Evidence map›Paper›PMID 32196499›Full record

ArticlePLoS genetics2020

E2f5 is a versatile transcriptional activator required for spermatogenesis and multiciliated cell differentiation in zebrafish.

Haibo Xie, Yunsi Kang, Shuo Wang, Pengfei Zheng, Zhe Chen, Sudipto Roy, Chengtian Zhao

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 45 citations in OpenAlex.

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  19. Cilia regulate meiotic recombination in zebrafish.Journal of molecular cell 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

7 authors at 2 institutions in 2 countries.

Haibo XieInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, Shandong, China.
Yunsi KangInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, Shandong, China.
Shuo WangInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, Shandong, China.
Pengfei ZhengInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, Shandong, China.
Zhe ChenInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, Shandong, China.
Sudipto RoyInstitute of Molecular and Cell Biology, Singapore, Singapore.ORCID 0000-0002-6636-1429
Chengtian ZhaoInstitute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao, Shandong, China.ORCID 0000-0003-1236-914X
Qingdao National Laboratory for Marine Science and Technology · CNNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

E2f5 is a member of the E2f family of transcription factors that play essential roles during many cellular processes. E2f5 was initially characterized as a transcriptional repressor in cell proliferation studies through its interaction with the Retinoblastoma (Rb) protein for inhibition of target gene transcription. However, the precise roles of E2f5 during embryonic and post-embryonic development remain incompletely investigated. Here, we report that zebrafish E2f5 plays critical roles during spermatogenesis and multiciliated cell (MCC) differentiation. Zebrafish e2f5 mutants develop exclusively as infertile males. In the mutants, spermatogenesis is arrested at the zygotene stage due to homologous recombination (HR) defects, which finally leads to germ cell apoptosis. Inhibition of cell apoptosis in e2f5;tp53 double mutants rescued ovarian development, although oocytes generated from the double mutants were still abnormal, characterized by aberrant distribution of nucleoli. Using transcriptome analysis, we identified dmc1, which encodes an essential meiotic recombination protein, as the major target gene of E2f5 during spermatogenesis. E2f5 can bind to the promoter of dmc1 to promote HR, and overexpression of dmc1 significantly increased the fertilization rate of e2f5 mutant males. Besides gametogenesis defects, e2f5 mutants failed to develop MCCs in the nose and pronephric ducts during early embryonic stages, but these cells recovered later due to redundancy with E2f4. Moreover, we demonstrate that ion transporting principal cells in the pronephric ducts, which remain intercalated with the MCCs, do not contain motile cilia in wild-type embryos, while they generate single motile cilia in the absence of E2f5 activity. In line with this, we further show that E2f5 activates the Notch pathway gene jagged2b (jag2b) to inhibit the acquisition of MCC fate as well as motile cilia differentiation by the neighboring principal cells. Taken together, our data suggest that E2f5 can function as a versatile transcriptional activator and identify novel roles of the protein in spermatogenesis as well as MCC differentiation during zebrafish development.

Indexed as

AnimalsCell Cycle ProteinsCell DifferentiationCiliaDNA-Binding ProteinsE2F5 Transcription FactorMaleReceptors, NotchSignal TransductionSpermatogenesisZebrafishZebrafish ProteinsCell Cycle ProteinsDNA-Binding ProteinsE2F5 Transcription FactorReceptors, NotchZebrafish Proteins

Identifiers

PMID32196499
PMCPMC7112233
OpenAlexW3011364173

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.