The cell cycle gene SKP1 is regulated by light in postnatal rat brain

被引:3
作者
Uro-Coste, E
Perret, E
Fonta, C
Mathieu, M
Delisle, MB
Caput, D
Imbert, M
机构
[1] Univ Toulouse 3, EHESS, CNRS UMR 5549, Fac Med Rangueil,Ctr Rech Cerveau & Cognit, F-31062 Toulouse, France
[2] CHU Rangueil, Inst Federatif Rech Louis Bugnard, INSERM466, F-31403 Toulouse 4, France
[3] Labege Innopole, Sanofi Rech, F-31676 Labege, France
[4] CHU Rangueil, Grp Rech Physiopathol Cellulaire & Mol Syst Nerve, F-31403 Toulouse 4, France
来源
MOLECULAR BRAIN RESEARCH | 1998年 / 56卷 / 1-2期
关键词
brain; dark-rearing; visual; critical period; SKP1; cell;
D O I
10.1016/S0169-328X(98)00011-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
During the early postnatal phase of high neuronal plasticity, an altered visual input leads to great modifications of visual cortex organization [Y. Fregnac, M. Imbert, Development of neuronal selectivity in primary visual cortex of cat, Physiol. Rev., 64 (1984) 375-434; D.H. Hubel, T.N. Wiesel, S. LeVay, Plasticity of ocular dominance columns in monkey striate cortex, Philos. Trans. R. Sec. London, Ser. B, 278 (1977) 377-409.]. We used refined differential screening of an organized cDNA library to identify the genes that may participate in this plasticity. We isolated a candidate plasticity gene encoding for a 163 aa protein that is closely related to the human and yeast Skplp, a key factor in cell cycle progression [C. Bai, K. Hofman, L. Ma, M. Goebl, J.W. Harper, S.J. Elledge, SKP1 connects cell cycle regulators to the ubiquitin proteolysis machinery through a novel motif, the F-box, Cell, 86 (1996) 263-274; C. Connelly, P. Hieter, Budding yeast SKP1 encodes an evolutionary conserved kinetochore protein required for cell cycle progression, Cell, 86 (1996) 275-285; H. Zhang, R. Kobayashi, K. Galaktionov, D. Beach, p19Skp1 and p45Skp2 are essential elements of the cyclin A-CDK2 S phase kinase, Cell, 82 (1995) 915-925.]. Northern blot analysis showed that the expression of SKP1 (Skplp gene) dramatically decreased after 2 h of light stimulation in the visual cortex of young dark-reared rats. This down regulation lasted at least 72 h. It was specific for the critical period as we did not observe any significant regulation of SKP1 mRNA by light in adult dark-reared rat brain. The down regulation was observed in the superior colliculus but also in the frontal cortex and in the hippocampus. The fact that this down regulation was not restricted to the visual system, suggested that it could be produced by dark rearing-induced hormonal changes. The significance of SKP1 expression in the brain and its regulation are discussed. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:192 / 199
页数:8
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