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Temperature-dependent splicing of β-globin pre-mRNA

机译:β-珠蛋白前体mRNA的温度依赖性剪接

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摘要

A T→G mutation at nucleotide 705 of human β-globin intron 2 creates an aberrant 5′ splice site and activates a cryptic 3′ splice site upstream. In consequence, the pre-mRNA is spliced via aberrant splice sites, despite the presence of the still functional correct sites. Surprisingly, when IVS2-705 HeLa or K562 cells were cultured at temperatures below 30°C, aberrant splicing was inhibited and correct splicing was restored. Similar temperature effects were seen for another β-globin pre-mRNA, IVS2-745, and in a construct in which a β-globin intron was inserted into a coding sequence of EGFP. Temperature-induced alternative splicing was affected by the nature of the internal aberrant splice sites flanking the correct sites and by exonic sequences. The results indicate that in the context of thalassemic splicing mutations and possibly in other alternatively spliced pre-mRNAs, temperature is one of the parameters that affect splice site selection.
机译:人β-珠蛋白内含子2的核苷酸705处的T→G突变产生异常的5'剪接位点并激活上游的隐秘3'剪接位点。结果,尽管仍存在功能正确的正确位点,但前mRNA仍通过异常的剪接位点进行剪接。出人意料的是,当IVS2-705 HeLa或K562细胞在低于30°C的温度下培养时,异常剪接受到抑制,正确的剪接得以恢复。对于另一种β-球蛋白前体mRNA IVS2-745,以及在将β-球蛋白内含子插入EGFP编码序列的构建体中,也观察到了类似的温度效应。温度诱导的选择性剪接受到正确位置两侧的内部异常剪接位点的性质和外显子序列的影响。结果表明,在地中海贫血剪接突变的情况下,以及可能在其他选择性剪接的pre-mRNA中,温度是影响剪接位点选择的参数之一。

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