HPV-mediated nuclear export of HP1γ drives cervical tumorigenesis by downregulation of p53

Sang Ah Yi, Dong Hoon Lee, Go Woon Kim, Hyun Wook Ryu, Jong Woo Park, Jaecheol Lee, Jihoon Han, Jee Hun Park, Hwamok Oh, Jieun Lee, Junjeong Choi, Hyun Soo Kim, Hyeok Gu Kang, Da Hyun Kim, Kyung Hee Chun, Jueng Soo You, Jeung Whan Han, So Hee Kwon

Research output: Contribution to journalArticlepeer-review

13 Citations (Scopus)


E6 oncoprotein derived from high-risk human papillomavirus (HPV) drives the development of cervical cancer through p53 degradation. Because cervical cancer therapies to inactivate HPV or E6 protein are not available, alternative strategies are required. Here, we show that HPV-mediated nuclear export of human heterochromatin protein 1γ (HP1γ) reduces the stability of p53 through UBE2L3-mediated p53 polyubiquitination during cervical cancer progression. In general, HP1 plays a key role in heterochromatin formation and transcription in the nucleus. However, our immunostaining data showed that the majority of HP1γ is localized in the cytoplasm in HPV-mediated cervical cancer. We found that HPV E6 protein drives unusual nuclear export of HP1γ through the interaction between the NES sequence of HP1γ and exportin-1. The mutation of the NES sequence in HP1γ led to nuclear retention of HP1γ and reduced cervical cancer cell growth and tumor generation. We further discovered that HP1γ directly suppresses the expression of UBE2L3 which drives E6-mediated proteasomal degradation of p53 in cervical cancer. Downregulation of UBE2L3 by overexpression of HP1γ suppressed UBE2L3-dependent p53 degradation-promoting apoptosis of cervical cancer cells. Our findings propose a useful strategy to overcome p53 degradation in cervical cancer through the blockage of nuclear export of HP1γ.

Original languageEnglish
Pages (from-to)2537-2551
Number of pages15
JournalCell Death and Differentiation
Issue number9
Publication statusPublished - 2020 Sept 1

Bibliographical note

Funding Information:
Acknowledgements Raw data have been deposited in Gene Expression Omnibus (GEO) profiles (accession no. GDS2416 and GDS3233). This research was supported by the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (2017R1A6A3A04001986 to SAY, 2017R1A2B3002186 and 2019R1A5A2027340 to JWH, 2018R1A6A1A03023718 and 2019R1A2C1008619 to SHK).

Publisher Copyright:
© 2020, The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare.

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Cell Biology


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