Evidence map›Paper›PMID 32412326›Full record

ReviewNucleus (Austin, Tex.)2020

Telomere-led meiotic chromosome movements: recent update in structure and function.

C Y Lee, C G Bisig, M N Conrad, Y Ditamo, L Previato de Almeida, M E Dresser, R J Pezza

Open access · goldAbstract readReview
In one paragraph

Review in Nucleus (Austin, Tex.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Identifying Chromosome Movement Patterns During Meiosis Using ChroMo.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  3. Article
  4. Cells · 2021
    Article
  5. Article
  6. Review
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

7 authors at 2 institutions in 2 countries.

C Y LeeCell Cycle and Cancer Biology Research Program, Oklahoma Medical Research Foundation , Oklahoma City, OK, USA.
C G BisigFacultad de Ciencias Químicas, Dpto. Química Biológica Ranwel Caputto-CIQUIBIC, Universidad Nacional de Córdoba , Córdoba, Argentina.
M N ConradCell Cycle and Cancer Biology Research Program, Oklahoma Medical Research Foundation , Oklahoma City, OK, USA.
Y DitamoFacultad de Ciencias Químicas, Dpto. Química Biológica Ranwel Caputto-CIQUIBIC, Universidad Nacional de Córdoba , Córdoba, Argentina.
L Previato de AlmeidaCell Cycle and Cancer Biology Research Program, Oklahoma Medical Research Foundation , Oklahoma City, OK, USA.
M E DresserCell Cycle and Cancer Biology Research Program, Oklahoma Medical Research Foundation , Oklahoma City, OK, USA.
R J PezzaCell Cycle and Cancer Biology Research Program, Oklahoma Medical Research Foundation , Oklahoma City, OK, USA.
Oklahoma Medical Research Foundation · USUniversidad Nacional de Córdoba · AR

Funding

Epigenetic control of meiotic recombination in mammals - Equipment SupplementR01GM125803 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI PEZZA, ROBERTO JOSE · 2018 to 2021
$1.8M
Development of a lacO/lacI based flourescence reporter-operator system to study chromosome dynamics in miceR21HD103562 · NICHD · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI PEZZA, ROBERTO JOSE · 2021 to 2022
$495k
NICHD NIH HHS R21 HD103562NIGMS NIH HHS R01 GM125803
6 · The paper itself

Abstract

In S. cerevisiae prophase meiotic chromosomes move by forces generated in the cytoplasm and transduced to the telomere via a protein complex located in the nuclear membrane. We know that chromosome movements require actin cytoskeleton [13,31] and the proteins Ndj1, Mps3, and Csm4. Until recently, the identity of the protein connecting Ndj1-Mps3 with the cytoskeleton components was missing. It was also not known the identity of a cytoplasmic motor responsible for interacting with the actin cytoskeleton and a protein at the outer nuclear envelope. Our recent work [36] identified Mps2 as the protein connecting Ndj1-Mps3 with cytoskeleton components; Myo2 as the cytoplasmic motor that interacts with Mps2; and Cms4 as a regulator of Mps2 and Myo2 interaction and activities (Figure 1). Below we present a model for how Mps2, Csm4, and Myo2 promote chromosome movements by providing the primary connections joining telomeres to the actin cytoskeleton through the LINC complex.

Indexed as

Chromosomes, FungalMeiosisActin CytoskeletonChromosome StructuresModels, MolecularSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTelomereSaccharomyces cerevisiae ProteinsCsm4LINCMps2Myo2rapid prophase movements (RPMs)

Identifiers

PMID32412326
PMCPMC7781623
OpenAlexW3025602696

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.