DNA damage targets PKCη to the nuclear membrane via its C1b domain

Ana Tamarkin, Udi Zurgil, Alex Braiman, Naama Hai, Ella Krasnitsky, Adva Maissel, Assaf Ben-Ari, Liat Yankelovich, Etta Livneh

Research output: Contribution to journalArticlepeer-review


Translocation to cellular membranes is one of the hallmarks of PKC activation, occurring as a result of the generation of lipid secondary messengers in target membrane compartments. The activation-induced translocation of PKCs and binding to membranes is largely directed by their regulatory domains. We have previously reported that PKCη, a member of the novel subfamily and an epithelial specific isoform, is localized at the cytoplasm and ER/Golgi and is translocated to the plasma membrane and the nuclear envelope upon short-term activation by PMA. Here we show that PKCη is shuttling between the cytoplasm and the nucleus and that upon etoposide induced DNA damage is tethered at the nuclear envelope. Although PKCη expression and its phosphorylation on the hydrophobic motif (Ser675) are increased by etoposide, this phosphorylation is not required for its accumulation at the nuclear envelope. Moreover, we demonstrate that the C1b domain is sufficient for translocation to the nuclear envelope. We further show that, similar to full-length PKCη, the C1b domain could also confer protection against etoposide-induced cell death. Our studies demonstrate translocation of PKCη to the nuclear envelope, and suggest that its spatial regulation could be important for its cellular functions including effects on cell death.

Original languageAmerican English
Pages (from-to)1465-1475
Number of pages11
JournalExperimental Cell Research
Issue number10
StatePublished - 1 Jan 2011


  • Cell death
  • Etoposide
  • Nuclear envelope
  • PKCη

All Science Journal Classification (ASJC) codes

  • Cell Biology


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