Evidence map›Paper›PMID 25139354›Full record

ArticleBlood2014

The DPY30 subunit in SET1/MLL complexes regulates the proliferation and differentiation of hematopoietic progenitor cells.

Zhenhua Yang, Jonathan Augustin, Chenbei Chang, Jing Hu, Kushani Shah, Chia-Wei Chang, Tim Townes, Hao Jiang

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 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

44 citing papers in PubMed, 70 citations in OpenAlex.

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  12. Wdr5 is essential for fetal erythropoiesis and hematopoiesis.Experimental hematology & oncology · 2023
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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

8 authors at 1 institution in 1 country.

Zhenhua YangDepartment of Biochemistry and Molecular Genetics, University of Alabama at Birmingham Stem Cell Institute, and.
Jonathan AugustinDepartment of Biochemistry and Molecular Genetics, University of Alabama at Birmingham Stem Cell Institute, and.
Chenbei ChangDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham School of Medicine, Birmingham, AL.
Jing HuDepartment of Biochemistry and Molecular Genetics, University of Alabama at Birmingham Stem Cell Institute, and.
Kushani ShahDepartment of Biochemistry and Molecular Genetics, University of Alabama at Birmingham Stem Cell Institute, and.
Chia-Wei ChangDepartment of Biochemistry and Molecular Genetics, University of Alabama at Birmingham Stem Cell Institute, and.
Tim TownesDepartment of Biochemistry and Molecular Genetics, University of Alabama at Birmingham Stem Cell Institute, and.
Hao JiangDepartment of Biochemistry and Molecular Genetics, University of Alabama at Birmingham Stem Cell Institute, and.
University of Alabama at Birmingham · US

Funding

Connecting signaling with cytoskeleton: Abl and Arg in vertebrate gastrulationR01GM098566 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CHANG, CHENBEI · 2012 to 2015
$1.3M
NIGMS NIH HHS R01 GM098566
6 · The paper itself

Abstract

Epigenetic mechanisms, including histone modifications, have emerged as important factors influencing cell fate determination. The functional role of H3K4 methylation, however, remains largely unclear in the maintenance and differentiation of hematopoietic stem cells (HSCs)/hematopoietic progenitor cells (HPCs). Here we show that DPY30, a shared core subunit of the SET1/MLL family methyltransferase complexes and a facilitator of their H3K4 methylation activity, is important for ex vivo proliferation and differentiation of human CD34(+) HPCs. DPY30 promotes HPC proliferation by directly regulating the expression of genes critical for cell proliferation. Interestingly, while DPY30 knockdown in HPCs impaired their differentiation into the myelomonocytic lineage, it potently promoted hemoglobin production and affected the kinetics of their differentiation into the erythroid lineage. In an in vivo model, we show that morpholino-mediated dpy30 knockdown resulted in severe defects in the development of the zebrafish hematopoietic system, which could be partially rescued by coinjection of dpy30 messenger RNA. Taken together, our results establish a critical role of DPY30 in the proliferation and appropriate differentiation of hematopoietic progenitor cells and in animal hematopoiesis. Finally, we also demonstrate a crucial role of DPY30 in the growth of several MLL1-fusion-mediated leukemia cell lines.

Indexed as

Cell DifferentiationAmino Acid SequenceAnimalsCell Line, TumorCell ProliferationCell Transformation, NeoplasticHematopoiesisHematopoietic Stem CellsHistone-Lysine N-MethyltransferaseHumansLeukemiaMolecular Sequence DataMultiprotein ComplexesMyeloid-Lymphoid Leukemia ProteinNuclear ProteinsOncogene Proteins, FusionDPY30 protein, humanHistone-Lysine N-MethyltransferaseMultiprotein ComplexesMyeloid-Lymphoid Leukemia ProteinNuclear ProteinsOncogene Proteins, FusionProtein SubunitsTranscription Factors

Identifiers

PMID25139354
PMCPMC4507038
OpenAlexW2085252297

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.