Recruiting substrates to cullin 4-dependent ubiquitin ligases by DDB1

Chad M. McCall, Jian Hu, Yue Xiong

Research output: Contribution to journalShort surveypeer-review

13 Scopus citations

Abstract

The ubiqutin-proteasome system is the major pathway by which cells target proteins for degradation in a specific manner. The E3 ubiquitin ligase, which brings targeted proteins (substrates) and activated ubiquitin in close proximity, enabling covalent conjugation of ubiquitin to the substrate, is an essential component of this system. Of the E3 ligases, the cullin (CUL) ligases are of high interest because of their capacity to form multiple distinct E3 complexes to ubiquitinate a potentially large number of substrates. Of the six closely related cullins, very little is known about how specific substrates are recruited to CUL4-dependent ligases. A recent paper in Nature Cell Biology may shed some light on this issue as well as on the function of DDB1, a damaged-DNA binding protein that has long been associated with DNA repair.

Original languageEnglish (US)
Pages (from-to)27-29
Number of pages3
JournalCell Cycle
Volume4
Issue number1
DOIs
StatePublished - Jan 2005

Keywords

  • CUL4
  • Cdt1
  • Culin
  • DDB1
  • DNA repair
  • Ubiquitin ligase
  • Ubiquitin-proteasome system

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology
  • Cell Biology

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