Molecular cloning of novel Monad binding protein containing tetratricopeptide repeat domains

FEBS Lett. 2008 Jul 9;582(16):2365-70. doi: 10.1016/j.febslet.2008.05.041. Epub 2008 Jun 5.

Abstract

We have previously reported that Monad, a novel WD40 repeat protein, potentiates apoptosis induced by tumor necrosis factor-alpha(TNF-alpha) and cycloheximide (CHX). By affinity purification and mass spectrometry, we identified RNA polymerase II-associated protein 3 (RPAP3) as a binding protein of Monad. Overexpression of RPAP3 in HEK 293 potentiated caspase-3 activation and apoptosis induced by TNF-alpha and CHX. In addition, knockdown of RPAP3 by RNA interference resulted in a significant reduction of apoptosis induced by TNF-alpha and CHX in HEK293 and HeLa cells. These results raise the possibility that RPAP3, together with Monad, may function as a novel modulator of apoptosis pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Apoptosis Regulatory Proteins / metabolism*
  • Apoptosis*
  • Carrier Proteins / chemistry
  • Carrier Proteins / genetics
  • Carrier Proteins / physiology*
  • Cell Line
  • Cloning, Molecular
  • Humans
  • Molecular Sequence Data
  • Protein Structure, Tertiary
  • RNA, Messenger / metabolism
  • Repetitive Sequences, Amino Acid
  • Tissue Distribution

Substances

  • Apoptosis Regulatory Proteins
  • Carrier Proteins
  • DNAAF10 protein, human
  • RNA, Messenger
  • RPAP3 protein, human