Evidence map›Paper›PMID 32499180›Full record

ArticleJournal of genetics and genomics = Yi chuan xue bao2020

Drosophila P75 safeguards oogenesis by preventing H3K9me2 spreading.

Kun Dou, Yanchao Liu, Yingpei Zhang, Chenhui Wang, Ying Huang, Zz Zhao Zhang

Open access · greenAbstract read
In one paragraph

Article in Journal of genetics and genomics = Yi chuan xue bao, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

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  5. Lysine-36 ofbioRxiv : the preprint server for biology · 2023
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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 4 institutions in 2 countries.

Kun DouDepartment of Embryology, Carnegie Institution for Science, Baltimore, MD, 21218, USA; School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China. Electronic address: doukun@shanghaitech.edu.cn.
Yanchao LiuState Key Laboratory of Molecular Biology, Shanghai Key Laboratory of Molecular Andrology, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai 200031, China.
Yingpei ZhangState Key Laboratory of Molecular Biology, Shanghai Key Laboratory of Molecular Andrology, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai 200031, China.
Chenhui WangDepartment of Embryology, Carnegie Institution for Science, Baltimore, MD, 21218, USA.
Ying HuangState Key Laboratory of Molecular Biology, Shanghai Key Laboratory of Molecular Andrology, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai 200031, China; State Key Laboratory of Oncogenes and Related Genes, Shanghai Key Laboratory of Biliary Tract Disease Research, Shanghai Research Center of Biliary Tract Disease, Department of General Surgery, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China. Electronic address: huangying@xinhuamed.com.cn.
Zz Zhao ZhangDepartment of Embryology, Carnegie Institution for Science, Baltimore, MD, 21218, USA; Department of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, NC, 27710, USA; Regeneration Next, Duke University, Durham, NC, 27710, USA. Electronic address: z.z@duke.edu.
Carnegie Institution for Science · USChinese Academy of Sciences · CNDuke University · USShanghai Jiao Tong University · CN

Funding

Somatic transposition-mediated genome variegation during development, disease and aging conditionsDP5OD021355 · OD · DUKE UNIVERSITY · PI ZHANG, ZHAO · 2015 to 2019
$2.0M
NIH HHS DP5 OD021355
6 · The paper itself

Abstract

Serving as a host factor for human immunodeficiency virus (HIV) integration, LEDGF/p75 has been under extensive study as a potential target for therapy. However, as a highly conserved protein, its physiological function remains to be thoroughly elucidated. Here, we characterize the molecular function of dP75, the Drosophila homolog of LEDGF/p75, during oogenesis. dP75 binds to transcriptionally active chromatin with its PWWP domain. The C-terminus integrase-binding domain-containing region of dP75 physically interacts with the histone kinase Jil-1 and stabilizes it in vivo. Together with Jil-1, dP75 prevents the spreading of the heterochromatin mark-H3K9me2-onto genes required for oogenesis and piRNA production. Without dP75, ectopical silencing of these genes disrupts oogenesis, activates transposons, and causes animal sterility. We propose that dP75, the homolog of an HIV host factor in Drosophila, partners with and stabilizes Jil-1 to ensure gene expression during oogenesis by preventing ectopic heterochromatin spreading.

Indexed as

AnimalsCell LineChromatinDrosophilaDrosophila ProteinsHeterochromatinHIVHumansInfertilityIntercellular Signaling Peptides and ProteinsOogenesisProtein Serine-Threonine KinasesRNA, Small InterferingVirus IntegrationChromatinDrosophila ProteinsHeterochromatinIntercellular Signaling Peptides and ProteinsJIL-1 protein, Drosophilalens epithelium-derived growth factorProtein Serine-Threonine KinasesRNA, Small InterferingDrosophilaH3K9me2Jil-1LEDGF/p75

Identifiers

PMID32499180
PMCPMC7416749
OpenAlexW3011968128

What OpenQuestion holds

Textmetadata
LicenceTDM
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.