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Published on: July 17, 2020
HPV18 E7 inhibits LATS1 kinase and activates YAP1 by degrading PTPN14
William J Blakely1, Joshua Hatterschide1, Elizabeth A White1
1Department of Otorhinolaryngology: Head and Neck Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Abstract:
High-risk human papillomavirus (HPV) oncoproteins inactivate cellular tumor suppressors to reprogram host cell signaling pathways. HPV E7 proteins bind and degrade the tumor suppressor PTPN14, thereby promoting the nuclear localization of the YAP1 oncoprotein and inhibiting keratinocyte differentiation. YAP1 is a transcriptional coactivator that drives epithelial cell stemness and self-renewal. YAP1 activity is inhibited by the highly conserved Hippo pathway, which is frequently inactivated in human cancers. MST1/2 and LATS1/2 kinases form the core of the Hippo kinase cascade. Active LATS1 kinase is phosphorylated on threonine 1079 and inhibits YAP1 by phosphorylating it on amino acids including serine 127. Here, we tested the effect of high-risk (carcinogenic) HPV18 E7 on Hippo pathway activity. We found that either PTPN14 knockout or PTPN14 degradation by HPV18 E7 decreased the phosphorylation of LATS1 T1079 and YAP1 S127 in human keratinocytes and inhibited keratinocyte differentiation. Conversely, PTPN14-dependent differentiation required LATS kinases and certain PPxY motifs in PTPN14. Neither MST1/2 kinases nor the putative PTPN14 phosphatase active sites were required for PTPN14 to promote differentiation. Together, these data support that PTPN14 inactivation or degradation of PTPN14 by HPV18 E7 reduce LATS1 activity, promoting active YAP1 and inhibiting keratinocyte differentiation.IMPORTANCEThe Hippo kinase cascade inhibits YAP1, an oncoprotein and driver of cell stemness and self-renewal. There is mounting evidence that the Hippo pathway is targeted by tumor viruses including human papillomavirus. The high-risk HPV E7 oncoprotein promotes YAP1 nuclear localization and the carcinogenic activity of high-risk HPV E7 requires YAP1 activity. Blocking HPV E7-dependent YAP1 activation could inhibit HPV-mediated carcinogenesis, but the mechanism by which HPV E7 activates YAP1 has not been elucidated. Here we report that by degrading the tumor suppressor PTPN14, HPV18 E7 inhibits LATS1 kinase, reducing inhibitory phosphorylation on YAP1. These data support that an HPV oncoprotein can inhibit Hippo signaling to activate YAP1 and strengthen the link between PTPN14 and Hippo signaling in human epithelial cells.
Insights
High-risk human papillomavirus (HPV) oncoprotein E7 degrades tumor suppressor PTPN14, inhibiting the Hippo pathway. This promotes YAP1 activity, driving keratinocyte stemness and blocking differentiation, thus contributing to HPV-driven carcinogenesis.
Area of Science:
- Cell Biology
- Molecular Oncology
- Virology
Background:
- High-risk human papillomavirus (HPV) oncoproteins disrupt cellular tumor suppressors, reprogramming host signaling.
- YAP1, a transcriptional coactivator driving epithelial stemness, is negatively regulated by the Hippo kinase pathway.
- The Hippo pathway is frequently inactivated in cancers, and HPV E7 oncoprotein activity requires YAP1.
Purpose of the Study:
- To investigate the effect of high-risk HPV18 E7 oncoprotein on Hippo pathway activity.
- To elucidate the mechanism by which HPV E7 activates YAP1 and promotes keratinocyte dedifferentiation.
Main Methods:
- Investigated HPV18 E7 effects on Hippo pathway components in human keratinocytes.
- Utilized PTPN14 knockout and assessed phosphorylation of LATS1 and YAP1.
- Examined the role of LATS kinases and PTPN14 motifs in keratinocyte differentiation.
Main Results:
- PTPN14 knockout or HPV18 E7-mediated degradation of PTPN14 reduced LATS1 T1079 and YAP1 S127 phosphorylation.
- This reduction in phosphorylation inhibited keratinocyte differentiation.
- PTPN14-dependent differentiation necessitated LATS kinases and specific PTPN14 motifs, but not MST1/2 kinases or PTPN14 phosphatase activity.
Conclusions:
- HPV18 E7 degrades PTPN14, leading to reduced LATS1 kinase activity.
- Inhibition of LATS1 kinase promotes YAP1 activation, driving keratinocyte stemness and inhibiting differentiation.
- These findings strengthen the link between PTPN14, Hippo signaling, and HPV-mediated carcinogenesis.
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