首页> 外文期刊>Nucleic Acids Research >Effects of the trinucleotide preceding the self-cleavage site on eggplant latent viroid hammerheads: differences in co- and post-transcriptional self-cleavage may explain the lack of trinucleotide AUC in most natural hammerheads
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Effects of the trinucleotide preceding the self-cleavage site on eggplant latent viroid hammerheads: differences in co- and post-transcriptional self-cleavage may explain the lack of trinucleotide AUC in most natural hammerheads

机译:自切割位点前的三核苷酸对茄子潜在类病毒锤头的影响:共转录和自转录后自切割的差异可能解释了大多数天然锤头中缺乏三核苷酸AUC

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摘要

Eggplant latent viroid (ELVd) can form stable hammerhead structures in its (+) and (-) strands. These ribozymes have the longest helices I reported in natural hammerheads, with that of the ELVd (+) hammerhead being particularly stable (5/7 bp are G-C). Moreover, the trinucleotide preceding the self-cleavage site of this hammerhead is AUA, which together with GUA also found in some natural hammerheads, deviate from the GUC present in most natural hammerheads including the ELVd (-) hammerhead. When the AUA trinucleotide preceding the self-cleavage site of the ELVd (+) hammerhead was substituted by GUA and GUC, as well as by AUC (essentially absent in natural hammerheads), the values of the self-cleavage rate constants at low magnesium of the purified hammerheads were: ELVd-(+)-AUC approximate to ELVd-(+)-GUC > ELVd-(+)-GUA > ELVd-(+)-AUA. However, the ELVd-(+)-AUC hammerhead was the catalytically less efficient during in vitro transcription, most likely because of the transient adoption of catalytically-inactive metastable structures. These results suggest that natural hammerheads have been evolutionary selected to function co-transcriptionally, and provide a model explaining the lack of trinucleotide AUC preceding the self-cleavage site of most natural hammerheads. Comparisons with other natural hammerheads showed that the ELVd-(+)-GUC and ELVd-(+)-AUC hammerheads are the catalytically most active in a post-transcriptional context with low magnesium.
机译:茄子潜在类病毒(ELVd)可以在其(+)和(-)链中形成稳定的锤头结构。这些核酶具有我在天然锤头中报道的最长螺旋,而ELVd(+)锤头则特别稳定(G-C为5/7 bp)。而且,在该锤头的自我切割位点之前的三核苷酸是AUA,它与GUA一起也在一些天然锤头中发现,与大多数天然锤头(包括ELVd(-)锤头)中存在的GUC不同。当ELVd(+)锤头的自我切割位点之前的AUA三核苷酸被GUA和GUC以及AUC(天然锤头中基本上不存在)取代时,在低镁下,自我切割速率常数的值纯化的锤头为:ELVd-(+)-AUC近似于ELVd-(+)-GUC> ELVd-(+)-GUA> ELVd-(+)-AUA。但是,ELVd-(+)-AUC锤头在体外转录过程中催化效率较低,这很可能是由于瞬态采用了催化失活的亚稳结构。这些结果表明,天然锤头已被进化选择为具有共转录功能,并提供了解释大多数天然锤头的自我切割位点之前缺乏三核苷酸AUC的模型。与其他天然锤头的比较表明,ELVd-(+)-GUC和ELVd-(+)-AUC锤头在低镁的转录后环境中催化活性最高。

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