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同源域相互作用蛋白激酶(HPK-1)调节秀丽隐杆线虫的应激反应和衰老。

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

作者信息

Berber Slavica, Wood Mallory, Llamosas Estelle, Thaivalappil Priya, Lee Karen, Liao Bing Mana, Chew Yee Lian, Rhodes Aaron, Yucel Duygu, Crossley Merlin, Nicholas Hannah R

机构信息

School of Molecular Bioscience, University of Sydney, Sydney, Australia.

School of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, Australia.

出版信息

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.

摘要

同源结构域相互作用蛋白激酶(HIPK)家族的蛋白质调控哺乳动物系统中的一系列过程,如DNA损伤反应、细胞增殖和凋亡。线虫秀丽隐杆线虫有一种名为HPK-1的单一HIPK同源物。先前的研究表明HPK-1参与寿命控制,并提示该蛋白质可能以应激依赖的方式受到调控。在此,我们通过研究HPK-1在寿命以及对热和氧化应激反应中的作用来扩展这些观察结果。我们发现HPK-1的水平受热应激调控,并且HPK-1有助于热应激或氧化应激后的存活。此外,我们表明正常寿命需要HPK-1,HPK-1功能丧失会导致反映过早衰老的生理过程更快衰退。通过微阵列分析,我们发现HPK-1调控的基因包括那些编码在应激反应中起重要作用的蛋白质的基因,如I相和II相解毒酶。与在寿命保障中的作用一致,HPK-1还调控年龄调控基因的表达。最后,我们表明HPK-1与DAF-16在同一途径中发挥作用以调控寿命,并揭示了HPK-1在发育中的新作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc5f/4726358/04013d8246c2/srep19582-f1.jpg

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