## Abstract Stable tubulin‐only polypeptide (STOP) proteins are microtubule‐associated proteins responsible for microtubule stabilization in neurons. STOP null mice show apparently normal cerebral anatomy but display synaptic defects associated with neuroleptic‐sensitive behavioral disorders. STOP
Open brain gene product Rab23: Expression pattern in the adult mouse brain and functional characterization
✍ Scribed by Anchen Guo; Ting Wang; Ee Ling Ng; Selina Aulia; Kooi Hoong Chong; Felicia Yu Hsuan Teng; Ya Wang; Bor Luen Tang
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 854 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0360-4012
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The gene mutated in the mouse open brain (opb) phenotype antagonizes sonic hedgehog‐mediated signaling and encodes a small GTPase of the Rab family, Rab23. To date, the brain expression profile and exact mechanism of function of the Rab23 protein has remained unknown. Specific antibodies generated against Rab23 showed that the protein is highly enriched in the adult rodent brain and present in low levels in multiple tissues of the adult rodent. Rab23 is found in the cytosol as well as being associated with the plasma and endosomal membranes. In the adult mouse brain, Rab23 is found in βIII tubulin (TuJ) positive neuronal cell bodies and are most prominent in the cortex, hypothalamus and the cerebellum. It is, however, absent from glial fibrillary acidic protein (GFAP) positive astrocytes or CNPase positive oligodendrocytes. Despite the plasma membrane/endosomal membrane localization of Rab23, neither overexpression of the GTP‐restricted nor the GDP‐bound mutant forms affect internalization of transferrin or epidermal growth factor. Exogenous overexpression of Rab23 or its mutants also did not affect the morphological differentiation of thalamic neurons in culture. Expression of Rab23 in the adult brain is suggestive, however, of having a postnatal function beyond its role in embryonic development. © 2006 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract To achieve inducible and reversible gene expression in the adult mouse brain, we exploited an improved version of the tetracycline‐controlled transactivator‐based system (rtTA2^S^‐M2, rtTA2 hereafter) and combined it with the forebrain‐specific CaMKIIα promoter. Several independent line
## Abstract Three genetic mouse models were examined to define effects of bone morphogenetic protein (BMP) signalling on gene expression in normal and injured adult brain. CaMKII‐Cre eliminated the BMP receptor Acvr1 (Alk2) and the common TGFβ superfamily signal mediator Smad4 or activated a consti