The in vivo minigene approach to analyze tissue-specific splicing

被引:51
作者
Stoss, O
Stoilov, P
Hartmann, AM
Nayler, O
Stamm, S
机构
[1] Max Planck Inst Neurobiol, D-82152 Martinsried, Germany
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
来源
BRAIN RESEARCH PROTOCOLS | 1999年 / 4卷 / 03期
关键词
alternative splicing; minigene; RT-PCR; transfection;
D O I
10.1016/S1385-299X(99)00043-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The exact mechanisms leading to alternative splice site selection are still poorly understood. However, recently cotransfection studies in eukaryotic cells were successfully used to decipher contributions of RNA elements (cis-factors), their interacting protein components (trans-factors) or the cell type to alternative pre-mRNA splicing. Splice factors often work in a concentration dependent manner, resulting in a gradual change of alternative splicing patterns of a minigene when the amount of a trans-acting protein is increased by cotransfections. Here, we give a detailed description of this technique that allows analysis of large gene fragments (up to 10-12 kb) under in vivo condition. Furthermore, we provide a summary of 44 genes currently investigated to demonstrate the general feasibility of this technique. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:383 / 394
页数:12
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