## Abstract Runx2 is a transcription factor controlling skeletal development, and is also expressed in extraskeletal tissues where its function is not well understood. Existing __Runx2__ mutant and transgenic mouse models do not allow the necessary control of __Runx2__ expression to understand its
Inducible expression of retrograde transynaptic genetic tracer in mice
โ Scribed by Hiromi Sano; Yumiko Nagai; Mineto Yokoi
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 309 KB
- Volume
- 45
- Category
- Article
- ISSN
- 1526-954X
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
A key step towards understanding the development and function of the central nervous system is by characterizing the connections between neurons. Tetanus toxin C fragment (TTC) is transynaptically and retrogradely transported without the toxin's pathogenic effect, and therefore, recently it has been used as a genetic tracer combined with ฮฒโgalactosidase or green fluorescent protein. Here, we introduce a new fusion construct, APTTC, consisting of the truncated human placental alkaline phosphatase with TTC, and generating the transgenic mouse line, (tetracycline operator) tetOโAPTTC, for inducible expression of APTTC regulated by tetO. We demonstrate that APTTC is transported retrogradely and transynaptically, and allows us to robustly visualize the inputs of the expressing neurons when transgenetically expressed in mice, exemplified in the striatal neuronal circuit. Therefore, tetOโAPTTC transgenic mouse line can be widely used for visualization of neuronal connectivity when combined with mice carrying tetracyclineโcontrolled transactivator (tTA) in any specific neurons. genesis 45:123โ128, 2007. ยฉ 2007 WileyโLiss, Inc.
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