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PMID: 15083520 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Generation of Pax2-Cre mice by modification of a Pax2 bacterial artificial chromosome.

Genesis (New York, N.Y. : 2000) ·Vol. 38 ·No. 4 ·2004-04-00 ·Pages 195-9

Ohyama T, Groves AK

Abstract

The Pax2 gene is expressed in the developing otocyst, kidney, and midbrain-hindbrain boundary. We generated Pax2-Cre transgenic lines by modification of a Pax2 bacterial artificial chromosome (BAC). In one Pax2-Cre line, Cre mRNA starts to be expressed in the otic placode at the late presomite stage. R26R reporter mouse analysis revealed that the Cre expression is sufficient to delete the loxP-flanked sequences in most of the cells in the inner ear. Reporter-positive cells are also detected in other Pax2-expressing tissues such as midbrain, cerebellum, olfactory bulb, and kidney, suggesting that these cells are the descendants of Pax2-expressing cells in these tissues and that Pax2-Cre transgenic mice can delete genes efficiently in these tissues.

MeSH Terms
Animals Chromosomes, Artificial, Bacterial/genetics DNA-Binding Proteins/genetics,metabolism Down-Regulation Embryo, Mammalian/embryology,metabolism Integrases/genetics,metabolism Mice Mice, Transgenic PAX2 Transcription Factor RNA, Messenger/genetics,metabolism Transcription Factors/genetics,metabolism
Chemicals
DNA-Binding Proteins PAX2 Transcription Factor Pax2 protein, mouse RNA, Messenger Transcription Factors Cre recombinase Integrases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ohyama Takahiro
Gonda Department of Cell and Molecular Biology, House Ear Institute, Los Angeles, California 90057, USA.
Groves Andrew K
Article Info
Journal
Genesis (New York, N.Y. : 2000)
Abbr.
Genesis
ISSN
1526-954X
Published
2004-04-00
Pages
195-9
Language
English
Region
United States
NLM ID
100931242
Subset
IM
Grants
NIDCD NIH HHS · DC04876 · United States
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