Evidence map›Paper›PMID 28943313›Full record

ArticleMolecular cell2017

The Role of N-α-acetyltransferase 10 Protein in DNA Methylation and Genomic Imprinting.

Chen-Cheng Lee, Shih-Huan Peng, Li Shen, Chung-Fan Lee, Ting-Huei Du, Ming-Lun Kang, Guo-Liang Xu, Anup K Upadhyay, Xiaodong Cheng, Yu-Ting Yan and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

38 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Conformational plasticity links structural instability of NAA10Computational and structural biotechnology journal · 2024
    Article
  7. Article
  8. Article
  9. A novelFrontiers in genetics · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Genetic Studies on Mammalian DNA Methyltransferases.Advances in experimental medicine and biology · 2022
    Article
  14. Article
  15. eLife · 2021
    Article
  16. Article
  17. International journal of molecular sciences · 2020
    Article
  18. Review
  19. Article
  20. Article
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 7 institutions in 3 countries.

Chen-Cheng LeeGenomics Research Center, Academia Sinica, Taipei 115, Taiwan, ROC.
Shih-Huan PengGenomics Research Center, Academia Sinica, Taipei 115, Taiwan, ROC; Institute of Molecular Medicine, National Taiwan University College of Medicine, Taipei 100, Taiwan, ROC.
Li ShenHoward Hughes Medical Institute, Harvard Medical School, Boston, MA 02115, USA.
Chung-Fan LeeGenomics Research Center, Academia Sinica, Taipei 115, Taiwan, ROC.
Ting-Huei DuGenomics Research Center, Academia Sinica, Taipei 115, Taiwan, ROC.
Ming-Lun KangGenomics Research Center, Academia Sinica, Taipei 115, Taiwan, ROC.
Guo-Liang XuInstitute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Anup K UpadhyayDepartment of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322, USA.
Xiaodong ChengDepartment of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322, USA; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Yu-Ting YanInstitute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan, ROC.
Yi ZhangHoward Hughes Medical Institute, Harvard Medical School, Boston, MA 02115, USA. Electronic address: yzhang@genetics.med.harvard.edu.
Li-Jung JuanGenomics Research Center, Academia Sinica, Taipei 115, Taiwan, ROC. Electronic address: ljjuan@gate.sinica.edu.tw.
Genomics Research Center, Academia Sinica · TWEmory University · USHarvard University · USHoward Hughes Medical Institute · USInstitute of Biomedical Sciences, Academia Sinica · TWShanghai Institutes for Biological Sciences · CNThe University of Texas MD Anderson Cancer Center · US

Funding

THREE-DIMENSIONAL STRUCTURE OF HHAI METHYLASER01GM049245 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CHENG, XIAODONG · 1993 to 2017
$6.6M
NIGMS NIH HHS R01 GM049245
6 · The paper itself

Abstract

Genomic imprinting is an allelic gene expression phenomenon primarily controlled by allele-specific DNA methylation at the imprinting control region (ICR), but the underlying mechanism remains largely unclear. N-α-acetyltransferase 10 protein (Naa10p) catalyzes N-α-acetylation of nascent proteins, and mutation of human Naa10p is linked to severe developmental delays. Here we report that Naa10-null mice display partial embryonic lethality, growth retardation, brain disorders, and maternal effect lethality, phenotypes commonly observed in defective genomic imprinting. Genome-wide analyses further revealed global DNA hypomethylation and enriched dysregulation of imprinted genes in Naa10p-knockout embryos and embryonic stem cells. Mechanistically, Naa10p facilitates binding of DNA methyltransferase 1 (Dnmt1) to DNA substrates, including the ICRs of the imprinted allele during S phase. Moreover, the lethal Ogden syndrome-associated mutation of human Naa10p disrupts its binding to the ICR of H19 and Dnmt1 recruitment. Our study thus links Naa10p mutation-associated Ogden syndrome to defective DNA methylation and genomic imprinting.

Indexed as

Epigenesis, GeneticGenomic ImprintingAnimalsDevelopmental DisabilitiesDisease Models, AnimalDNADNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesDNA MethylationEmbryo, MammalianFemaleGene DeletionGenes, LethalGenome-Wide Association StudyMaleMiceDNADNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesDNMT1 protein, humanDnmt1 protein, mouseH19 long non-coding RNANaa10 protein, mouseN-Terminal Acetyltransferase AN-Terminal Acetyltransferase ERNA, Long Noncodingdevelopmentdevelopmental delayDNA methylationDnmt1genomic imprintingNaa10pN-α-acetyltransferaseOgden syndrome

Identifiers

PMID28943313
PMCPMC6322414
OpenAlexW2756784367

What OpenQuestion holds

Textmetadata
LicenceTDM
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.