Lens epithelium-derived growth factor deSumoylation by Sumo-specific protease-1 regulates its transcriptional activation of small heat shock protein and the cellular response

Keiichi Ishihara, Nigar Fatma, Biju Bhargavan, Bhavana Chhunchha, Eri Kubo, Sanjib Dey, Yoshihiro Takamura, Anil Kumar, Dhirendra P. Singh

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Lens epithelium-derived growth factor (LEDGF), a ubiquitously expressed nuclear protein, acts by interacting with DNA and protein and is involved in widely varying cellular functions. Despite its importance, the mechanism(s) that regulate naturally occurring LEDGF activity are unidentified. In the present study, we report that LEDGF is constitutively Sumoylated, and that the dynamical regulatory mechanism(s) (i.e. Sumoylation and deSumoylation) act as a molecular switch in modulating the DNA-binding and transcriptional activity of LEDGF with the functional consequences. Using bioinformatics analysis coupled with in vitro and in vivo Sumoylation assays, we found that lysine (K) 364 of LEDGF was Sumoylated, repressing its transcriptional activity. Conversely, mutation of K364 to arginine (R) or deSumoylation by small ubiquitin-like modifier (Sumo)-specific protease-1, a nuclear deSumoylase, enhanced the transactivation capacity of LEDGF and its cellular abundance. The enhancements were directly correlated with an increase in the DNA-binding activity and small heat shock protein transcription of LEDGF, whereas the process was reversed in cells overexpressing Sumo1. Interestingly, cells expressing Sumoylation-deficient pEGFP-K364R protein showed increased cellular survival compared to wild-type LEDGF protein. The findings provide insights into the regulation and regulatory functions of LEDGF in Sumoylation-dependent transcriptional control that may be essential for modifying the physiology of cells to maintain cellular homeostasis. These studies also provide new evidence of the important role of post-translational modification in controlling LEDGF function.

Original languageEnglish (US)
Pages (from-to)3048-3070
Number of pages23
JournalFEBS Journal
Volume279
Issue number17
DOIs
StatePublished - Sep 1 2012

Fingerprint

Small Heat-Shock Proteins
Ubiquitin
Transcriptional Activation
Peptide Hydrolases
Chemical activation
Sumoylation
DNA
lens epithelium-derived growth factor
Cell Physiological Phenomena
Proteins
Physiology
Transcription
Post Translational Protein Processing
Bioinformatics
Nuclear Proteins
Computational Biology
Lysine
Arginine
Assays
Homeostasis

Keywords

  • HSP27
  • LEDGF
  • Senp-1
  • Sp1
  • Sumo1

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

Lens epithelium-derived growth factor deSumoylation by Sumo-specific protease-1 regulates its transcriptional activation of small heat shock protein and the cellular response. / Ishihara, Keiichi; Fatma, Nigar; Bhargavan, Biju; Chhunchha, Bhavana; Kubo, Eri; Dey, Sanjib; Takamura, Yoshihiro; Kumar, Anil; Singh, Dhirendra P.

In: FEBS Journal, Vol. 279, No. 17, 01.09.2012, p. 3048-3070.

Research output: Contribution to journalArticle

Ishihara, Keiichi ; Fatma, Nigar ; Bhargavan, Biju ; Chhunchha, Bhavana ; Kubo, Eri ; Dey, Sanjib ; Takamura, Yoshihiro ; Kumar, Anil ; Singh, Dhirendra P. / Lens epithelium-derived growth factor deSumoylation by Sumo-specific protease-1 regulates its transcriptional activation of small heat shock protein and the cellular response. In: FEBS Journal. 2012 ; Vol. 279, No. 17. pp. 3048-3070.
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AU - Chhunchha, Bhavana

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AU - Takamura, Yoshihiro

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