Evidence map›Paper›PMID 16717126›Full record

ArticleThe Journal of cell biology2006

Mouse SYCP2 is required for synaptonemal complex assembly and chromosomal synapsis during male meiosis.

Fang Yang, Rabindranath De La Fuente, N Adrian Leu, Claudia Baumann, K John McLaughlin, P Jeremy Wang

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 153 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
153citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

153 citing papers in PubMed, 1 synthesis or guideline pooled it, 281 citations in OpenAlex.

  1. Pooled it
  2. Controlling Meiotic Double-Strand Break Formation in Mice: A Web of Multivalent Protein-Protein Interactions.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Review
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  8. Review
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  10. Article
  11. Article
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  14. Topographic Axes of Wiring Space Converge to Genetic Topography in Shaping the Human Cortical Layout.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  15. Article
  16. Article
  17. A novel loss-of-functionFrontiers in genetics · 2025
    Article
  18. Article
  19. Article
  20. Article

93 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Fang YangDepartment of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Rabindranath De La Fuente
N Adrian Leu
Claudia Baumann
K John McLaughlin
P Jeremy Wang
University of Pennsylvania · US

Funding

Epigenetic Control of Heterochromatin FormationR01HD042740 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI DE LA FUENTE, RABINDRANATH · 2004 to 2010
$1.6M
Regulation of Spermiogenesis in MiceU01HD045866 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI WANG, PEIJING JEREMY · 2004 to 2008
$1.4M
NICHD NIH HHS HD042740NICHD NIH HHS R01 HD042740NICHD NIH HHS U01 HD045866
6 · The paper itself

Abstract

During meiosis, the arrangement of homologous chromosomes is tightly regulated by the synaptonemal complex (SC). Each SC consists of two axial/lateral elements (AEs/LEs), and numerous transverse filaments. SC protein 2 (SYCP2) and SYCP3 are integral components of AEs/LEs in mammals. We find that SYCP2 forms heterodimers with SYCP3 both in vitro and in vivo. An evolutionarily conserved coiled coil domain in SYCP2 is required for binding to SYCP3. We generated a mutant Sycp2 allele in mice that lacks the coiled coil domain. The fertility of homozygous Sycp2 mutant mice is sexually dimorphic; males are sterile because of a block in meiosis, whereas females are subfertile with sharply reduced litter size. Sycp2 mutant spermatocytes exhibit failure in the formation of AEs and chromosomal synapsis. Strikingly, the mutant SYCP2 protein localizes to axial chromosomal cores in both spermatocytes and fetal oocytes, but SYCP3 does not, demonstrating that SYCP2 is a primary determinant of AEs/LEs and, thus, is required for the incorporation of SYCP3 into SCs.

Indexed as

AnimalsCell Cycle ProteinsChromosomal Proteins, Non-HistoneChromosome PairingChromosomesConserved SequenceDNA-Binding ProteinsFemaleInfertility, FemaleInfertility, MaleMaleMeiosisMiceMice, KnockoutMolecular Sequence DataMutationCell Cycle ProteinsChromosomal Proteins, Non-HistoneDNA-Binding ProteinsNuclear ProteinsSycp2 protein, mouseSycp3 protein, mouse

Identifiers

PMID16717126
PMCPMC2063860
OpenAlexW2099448734

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.