Evidence map›Paper›PMID 24591581›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Transcriptional divergence and conservation of human and mouse erythropoiesis.

Novalia Pishesha, Prathapan Thiru, Jiahai Shi, Jennifer C Eng, Vijay G Sankaran, Harvey F Lodish

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

61 citing papers in PubMed, 87 citations in OpenAlex.

  1. Review
  2. Orai1 acts as a novel CaExperimental & molecular medicine · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Erythropoiesis: insights from a genomic perspective.Experimental & molecular medicine · 2024
    Review
  8. Article
  9. Article
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  11. Article
  12. Article
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  19. Review
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1 more citing papers are in PubMed but not listed here.

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 1 country.

Novalia PisheshaWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Prathapan Thiru
Jiahai Shi
Jennifer C Eng
Vijay G Sankaran
Harvey F Lodish
Whitehead Institute for Biomedical Research · USMassachusetts Institute of Technology · USDana-Farber Cancer Institute · US

Funding

TRANSCRIPTION FACTOR GATA-1 IN TERMINAL ERYTHROID DEVELOPMENTP01HL032262 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI ORKIN, STUART H · 1985 to 2021
$38.9M
PATHOPHYSIOLOGY OF HUMAN BLOOD CELLST32HL007574 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI Daniel Evan Bauer · 1985 to 2026
$18.4M
NHLBI NIH HHS P01 HL032262NHLBI NIH HHS P01 HL32262NHLBI NIH HHS T32 HL007574NHLBI NIH HHS T32 HL007574-30
6 · The paper itself

Abstract

Mouse models have been used extensively for decades and have been instrumental in improving our understanding of mammalian erythropoiesis. Nonetheless, there are several examples of variation between human and mouse erythropoiesis. We performed a comparative global gene expression study using data from morphologically identical stage-matched sorted populations of human and mouse erythroid precursors from early to late erythroblasts. Induction and repression of major transcriptional regulators of erythropoiesis, as well as major erythroid-important proteins, are largely conserved between the species. In contrast, at a global level we identified a significant extent of divergence between the species, both at comparable stages and in the transitions between stages, especially for the 500 most highly expressed genes during development. This suggests that the response of multiple developmentally regulated genes to key erythroid transcriptional regulators represents an important modification that has occurred in the course of erythroid evolution. In developing a systematic framework to understand and study conservation and divergence between human and mouse erythropoiesis, we show how mouse models can fail to mimic specific human diseases and provide predictions for translating findings from mouse models to potential therapies for human disease.

Indexed as

AnimalsBlotting, WesternErythroid Precursor CellsErythropoiesisFlow CytometryGene Expression ProfilingGene Expression Regulation, DevelopmentalHumansMiceMicroarray AnalysisSpecies SpecificityTranscriptomecomparative genomicshematopoiesismicroarray

Identifiers

PMID24591581
PMCPMC3964037
OpenAlexW2014968377

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.