Evidence map›Paper›PMID 36504011›Full record

ArticleNucleic acids research2022

ZYP1-mediated recruitment of PCH2 to the synaptonemal complex remodels the chromosome axis leading to crossover restriction.

Chao Yang, Kostika Sofroni, Yuki Hamamura, Bingyan Hu, Hasibe Tunçay Elbasi, Martina Balboni, Lei Chu, Dagmar Stang, Maren Heese, Arp Schnittger

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

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  13. Meiosis in bulbous flower speciesFrontiers in plant science · 2025
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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

10 authors at 2 institutions in 2 countries.

Chao YangNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan 430070, China.ORCID 0000-0002-4035-6453
Kostika SofroniDepartment of Developmental Biology, Institute of Plant Science and Microbiology, University of Hamburg, Hamburg 22609, Germany.
Yuki HamamuraDepartment of Developmental Biology, Institute of Plant Science and Microbiology, University of Hamburg, Hamburg 22609, Germany.
Bingyan HuDepartment of Developmental Biology, Institute of Plant Science and Microbiology, University of Hamburg, Hamburg 22609, Germany.
Hasibe Tunçay ElbasiDepartment of Developmental Biology, Institute of Plant Science and Microbiology, University of Hamburg, Hamburg 22609, Germany.ORCID 0000-0001-5492-5920
Martina BalboniDepartment of Developmental Biology, Institute of Plant Science and Microbiology, University of Hamburg, Hamburg 22609, Germany.
Lei ChuNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan 430070, China.
Dagmar StangDepartment of Developmental Biology, Institute of Plant Science and Microbiology, University of Hamburg, Hamburg 22609, Germany.
Maren HeeseDepartment of Developmental Biology, Institute of Plant Science and Microbiology, University of Hamburg, Hamburg 22609, Germany.
Arp SchnittgerDepartment of Developmental Biology, Institute of Plant Science and Microbiology, University of Hamburg, Hamburg 22609, Germany.ORCID 0000-0001-7067-0091
Universität Hamburg · DEHuazhong Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromosome axis-associated HORMA domain proteins (HORMADs), e.g. ASY1 in Arabidopsis, are crucial for meiotic recombination. ASY1, as other HORMADs, is assembled on the axis at early meiosis and depleted when homologous chromosomes synapse. Puzzlingly, both processes are catalyzed by AAA+ ATPase PCH2 together with its cofactor COMET. Here, we show that the ASY1 remodeling complex is temporally and spatially differently assembled. While PCH2 and COMET appear to directly interact in the cytoplasm in early meiosis, PCH2 is recruited by the transverse filament protein ZYP1 and brought to the ASY1-bound COMET assuring the timely removal of ASY1 during chromosome synapsis. Since we found that the PCH2 homolog TRIP13 also binds to the ZYP1 homolog SYCP1 in mouse, we postulate that this mechanism is conserved among eukaryotes. Deleting the PCH2 binding site of ZYP1 led to a failure of ASY1 removal. Interestingly, the placement of one obligatory crossover per homologous chromosome pair, compromised by ZYP1 depletion, is largely restored in this separation-of-function zyp1 allele suggesting that crossover assurance is promoted by synapsis. In contrast, this zyp1 allele, similar to the zyp1 null mutant, showed elevated type I crossover numbers indicating that PCH2-mediated eviction of ASY1 from the axis restricts crossover formation.

Indexed as

ArabidopsisArabidopsis ProteinsChromosome PairingAdenosine TriphosphatasesAnimalsBinding SitesMeiosisMiceSynaptonemal ComplexAdenosine TriphosphatasesArabidopsis ProteinsPCH2 protein, Arabidopsis

Identifiers

PMID36504011
PMCPMC9825157
OpenAlexW4311153976

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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.