Identification of a mouse synaptic glycoprotein gene in cultured neurons

被引:9
作者
Yu, ACH
Sun, CX
Li, Q
Liu, HD
Wang, CR
Zhao, GP
Jin, ML
Lau, LT
Fung, YWW
Liu, SA
机构
[1] Peking Univ, Neurosci Res Inst, Beijing 100871, Peoples R China
[2] Minist Educ Res, Key Lab Neurosci, Beijing, Peoples R China
[3] Peking Univ, Dept Neurobiol, Hlth Sci Ctr, Beijing 100871, Peoples R China
[4] Chinese Acad Sci, Shanghai Brain Res Inst, Shanghai Res Ctr Life Sci, Shanghai, Peoples R China
[5] Hong Kong DNA Chips Ltd, Hong Kong, Hong Kong, Peoples R China
[6] Chinese Acad Sci, Shanghai Res Ctr Biotechnol, Shanghai Inst Biol Sci, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
primary culture; cerebral cortical neurons; synaptic glycoprotein; bioinformatics;
D O I
10.1007/s11064-005-8800-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Neuronal differentiation and aging are known to involve many genes, which may also be differentially expressed during these developmental processes. From primary cultured cerebral cortical neurons, we have previously identified various differentially expressed gene transcripts from cultured cortical neurons using the technique of arbitrarily primed PCR (RAP-PCR). Among these transcripts, clone 0-2 was found to have high homology to rat and human synaptic glycoprotein. By in silico analysis using an EST database and the FACTURA software, the full-length sequence of 0-2 was assembled and the clone was named as mouse synaptic glycoprotein homolog 2 (mSC2). DNA sequencing revealed transcript size of mSC2 being smaller than the human and rat homologs. RT-PCR indicated that mSC2 was expressed differentially at various culture days. The mSC2 gene was located in various tissues with higher expression in brain, lung, and liver. Functions of mSC2 in neurons and other tissues remain elusive and will require more investigation.
引用
收藏
页码:1289 / 1294
页数:6
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