# HCV infection induces ubiquitin-dependent degradation of LATS1, inactivating the Hippo pathway and upregulating transcription of the CYR61 and CTGF genes

## TL;DR

HCV infection causes degradation of a key protein in the Hippo pathway, leading to increased activity of genes linked to liver disease.

## Contribution

The study reveals that HCV induces ubiquitin-dependent degradation of LATS1, linking Hippo pathway suppression to CYR61 and CTGF upregulation.

## Key findings

- HCV promotes proteasomal degradation of LATS1 via the Itch ubiquitin ligase.
- HCV infection causes nuclear translocation of YAP1 and upregulation of CYR61 and CTGF genes.
- These changes may contribute to HCV-related liver pathogenesis.

## Abstract

Hepatitis C virus (HCV) is often associated with chronic liver diseases and significant alterations in host cellular signalling. However, the molecular mechanisms underlying HCV-related liver pathogenesis remain to be elucidated. The Hippo signalling pathway, a key regulator of cell proliferation and survival, plays a critical role in maintaining liver homeostasis. Here, we investigated the role of the Hippo pathway in HCV-related pathogenesis. We demonstrated that HCV infection induces degradation of LATS1, a key regulator of the Hippo pathway. Degradation of LATS1 protein was restored by a proteasomal inhibitor, but not a lysosome inhibitor, indicating that HCV promotes proteasomal degradation of LATS1 protein. HCV-induced degradation of LATS1 protein was suppressed in si-Itch-transfected Huh-7.5 cells. These results suggest that Itch ubiquitin ligase is involved in ubiquitin-dependent degradation of LATS1 protein. Cell fractionation assays and immunofluorescence staining revealed that HCV infection promoted nuclear translocation of YAP1 protein, suggesting that HCV infection suppresses the Hippo pathway. Furthermore, the transcription of YAP1 target genes, CYR61 and CTGF, that are involved in tissue remodelling and proliferation, was upregulated in HCV-infected Huh-7.5 cells and in HCV-infected patients. Taken together, we propose that HCV promotes the ubiquitin-dependent proteasomal degradation of LATS1 protein, leading to suppression of the Hippo pathway, thereby upregulating transcription of CYR61 and CTGF genes, which may contribute to HCV-related pathogenesis.