A PtdIns4,5P2-regulated nuclear poly(A) polymerase controls expression of select mRNAs

A new polyadenylation polymerase, called Star-PAP, is identified, the activity of which is regulated by nuclear phosphoinositides generated by the kinase PIPKIα. Phosphoinositides are a family of lipid signalling molecules that regulate many cellular functions in eukaryotes. Phosphatidylinositol-4,5-bisphosphate (PtdIns4,5P 2 ), the central component in the phosphoinositide signalling circuitry, is generated primarily by type I phosphatidylinositol 4-phosphate 5-kinases (PIPKIα, PIPKIβ and PIPKIγ) 1 . In addition to functions in the cytosol, phosphoinositides are present in the nucleus 2 , 3 , where they modulate several functions 4 , 5 , 6 ; however, the mechanism by which they directly regulate nuclear functions remains unknown. PIPKIs regulate cellular functions through interactions with protein partners, often PtdIns4,5P 2 effectors, that target PIPKIs to discrete subcellular compartments, resulting in the spatial and temporal generation of PtdIns4,5P 2 required for the regulation of specific signalling pathways 1 , 7 . Therefore, to determine roles for nuclear PtdIns4,5P 2 we set out to identify proteins that interacted with the nuclear PIPK, PIPKIα. Here we show that PIPKIα co-localizes at nuclear speckles and interacts with a newly identified non-canonical poly(A) polymerase, which we have termed Star-PAP (nuclear speckle targeted PIPKIα regulated-poly(A) polymerase) and that the activity of Star-PAP can be specifically regulated by PtdIns4,5P 2 . Star-PAP and PIPKIα function together in a complex to control the expression of select mRNAs, including the transcript encoding the key cytoprotective enzyme haem oxygenase-1 (refs 8 , 9 ) and other oxidative stress response genes by regulating the 3′-end formation of their mRNAs. Taken together, the data demonstrate a model by which phosphoinositide signalling works in tandem with complement pathways to regulate the activity of Star-PAP and the subsequent biosynthesis of its target mRNA. The results reveal a mechanism for the integration of nuclear phosphoinositide signals and a method for regulating gene expression.