Overexpression of small glutamine-rich TPR-containing protein promotes apoptosis in 7721 cells.

Hongliang Zong

Research output: Contribution to journalArticlepeer-review

30 Citations (Scopus)

Abstract

It is known that small glutamine-rich TPR-containing protein (SGT) is the member of TPR motif family. However, the biological functions of SGT remain unclear. In this paper, we report that SGT plays a role in apoptotic signaling. Ectopic expression of SGT enhances DNA fragment and nucleus breakage after the induction of apoptosis. Increasing mRNA level of SGT is also observed in 7721 cells undergoing apoptosis, knockdown the expression of endogenous SGT contributes to the decrease of apoptosis of 7721 cells. Deletion analysis reveals that TPR domain is critical to pro-apoptotic function of SGT. Furthermore, we demonstrated that the PARP cleavage and cytochrome c release are enhanced when SGT is overexpressed in 7721 cells during apoptosis. Collectively, our results indicate that SGT is a new pro-apoptotic factor.
Original languageEnglish
Pages (from-to)1279-1284
Number of pages6
JournalFEBS Letters
Volume579(5)
Issue number5
DOIs
Publication statusPublished - 14 Feb 2005

ASJC Scopus subject areas

  • Biochemistry
  • Biophysics
  • Molecular Biology

Fingerprint

Dive into the research topics of 'Overexpression of small glutamine-rich TPR-containing protein promotes apoptosis in 7721 cells.'. Together they form a unique fingerprint.

Cite this