Evidence map›Paper›PMID 32807903›Full record

ArticleNature cell biology2020

Decapping enzyme 1A breaks X-chromosome symmetry by controlling Tsix elongation and RNA turnover.

Eric Aeby, Hun-Goo Lee, Yong-Woo Lee, Andrea Kriz, Brian C Del Rosario, Hyun Jung Oh, Myriam Boukhali, Wilhelm Haas, Jeannie T Lee

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Control of RNA degradation in cell fate decision.Frontiers in cell and developmental biology · 2023
    Review
  11. Article
  12. Gene regulation in time and space during X-chromosome inactivation.Nature reviews. Molecular cell biology · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Revisiting the consequences of deleting the X inactivation center.Proceedings of the National Academy of Sciences of the United States of America · 2021
    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

9 authors at 1 institution in 1 country.

Eric AebyDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA.
Hun-Goo Lee *Department of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-2840-7684
Yong-Woo Lee *Department of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA.
Andrea KrizDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-3395-4498
Brian C Del RosarioDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA.
Hyun Jung OhDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA.
Myriam BoukhaliMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Wilhelm HaasMassachusetts General Hospital Cancer Center, Boston, MA, USA.
Jeannie T LeeDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA. lee@molbio.mgh.harvard.edu.ORCID http://orcid.org/0000-0001-7786-8850
Harvard University · US

Funding

Regulation of X-Inactivation by Non-Coding RNA LociR01GM058839 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, JEANNIE T · 1999 to 2025
$6.7M
Regulation of X-chromosome Inactivation and Imprinting by Non-coding ElementsR37GM058839 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, JEANNIE T · 2012 to 2021
$4.1M
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM058839NIGMS NIH HHS R37 GM058839
6 · The paper itself

Abstract

How allelic asymmetry is generated remains a major unsolved problem in epigenetics. Here we model the problem using X-chromosome inactivation by developing "BioRBP", an enzymatic RNA-proteomic method that enables probing of low-abundance interactions and an allelic RNA-depletion and -tagging system. We identify messenger RNA-decapping enzyme 1A (DCP1A) as a key regulator of Tsix, a noncoding RNA implicated in allelic choice through X-chromosome pairing. DCP1A controls Tsix half-life and transcription elongation. Depleting DCP1A causes accumulation of X-X pairs and perturbs the transition to monoallelic Tsix expression required for Xist upregulation. While ablating DCP1A causes hyperpairing, forcing Tsix degradation resolves pairing and enables Xist upregulation. We link pairing to allelic partitioning of CCCTC-binding factor (CTCF) and show that tethering DCP1A to one Tsix allele is sufficient to drive monoallelic Xist expression. Thus, DCP1A flips a bistable switch for the mutually exclusive determination of active and inactive Xs.

Indexed as

AllelesAnimalsCCCTC-Binding FactorCell LineEndoribonucleasesFemaleGene Expression Regulation, DevelopmentalMiceMice, Inbred C57BLRNARNA, MessengerTrans-ActivatorsTranscription, GeneticUp-RegulationX ChromosomeX Chromosome InactivationCCCTC-Binding FactorEndoribonucleasesmRNA decapping enzymesRNARNA, Messengersmad4-interacting protein SMIF, mouseTrans-Activators

Identifiers

PMID32807903
PMCPMC12082808
OpenAlexW3048975439

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.