𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Generation of novel conditional and hypomorphic alleles of the Smad2 gene

✍ Scribed by Ye Liu; Maria H. Festing; Mark Hester; John C. Thompson; Michael Weinstein


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
249 KB
Volume
40
Category
Article
ISSN
1526-954X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Smad2 is an intracellular mediator of the transforming growth factor beta signaling (TGFΞ²) pathway. It has been previously shown that, in the mouse, ablation of functional Smad2 results in embryonic lethality due to gastrulation defects. To circumvent the early lethality and study the spatially and temporally specific functions of Smad2, we utilized the Cre‐loxP system to generate a Smad2 conditional allele. Here we show that a conditional allele, Smad2^flox^, was generated. In this allele, exons 9 and 10 are flanked by loxP sites and the gene is functionally wildtype. Cre‐mediated recombination results in a deletion allele which phenocopies our previously reported Smad2^Ξ”__C__^ null mutation. To generate this conditional allele, we first made a targeted mutation which introduced a floxed neo cassette into intron 10. This allele (Smad2^3loxP^) functions hypomorphically when placed opposite a null allele, and unlike the other published Smad2 hypomorphic allele, can be maintained in the homozygous state. genesis 40:118–123, 2004. Β© 2004 Wiley‐Liss, Inc.


πŸ“œ SIMILAR VOLUMES


Generation of conditional Cited2 null al
✍ Jost I. Preis; Natalie Wise; Mark J. Solloway; Richard P. Harvey; Duncan B. Spar πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 224 KB πŸ‘ 1 views
Generation of a conditional allele of th
✍ Paloma GarcΓ­a; Oscar Berlanga; Roger Watson; Jon Frampton πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 630 KB

## Abstract B‐Myb is an essential transcription factor involved in control of the cell cycle and the regulation of tissue‐specific gene expression in a wide range of cell types. Loss of both alleles results in early embryonic lethality at E4.5–6.5. To address the function of B‐Myb in later stages o