Format

Send to

Choose Destination
J Mol Evol. 1994 Mar;38(3):211-4.

Polycytidylate and poly(7-deazaguanylate): a pair of complementary templates.

Author information

1
BYK-Gulden-Lomberg, Department FC1, Konstanz, Germany.
2
U CA San Diego, La Jolla

Abstract

We have studied the template-directed oligomerization on polycytidylic acid of the 5'-phosphoro(2-methyl)imidazolides of a number of analogues of guanosine. None of the analogues reacted as efficiently as the original guanosine compound, and only the 7-deazaguanosine analogue gives a detectable yield of oligomers. Similar results are described for a reaction involving the intramolecular template-directed elongation of a short oligocytidylate primer. Oligocytidylates containing five or more cytidylate residues are extended on the single-stranded regions of poly(G). In the present study we show that these oligocytidylates are extended efficiently by reaction with cytidine-5'-phosphoro(2-methyl)imidazolide on a poly(7-deazaguanylic acid) template. The products are considerably longer than those obtained using a polyguanylic acid template. We believe that the formation of a tetrahelix inhibits the latter reaction, while poly(7-deazaguanylate) does not aggregate and, therefore, acts as a more efficient template. This work identifies for the first time a pair of homopolymers each of which facilitates the template-directed elongation of the other.

PMID:
8006989
[Indexed for MEDLINE]

Supplemental Content

Loading ...
Support Center