Literature DB >> 11377750

Neuron-specific expression of Cre recombinase during the late phase of brain development.

M Hirasawa1, A Cho, T Sreenath, B Sauer, J P Julien, A B Kulkarni.   

Abstract

Gene targeting to disrupt gene expression in a temporal and spatial manner in a specific tissue using Cre recombinase-mediated gene inactivation has been proven to be useful to study in vivo gene function. To delete genes specifically in neurons during the late phase of brain development, we have generated transgenic mouse lines that express Cre recombinase under the control of the murine neurofilament-H (mNF-H) gene promoter. In this study, we report that one of these mouse lines expresses Cre recombinase specifically in the neurons of the brain and spinal cord during the late stage of their development. The transgenic line displays specific excision of the loxP-flanked gene in the neurons just after embryonic day 18.5 (E.18.5), which coincides with the later phase of brain maturation including spinal cord and olfactory bulb area. This mNF-H-cre transgenic mouse line will be valuable for studying in vivo functions of neuron-specific genes, particularly, defining their precise roles in the mature nervous system using conditional gene targeting strategies.

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Year:  2001        PMID: 11377750     DOI: 10.1016/s0168-0102(01)00216-4

Source DB:  PubMed          Journal:  Neurosci Res        ISSN: 0168-0102            Impact factor:   3.304


  10 in total

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4.  Perinatal abrogation of Cdk5 expression in brain results in neuronal migration defects.

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5.  Neuron-specific (pro)renin receptor knockout prevents the development of salt-sensitive hypertension.

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10.  Neuron-Specific Deletion of the Nf2 Tumor Suppressor Impairs Functional Nerve Regeneration.

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  10 in total

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