Coronavirus mRNA synthesis: identification of novel transcription initiation signals which are differentially regulated by different leader sequences
- PMID: 1566582
- PMCID: PMC7131442
- DOI: 10.1016/0042-6822(92)90774-j
Coronavirus mRNA synthesis: identification of novel transcription initiation signals which are differentially regulated by different leader sequences
Abstract
The mRNA synthesis of mouse hepatitis virus (MHV) has been proposed to be the result of interaction between the leader RNA and the intergenic sites. Previously, we have identified a transcription initiation site (for mRNA 2-1), which is more efficiently transcribed by viruses containing two copies of UCUAA sequence in the leader RNA than by those with three copies. In this study, we have identified several sites which are regulated in the opposite way, namely, they are efficiently transcribed by the leader RNA with three UCUAA copies but not by those with two copies. These sites were characterized by primer extension and amplification by polymerase chain reaction. One of these sites is in the gene 3 region of a recombinant virus between A59 and JHM strains of MHV. Another is in the gene 2 region of MHV-1 strain. Both of these sites have a sequence similar to but different from the consensus transcription initiation signal (UCUAAUCUAUC and UUUAAUCUU, as opposed to UCUAAAC). These two novel intergenic sequences are not present in the genome of the JHM strain, consistent with the absence of these mRNAs in the JHM-infected cells. The discovery of this type of transcription initiation site provides additional evidence for the importance of the leader RNA in the transcription initiation of MHV mRNAs.
Similar articles
-
Coronavirus leader RNA regulates and initiates subgenomic mRNA transcription both in trans and in cis.J Virol. 1994 Aug;68(8):4738-46. doi: 10.1128/JVI.68.8.4738-4746.1994. J Virol. 1994. PMID: 8035476 Free PMC article.
-
Heterogeneity of gene expression of the hemagglutinin-esterase (HE) protein of murine coronaviruses.Virology. 1991 Aug;183(2):647-57. doi: 10.1016/0042-6822(91)90994-m. Virology. 1991. PMID: 1649505 Free PMC article.
-
Requirement of the 5'-end genomic sequence as an upstream cis-acting element for coronavirus subgenomic mRNA transcription.J Virol. 1994 Aug;68(8):4727-37. doi: 10.1128/JVI.68.8.4727-4737.1994. J Virol. 1994. PMID: 8035475 Free PMC article.
-
Coronaviruses use discontinuous extension for synthesis of subgenome-length negative strands.Adv Exp Med Biol. 1995;380:499-506. doi: 10.1007/978-1-4615-1899-0_79. Adv Exp Med Biol. 1995. PMID: 8830530 Review.
-
Background paper. Transcription and replication of coronavirus RNA: a 1989 update.Adv Exp Med Biol. 1990;276:327-33. doi: 10.1007/978-1-4684-5823-7_44. Adv Exp Med Biol. 1990. PMID: 2103099 Review. No abstract available.
Cited by
-
Comparative analysis of bioinformatics tools to characterize SARS-CoV-2 subgenomic RNAs.Life Sci Alliance. 2023 Sep 25;6(12):e202302017. doi: 10.26508/lsa.202302017. Print 2023 Dec. Life Sci Alliance. 2023. PMID: 37748810 Free PMC article.
-
sgRNAs: A SARS-CoV-2 emerging issue.Asp Mol Med. 2023;1:100008. doi: 10.1016/j.amolm.2023.100008. Epub 2023 Apr 16. Asp Mol Med. 2023. PMID: 37519862 Free PMC article. Review.
-
Analysis of SARS-CoV-2 known and novel subgenomic mRNAs in cell culture, animal model, and clinical samples using LeTRS, a bioinformatic tool to identify unique sequence identifiers.Gigascience. 2022 May 26;11:giac045. doi: 10.1093/gigascience/giac045. Gigascience. 2022. PMID: 35639883 Free PMC article.
-
New insights about the regulation of Nidovirus subgenomic mRNA synthesis.Virology. 2018 Apr;517:38-43. doi: 10.1016/j.virol.2018.01.026. Epub 2018 Feb 21. Virology. 2018. PMID: 29475599 Free PMC article.
-
Expanded subgenomic mRNA transcriptome and coding capacity of a nidovirus.Proc Natl Acad Sci U S A. 2017 Oct 17;114(42):E8895-E8904. doi: 10.1073/pnas.1706696114. Epub 2017 Oct 4. Proc Natl Acad Sci U S A. 2017. PMID: 29073030 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources