Evidence map›Paper›PMID 28003475›Full record

ArticleNucleic acids research2017

Single cell transcriptomics reveals unanticipated features of early hematopoietic precursors.

Jennifer Yang, Yoshiaki Tanaka, Montrell Seay, Zhen Li, Jiaqi Jin, Lana Xia Garmire, Xun Zhu, Ashley Taylor, Weidong Li, Ghia Euskirchen and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  8. Tumorigenicity risk of iPSCsPrecision clinical medicine · 2022
    Review
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  16. Spatial-omics: Novel approaches to probe cell heterogeneity and extracellular matrix biology.Matrix biology : journal of the International Society for Matrix Biology · 2020
    Review
  17. Article
  18. Review
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  20. Review
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

16 authors at 8 institutions in 2 countries.

Jennifer YangDepartment of Genetics, Yale School of Medicine, New Haven, CT, USA.
Yoshiaki TanakaYale Stem Cell Center, Yale School of Medicine, New Haven, CT, USA.
Montrell SeayDepartment of Genetics, Yale School of Medicine, New Haven, CT, USA.
Zhen LiDepartment of Neurobiology, Yale School of Medicine, New Haven, CT, USA.
Jiaqi JinDepartment of Genetics, Yale School of Medicine, New Haven, CT, USA.
Lana Xia GarmireEpidemiology Program, University of Hawaii Cancer Center, HI, USA.
Xun ZhuEpidemiology Program, University of Hawaii Cancer Center, HI, USA.
Ashley TaylorHematology, Yale Comprehensive Cancer Center and Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
Weidong LiDepartment of Genetics, Yale School of Medicine, New Haven, CT, USA.
Ghia EuskirchenDepartment of Genetics, Stanford University, Palo, Alto, CA, USA.
Stephanie HaleneHematology, Yale Comprehensive Cancer Center and Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
Yuval KlugerDepartment of Pathology, Yale School of Medicine, New Haven, CT, USA.
Michael P SnyderDepartment of Genetics, Stanford University, Palo, Alto, CA, USA.
In-Hyun ParkYale Stem Cell Center, Yale School of Medicine, New Haven, CT, USA.
Xinghua PanDepartment of Genetics, Yale School of Medicine, New Haven, CT, USA.
Sherman Morton WeissmanDepartment of Genetics, Yale School of Medicine, New Haven, CT, USA.
Yale University · USYale Cancer Center · USCancer Center of Hawaii · USJiujiang University · CNPalo Alto University · USSouthern Medical University · CNStanford University · USUniversity of Hawaiʻi at Mānoa · US

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI MEGAN C KING · 1985 to 2026
$85.0M
Special EquipmentP50HG007735 · NHGRI · STANFORD UNIVERSITY · PI CHANG, HOWARD Y · 2014 to 2018
$15.2M
Transgenic Mouse, ICSI and IVF CoreP20GM103457 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI URSCHITZ, JOHANN · 2012 to 2018
$12.9M
Cancer precision medicine through spatially informative single cell image and transcriptomics data analysisR01LM012373 · NLM · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GARMIRE, LANA X · 2016 to 2024
$2.4M
EFFICIENT SPECTRAL APPROACHES FOR FINDING UNDERLYING STRUCTURES IN BIG DATAR01HG008383 · NHGRI · YALE UNIVERSITY · PI KLUGER, YUVAL · 2016 to 2018
$1.2M
Predicting Metastisis to Lymph NodesR33CA110511 · NCI · YALE UNIVERSITY · PI RIMM, DAVID L · 2005 to 2008
$1.0M
An Integrative Bioinformatics Approach to Study Single Cancer Cell HeterogeneityK01ES025434 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GARMIRE, LANA X · 2014 to 2018
$905k
NCI NIH HHS P30 CA016359NCI NIH HHS R33 CA110511NHGRI NIH HHS P50 HG007735NHGRI NIH HHS R01 HG008383NIEHS NIH HHS K01 ES025434NIGMS NIH HHS P20 GM103457NLM NIH HHS R01 LM012373
6 · The paper itself

Abstract

Molecular changes underlying stem cell differentiation are of fundamental interest. scRNA-seq on murine hematopoietic stem cells (HSC) and their progeny MPP1 separated the cells into 3 main clusters with distinct features: active, quiescent, and an un-characterized cluster. Induction of anemia resulted in mobilization of the quiescent to the active cluster and of the early to later stage of cell cycle, with marked increase in expression of certain transcription factors (TFs) while maintaining expression of interferon response genes. Cells with surface markers of long term HSC increased the expression of a group of TFs expressed highly in normal cycling MPP1 cells. However, at least Id1 and Hes1 were significantly activated in both HSC and MPP1 cells in anemic mice. Lineage-specific genes were differently expressed between cells, and correlated with the cell cycle stages with a specific augmentation of erythroid related genes in the G2/M phase. Most lineage specific TFs were stochastically expressed in the early precursor cells, but a few, such as Klf1, were detected only at very low levels in few precursor cells. The activation of these factors may correlate with stages of differentiation. This study reveals effects of cell cycle progression on the expression of lineage specific genes in precursor cells, and suggests that hematopoietic stress changes the balance of renewal and differentiation in these homeostatic cells.

Indexed as

AnemiaAnimalsCell LineageErythropoiesisFemaleGene Expression ProfilingGene Expression RegulationHematopoietic Stem CellsMaleMice, Inbred C57BLSequence Analysis, RNASingle-Cell AnalysisTranscription Factor HES-1Transcription FactorsHes1 protein, mouseTranscription Factor HES-1Transcription Factors

Identifiers

PMID28003475
PMCPMC5388401
OpenAlexW2567309032

What OpenQuestion holds

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LicenceCC BY-NC
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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.