Evidence map›Paper›PMID 35301318›Full record

ArticleNature communications2022

The Oligodendrocyte Transcription Factor 2 OLIG2 regulates transcriptional repression during myelinogenesis in rodents.

Kunkun Zhang, Shaoxuan Chen, Qihua Yang, Shuanghui Guo, Qiang Chen, Zhixiong Liu, Li Li, Mengyun Jiang, Hongda Li, Jin Hu and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
8.3field-weighted citation impact, top 1% 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

50 citing papers in PubMed, 72 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 2 institutions in 1 country.

Kunkun Zhang *Department of Neurosurgery and Department of Neuroscience, the First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, School of Medicine, Xiamen University, Fujian, China.
Shaoxuan Chen *Department of Neurosurgery and Department of Neuroscience, the First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, School of Medicine, Xiamen University, Fujian, China.
Qihua YangSchool of Life Sciences, Innovation Center for Cell Signaling Network, Xiamen University, Fujian, China.
Shuanghui GuoSchool of Life Sciences, Innovation Center for Cell Signaling Network, Xiamen University, Fujian, China.
Qiang ChenDepartment of Neurosurgery and Department of Neuroscience, the First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, School of Medicine, Xiamen University, Fujian, China.
Zhixiong LiuDepartment of Neurosurgery and Department of Neuroscience, the First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, School of Medicine, Xiamen University, Fujian, China.ORCID http://orcid.org/0000-0002-9838-7527
Li LiSchool of Life Sciences, Innovation Center for Cell Signaling Network, Xiamen University, Fujian, China.
Mengyun JiangSchool of Life Sciences, Innovation Center for Cell Signaling Network, Xiamen University, Fujian, China.
Hongda LiSchool of Life Sciences, Innovation Center for Cell Signaling Network, Xiamen University, Fujian, China.
Jin HuSchool of Life Sciences, Innovation Center for Cell Signaling Network, Xiamen University, Fujian, China.
Xu PanSchool of Pharmaceutical Sciences, Xiamen University, Xiamen, Fujian, 361102, China.
Wenbo DengXiamen Key Laboratory of Brain Center, the First Affiliated Hospital of Xiamen University, Fujian, China.ORCID http://orcid.org/0000-0001-7222-372X
Naian XiaoDepartment of Neurosurgery and Department of Neuroscience, the First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, School of Medicine, Xiamen University, Fujian, China.
Bo WangSchool of Life Sciences, Innovation Center for Cell Signaling Network, Xiamen University, Fujian, China.
Zhan-Xiang WangDepartment of Neurosurgery and Department of Neuroscience, the First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, School of Medicine, Xiamen University, Fujian, China. wangzx@xmu.edu.cn.
Liang ZhangDepartment of Neurosurgery and Department of Neuroscience, the First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, School of Medicine, Xiamen University, Fujian, China. lzhangxmu@xmu.edu.cn.ORCID http://orcid.org/0000-0003-4528-2403
Wei MoDepartment of Neurosurgery and Department of Neuroscience, the First Affiliated Hospital of Xiamen University, State Key Laboratory of Cellular Stress Biology, School of Medicine, Xiamen University, Fujian, China. wmo@xmu.edu.cn.ORCID http://orcid.org/0000-0002-8165-4473
Xiamen University · CNFirst Affiliated Hospital of Xiamen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OLIG2 is a transcription factor that activates the expression of myelin-associated genes in the oligodendrocyte-lineage cells. However, the mechanisms of myelin gene inactivation are unclear. Here, we uncover a non-canonical function of OLIG2 in transcriptional repression to modulate myelinogenesis by functionally interacting with tri-methyltransferase SETDB1. Immunoprecipitation and chromatin-immunoprecipitation assays show that OLIG2 recruits SETDB1 for H3K9me3 modification on the Sox11 gene, which leads to the inhibition of Sox11 expression during the differentiation of oligodendrocytes progenitor cells (OPCs) into immature oligodendrocytes (iOLs). Tissue-specific depletion of Setdb1 in mice results in the hypomyelination during development and remyelination defects in the injured rodents. Knockdown of Sox11 by siRNA in rat primary OPCs or depletion of Sox11 in the oligodendrocyte lineage in mice could rescue the hypomyelination phenotype caused by the loss of OLIG2. In summary, our work demonstrates that the OLIG2-SETDB1 complex can mediate transcriptional repression in OPCs, affecting myelination.

Indexed as

Basic Helix-Loop-Helix ProteinsRodentiaAnimalsCell DifferentiationMiceMyelin SheathNerve Tissue ProteinsOligodendrocyte Transcription Factor 2OligodendrogliaRatsBasic Helix-Loop-Helix ProteinsNerve Tissue ProteinsOlig2 protein, mouseOlig2 protein, ratOligodendrocyte Transcription Factor 2

Identifiers

PMID35301318
PMCPMC8931116
OpenAlexW4221003986

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.