show that this result is due to the inability of the mel CENP-A chaperone, CAL1, to deposit bip CENP-A into chromatin. Co-expression of bip CENP-A and bip CAL1 in mel cells restores centromeric localization, and similar findings apply to other Drosophila species. We identify two co-evolving regions, CENP-A L1 and the CAL1 N terminus, as critical for lineage-specific CENP-A incorporation. Collectively, our data show that the rapid evolution of L1 modulates CAL1-mediated CENP-A assembly, suggesting an alternative mechanism for the suppression of centromere drive.

Indexed as

AnimalsCentromereCentromere Protein AChromatinChromosome SegregationDNA-Binding ProteinsDrosophilaDrosophila ProteinsHistonesMitosisCal1 protein, DrosophilaCentromere Protein AChromatinCid protein, DrosophilaDNA-Binding ProteinsDrosophila ProteinsHistones

Identifiers

PMID27093083
PMCPMC4861639

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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.