AI Article Synopsis

  • ETS1 is a transcription factor involved in key cellular processes like cell growth and movement, and its function is influenced by various protein interactions.
  • A study revealed that SP100 interacts with ETS1, affecting its activity and altering the morphology of nuclear bodies within the cell.
  • SP100 negatively regulates ETS1's ability to activate certain genes linked to cancer invasion, showcasing its role in controlling processes relevant to breast cancer cell invasion.

Article Abstract

The ETS1 transcription factor is a member of the Ets family of conserved sequence-specific DNA-binding proteins. ETS1 has been shown to play important roles in various cellular processes such as proliferation, differentiation, lymphoid development, motility, invasion and angiogenesis. These diverse roles of ETS1 are likely to be dependent on specific protein interactions. To identify proteins that interact with ETS1, a yeast two-hybrid screen was conducted. Here, we describe the functional interaction between SP100 and ETS1. SP100 protein interacts with ETS1 both in vitro and in vivo. SP100 is localized to nuclear bodies and ETS1 expression alters the nuclear body morphology in living cells. SP100 negatively modulates ETS1 transcriptional activation of the MMP1 and uPA promoters in a dose-dependent manner, decreases the expression of these endogenous genes, and reduces ETS1 DNA binding. Expression of SP100 inhibits the invasion of breast cancer cells and is induced by Interferon-alpha, which has been shown to inhibit the invasion of cancer cells. These data demonstrate that SP100 modulates ETS1-dependent biological processes.

Download full-text PDF

Source
http://dx.doi.org/10.1038/sj.onc.1207891DOI Listing

Publication Analysis

Top Keywords

ets1
10
modulates ets1
8
ets1 transcriptional
8
cancer cells
8
sp100
7
sp100 expression
4
expression modulates
4
transcriptional activity
4
activity inhibits
4
inhibits cell
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!