造血
生物
髓样
突变体
祖细胞
转录因子
IRF8
遗传学
胚胎
细胞生物学
红细胞
基因座(遗传学)
基因
分子生物学
免疫学
干细胞
作者
Edward W. Scott,M. Celeste Simon,John Anastasi,Harinder Singh
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1994-09-09
卷期号:265 (5178): 1573-1577
被引量:1508
标识
DOI:10.1126/science.8079170
摘要
The transcription factor PU.1 is a hematopoietic-specific member of the ets family. Mice carrying a mutation in the PU.1 locus 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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