Abstract
The transcription factor PU.1 is a hematopoietic-specific member of theetsfamily. Mice carrying a mutation in thePU.1locus were generated by gene targeting. Homozygous mutant embryos died at a late gestational stage. Mutant embryos produced normal numbers of megakaryocytes and erythroid progenitors, but some showed an impairment of erythroblast maturation. An invariant consequence of the mutation was a multilineage defect in the generation of progenitors for B and T lymphocytes, monocytes, and granulocytes. Thus, the developmental programs of lymphoid and myeloid lineages require a common genetic function likely acting at the level of a multipotential progenitor.
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Dates
Type | When |
---|---|
Created | 18 years, 11 months ago (Oct. 5, 2006, 8:01 p.m.) |
Deposited | 7 months, 3 weeks ago (Jan. 11, 2025, 3:42 a.m.) |
Indexed | 2 days, 15 hours ago (Sept. 3, 2025, 6:19 a.m.) |
Issued | 30 years, 11 months ago (Sept. 9, 1994) |
Published | 30 years, 11 months ago (Sept. 9, 1994) |
Published Print | 30 years, 11 months ago (Sept. 9, 1994) |
@article{Scott_1994, title={Requirement of Transcription Factor PU.1 in the Development of Multiple Hematopoietic Lineages}, volume={265}, ISSN={1095-9203}, url={http://dx.doi.org/10.1126/science.8079170}, DOI={10.1126/science.8079170}, number={5178}, journal={Science}, publisher={American Association for the Advancement of Science (AAAS)}, author={Scott, Edward W. and Simon, M. Celeste and Anastasi, John and Singh, Harinder}, year={1994}, month=sep, pages={1573–1577} }