Differential Spatial Expression and Subcellular Localization of CtBP Family Members in Rodent Brain

被引:32
|
作者
Huebler, Diana [1 ]
Rankovic, Marija [1 ]
Richter, Karin [2 ]
Lazarevic, Vesna [1 ,3 ]
Altrock, Wilko D. [1 ]
Fischer, Klaus-Dieter [2 ]
Gundelfinger, Eckart D. [1 ]
Fejtova, Anna [1 ]
机构
[1] Leibniz Inst Neurobiol, Dept Neurochem & Mol Biol, Magdeburg, Germany
[2] Univ Magdeburg, Inst Biochem & Cell Biol, D-39106 Magdeburg, Germany
[3] German Ctr Neurodegenerat Disorders DZNE, Magdeburg Branch, Magdeburg, Germany
来源
PLOS ONE | 2012年 / 7卷 / 06期
关键词
SYNAPTIC RIBBONS; MOLECULAR-CLONING; MEMBRANE FISSION; PROTEIN BASSOON; GOLGI MEMBRANE; ROLES; CTBP/BARS; CTBP3/BARS; REPRESSION; INTERACTS;
D O I
10.1371/journal.pone.0039710
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
C-terminal binding proteins (CtBPs) are well-characterized nuclear transcriptional co-regulators. In addition, cytoplasmic functions were discovered for these ubiquitously expressed proteins. These include the involvement of the isoform CtBP1-S/BARS50 in cellular membrane-trafficking processes and a role of the isoform RIBEYE as molecular scaffolds in ribbons, the presynaptic specializations of sensory synapses. CtBPs were suggested to regulate neuronal differentiation and they were implied in the control of gene expression during epileptogenesis. However, the expression patterns of CtBP family members in specific brain areas and their subcellular localizations in neurons in situ are largely unknown. Here, we performed comprehensive assessment of the expression of CtBP1 and CtBP2 in mouse brain at the microscopic and the ultra-structural levels using specific antibodies. We quantified and compared expression levels of both CtBPs in biochemically isolated brain fractions containing cellular nuclei or synaptic compartment. Our study demonstrates differential regional and subcellular expression patterns for the two CtBP family members in brain and reveals a previously unknown synaptic localization for CtBP2 in particular brain regions. Finally, we propose a mechanism of differential synapto-nuclear targeting of its splice variants CtBP2-S and CtBP2-L in neurons.
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页数:15
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