Hypoxia inducible factors (HIFs) are key regulators of the transcriptional response to hypoxic stress. Three inducible isoforms of HIF are present in mammals. HIF1? and HIF2? are the best characterized and structurally similar isoforms, while HIF3? is the most distantly related and is less studied. The HIF3? gene undergoes complex regulation and produces a large number of long and short mRNA splice variants, which are translated into different polypeptides. These molecules primarly act as negative regulators of HIF1? and HIF2? activity and transcriptional activators of target genes, according to the variant and the biological context. The present review provides an overview of the available, fragmented and sometimes contradictory, information concerning the structure, expression and distinct roles of the HIF3? variants, in both hypoxic adaptation and in hypoxia-unrelated activities. The pathological consequences of HIF3? deregulation are also illustrated.

HIF3a: the little we know

Luisa Salvatori;
2015

Abstract

Hypoxia inducible factors (HIFs) are key regulators of the transcriptional response to hypoxic stress. Three inducible isoforms of HIF are present in mammals. HIF1? and HIF2? are the best characterized and structurally similar isoforms, while HIF3? is the most distantly related and is less studied. The HIF3? gene undergoes complex regulation and produces a large number of long and short mRNA splice variants, which are translated into different polypeptides. These molecules primarly act as negative regulators of HIF1? and HIF2? activity and transcriptional activators of target genes, according to the variant and the biological context. The present review provides an overview of the available, fragmented and sometimes contradictory, information concerning the structure, expression and distinct roles of the HIF3? variants, in both hypoxic adaptation and in hypoxia-unrelated activities. The pathological consequences of HIF3? deregulation are also illustrated.
2015
Istituto di Biologia e Patologia Molecolari - IBPM
HIF ; HIF3?; hypoxia; pathology; splice variants; transcriptional regulation
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/304170
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