Evidence map›Paper›PMID 24869935›Full record

ArticleBlood2014

Muscleblind-like 1 (Mbnl1) regulates pre-mRNA alternative splicing during terminal erythropoiesis.

Albert W Cheng, Jiahai Shi, Piu Wong, Katherine L Luo, Paula Trepman, Eric T Wang, Heejo Choi, Christopher B Burge, Harvey F Lodish

Abstract read
In one paragraph

Article in Blood, 2014. 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
2.4field-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

38 citing papers in PubMed, 54 citations in OpenAlex.

  1. Insects · 2026
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  9. Post-transcriptional regulation of erythropoiesis.Blood science (Baltimore, Md.) · 2023
    Review
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  15. Inhibition of lncRNA MAAT Controls Multiple Types of Muscle Atrophy by cis- and trans-Regulatory Actions.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  16. Article
  17. Regulators of cardiac fibroblast cell state.Matrix biology : journal of the International Society for Matrix Biology · 2020
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Albert W ChengWhitehead Institute for Biomedical Research, Cambridge, MA; Computational and Systems Biology Program, and.
Jiahai ShiWhitehead Institute for Biomedical Research, Cambridge, MA;ORCID http://orcid.org/0000-0002-6467-8289
Piu WongWhitehead Institute for Biomedical Research, Cambridge, MA;
Katherine L LuoDepartments of Biology and Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA; and.
Paula TrepmanDepartments of Biology and Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA; and.
Eric T WangDepartments of Biology and Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA; and Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA.
Heejo ChoiDepartments of Biology and Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA; and.
Christopher B BurgeDepartments of Biology and Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA; and.
Harvey F LodishWhitehead Institute for Biomedical Research, Cambridge, MA; Departments of Biology and Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA; and.
Massachusetts Institute of Technology · USWhitehead Institute for Biomedical Research · USHarvard–MIT Division of Health Sciences and Technology · US

Funding

TRANSCRIPTION FACTOR GATA-1 IN TERMINAL ERYTHROID DEVELOPMENTP01HL032262 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI ORKIN, STUART H · 1985 to 2021
$38.9M
MicroRNAs and hematopoietic differentiationR01DK068348 · NIDDK · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI LODISH, HARVEY F · 2004 to 2019
$8.3M
NHLBI NIH HHS P01 HL032262NHLBI NIH HHS P01 HL032262-25NIDDK NIH HHS R01 DK068348NIDDK NIH HHS R01DK068348-07
6 · The paper itself

Abstract

The scope and roles of regulated isoform gene expression during erythroid terminal development are poorly understood. We identified hundreds of differentiation-associated isoform changes during terminal erythropoiesis. Sequences surrounding cassette exons of skipped exon events are enriched for motifs bound by the Muscleblind-like (MBNL) family of splicing factors. Knockdown of Mbnl1 in cultured murine fetal liver erythroid progenitors resulted in a strong block in erythroid differentiation and disrupted the developmentally regulated exon skipping of Ndel1 mRNA, which is bound by MBNL1 and critical for erythroid terminal proliferation. These findings reveal an unanticipated scope of the alternative splicing program and the importance of Mbnl1 during erythroid terminal differentiation.

Indexed as

Alternative SplicingCell DifferentiationGene Expression RegulationAnimalsBlotting, WesternCarrier ProteinsCell ProliferationDNA-Binding ProteinsErythropoiesisExonsHEK293 CellsHumansImmunoprecipitationMiceProtein IsoformsReal-Time Polymerase Chain ReactionCarrier ProteinsDNA-Binding ProteinsMbnl1 protein, mouseNdel1 protein, mouseProtein IsoformsRNA-Binding ProteinsRNA, MessengerRNA PrecursorsRNA, Small Interfering

Identifiers

PMID24869935
PMCPMC4110662
OpenAlexW1991898382

What OpenQuestion holds

Textmetadata
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.