8TDY
16mer self-complementary duplex RNA with D:U pair sequence 1
Summary for 8TDY
Entry DOI | 10.2210/pdb8tdy/pdb |
Descriptor | RNA, MAGNESIUM ION (3 entities in total) |
Functional Keywords | diaminopurine, rna, non-canonical base pair |
Biological source | synthetic construct |
Total number of polymer chains | 1 |
Total formula weight | 5146.69 |
Authors | Fang, Z.,Jia, X.,Szostak, J.W. (deposition date: 2023-07-05, release date: 2024-06-12, Last modification date: 2024-06-26) |
Primary citation | Jia, X.,Fang, Z.,Kim, S.C.,Ding, D.,Zhou, L.,Szostak, J.W. Diaminopurine in Nonenzymatic RNA Template Copying. J.Am.Chem.Soc., 146:15897-15907, 2024 Cited by PubMed Abstract: In the RNA World before the emergence of an RNA polymerase, nonenzymatic template copying would have been essential for the transmission of genetic information. However, the products of chemical copying with the canonical nucleotides (A, U, C, and G) are heavily biased toward the incorporation of G and C, which form a more stable base pair than A and U. We therefore asked whether replacing adenine (A) with diaminopurine (D) might lead to more efficient and less biased nonenzymatic template copying by making a stronger version of the A:U pair. As expected, primer extension substrates containing D bound to U in the template more tightly than substrates containing A. However, primer extension with D exhibited elevated reaction rates on a C template, leading to concerns about fidelity. Our crystallographic studies revealed the nature of the D:C mismatch by showing that D can form a wobble-type base pair with C. We then asked whether competition with G would decrease the mismatched primer extension. We performed nonenzymatic primer extension with all four activated nucleotides on randomized RNA templates containing all four letters and used deep sequencing to analyze the products. We found that the DUCG genetic system exhibited a more even product distribution and a lower mismatch frequency than the canonical AUCG system. Furthermore, primer extension is greatly reduced following all mismatches, including the D:C mismatch. Our study suggests that D deserves further attention for its possible role in the RNA World and as a potentially useful component of artificial nonenzymatic RNA replication systems. PubMed: 38818863DOI: 10.1021/jacs.4c02560 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.66 Å) |
Structure validation
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