Homeodomain-Interacting Protein Kinase (HPK-1) regulates stress responses and ageing in C. elegans

Sci Rep. 2016 Jan 21:6:19582. doi: 10.1038/srep19582.

Abstract

Proteins of the Homeodomain-Interacting Protein Kinase (HIPK) family regulate an array of processes in mammalian systems, such as the DNA damage response, cellular proliferation and apoptosis. The nematode Caenorhabditis elegans has a single HIPK homologue called HPK-1. Previous studies have implicated HPK-1 in longevity control and suggested that this protein may be regulated in a stress-dependent manner. Here we set out to expand these observations by investigating the role of HPK-1 in longevity and in the response to heat and oxidative stress. We find that levels of HPK-1 are regulated by heat stress, and that HPK-1 contributes to survival following heat or oxidative stress. Additionally, we show that HPK-1 is required for normal longevity, with loss of HPK-1 function leading to a faster decline of physiological processes that reflect premature ageing. Through microarray analysis, we have found that HPK-1-regulated genes include those encoding proteins that serve important functions in stress responses such as Phase I and Phase II detoxification enzymes. Consistent with a role in longevity assurance, HPK-1 also regulates the expression of age-regulated genes. Lastly, we show that HPK-1 functions in the same pathway as DAF-16 to regulate longevity and reveal a new role for HPK-1 in development.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / genetics*
  • Animals
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans / metabolism*
  • Gene Expression Regulation*
  • Gene Knockout Techniques
  • Heat-Shock Response / genetics
  • Insulin / metabolism
  • Insulin-Like Growth Factor I / metabolism
  • Intestinal Mucosa / metabolism
  • Longevity / genetics
  • Oxidative Stress / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Signal Transduction
  • Stress, Physiological / genetics*

Substances

  • Insulin
  • Insulin-Like Growth Factor I
  • hematopoietic progenitor kinase 1
  • Protein Serine-Threonine Kinases