## Abstract Summary: Conditional and tissue specific gene targeting using the Cre‐loxP recombination system in combination with established ES cell techniques has become a standard for in vivo loss of function studies. In a typical flox and delete gene targeting strategy, the loxP‐neo‐loxP cassette
Direct removal in the mouse of a floxed neo gene from a three-loxp conditional knockout allele by two novel approaches
✍ Scribed by Xiaoling Xu; Cuiling Li; Lisa Garrett-Beal; Denise Larson; Anthony Wynshaw-Boris; Chu-Xia Deng
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 339 KB
- Volume
- 30
- Category
- Article
- ISSN
- 1526-954X
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✦ Synopsis
Abstract
Summary: The presence in an intron of the ploxP‐neo‐loxP cassette often results in severe interference with gene expression. Consequently, many investigators selectively remove the ploxP‐neo‐loxP cassette by transient expression of Cre in ES cells. Although effective, the added manipulation of the ES cells may reduce the likelihood that a clone will be able to transmit via the germline. Therefore, we developed two novel approaches that remove the ploxP‐neo‐loxP by Cre‐mediated recombination in mouse. First, the ploxP‐neo‐loxP‐containing mice were crossed with EIIa‐Cre transgenic mice. Second, a Cre‐expression plasmid was injected into pronuclei of fertilized eggs bearing the ploxP‐neo‐loxP allele. Both approaches produced mosaic mice with partial and complete excision. These mosaic mice were then mated, and the neo‐less conditional knockout allele was found in the offspring after screening only a few litters. These procedures provide options for removing neo directly in the mouse in addition to the commonly used approach that deletes neo in ES cells. genesis 30:1–6, 2001. © 2001 Wiley‐Liss, Inc.
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