Evidence map›Paper›PMID 29742103›Full record

ArticlePLoS genetics2018

SHOC1 is a ERCC4-(HhH)2-like protein, integral to the formation of crossover recombination intermediates during mammalian meiosis.

Michel F Guiraldelli, Anna Felberg, Luciana P Almeida, Aniruddha Parikh, Rodrigo O de Castro, Roberto J Pezza

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

41 citing papers in PubMed, 56 citations in OpenAlex.

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  9. HEIP1 orchestrates pro-crossover protein activity during mammalian meiosis.Proceedings of the National Academy of Sciences of the United States of America · 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

6 authors at 1 institution in 1 country.

Michel F GuiraldelliOklahoma Medical Research Foundation, Oklahoma City, Oklahoma, United States of America.
Anna FelbergOklahoma Medical Research Foundation, Oklahoma City, Oklahoma, United States of America.
Luciana P AlmeidaOklahoma Medical Research Foundation, Oklahoma City, Oklahoma, United States of America.
Aniruddha ParikhOklahoma Medical Research Foundation, Oklahoma City, Oklahoma, United States of America.
Rodrigo O de CastroOklahoma Medical Research Foundation, Oklahoma City, Oklahoma, United States of America.
Roberto J PezzaOklahoma Medical Research Foundation, Oklahoma City, Oklahoma, United States of America.ORCID 0000-0003-0279-5516
Oklahoma Medical Research Foundation · US

Funding

Understanding connective tissue development and disease with PDGFR-driven..... P20GM103636 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI THOMPSON, LINDA F · 2013 to 2023
$26.9M
Epigenetic control of meiotic recombination in mammals - Equipment SupplementR01GM125803 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI PEZZA, ROBERTO JOSE · 2018 to 2021
$1.8M
NIGMS NIH HHS P20 GM103636NIGMS NIH HHS R01 GM125803
6 · The paper itself

Abstract

Chromosome segregation errors during meiosis result in the formation of aneuploid gametes and are the leading cause of pregnancy loss and birth defects in humans. Proper chromosome segregation requires pairwise associations of maternal and paternal homologous chromosomes. Chiasmata, which are the cytological manifestations of crossovers (COs), provide a physical link that holds the homologs together as a pair, facilitating their orientation on the spindle at meiosis I. Although CO-promoting activities ensure a balanced number and position of COs, their identity and mechanism of action in mammals remain understudied. Previous work in yeast and Arabidopsis has shown that Zip2 and Shoc1 are ortholog proteins with an important role in promoting the formation of COs. Our work is the first study in mammals showing the in vivo and in vitro function of mouse and human SHOC1. We show that purified recombinant human SHOC1, an XPF/MUS81 family member, preferentially binds branched DNA molecules but apparently lacks in vitro endonuclease activity, despite its conserved ERCC4-(HhH)2 core structure. Cytological observations suggest that initial steps of recombination are normal in a majority of spermatocytes from SHOC1 hypomorphic mice. However, late stages of recombination appear abnormal, as chromosomal localization of MLH1 is reduced. In agreement, chiasma formation is reduced, and cells arrest at metaphase I with a few lagging chromosomes and subsequent apoptosis. This analysis of SHOC1-deficient mice and the selective localization of SHOC1 to a subset of recombination sites show that SHOC1 acts at key mid-stage steps of the CO formation process. The formation of chromosome axial elements and homologous pairing are apparently normal, but synapsis is altered with SYCP1 frequently failing to extend the full length of the chromosome axes. Finally, we describe that SHOC1 interacts with TEX11, another protein important for the formation of COs, connecting SHOC1 to chromosome axis and structure.

Indexed as

Crossing Over, GeneticAnimalsChromosome PairingChromosome SegregationDNA-Binding ProteinsEndonucleasesFemaleHumansMaleMeiosisMice, Inbred C57BLMice, KnockoutRecombination, GeneticSpermatocytesDNA-Binding ProteinsEndonucleasesShoc1 protein, mouse

Identifiers

PMID29742103
PMCPMC5962103
OpenAlexW2802128904

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LicenceCC BY
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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.