Evidence map›Paper›PMID 38459149›Full record

ArticleCellular and molecular life sciences : CMLS2024

PRMT5-mediated homologous recombination repair is essential to maintain genomic integrity of neural progenitor cells.

Ya-Jun Wang, Jian-Bo Cao, Jing Yang, Tong Liu, Hua-Li Yu, Zi-Xuan He, Shi-Lai Bao, Xiao-Xiao He, Xiao-Juan Zhu

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 7 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Ya-Jun WangKey Laboratory of Molecular Epigenetics, Ministry of Education, Institute of Genetics and Cytology, Northeast Normal University, Changchun, 130024, China.
Jian-Bo CaoKey Laboratory of Molecular Epigenetics, Ministry of Education, Institute of Genetics and Cytology, Northeast Normal University, Changchun, 130024, China.
Jing YangKey Laboratory of Molecular Epigenetics, Ministry of Education, Institute of Genetics and Cytology, Northeast Normal University, Changchun, 130024, China.
Tong LiuKey Laboratory of Molecular Epigenetics, Ministry of Education, Institute of Genetics and Cytology, Northeast Normal University, Changchun, 130024, China.
Hua-Li YuKey Laboratory of Molecular Epigenetics, Ministry of Education, Institute of Genetics and Cytology, Northeast Normal University, Changchun, 130024, China.
Zi-Xuan HeKey Laboratory of Molecular Epigenetics, Ministry of Education, Institute of Genetics and Cytology, Northeast Normal University, Changchun, 130024, China.
Shi-Lai BaoState Key Laboratory of Molecular and Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China.
Xiao-Xiao HeKey Laboratory of Molecular Epigenetics, Ministry of Education, Institute of Genetics and Cytology, Northeast Normal University, Changchun, 130024, China. hexx100@nenu.edu.cn.
Xiao-Juan ZhuKey Laboratory of Molecular Epigenetics, Ministry of Education, Institute of Genetics and Cytology, Northeast Normal University, Changchun, 130024, China. zhuxj720@nenu.edu.cn.ORCID http://orcid.org/0000-0001-8386-8064
Northeast Normal University · CNChinese Academy of Sciences · CN

Funding

Ministry of Science and Technology of the People's Republic of China 2021ZD0204003National Natural Science Foundation of China 32070809National Natural Science Foundation of China 32170973
6 · The paper itself

Abstract

Maintaining genomic stability is a prerequisite for proliferating NPCs to ensure genetic fidelity. Though histone arginine methylation has been shown to play important roles in safeguarding genomic stability, the underlying mechanism during brain development is not fully understood. Protein arginine N-methyltransferase 5 (PRMT5) is a type II protein arginine methyltransferase that plays a role in transcriptional regulation. Here, we identify PRMT5 as a key regulator of DNA repair in response to double-strand breaks (DSBs) during NPC proliferation. Prmt5

Indexed as

Neural Stem CellsRecombinational DNA RepairAnimalsArginineDNA RepairGenomic InstabilityGenomicsHistonesMiceProtein-Arginine N-MethyltransferasesArginineHistonesPrmt5 protein, mouseProtein-Arginine N-MethyltransferasesApoptosisDNA double-strand breakDNA repairGenomic integrityHistone arginine methylationMicrocephaly

Identifiers

PMID38459149
PMCPMC10923982
OpenAlexW4392583178

What Socratic 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 Socratic graph.