Evidence map›Paper›PMID 24831702›Full record

ArticleGenes & development2014

E3 ligase Hei10: a multifaceted structure-based signaling molecule with roles within and beyond meiosis.

Arnaud De Muyt, Liangran Zhang, Tristan Piolot, Nancy Kleckner, Eric Espagne, Denise Zickler

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing 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

76 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. HEIP1 orchestrates pro-crossover protein activity during mammalian meiosis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. The histone variant H2A.W restricts heterochromatic crossovers inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Article
  15. Article
  16. Distinct and interdependent functions of three RING proteins regulate recombination during mammalian meiosis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Review
  18. Article
  19. Article
  20. Article

16 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 3 institutions in 2 countries.

Arnaud De MuytUMR 8621, Institut de Génétique et Microbiologie, Université Paris-Sud, 91405 Orsay, France; Institut Curie, 75248 Paris Cedex 05, France;
Liangran ZhangDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA;
Tristan PiolotUMR 3215, INSERM U934, Institut Curie, 75005 Paris, France.
Nancy KlecknerDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA;
Eric EspagneUMR 8621, Institut de Génétique et Microbiologie, Université Paris-Sud, 91405 Orsay, France;
Denise ZicklerUMR 8621, Institut de Génétique et Microbiologie, Université Paris-Sud, 91405 Orsay, France;
Université Paris-Sud · FRHarvard University · USInserm · FR

Funding

MEIOTIC CHROMOSOME SYNAPSIS AND RECOMBINATION IN YEASTR01GM044794 · NIGMS · HARVARD UNIVERSITY · PI KLECKNER, NANCY E · 1990 to 2018
$13.8M
NIGMS NIH HHS GM044794NIGMS NIH HHS R01 GM044794
6 · The paper itself

Abstract

Human enhancer of invasion-10 (Hei10) mediates meiotic recombination and also plays roles in cell proliferation. Here we explore Hei10's roles throughout the sexual cycle of the fungus Sordaria with respect to localization and effects of null, RING-binding, and putative cyclin-binding (RXL) domain mutations. Hei10 makes three successive types of foci. Early foci form along synaptonemal complex (SC) central regions. At some of these positions, depending on its RING and RXL domains, Hei10 mediates development and turnover of two sequential types of recombination complexes, each demarked by characteristic amplified Hei10 foci. Integration with ultrastructural data for recombination nodules further reveals that recombination complexes differentiate into three types, one of which corresponds to crossover recombination events during or prior to SC formation. Finally, Hei10 positively and negatively modulates SUMO localization along SCs by its RING and RXL domains, respectively. The presented findings suggest that Hei10 integrates signals from the SC, associated recombination complexes, and the cell cycle to mediate both the development and programmed turnover/evolution of recombination complexes via SUMOylation/ubiquitination. Analogous cell cycle-linked assembly/disassembly switching could underlie localization and roles for Hei10 in centrosome/spindle pole body dynamics and associated nuclear trafficking. We suggest that Hei10 is a unique type of structure-based signal transduction protein.

Indexed as

Signal TransductionFungal ProteinsMeiosisMutationProtein Structure, TertiaryRecombination, GeneticSordarialesSUMO-1 ProteinSynaptonemal ComplexUbiquitin-Protein LigasesFungal ProteinsSUMO-1 ProteinUbiquitin-Protein LigasesHei10meiosisrecombinationspindle pole body/centrosomesynaptonemal complex

Identifiers

PMID24831702
PMCPMC4035539
OpenAlexW2137314232

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.