Evidence map›Paper›PMID 41879670›Full record

ReviewThe Journal of cell biology2026

Structure and function of the synaptonemal complex.

Brenda I Cesar, Yumi Kim

Abstract readReview
In one paragraph

Review in The Journal of cell biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

2 authors.

Brenda I CesarDepartment of Biology, Johns Hopkins University, Baltimore, MD, USA.ORCID 0009-0004-3762-0032
Yumi KimDepartment of Biology, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0002-6110-5936

Funding

Molecular Control of Meiotic Chromosome DynamicsR35GM124895 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Yumi Kim · 2017 to 2026
$4.3M
In vitro Reconstitution of the C. elegans Synaptonemal ComplexF31GM153163 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CESAR-HERNANDEZ, BRENDA I · 2024 to 2025
$99k
NIGMS NIH HHS F31 GM153163NIGMS NIH HHS R35 GM124895NIH HHS F31GM153163NIH HHS R35GM124895
6 · The paper itself

Abstract

A defining feature of meiosis is the synaptonemal complex (SC), a zipper-like protein structure that forms between homologous chromosomes to regulate their recombination and segregation. Historically viewed as an enigmatic electron-dense scaffold, the SC is now recognized as a dynamic signaling platform that coordinates key meiotic processes. Here, we review recent advances in understanding SC structure and function. We describe diverse complementary approaches that have expanded the catalog of SC components and their network of interactions within this architecture. We highlight striking conservation in structural organization and ancient molecular modules that couple SC structure to crossover regulation and further discuss how the SC implements feedback mechanisms controlling meiotic DNA break formation and repair capacity to ensure faithful chromosome segregation across generations.

Indexed as

MeiosisSynaptonemal ComplexAnimalsChromosome SegregationHumans

Identifiers

PMID41879670
PMCPMC13265054

What OpenQuestion holds

Textmetadata
LicenceTDM
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.