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Multiple Distinct Splicing Enhancers in the Protein-Coding Sequences of a Constitutively Spliced Pre-mRNA

机译:组成型拼接前mRNA的蛋白质编码序列中的多个不同的拼接增强子。

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摘要

We have identified multiple distinct splicing enhancer elements within protein-coding sequences of the constitutively spliced human β-globin pre-mRNA. Each of these highly conserved sequences is sufficient to activate the splicing of a heterologous enhancer-dependent pre-mRNA. One of these enhancers is activated by and binds to the SR protein SC35, whereas at least two others are activated by the SR protein SF2/ASF. A single base mutation within another enhancer element inactivates the enhancer but does not change the encoded amino acid. Thus, overlapping protein coding and RNA recognition elements may be coselected during evolution. These studies provide the first direct evidence that SR protein-specific splicing enhancers are located within the coding regions of constitutively spliced pre-mRNAs. We propose that these enhancers function as multisite splicing enhancers to specify 3′ splice-site selection.
机译:我们已经鉴定出组成型人β-珠蛋白pre-mRNA的蛋白质编码序列内的多个不同的剪接增强子元件。这些高度保守的序列中的每一个都足以激活异源增强子依赖性pre-mRNA的剪接。这些增强子之一被SR蛋白SC35激活并与之结合,而至少另外两个被SR蛋白SF2 / ASF激活。另一个增强子元件内的单碱基突变使该增强子失活,但不改变编码的氨基酸。因此,在进化过程中可以共同选择重叠的蛋白质编码和RNA识别元件。这些研究提供了第一个直接证据,表明SR蛋白特异性剪接增强子位于组成性剪接的pre-mRNA的编码区内。我们建议这些增强子作为多位点拼接增强子来指定3'拼接位点的选择。

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