Gemignani Federica, Sazani Peter, Morcos Paul, Kole Ryszard
Lineberger Comprehensive Cancer Center and Department of Pharmacology, CB 7295, University of North Carolina, Chapel Hill, NC 27599-7295, USA.
Nucleic Acids Res. 2002 Nov 1;30(21):4592-8. doi: 10.1093/nar/gkf607.
A T-->G mutation at nucleotide 705 of human beta-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 degrees C, aberrant splicing was inhibited and correct splicing was restored. Similar temperature effects were seen for another beta-globin pre-mRNA, IVS2-745, and in a construct in which a beta-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.
人类β-珠蛋白内含子2第705位核苷酸处的T→G突变产生了一个异常的5'剪接位点,并激活了上游一个隐蔽的3'剪接位点。结果,尽管存在仍具功能的正确剪接位点,前体mRNA仍通过异常剪接位点进行剪接。令人惊讶的是,当IVS2-705 HeLa或K562细胞在低于30摄氏度的温度下培养时,异常剪接受到抑制,正确剪接得以恢复。对于另一种β-珠蛋白前体mRNA(IVS2-745)以及在将β-珠蛋白内含子插入EGFP编码序列的构建体中,也观察到了类似的温度效应。温度诱导的可变剪接受正确剪接位点两侧内部异常剪接位点的性质以及外显子序列的影响。结果表明,在地中海贫血剪接突变的背景下,以及可能在其他可变剪接的前体mRNA中,温度是影响剪接位点选择的参数之一。