Hall K B, Konarska M M
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO 63110.
Proc Natl Acad Sci U S A. 1992 Nov 15;89(22):10969-73. doi: 10.1073/pnas.89.22.10969.
A short RNA oligonucleotide comprising the 5' splice site consensus sequence (5'SS RNA oligo) efficiently inhibits splicing of mRNA precursors in HeLa cell nuclear extracts. Addition of 5'SS RNA oligo inhibits early, but not late, steps in the splicing reaction, affecting the process of spliceosome assembly. In the presence of 5'SS RNA oligo a majority of U4/U5/U6 triple small nuclear ribonucleoprotein (snRNP) complex present in HeLa nuclear extracts associates with U2 snRNP to form a multi-snRNP complex, which could account for the observed inhibition of splicing by the oligo. This same set of snRNPs has been shown to assemble on pre-mRNAs during in vitro splicing to form splicing complex B. Removal of the 5' end of U1 snRNA, which is complementary to the 5' splice site, does not prevent association of snRNPs into U2/U4/U5/U6 complex in the presence of 5'SS RNA oligo. This suggests that interactions other than U1 snRNA.5'SS RNA oligo base pairing are used in recognition of the oligo sequence. 5'SS RNA oligo-induced assembly of the multi-snRNP complex may thus serve as a model to study the mechanism of 5' splice site recognition during splicing.
一种包含5'剪接位点共有序列的短RNA寡核苷酸(5'SS RNA寡核苷酸)能有效抑制HeLa细胞核提取物中mRNA前体的剪接。添加5'SS RNA寡核苷酸会抑制剪接反应的早期步骤,但不影响后期步骤,从而影响剪接体组装过程。在存在5'SS RNA寡核苷酸的情况下,HeLa细胞核提取物中存在的大多数U4/U5/U6三联小核核糖核蛋白(snRNP)复合物会与U2 snRNP结合形成多snRNP复合物,这可以解释该寡核苷酸对剪接的抑制作用。已证明同一组snRNP在体外剪接过程中会组装在mRNA前体上,形成剪接复合物B。去除与5'剪接位点互补的U1 snRNA的5'端,在存在5'SS RNA寡核苷酸的情况下,并不妨碍snRNP组装成U2/U4/U5/U6复合物。这表明在识别该寡核苷酸序列时,除了U1 snRNA-5'SS RNA寡核苷酸碱基配对之外,还利用了其他相互作用。因此,5'SS RNA寡核苷酸诱导的多snRNP复合物组装可作为研究剪接过程中5'剪接位点识别机制的模型。