Evidence map›Paper›PMID 16024775›Full record

ArticleMolecular and cellular biology2005

Functional but abnormal adult erythropoiesis in the absence of the stem cell leukemia gene.

Mark A Hall, Nicholas J Slater, C Glenn Begley, Jessica M Salmon, Leonie J Van Stekelenburg, Matthew P McCormack, Stephen M Jane, David J Curtis

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.5field-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

26 citing papers in PubMed, 48 citations in OpenAlex.

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  8. Review
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  12. Epigenetic and genetic mechanisms in red cell biology.Current opinion in hematology · 2014
    Review
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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 2 institutions in 2 countries.

Mark A HallRotary Bone Marrow Research Laboratories, P.O. Royal Melbourne Hospital, Grattan St., Parkville, Melbourne 3050, Australia.
Nicholas J Slater
C Glenn Begley
Jessica M Salmon
Leonie J Van Stekelenburg
Matthew P McCormack
Stephen M Jane
David J Curtis
The Royal Melbourne Hospital · AUAmgen (United States) · US

Funding

VIROSOME/PROTEOLIPOSOME MEDIATED GENE TRANSFERP01HL053749 · NHLBI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI WEISS, MITCHELL J · 1994 to 2022
$43.6M
Role of LBP-1a and p14 NF-E4 in gamma globin gene expre*R01HL069232 · NHLBI · ROYAL MELBOURNE HOSPITAL · PI JANE, STEPHEN M. · 2001 to 2004
$700k
NHLBI NIH HHS P01 HL053749NHLBI NIH HHS P01 HL53749-03NHLBI NIH HHS R01 HL069232NHLBI NIH HHS R01 HL69232-01
6 · The paper itself

Abstract

Previous studies have indicated that the stem cell leukemia gene (SCL) is essential for both embryonic and adult erythropoiesis. We have examined erythropoiesis in conditional SCL knockout mice for at least 6 months after loss of SCL function and report that SCL was important but not essential for the generation of mature red blood cells. Although SCL-deleted mice were mildly anemic with increased splenic erythropoiesis, they responded appropriately to endogenous erythropoietin and hemolytic stress, a measure of late erythroid progenitors. However, SCL was more important for the proliferation of early erythroid progenitors because the predominant defects in SCL-deleted erythropoiesis were loss of in vitro growth of the burst-forming erythroid unit and an in vivo growth defect revealed by transplant assays. With respect to erythroid maturation, SCL-deleted proerythroblasts could generate more mature erythroblasts and circulating red blood cells. However, SCL was required for normal expression of TER119, one of the few proposed target genes of SCL. The unexpected finding that SCL-independent erythropoiesis can proceed in the adult suggests that alternate factors can replace the essential functions of SCL and raises the possibility that similar mechanisms also explain the relatively minor defects previously observed in SCL-null hematopoietic stem cells.

Indexed as

AgingAnimalsBasic Helix-Loop-Helix ProteinsBone Marrow TransplantationDNA-Binding ProteinsErythroid Precursor CellsErythropoiesisHematopoietic Stem CellsMiceMice, KnockoutMice, TransgenicProto-Oncogene ProteinsT-Cell Acute Lymphocytic Leukemia Protein 1Transcription FactorsBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsProto-Oncogene ProteinsTal1 protein, mouseT-Cell Acute Lymphocytic Leukemia Protein 1Transcription Factors

Identifiers

PMID16024775
PMCPMC1190361
OpenAlexW2151526704

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.