Mouse DREAM/Calsenilin/KChIP3: Gene structure, coding potential, and expression

被引:57
作者
Spreafico, F
Barski, JJ
Farina, C
Meyer, M
机构
[1] Max Planck Inst Neurobiol, D-82152 Martinsried, Germany
[2] IRCCS, Eugenio Medea Sci Inst, I-23842 Bosisio Parini, LC, Italy
[3] Med Univ Silesia, Dept Physiol, PL-40752 Katowice, Poland
关键词
D O I
10.1006/mcne.2000.0913
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ca2+-binding proteins containing EF-hands are important constituents of intracellular signaling pathways. Recently, three new members of the Neuronal Calcium Sensor subgroup have been cloned in humans. Calsenilin interacts with presenilins, DREAM is a calcium-regulated transcriptional repressor and KChlP3 binds and modulates A-type potassium channels. Here we describe the mouse full-length cDNA and the genomic locus, demonstrating that the three proteins are encoded by the same unique gene. Various mechanisms contribute to the coding potential of this locus. These include alternate translation starts in the first exon and alternative splicing yielding transcripts lacking the EF-hand domains. In situ hybridization, RT-PCR, and Northern blotting reveal nervous system-restricted expression largely coinciding with the distribution of the Kv4.2 alpha -subunit of potassium channels. The presence of transcripts in early embryonic stages suggests roles for the protein also during development.
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页码:1 / 16
页数:16
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