Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities

被引:913
作者
McKercher, SR
Torbett, BE
Anderson, KL
Henkel, GW
Vestal, DJ
Baribault, H
Klemsz, M
Feeney, AJ
Wu, GE
Paige, CJ
Maki, RA
机构
[1] UNIV TORONTO, DEPT IMMUNOL, TORONTO, ON, CANADA
[2] WELLESLEY HOSP, RES INST, TORONTO, ON, CANADA
[3] SCRIPPS RES INST, LA JOLLA, CA 92037 USA
[4] BURNHAM INST, LA JOLLA, CA 92037 USA
关键词
ets family; hematopoiesis; PU-1; transcription factor;
D O I
10.1002/j.1460-2075.1996.tb00949.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
PU.1 is a member of the ets family of transcription factors and is expressed exclusively in cells of the hematopoietic lineage, Mice homozygous for a disruption in the PU.1 DNA binding domain are born alive but die of severe septicemia within 48 h, The analysis of these neonates revealed a lack of mature macrophages, neutrophils, B cells and T cells, although erythrocytes and megakaryocytes were present. The absence of lymphoid commitment and development in null mice was not absolute, since mice maintained on antibiotics began to develop normal appearing T cells 3-5 days after birth, In contrast, mature B cells remained undetectable in these older mice, Within the myeloid lineage, despite a lack of macrophages in the older antibiotic-treated animals, a few cells with the characteristics of neutrophils began to appear by day 3, While the PU.1 protein appears not to be essential for myeloid and lymphoid lineage commitment, it is absolutely required for the normal differentiation of B cells and macrophages.
引用
收藏
页码:5647 / 5658
页数:12
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