Evidence map›Paper›PMID 27742779›Full record

ArticleHuman molecular genetics2016

Zfy genes are required for efficient meiotic sex chromosome inactivation (MSCI) in spermatocytes.

Nadège Vernet, Shantha K Mahadevaiah, Dirk G de Rooij, Paul S Burgoyne, Peter J I Ellis

Open access · hybridAbstract read
In one paragraph

Article in Human molecular genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.9field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 29 citations in OpenAlex.

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  10. MRNIP interacts with sex body chromatin to support meiotic progression, spermatogenesis, and male fertility in mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
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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

5 authors at 4 institutions in 3 countries.

Nadège VernetDivision of Stem Cell Biology and Developmental Genetics, MRC National Institute for Medical Research, Mill Hill, London, UK.
Shantha K MahadevaiahDivision of Stem Cell Biology and Developmental Genetics, MRC National Institute for Medical Research, Mill Hill, London, UK.
Dirk G de RooijReproductive Biology Group, Division of Developmental Biology, Department of Biology, Faculty of Science, Utrecht University, Utrecht, The Netherlands.
Paul S BurgoyneDivision of Stem Cell Biology and Developmental Genetics, MRC National Institute for Medical Research, Mill Hill, London, UK.
Peter J I EllisDepartment of Pathology, University of Cambridge, Cambridge, UK.
The Francis Crick Institute · GBInstitut de génétique et de biologie moléculaire et cellulaire · FRUniversity of Kent · GBUtrecht University · NL

Funding

Biotechnology and Biological Sciences Research Council BB/F007434/1Biotechnology and Biological Sciences Research Council BB/J00877X/1Biotechnology and Biological Sciences Research Council BB/N000463/1Medical Research Council U117532009
6 · The paper itself

Abstract

During spermatogenesis, germ cells that fail to synapse their chromosomes or fail to undergo meiotic sex chromosome inactivation (MSCI) are eliminated via apoptosis during mid-pachytene. Previous work showed that Y-linked genes Zfy1 and Zfy2 act as 'executioners' for this checkpoint, and that wrongful expression of either gene during pachytene triggers germ cell death. Here, we show that in mice, Zfy genes are also necessary for efficient MSCI and the sex chromosomes are not correctly silenced in Zfy-deficient spermatocytes. This unexpectedly reveals a triple role for Zfy at the mid-pachytene checkpoint in which Zfy genes first promote MSCI, then monitor its progress (since if MSCI is achieved, Zfy genes will be silenced), and finally execute cells with MSCI failure. This potentially constitutes a negative feedback loop governing this critical checkpoint mechanism.

Indexed as

AnimalsDNA-Binding ProteinsMaleMeiosisMiceSpermatocytesSpermatogenesisTranscription FactorsX ChromosomeX Chromosome InactivationDNA-Binding ProteinsTranscription FactorsZfy1 protein, mouseZfy2 protein, mouse

Identifiers

PMID27742779
PMCPMC5418838
OpenAlexW2531358790

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.