Nelson K K, Green M R
Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, MA 02138.
Proc Natl Acad Sci U S A. 1990 Aug;87(16):6253-7. doi: 10.1073/pnas.87.16.6253.
The 5' splice site of a pre-mRNA is recognized by U1 small nuclear ribonucleoprotein particles (snRNP) through base pairing with the 5' end of U1 small nuclear RNA (snRNA). Single-base substitutions within a 9-nucleotide 5'-splice-site sequence can abolish or attenuate use of that site and, in higher eukaryotes, can also activate nearby "cryptic" 5' splice sites. Here we show that the effects of single-base substitutions within a 5' splice site can be completely or partially suppressed by cis mutations that improve the overall complementarity of the site to U1 snRNA. We further show that in the presence of the normal 5' splice site, a cryptic 5' splice site can be activated by increasing its complementarity to U1 snRNA. U1 snRNP binding experiments confirm that cryptic 5' splice sites are activated when their affinity for U1 snRNP approaches that of the authentic 5' splice site. Based upon these results, we propose a spliceosome competition model for 5'-splice-site selection and cryptic 5'-splice-site activation. We discuss our results with regard to the factors involved in 5'-splice-site recognition.
前体mRNA的5'剪接位点通过与U1小核RNA(snRNA)的5'末端碱基配对,被U1小核糖核蛋白颗粒(snRNP)识别。9核苷酸5'剪接位点序列内的单碱基替换可消除或减弱该位点的使用,并且在高等真核生物中,还可激活附近的“隐蔽”5'剪接位点。在此我们表明,5'剪接位点内单碱基替换的效应可被顺式突变完全或部分抑制,这些顺式突变可提高该位点与U1 snRNA的整体互补性。我们进一步表明,在正常5'剪接位点存在的情况下,隐蔽的5'剪接位点可通过增加其与U1 snRNA的互补性而被激活。U1 snRNP结合实验证实,当隐蔽的5'剪接位点对U1 snRNP的亲和力接近真实5'剪接位点的亲和力时,它们就会被激活。基于这些结果,我们提出了一个用于5'剪接位点选择和隐蔽5'剪接位点激活的剪接体竞争模型。我们讨论了我们关于参与5'剪接位点识别的因素的结果。