Böhler C, Nielsen P E, Orgel L E
Salk Institute for Biological Studies, San Diego, California 92186, USA.
Nature. 1995 Aug 17;376(6541):578-81. doi: 10.1038/376578a0.
The origin of the RNA world is not easily understood, as effective prebiotic syntheses of the components of RNA, the beta-ribofuranoside-5'-phosphates, are hard to envisage. Recognition of this difficulty has led to the proposal that other genetic systems, the components of which are more easily formed, may have preceded RNA. This raises the question of how transitions between one genetic system and another could occur. Peptide nucleic acid (PNA) resembles RNA in its ability to form double-helical complexes stabilized by Watson-Crick hydrogen bonding between adenine and thymine and between cytosine and guanine, but has a backbone that is held together by amide rather than by phosphodiester bonds. Oligonucleotides bases on RNA are known to act as templates that catalyse the non-enzymatic synthesis of their complements from activated mononucleotides, we now show that RNA oligonucleotides facilitate the synthesis of complementary PNA strands and vice versa. This suggests that a transition between different genetic systems can occur without loss of information.
RNA世界的起源并不容易理解,因为难以设想出有效的RNA成分(β-D-呋喃核糖核苷-5'-磷酸)的益生元合成过程。认识到这一困难后,有人提出可能存在其他更容易形成的遗传系统,这些系统先于RNA出现。这就引出了一个问题:一个遗传系统与另一个遗传系统之间的转变是如何发生的。肽核酸(PNA)在通过腺嘌呤与胸腺嘧啶以及胞嘧啶与鸟嘌呤之间的沃森-克里克氢键形成稳定的双螺旋复合物的能力方面类似于RNA,但它的主链是由酰胺键而非磷酸二酯键连接在一起的。已知基于RNA的寡核苷酸可作为模板,催化从活化的单核苷酸非酶促合成其互补物,我们现在表明RNA寡核苷酸促进互补PNA链的合成,反之亦然。这表明不同遗传系统之间的转变可以在不丢失信息的情况下发生。