1. Academic Validation
  2. SIAH-1 interacts with CtIP and promotes its degradation by the proteasome pathway

SIAH-1 interacts with CtIP and promotes its degradation by the proteasome pathway

  • Oncogene. 2003 Dec 4;22(55):8845-51. doi: 10.1038/sj.onc.1206994.
Antonia Germani 1 Audrey Prabel Samia Mourah Marie-Pierre Podgorniak Anna Di Carlo Ricardo Ehrlich Sylvie Gisselbrecht Nadine Varin-Blank Fabien Calvo Heriberto Bruzzoni-Giovanelli
Affiliations

Affiliation

  • 1 Laboratory of Vascular Biology and Gene Therapy, Centro Cardiologico Fondazione-IRCCS, Via Parea 4, 20138 Milano, Italy.
Abstract

SIAH-1 and SIAH-2 are the human members of an evolutionary highly conserved E3 ligase family. SIAH-1 is a p53 and p21(Waf-1/Cip-1) induced gene during Apoptosis and tumor suppression. In stable-transfected clones of MCF-7 cells, SIAH-1 overexpression was associated with Apoptosis, mitotic alterations and p21(Waf-1/Cip-1) induction of expression. Using a two-hybrid screening, we identified here the transcriptional corepressor CtBP-interacting protein (CtIP) as a SIAH-1-interacting protein. CtIP has been proposed as a regulator of p21(Waf-1/Cip-1) gene transcription through a protein complex involving BRCA1. We demonstrate that SIAH-1 associates with CtIP both in vitro and in vivo. This interaction led to CtIP degradation by the ubiquitin-proteasome pathway. As expected, SIAH-1 induced p21(Waf-1/Cip-1) transcription in Jurkat-T cell. Surprisingly, a SIAH protein deleted of its RING finger, SIAH-1DeltaN, which is able to interact with CtIP but does not promote its degradation, also induced transcription from the p21(Waf-1) promoter in a similar extent as did SIAH-1. Our results suggest that p21(Waf-1/Cip-1) induction by SIAH-1 could not be mediated by CtIP degradation.

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