Scotland G, Beard M, Erdogan S, Huston E, McCallum F, MacKenzie S J, Peden A H, Pooley L, Rena N G, Ross A H, Yarwood S J, Houslay M D
Division of Biochemistry and Molecular Biology, Institute of Life and Biomedical Sciences, Davidson Building, Glasgow, G12 8QQ, Scotland.
Methods. 1998 Jan;14(1):65-79. doi: 10.1006/meth.1997.0566.
The PDE4 cyclic AMP-specific phosphodiesterase family comprises a large number of different isoforms encoded by four distinct genes, with additional complexity arising through alternate mRNA splicing. This generates a number of distinct PDE4 isoforms with unique N-terminal regions. The range of such splice variants emanating from the four PDE4 genes appears to be highly conserved across species. One key role for such regions appears to be their potential to target isoforms to specific intracellular sites. Evidence for such a targeting role for these N-terminal regions can be gleaned by a variety of techniques. These include subcellular fractionation, confocal microscopy, binding assays to show association with proteins having src homology 3 (SH3) domains, and generation of chimeric constructs of these N-terminal regions with proteins that are normally expressed in the cytosol.
磷酸二酯酶4(PDE4)环磷酸腺苷特异性磷酸二酯酶家族由四个不同基因编码的大量不同亚型组成,通过可变mRNA剪接产生额外的复杂性。这产生了许多具有独特N端区域的不同PDE4亚型。来自四个PDE4基因的此类剪接变体范围在物种间似乎高度保守。这些区域的一个关键作用似乎是它们将亚型靶向特定细胞内位点的潜力。通过多种技术可以收集到这些N端区域具有这种靶向作用的证据。这些技术包括亚细胞分级分离、共聚焦显微镜、用于显示与具有src同源3(SH3)结构域的蛋白质结合的结合测定,以及这些N端区域与通常在细胞质中表达的蛋白质的嵌合构建体的生成。