Evidence map›Paper›PMID 8642256›Full record

ArticleThe Journal of experimental medicine1996

Genetic control of the frequency of hematopoietic stem cells in mice: mapping of a candidate locus to chromosome 1.

C E Müller-Sieburg, R Riblet

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 1996. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. A quantitative trait locus on chr.4 regulates thymic involution.The journals of gerontology. Series A, Biological sciences and medical sciences · 2010
    Article
  8. Stem cell aging: survival of the laziest?Cell cycle (Georgetown, Tex.) · 2008
    Review
  9. Article
  10. Review
  11. Article
  12. QTL analyses of lineage-negative mouse bone marrow cells labeled with Sca-1 and c-Kit.Mammalian genome : official journal of the International Mammalian Genome Society · 2008
    Article
  13. Article
  14. Analysis of expansion of myeloid progenitors in mice to identify leukemic susceptibility genes.Mammalian genome : official journal of the International Mammalian Genome Society · 2006
    Article
  15. QTL influencing baseline hematocrit in the C57BL/6J and DBA/2J lineage: age-related effects.Mammalian genome : official journal of the International Mammalian Genome Society · 2006
    Article
  16. Article
  17. Article
  18. Senescence of hematopoietic stem cells and bone marrow failure.International journal of hematology · 2005
    Review
  19. Article
  20. Regulation of hematopoietic stem cell aging in vivo by a distinct genetic element.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
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

2 authors.

C E Müller-SieburgMedical Biology Institute, La Jolla, California 92037, USA.
R Riblet

Funding

GENETIC ANALYSIS OF THE IMMUNE SYSTEMR01AI023548 · NIAID · TORREY PINES INST FOR MOLECULAR STUDIES · PI RIBLET, ROY · 1985 to 2008
$1.9M
ISOLATION OF HEMATOPOIETIC AND STROMAL CELL PRECURSORSR01DK041214 · NIDDK · MEDICAL BIOLOGY INSTITUTE · PI MULLER-SIEBURG, CHRISTA E. · 1989 to 1993
–
NIAID NIH HHS AI-23548NIDDK NIH HHS DK-41214
6 · The paper itself

Abstract

The genetic elements that govern the differentiation and proliferation of hematopoietic stem cells remain to be defined. We describe here marked strain-specific differences in the frequency of long-term culture-initiating cells (LTC-IC) in the bone marrow of different strains of mice. Mice of C57Bl/6 background showed the lowest levels of stem cells in marrow, averaging 2.4 +/- .06 LTC-IC/10(5) cells, BALB/c is intermediate (9.1 +/- 4.2/10(5) cells), and DBA/2 mice contained a 11-fold higher frequency of LTC-IC (28.1 +/- 16.5/10(5) cells) than C57Bl/6 mice. The genetic factors affecting the size of the stem cell pool were analyzed in the C57Bl/6 X DBA/2 recombinant inbred strains; LTC-IC frequencies ranged widely, indicating that stem cell frequencies are controlled by multiple genes. Quantitative trait linkage analysis suggested that two loci that have major quantitative effects are located on chromosome 1 near Adprp and Acrg, respectively. The mapping of the locus near Adprp was confirmed by finding an elevated stem cell frequency in B6.C-H25, a C57Bl/6 congenic strain that carries a portion of chromosome 1 derived from BALB/c mice. We have named this gene Scfr1 (stem cell frequency regulator 1). The allelic forms of this gene may be an important predictor of stem cell number and thus would be useful for evaluating cell sources in clinical stem cell transplantation.

Indexed as

Bone Marrow CellsChromosome MappingAnimalsCell DifferentiationCell DivisionCell LineCells, CulturedColony-Forming Units AssayGenotypeGranulocytesHematopoietic Stem CellsKineticsMiceMice, Inbred BALB CMice, Inbred C57BLMice, Mutant Strains

Identifiers

PMID8642256
PMCPMC2192322

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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.