TY - JOUR
T1 - Chemical and enzymatic probing of spatial structure of the omega leader of tobacco mosaic virus RNA
AU - Shirokikh, N. E.
AU - Ch. Agalarov, S.
AU - Spirin, A. S.
PY - 2010/4
Y1 - 2010/4
N2 - The 5'-untranslated sequence of tobacco mosaic virus RNA - the so-called omega leader - exhibits features of a translational enhancer of homologous and heterologous mRNAs. The absence of guanylic residues, the presence of multi- ple trinucleotide CAA repeats in its central region, and the low predictable probability of the formation of an extensive sec- ondary structure of the Watson-Crick type were reported as the peculiarities of the primary structure of the omega leader. In this work we performed chemical and enzymatic probing of the secondary structure of the omega leader. The isolated RNA comprising omega leader sequence was subjected to partial modifications with dimethyl sulfate and diethyl pyrocar- bonate and partial hydrolyses with RNase A and RNase V1. The sites and the intensities of the modifications or the cleav- ages were detected and measured by the primer extension inhibition technique. The data obtained have demonstrated that RNase A, which attacks internucleotide bonds at the 3' side of pyrimidine nucleotides, and diethyl pyrocarbonate, which modifies N7 of adenines not involved in stacking interactions, weakly affected the core region of omega leader sequence enriched with CAA-repeats, this directly indicating the existence of a stable spatial structure. The significant stability of the core region structure to RNase A and diethyl pyrocarbonate was accompanied by its complete resistance against RNase V1, which cleaves a polyribonucleotide chain involved in Watson-Crick double helices and generally all A-form RNA helices, thus being an evidence in favor of a non-Watson-Crick structure. The latter was confirmed by the full susceptibility of all adenines and cytosines of the omega polynucleotide chain to dimethyl sulfate, which exclusively modifies N1 of adenines and N3 of cytosines not involved in Watson-Crick interactions. Thus, our data have confirmed that (1) the regular (CAA)n sequence characteristic of the core region of the omega leader does form stable secondary structure, and (2) the structure formed is not the canonical double helix of the Watson-Crick type.
AB - The 5'-untranslated sequence of tobacco mosaic virus RNA - the so-called omega leader - exhibits features of a translational enhancer of homologous and heterologous mRNAs. The absence of guanylic residues, the presence of multi- ple trinucleotide CAA repeats in its central region, and the low predictable probability of the formation of an extensive sec- ondary structure of the Watson-Crick type were reported as the peculiarities of the primary structure of the omega leader. In this work we performed chemical and enzymatic probing of the secondary structure of the omega leader. The isolated RNA comprising omega leader sequence was subjected to partial modifications with dimethyl sulfate and diethyl pyrocar- bonate and partial hydrolyses with RNase A and RNase V1. The sites and the intensities of the modifications or the cleav- ages were detected and measured by the primer extension inhibition technique. The data obtained have demonstrated that RNase A, which attacks internucleotide bonds at the 3' side of pyrimidine nucleotides, and diethyl pyrocarbonate, which modifies N7 of adenines not involved in stacking interactions, weakly affected the core region of omega leader sequence enriched with CAA-repeats, this directly indicating the existence of a stable spatial structure. The significant stability of the core region structure to RNase A and diethyl pyrocarbonate was accompanied by its complete resistance against RNase V1, which cleaves a polyribonucleotide chain involved in Watson-Crick double helices and generally all A-form RNA helices, thus being an evidence in favor of a non-Watson-Crick structure. The latter was confirmed by the full susceptibility of all adenines and cytosines of the omega polynucleotide chain to dimethyl sulfate, which exclusively modifies N1 of adenines and N3 of cytosines not involved in Watson-Crick interactions. Thus, our data have confirmed that (1) the regular (CAA)n sequence characteristic of the core region of the omega leader does form stable secondary structure, and (2) the structure formed is not the canonical double helix of the Watson-Crick type.
KW - Chemical modification of RNA
KW - Diethyl pyrocarbonate
KW - Dimethyl sulfate
KW - Enzymatic cleavage of RNA
KW - Omega leader of TMV RNA
KW - Primer extension inhibition
KW - RNA triple helix
KW - RNase A
KW - RNase V1
UR - http://www.scopus.com/inward/record.url?scp=77951687033&partnerID=8YFLogxK
U2 - 10.1134/S0006297910040024
DO - 10.1134/S0006297910040024
M3 - Article
SN - 0006-2979
VL - 75
SP - 405
EP - 411
JO - Biochemistry (Moscow)
JF - Biochemistry (Moscow)
IS - 4
ER -