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Conserved motifs in the invertebrate iridescent virus 6 (IIV6) genome regulate virus transcription.

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TLDR
The transcriptional class of all IIV6 genes that had not been classified until now is investigated and single nucleotide mutations in the highly conserved nucleotides at the end of the second motif showed that this motif acted as a repressor sequence for late genes in the IIV 6 genome.
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This article is published in Journal of Invertebrate Pathology.The article was published on 2020-11-01 and is currently open access. It has received 0 citations till now.

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Journal ArticleDOI

Transcriptome analysis of Frog virus 3, the type species of the genus Ranavirus, family Iridoviridae.

TL;DR: An oligonucleotide microarray containing 70-mer probes corresponding to each of the 98 FV3 ORFs was designed and used to examine viral gene expression, and genes encoding putative regulatory factors, or proteins that played a part in nucleic acid metabolism and immune evasion were classified as IE and DE genes, whereas those involved in DNA packaging and virion assembly were considered L genes.
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A cis Repression Sequence Adjacent to the Transcription Start Site of the Human Cytomegalovirus US3 Gene Is Required To Down Regulate Gene Expression at Early and Late Times after Infection

TL;DR: The CRS in the enhancer-containing US3 promoter appears to allow for a short burst of US3 gene expression followed by repression at early and late times after infection, which is detrimental to viral replication.
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Promoter analysis of the Chilo iridescent virus DNA polymerase and major capsid protein genes.

TL;DR: Infection of Bombyx mori SPC-BM-36 cells in the presence of inhibitors of DNA or protein synthesis showed that DNApol, as well as helicase, is an immediate-early gene and confirmed that the major capsid protein (MCP) is a late gene.
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Q1. What are the contributions in "Conserved motifs in the invertebrate iridescent virus 6 (iiv6) genome regulate virus transcription" ?

In this study, the authors investigated the transcriptional class of all IIV6 genes that had not been classified until now. Conversely, the presence of these two sequences upstream of the reporter decreased its expression. Next, upstream sequences of IIV6 L genes from which the authors removed this second motif in silico, were re-analyzed for the presence of potential conserved promoter sequences.