Evidence map›Paper›PMID 31006037›Full record

ArticleCellular and molecular life sciences : CMLS2019

NEAT1 regulates neuroglial cell mediating Aβ clearance via the epigenetic regulation of endocytosis-related genes expression.

Ziqiang Wang, Yiwan Zhao, Naihan Xu, Shikuan Zhang, Songmao Wang, Yunhao Mao, Yuanchang Zhu, Bing Li, Yuyang Jiang, Ying Tan and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
10.4field-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

96 citing papers in PubMed, 134 citations in OpenAlex.

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  18. Integrative multiomics elucidate crotonylation-associated GCDH in Parkinson's disease pathogenesis via metabolome remodeling.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
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36 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 2 countries.

Ziqiang WangSchool of Life Sciences, Tsinghua University, Beijing, 100084, China.
Yiwan ZhaoSchool of Life Sciences, Tsinghua University, Beijing, 100084, China.
Naihan XuKey Laboratory in Health Science and Technology, Division of Life Science, Graduate School at Shenzhen, Tsinghua University, Shenzhen, 518055, China.
Shikuan ZhangSchool of Life Sciences, Tsinghua University, Beijing, 100084, China.
Songmao WangKey Laboratory in Health Science and Technology, Division of Life Science, Graduate School at Shenzhen, Tsinghua University, Shenzhen, 518055, China.
Yunhao MaoKey Laboratory in Health Science and Technology, Division of Life Science, Graduate School at Shenzhen, Tsinghua University, Shenzhen, 518055, China.
Yuanchang ZhuSchool of Life Sciences, Tsinghua University, Beijing, 100084, China.
Bing LiSchool of Life Sciences, Tsinghua University, Beijing, 100084, China.
Yuyang JiangState Key Laboratory of Chemical Oncogenomics, Graduate School at Shenzhen, Tsinghua University, Shenzhen, 518055, China.
Ying TanKey Laboratory in Health Science and Technology, Division of Life Science, Graduate School at Shenzhen, Tsinghua University, Shenzhen, 518055, China.
Weidong XieKey Laboratory in Health Science and Technology, Division of Life Science, Graduate School at Shenzhen, Tsinghua University, Shenzhen, 518055, China.
Burton B YangSchool of Life Sciences, Tsinghua University, Beijing, 100084, China. byang@sri.utoronto.ca.
Yaou ZhangSchool of Life Sciences, Tsinghua University, Beijing, 100084, China. zhangyo@sz.tsinghua.edu.cn.ORCID http://orcid.org/0000-0002-2501-8093
University Town of Shenzhen · CNSunnybrook Health Science Centre · CASun Yat-sen University · CN

Funding

National Natural Science Foundation of China 31571400Postdoctoral Research Foundation of China 2018M633216Shenzhen Science and Technology Innovation Committee JCYJ20160226185623304Shenzhen Science and Technology Innovation Committee JCYJ20170405103953336
6 · The paper itself

Abstract

The accumulation of intracellular β-amyloid peptide (Aβ) is important pathological characteristic of Alzheimer's disease (AD). However, the exact underlying molecular mechanism remains to be elucidated. Here, we reported that Nuclear Paraspeckle Assembly Transcript 1 (NEAT1), a long n on-coding RNA, exhibits repressed expression in the early stage of AD and its down-regulation declines neuroglial cell mediating Aβ clearance via inhibiting expression of endocytosis-related genes. We find that NEAT1 is associated with P300/CBP complex and its inhibition affects H3K27 acetylation (H3K27Ac) and H3K27 crotonylation (H3K27Cro) located nearby to the transcription start site of many genes, including endocytosis-related genes. Interestingly, NEAT1 inhibition down-regulates H3K27Ac but up-regulates H3K27Cro through repression of acetyl-CoA generation. NEAT1 also mediates the binding between STAT3 and H3K27Ac but not H3K27Cro. Therefore, the decrease of H3K27Ac and/or the increase of H3K27Cro declines expression of multiple related genes. Collectively, this study first reveals the different roles of H3K27Ac and H3K27Cro in regulation of gene expression and provides the insight of the epigenetic regulatory mechanism of NEAT1 in gene expression and AD pathology.

Indexed as

AcetylationAcetyl Coenzyme AAlzheimer DiseaseAmyloid beta-PeptidesAnimalsCaveolin 2Disease Models, AnimalEpigenesis, GeneticGene ExpressionHistonesMiceMice, TransgenicNeurogliap300-CBP Transcription FactorsPeptide FragmentsReceptor, Transforming Growth Factor-beta Type IAcetyl Coenzyme AAmyloid beta-Peptidesamyloid beta-protein (1-42)Cav2 protein, mouseCaveolin 2HistonesNEAT1 long non-coding RNA, mousep300-CBP Transcription FactorsPeptide FragmentsReceptor, Transforming Growth Factor-beta Type IRNA, Long NoncodingRNA, Small InterferingSTAT3 Transcription FactorTgfb2 protein, mouseTgfbr1 protein, mouseTransforming Growth Factor beta2Alzheimer’s diseaseAβHistone modificationNEAT1P300

Identifiers

PMID31006037
PMCPMC6647258
OpenAlexW2939742915

What OpenQuestion holds

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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.