vavCre Transgenic mice: A tool for mutagenesis in hematopoietic and endothelial lineages

Genesis - Tập 34 Số 4 - Trang 251-256 - 2002
Pantelis Georgiades1, Sarah Ogilvy2, Hélène Duval1, Diana R. Licence1, D. Stephen Charnock‐Jones3,1, S. K. Smith3,1, Cristin G. Print1
1Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge, UK
2Department of Haematology, University of Cambridge, Cambridge Institute for Medical Research, Cambridge, UK
3Department of Obstetrics and Gynaecology, University of Cambridge, Rosie Hospital, Cambridge, UK

Tóm tắt

Abstract

Summary: Cre transgenic mice can be used to delete gene sequences flanked by loxP sites in specific somatic tissues. We have generated vavCre transgenic mice, which can be used to inactivate genes specifically in adult hematopoietic and endothelial cells. In these animals, a Cre transgene is expressed under control of murine vav gene regulatory elements. To assess their usefulness, vavCre transgenic mice were bred with R26R mice, which express a lacZ reporter gene only in cells where Cre‐mediated recombination has occurred. VavCre/R26R double‐heterozygous offspring were analyzed by β‐galactosidase histochemistry and flow cytometry. VavCre‐mediated recombination occurred in most hematopoietic cells of all hematopoietic organs, including the hematopoietic progenitor‐rich bone marrow. Recombination also occurred in most endothelial and germ cells, but only rarely in other cell types. The recombination in both hematopoietic and endothelial lineages may partly reflect their putative shared ontogeny and provides a unique tool for simultaneous pan‐hematopoietic and endothelial mutagenesis. genesis 34:251–256, 2002. © 2002 Wiley‐Liss, Inc.

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Tài liệu tham khảo

Bustelo XR, 1993, Developmental expression of the vav protooncogene, Cell Growth Diff, 4, 297

10.1242/dev.125.4.725

10.1023/A:1008942828960

10.1073/pnas.92.26.12070

Hogan B, 1994, Manipulating the mouse embryo

10.1182/blood.V98.7.2248

10.1016/S0092-8674(01)00328-2

10.1038/nm1101-1194

10.1002/(SICI)1526-968X(200002)26:2<99::AID-GENE1>3.0.CO;2-B

10.1182/blood.V91.2.419

10.1182/blood.V94.6.1855

10.1073/pnas.96.26.14943

Ohmura K, 1999, Emergence of T, B, and myeloid lineage‐committed as well as multipotent hemopoietic progenitors in the aorta‐gonad‐mesonephros region of day 10 fetuses of the mouse, J Immunol, 163, 4788, 10.4049/jimmunol.163.9.4788

10.1038/sj.onc.1202151

10.1038/sj.onc.1200878

10.1093/nar/25.6.1317

10.1016/S1046-2023(05)80067-2

Schuebel KE, 1996, Isolation and characterization of murine vav2, a member of the vav family of proto‐oncogenes, Oncogene, 13, 363

10.1038/5007

10.1002/(SICI)1521-4141(199807)28:07<2159::AID-IMMU2159>3.0.CO;2-B

10.1002/j.1460-2075.1995.tb06969.x