Expression trapping: Identification of novel genes expressed in hematopoietic and endothelial lineages by gene trapping in ES cells

被引:58
作者
Stanford, WL
Caruana, G
Vallis, KA
Inamdar, M
Hidaka, M
Bautch, VL
Bernstein, A
机构
[1] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Program Mol Biol & Canc, Toronto, ON M5G 1X5, Canada
[2] Ontario Canc Inst, Toronto, ON M4X 1K9, Canada
[3] Univ Toronto, Dept Mol & Med Genet, Toronto, ON, Canada
[4] Univ N Carolina, Dept Biol, Chapel Hill, NC USA
关键词
D O I
10.1182/blood.V92.12.4622.424k23_4622_4631
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have developed a large-scale, expression-based gene trap strategy to perform genome-wide functional analysis of the murine hematopoietic and vascular systems. Using two different gene trap vectors, we have isolated embryonic stem (ES) cell clones containing lacZ reporter gene insertions in genes expressed in blood island and vascular cells, muscle, stromal cells, and unknown cell types. Of 79 clones demonstrating specific expression patterns, 49% and 16% were preferentially expressed in blood islands and/or the vasculature, respectively. The majority of ES clones that expressed lacZ in blood islands also expressed lacZ upon differentiation into hematopoietic cells on OP9 stromal layers. Importantly, the in vivo expression of the lacZ fusion products accurately recapitulated the observed in vitro expression patterns. Expression and sequence analysis of representative clones suggest that this approach will be useful for identifying and mutating novel genes expressed in the developing hematopoietic and vascular systems. (C) 1998 by The American Society of Hematology.
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收藏
页码:4622 / 4631
页数:10
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