Evidence map›Paper›PMID 32374864›Full record

ArticleNucleic acids research2020

DXO/Rai1 enzymes remove 5'-end FAD and dephospho-CoA caps on RNAs.

Selom K Doamekpor, Ewa Grudzien-Nogalska, Agnieszka Mlynarska-Cieslak, Joanna Kowalska, Megerditch Kiledjian, Liang Tong

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

31 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. RNA regulation in plants.Science China. Life sciences · 2026
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  12. Application of Mammalian Nudix Enzymes to Capped RNA Analysis.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  13. Article
  14. Article
  15. Review
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  17. Article
  18. Article
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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

6 authors at 3 institutions in 2 countries.

Selom K DoamekporDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.
Ewa Grudzien-NogalskaDept. Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.
Agnieszka Mlynarska-CieslakDivision of Biophysics, Institute of Experimental Physics, Faculty of Physics, University of Warsaw, 02-093 Warsaw, Poland.
Joanna KowalskaDivision of Biophysics, Institute of Experimental Physics, Faculty of Physics, University of Warsaw, 02-093 Warsaw, Poland.
Megerditch KiledjianDept. Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.
Liang TongDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.
Columbia University · USRutgers, The State University of New Jersey · USUniversity of Warsaw · PL

Funding

Overall EvaluationP41GM103403 · NIGMS · CORNELL UNIVERSITY · PI EALICK, STEVEN E · 2012 to 2017
$14.3M
Structural and functional studies of mRNA processing, stability and quality controlR35GM118093 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI LIANG TONG · 2016 to 2026
$8.5M
Regulation of Mammalian mRNA DecayR01GM067005 · NIGMS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI KILEDJIAN, MEGERDITCH · 2004 to 2022
$5.5M
Replacement of an aging X-ray diffraction system for protein crystallographyS10OD012018 · OD · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI TONG, LIANG · 2012 to 2012
$405k
NIGMS NIH HHS P41 GM103403NIGMS NIH HHS R01 GM067005NIGMS NIH HHS R35 GM118093NIH HHS S10 OD012018
6 · The paper itself

Abstract

In eukaryotes, the DXO/Rai1 enzymes can eliminate most of the incomplete and non-canonical NAD caps through their decapping, deNADding and pyrophosphohydrolase activities. Here, we report that these enzymes can also remove FAD and dephospho-CoA (dpCoA) non-canonical caps from RNA, and we have named these activities deFADding and deCoAping. The crystal structures of mammalian DXO with 3'-FADP or CoA and fission yeast Rai1 with 3'-FADP provide elegant insight to these activities. FAD and CoA are accommodated in the DXO/Rai1 active site by adopting folded conformations. The flavin of FAD and the pantetheine group of CoA contact the same region at the bottom of the active site tunnel, which undergoes conformational changes to accommodate the different cap moieties. We have developed FAD-capQ to detect and quantify FAD-capped RNAs and determined that FAD caps are present on short RNAs (with less than ∼200 nucleotides) in human cells and that these RNAs are stabilized in the absence of DXO.

Indexed as

AnimalsCoenzyme AExoribonucleasesFlavin-Adenine DinucleotideHEK293 CellsHumansIn Vitro TechniquesKluyveromycesMiceModels, MolecularNADNuclear ProteinsRNA CapsRNA, MessengerSchizosaccharomyces pombe ProteinsSubstrate SpecificityCoenzyme Adephosphocoenzyme ADxo protein, mouseExoribonucleasesFlavin-Adenine DinucleotideNADNuclear ProteinsRai1 protein, S pombeRNA CapsRNA, MessengerSchizosaccharomyces pombe Proteins

Identifiers

PMID32374864
PMCPMC7293010
OpenAlexW3021812109

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.