TY - JOUR
T1 - Leader sequences of murine coronavirus mRNAs can be freely reassorted
T2 - Evidence for the role of free leader RNA in transcription
AU - Makino, S.
AU - Stohlman, S. A.
AU - Lai, M. M.C.
PY - 1986
Y1 - 1986
N2 - Mouse hepatitis virus (MHV), which replicates in cytoplasm of infected cells, contains an identical leader RNA sequence at the 5' end of each of the virus-specific mRNAs. Previous studies suggested that the synthesis of these mRNAs does not involve conventional RNA splicing and may instead require priming by a free leader RNA. In this communication, we demonstrate that, during a mixed infection with two different MHVs, the leader RNA sequences from one virus could be detected on the mRNAs of the coinfecting virus at a high frequency, as if the leader sequence and mRNAs were joined together from two randomly segregating RNA segments. This findings demonstrates that MHV mRNA transcription utilizes independently transcribed leader RNA species that possess the trans-acting property. This study thus provides further evidence in support of the unique model of 'leader-primed transcription' for coronavirus mRNA synthesis.
AB - Mouse hepatitis virus (MHV), which replicates in cytoplasm of infected cells, contains an identical leader RNA sequence at the 5' end of each of the virus-specific mRNAs. Previous studies suggested that the synthesis of these mRNAs does not involve conventional RNA splicing and may instead require priming by a free leader RNA. In this communication, we demonstrate that, during a mixed infection with two different MHVs, the leader RNA sequences from one virus could be detected on the mRNAs of the coinfecting virus at a high frequency, as if the leader sequence and mRNAs were joined together from two randomly segregating RNA segments. This findings demonstrates that MHV mRNA transcription utilizes independently transcribed leader RNA species that possess the trans-acting property. This study thus provides further evidence in support of the unique model of 'leader-primed transcription' for coronavirus mRNA synthesis.
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U2 - 10.1073/pnas.83.12.4204
DO - 10.1073/pnas.83.12.4204
M3 - Article
C2 - 3012558
AN - SCOPUS:0022457098
SN - 0027-8424
VL - 83
SP - 4204
EP - 4208
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 12
ER -