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Acridine‐Labeled Primers as Tools for the Study of Nonenzymatic RNA Oligomerization
Author(s) -
Kurz Markus,
Göbel Karin,
Hartel Christian,
Göbel Michael W.
Publication year - 1998
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19980810528
Subject(s) - chemistry , nucleic acid , oligonucleotide , rna , acridine , guanosine , cytidine , primer extension , polymerization , duplex (building) , primer (cosmetics) , dna , combinatorial chemistry , nucleotide , stereochemistry , biochemistry , organic chemistry , enzyme , gene , polymer
Short, dye‐labeled oligonucleotides have been used as primers in template‐controlled polymerization reactions of RNA. The synthesis of appropriate acridine derivatives and their attachments to nucleic acids is described. In the nonenzymatic oligomerization of 2‐methyl‐1 H ‐imidazole‐activated guanosine 5′‐monophosphate, two observations deserve special notice: ( 1 ) reaction rates are almost unchanged by variations of the Na + concentration; ( 2 ) the conformational type of the primer‐template duplex (A vs. B) has considerable influence on the rates and yields of RNA oligomerization. When the incorporation of cytidine was studied in the presence of 1 M Na + or K + , the process was almost inhibited by quadruplex formation of the oligo‐dG template. However, if these cations were omitted, an efficient primer extension could be observed using template concentrations as high as 100 μ M . The chances for nonenzymatic self‐replication of RNA thus might be distinctly better than previously assumed.