Journal of Virology · 2008 · 16 citations · 42 references
MedicineMolecular BiologyOncologyGene ExpressionTranscriptionTranscriptional RegulationOncogene ActivationOncogenic Signaling PathwaysProto-oncogene ActivationTranscription Factor OncogenesViral OncogenesViral OncogenesisAcute Lymphoblastic Leukemia BiologyHuman T-cell Leukemia Virus OncogenesisHuman T-cell Leukemia Virus Type 1 OncogenesisNf-κb SignalingOncogenic TransformationPositive Feedback LoopsPositive Feedback MechanismsT-cell Acute Lymphoblastic Leukemia
The human T-cell leukemia virus type 1 (HTLV-1) Tax transactivator is known to induce or repress various cellular genes, several of them encoding transcription factors. As Tax is known to deregulate various basic bHLH factors, we looked more specifically at its effect on TAL1 (T-cell acute lymphoblastic leukemia 1), also known as SCL (stem cell leukemia). Indeed, TAL1 is deregulated in a high percentage of T-cell acute lymphoblastic leukemia cells, and its oncogenic properties are well-established. Here we show that Tax induces transcription of this proto-oncogene by stimulating the activity of the TAL1 gene promoter 1b, through both the CREB and NF-kappaB pathways. It was also observed that TAL1 upregulates HTLV-1 promoter activity, in either the presence or the absence of Tax. The viral promoter is inhibited in trans by expression of the E2A protein E47, and TAL1 is able to abrogate this inhibition. These data show the existence of a positive feedback loop between Tax and TAL1 expression and support the notion that this proto-oncogene participates in generation of adult T-cell leukemia/lymphoma by increasing the amount of the Tax oncoprotein but also possibly by its own transforming activities.
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