Evidence map›Paper›PMID 30566428›Full record

ArticlePLoS biology2018

MEKK3 coordinates with FBW7 to regulate WDR62 stability and neurogenesis.

Dan Xu, Minghui Yao, Yaqing Wang, Ling Yuan, Joerg D Hoeck, Jingwen Yu, Liang Liu, Yvonne Y C Yeap, Weiya Zhang, Feng Zhang and 8 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 21 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

18 authors at 6 institutions in 4 countries.

Dan XuState Key Laboratory of Molecular Developmental Biology, CAS Center for Excellence in Brain Science and Intelligence Technology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Minghui YaoState Key Laboratory of Molecular Developmental Biology, CAS Center for Excellence in Brain Science and Intelligence Technology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Yaqing WangState Key Laboratory of Molecular Developmental Biology, CAS Center for Excellence in Brain Science and Intelligence Technology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Ling YuanCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Joerg D HoeckCR-UK London Research Institute, London, United Kingdom.
Jingwen YuState Key Laboratory of Molecular Developmental Biology, CAS Center for Excellence in Brain Science and Intelligence Technology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Liang LiuState Key Laboratory of Molecular Developmental Biology, CAS Center for Excellence in Brain Science and Intelligence Technology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Yvonne Y C YeapSchool of Biomedical Science, Faculty of Medicine, University of Queensland, St Lucia, Australia.
Weiya ZhangState Key Laboratory of Molecular Developmental Biology, CAS Center for Excellence in Brain Science and Intelligence Technology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Feng ZhangState Key Laboratory of Molecular Developmental Biology, CAS Center for Excellence in Brain Science and Intelligence Technology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Yinghang FengSino-Danish College, University of Chinese Academy of Science, Beijing, China.
Tiantian MaState Key Laboratory of Molecular Developmental Biology, CAS Center for Excellence in Brain Science and Intelligence Technology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Yujie WangCollege of Biological Science and Engineering, Institute of Life Sciences, Fuzhou University, Fuzhou, China.
Dominic C H NgSchool of Biomedical Science, Faculty of Medicine, University of Queensland, St Lucia, Australia.
Xiaoyin NiuShanghai Institute of Immunology, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Bing SuShanghai Institute of Immunology, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Axel BehrensAdult Stem Cell Laboratory, The Francis Crick Institute, London, United Kingdom.
Zhiheng XuState Key Laboratory of Molecular Developmental Biology, CAS Center for Excellence in Brain Science and Intelligence Technology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.ORCID 0000-0002-4809-2851
Chinese Academy of Sciences · CNShanghai Jiao Tong University · CNThe University of Queensland · AUCentral South University · CNKing's College London · GBSino-Danish Centre for Education and Research · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations of WD repeat domain 62 (WDR62) lead to autosomal recessive primary microcephaly (MCPH), and down-regulation of WDR62 expression causes the loss of neural progenitor cells (NPCs). However, how WDR62 is regulated and hence controls neurogenesis and brain size remains elusive. Here, we demonstrate that mitogen-activated protein kinase kinase kinase 3 (MEKK3) forms a complex with WDR62 to promote c-Jun N-terminal kinase (JNK) signaling synergistically in the control of neurogenesis. The deletion of Mekk3, Wdr62, or Jnk1 resulted in phenocopied defects, including premature NPC differentiation. We further showed that WDR62 protein is positively regulated by MEKK3 and JNK1 in the developing brain and that the defects of wdr62 deficiency can be rescued by the transgenic expression of JNK1. Meanwhile, WDR62 is also negatively regulated by T1053 phosphorylation, leading to the recruitment of F-box and WD repeat domain-containing protein 7 (FBW7) and proteasomal degradation. Our findings demonstrate that the coordinated reciprocal and bidirectional regulation among MEKK3, FBW7, WDR62, and JNK1, is required for fine-tuned JNK signaling for the control of balanced NPC self-renewal and differentiation during cortical development.

Indexed as

AnimalsCell Cycle ProteinsCell DifferentiationF-Box-WD Repeat-Containing Protein 7FemaleHEK293 CellsHumansMaleMAP Kinase Kinase Kinase 3MAP Kinase Signaling SystemMiceMice, KnockoutMice, TransgenicMicrocephalyMicrotubule-Associated ProteinsMitogen-Activated Protein Kinase 8Cell Cycle ProteinsF-Box-WD Repeat-Containing Protein 7MAP Kinase Kinase Kinase 3Microtubule-Associated ProteinsMitogen-Activated Protein Kinase 8Nerve Tissue ProteinsWDR62 protein, mouse

Identifiers

PMID30566428
PMCPMC6347294
OpenAlexW2904854839

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.