Evidence map›Paper›PMID 33293536›Full record

ArticleNature communications2020

Pontin arginine methylation by CARM1 is crucial for epigenetic regulation of autophagy.

Young Suk Yu, Hijai R Shin, Dongha Kim, Seon Ah Baek, Seon Ah Choi, Hyejin Ahn, Amen Shamim, Jeonghwan Kim, Ik Soo Kim, Kyeong Kyu Kim and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

39 citing papers in PubMed, 55 citations in OpenAlex.

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  13. The emerging role of CARM1 in cancer.Cellular oncology (Dordrecht, Netherlands) · 2024
    Review
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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

12 authors at 4 institutions in 4 countries.

Young Suk YuCreative Research Initiatives Center for Epigenetic Code and Diseases, Department of Biological Sciences, Seoul National University, Seoul, 08826, South Korea.
Hijai R ShinCreative Research Initiatives Center for Epigenetic Code and Diseases, Department of Biological Sciences, Seoul National University, Seoul, 08826, South Korea.ORCID 0000-0001-5642-4441
Dongha KimDepartment of Anatomy, College of Medicine, The Catholic University of Korea, Seoul, 06591, South Korea.ORCID 0000-0002-3454-6605
Seon Ah BaekCreative Research Initiatives Center for Epigenetic Code and Diseases, Department of Biological Sciences, Seoul National University, Seoul, 08826, South Korea.ORCID 0000-0002-9273-4129
Seon Ah ChoiCreative Research Initiatives Center for Epigenetic Code and Diseases, Department of Biological Sciences, Seoul National University, Seoul, 08826, South Korea.
Hyejin AhnCreative Research Initiatives Center for Epigenetic Code and Diseases, Department of Biological Sciences, Seoul National University, Seoul, 08826, South Korea.ORCID 0000-0002-3773-2737
Amen ShamimDepartment of Molecular Cell Biology, School of Medicine, Sungkyunkwan University, Suwon, 16419, South Korea.
Jeonghwan KimBiotech Research and Innovation Centre (BRIC), University of Copenhagen, 2200, Copenhagen N, Denmark.
Ik Soo KimCreative Research Initiatives Center for Epigenetic Code and Diseases, Department of Biological Sciences, Seoul National University, Seoul, 08826, South Korea.ORCID 0000-0002-0767-0766
Kyeong Kyu KimDepartment of Molecular Cell Biology, School of Medicine, Sungkyunkwan University, Suwon, 16419, South Korea.ORCID 0000-0003-2515-8894
Kyoung-Jae WonBiotech Research and Innovation Centre (BRIC), University of Copenhagen, 2200, Copenhagen N, Denmark.
Sung Hee BaekCreative Research Initiatives Center for Epigenetic Code and Diseases, Department of Biological Sciences, Seoul National University, Seoul, 08826, South Korea. sbaek@snu.ac.kr.
Seoul National University · KRSungkyunkwan University · KRUniversity of Copenhagen · DKCatholic University of Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a catabolic process through which cytoplasmic components are degraded and recycled in response to various stresses including starvation. Recently, transcriptional and epigenetic regulations of autophagy have emerged as essential mechanisms for maintaining homeostasis. Here, we identify that coactivator-associated arginine methyltransferase 1 (CARM1) methylates Pontin chromatin-remodeling factor under glucose starvation, and methylated Pontin binds Forkhead Box O 3a (FOXO3a). Genome-wide analyses and biochemical studies reveal that methylated Pontin functions as a platform for recruiting Tip60 histone acetyltransferase with increased H4 acetylation and subsequent activation of autophagy genes regulated by FOXO3a. Surprisingly, CARM1-Pontin-FOXO3a signaling axis can work in the distal regions and activate autophagy genes through enhancer activation. Together, our findings provide a signaling axis of CARM1-Pontin-FOXO3a and further expand the role of CARM1 in nuclear regulation of autophagy.

Indexed as

Epigenesis, GeneticAcetylationAnimalsArginineATPases Associated with Diverse Cellular ActivitiesAutophagyDNA HelicasesFibroblastsForkhead Box Protein O3Gene Knockdown TechniquesGene Knockout TechniquesGlucoseHEK293 CellsHeLa CellsHep G2 CellsHistonesArginineATPases Associated with Diverse Cellular Activitiescoactivator-associated arginine methyltransferase 1DNA HelicasesForkhead Box Protein O3FoxO3 protein, mouseGlucoseHistonesKat5 protein, mouseLysine Acetyltransferase 5Protein-Arginine N-MethyltransferasesRUVBL1 protein, mouseTrans-Activators

Identifiers

PMID33293536
PMCPMC7722926
OpenAlexW3111840185

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.