Min H, Turck C W, Nikolic J M, Black D L
Molecular Biology Institute, University of California at Los Angeles, 90095-1662, USA.
Genes Dev. 1997 Apr 15;11(8):1023-36. doi: 10.1101/gad.11.8.1023.
We have purified and cloned a new splicing factor, KSRP. KSRP is a component of a multiprotein complex that binds specifically to an intronic splicing enhancer element downstream of the neuron-specific c-src N1 exon. This 75-kD protein induces the assembly of five other proteins, including the heterogeneous nuclear ribonucleoprotein F, onto the splicing enhancer. The sequence of the KSRP cDNA indicates that the protein contains four K homology RNA-binding domains and an unusual carboxy-terminal domain. KSRP is similar to two proteins, FUSE-binding protein and P-element somatic inhibitor. KSRP is expressed in both neural and non-neural cell lines, although it is present at higher levels in neural cells. Antibodies specific for KSRP inhibit the splicing of the N1 exon in vitro. Moreover, this inhibition of N1 splicing can be rescued by the addition of purified KSRP. KSRP is likely to regulate splicing from a number of intronic splicing enhancer sequences.
我们已经纯化并克隆了一种新的剪接因子KSRP。KSRP是一种多蛋白复合物的组成成分,该复合物特异性结合于神经元特异性c-src N1外显子下游的内含子剪接增强子元件。这种75kD的蛋白质诱导包括异质性核核糖核蛋白F在内的其他五种蛋白质组装到剪接增强子上。KSRP cDNA的序列表明该蛋白质含有四个K同源RNA结合结构域和一个不寻常的羧基末端结构域。KSRP与两种蛋白质,即FUSE结合蛋白和P因子体细胞抑制剂相似。KSRP在神经细胞系和非神经细胞系中均有表达,尽管其在神经细胞中的含量更高。针对KSRP的特异性抗体在体外抑制N1外显子的剪接。此外,通过添加纯化的KSRP可以挽救这种对N1剪接的抑制。KSRP可能从多个内含子剪接增强子序列调节剪接。