Literature DB >> 24211575

SIRT1 negatively regulates the protein stability of HIPK2.

Joohyun Hwang1, Seo-Young Lee, Jong-Ryoul Choi, Ki Soon Shin, Cheol Yong Choi, Shin Jung Kang.   

Abstract

In the present study, we investigated whether a histone deacetylase sirtuin 1 (SIRT1) can regulate the protein stability of homeodomain-interacting protein kinase 2 (HIPK2). We observed the evidence of molecular interaction between SIRT1 and HIPK2. Interestingly, overexpression or pharmacological activation of SIRT1 promoted ubiquitination and the proteasomal degradation of HIPK2 whereas inhibition of SIRT1 activity increased the protein level of HIPK2. Furthermore, a SIRT1 activator decreased the level of HIPK2 acetylation whereas an inhibitor increased the acetylation level. These results suggest that SIRT1 may deacetylate and promote the ubiquitination and subsequent proteasomal degradation of HIPK2.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Deacetylation; HIPK2; Proteasomal degradation; SIRT1; Ubiquitination

Mesh:

Substances:

Year:  2013        PMID: 24211575     DOI: 10.1016/j.bbrc.2013.10.133

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

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Journal:  Cell Death Differ       Date:  2015-06-26       Impact factor: 15.828

3.  p300-mediated acetylation increased the protein stability of HIPK2 and enhanced its tumor suppressor function.

Authors:  Jong-Ryoul Choi; Seo-Young Lee; Ki Soon Shin; Cheol Yong Choi; Shin Jung Kang
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4.  SIRT6 overexpression retards renal interstitial fibrosis through targeting HIPK2 in chronic kidney disease.

Authors:  Xiaoxue Li; Wenxin Li; Zhengzhipeng Zhang; Weidong Wang; Hui Huang
Journal:  Front Pharmacol       Date:  2022-09-12       Impact factor: 5.988

  4 in total

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