Jankowsky E, Strunk G, Schwenzer B
Institut für Biochemie, Technische Universität Dresden, Mommsenstrasse 13, 01069 Dresden, Germany.
Nucleic Acids Res. 1997 Jul 15;25(14):2690-3. doi: 10.1093/nar/25.14.2690.
Long RNA substrates are inefficiently cleaved by hammerhead ribozymes in trans. Oligonucleotide facilitators capable of affecting the ribozyme activity by interacting with the substrates at the termini of the ribozyme provide a possibility to improve ribozyme mediated cleavage of long RNA substrates. We have examined the effect of PNA as facilitator in vitro in order to test if even artificial compounds have facilitating potential. Effects of 12mer PNA- (peptide nucleic acid), RNA- and DNA-facilitators of identical sequence were measured with three substrates containing either 942, 452 or 39 nucleotides. The PNA facilitator enhances the ribozyme activity with both, the 942mer and the 452mer substrate to a slightly smaller extent than RNA and DNA facilitators. This effect was observed up to PNA facilitator:substrate ratios of 200:1. The enhancement becomes smaller as the PNA facilitator:substrate ratio exceeds 200:1. With the 39mer substrate, the PNA facilitator decreases the ribozyme activity by more than 100-fold, even at PNA facilitator:substrate ratios of 1:1. Although with long substrates the effect of the PNA facilitator is slightly smaller than the effect of identical RNA or DNA facilitators, PNA may be a more practical choice for potential applications in vivo because PNA is much more resistant to degradation by cellular enzymes.
长链RNA底物在体外被锤头状核酶切割的效率较低。能够通过与核酶末端的底物相互作用来影响核酶活性的寡核苷酸促进剂为提高核酶介导的长链RNA底物切割提供了一种可能。我们在体外研究了肽核酸(PNA)作为促进剂的作用,以测试即使是人工合成的化合物是否也具有促进潜力。使用三种分别含有942、452或39个核苷酸的底物,测量了相同序列的12聚体PNA促进剂、RNA促进剂和DNA促进剂的作用。PNA促进剂对942聚体和452聚体底物的核酶活性增强作用,其程度略小于RNA促进剂和DNA促进剂。在PNA促进剂与底物的比例达到200:1之前,都能观察到这种效果。当PNA促进剂与底物的比例超过200:1时,增强作用变小。对于39聚体底物,即使在PNA促进剂与底物的比例为1:1时,PNA促进剂也会使核酶活性降低100倍以上。尽管对于长链底物,PNA促进剂的作用略小于相同的RNA或DNA促进剂,但由于PNA对细胞酶的降解具有更强的抗性,在体内的潜在应用中,PNA可能是一种更实际的选择。