Abstract
The genome of bovine leukemia virus (BLV) encodes a transcriptional trans-activator p38tax (also referred to as pXBL-I) which amplifies the virus gene expression driven by its long terminal repeat (LTR). It was proposed that activation of cellular gene expression by p38tax might be involved in the mechanism of B-cell transformation caused in vivo by BLV infection. Here, we report that the U3 region of BLV LTR contains multiple regulatory elements responsive to p38tax. A core element composing the p38tax-inducible U3 structure is suggested to be a heptanucleotide motif of 5'TGACGTCA3', the consensus sequence proposed for a cAMP-responsive element (CRE) and for the binding sites of a cellular transcription factor (ATF). Adenovirus-5 E3 and E4, c-fos and somatostatin regulatory regions containing CRE/ATF-element exhibited responsiveness to p38tax in a chloramphenicol acetyltransferase transient expression assay. These suggest that in BLV-infected cells, cellular gene expression might be induced abnormally by the virus trans-activator through ATF or ATF-like factors.
MeSH Terms
Activating Transcription Factors
Animals
Base Sequence
Binding Sites
Blood Proteins/genetics,metabolism
Chloramphenicol O-Acetyltransferase/genetics
Cyclic AMP/genetics,metabolism
DNA, Viral/genetics
Enhancer Elements, Genetic
Gene Expression Regulation
Gene Products, tax
Leukemia Virus, Bovine/genetics
Promoter Regions, Genetic/drug effects
Proto-Oncogenes
Retroviridae/genetics
Retroviridae Proteins/genetics,pharmacology
Retroviridae Proteins, Oncogenic
Transcription Factors/genetics,metabolism
Chemicals
Activating Transcription Factors
Blood Proteins
DNA, Viral
Gene Products, tax
Retroviridae Proteins
Retroviridae Proteins, Oncogenic
Transcription Factors
transactivator protein p38(tax)
Cyclic AMP
Chloramphenicol O-Acetyltransferase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Katoh I
Tsukuba Life Science Center, Institute of Chemical and Physical Research, Ibaraki, Japan.
Yoshinaka Y
Ikawa Y
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