TY - JOUR
T1 - Functional analysis of the stem-loop structures at the 5′ end of the Aichi virus genome
AU - Nagashima, Shigeo
AU - Sasaki, Jun
AU - Taniguchi, Koki
N1 - Funding Information:
This work was supported in part by a grant from the Human Science Research Foundation of Japan and a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, and Culture, Tokyo, Japan.
PY - 2003/8/15
Y1 - 2003/8/15
N2 - Aichi virus is a member of the family Picornaviridae. Computer-assisted secondary structure prediction suggested the formation of three stem-loop structures (SL-A, SL-B, and SL-C from the 5′ end) within the 5′-end 120 nucleotides of the genome. We have already shown that the most 5′-end stem-loop, SL-A, is critical for viral RNA replication. Here, using an infectious cDNA clone and a replicon harboring a luciferase gene, we revealed that formation of SL-B and SL-C on the positive strand is essential for viral RNA replication. In addition, the specific nucleotide sequence of the loop segment of SL-B was also shown to be critical for viral RNA replication. Mutations of the upper and lower stems of SL-C that do not disrupt the base-pairings hardly affected RNA replication, but decreased the yields of viable viruses significantly compared with for the wild-type. This suggests that SL-C plays a role at some step besides RNA replication during virus infection.
AB - Aichi virus is a member of the family Picornaviridae. Computer-assisted secondary structure prediction suggested the formation of three stem-loop structures (SL-A, SL-B, and SL-C from the 5′ end) within the 5′-end 120 nucleotides of the genome. We have already shown that the most 5′-end stem-loop, SL-A, is critical for viral RNA replication. Here, using an infectious cDNA clone and a replicon harboring a luciferase gene, we revealed that formation of SL-B and SL-C on the positive strand is essential for viral RNA replication. In addition, the specific nucleotide sequence of the loop segment of SL-B was also shown to be critical for viral RNA replication. Mutations of the upper and lower stems of SL-C that do not disrupt the base-pairings hardly affected RNA replication, but decreased the yields of viable viruses significantly compared with for the wild-type. This suggests that SL-C plays a role at some step besides RNA replication during virus infection.
UR - http://www.scopus.com/inward/record.url?scp=0042389497&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0042389497&partnerID=8YFLogxK
U2 - 10.1016/S0042-6822(03)00346-5
DO - 10.1016/S0042-6822(03)00346-5
M3 - Article
C2 - 12951021
AN - SCOPUS:0042389497
SN - 0042-6822
VL - 313
SP - 56
EP - 65
JO - Virology
JF - Virology
IS - 1
ER -