Biochemical and Biophysical Research Communications, Vol.343, No.1, 260-268, 2006
Spectroscopic characterization of the tumor antigen NY-REN-21 and identification of heterodimer formation with SCAND1
Human NY-REN-21 is a C2H2 type mufti-finger protein, with a SCAN domain in the N-terminal region and a predicted coil central region. It represents a putative ortholog of mouse ZFP38, a transcriptional factor that recognizes a bipartite DNA motif and is unable to form homodimers. As shown in this work, NY-REN-21 contains a SCAN domain able to form homodimers and a central region that behaves as an intrinsically disordered protein. The SCAN domain is found in 71 human proteins and its ability to form homo- and heterodimers widens the number of genes that are regulated by this group of transcription factors. NY-REN-21 interaction with SCAND1 was identified using the yeast two-hybrid system and confirmed using recombinant proteins. SCAND1 is a truncated SCAN box protein, lacking the zinc finger region and the NY-REN-21/SCAND1 heterodimer is asymmetric concerning the DNA binding region. This result indicates that NY-REN-21 can function either as a homodimer or as a heterodimer with SCAND1. (c) 2006 Elsevier Inc. All rights reserved.
Keywords:SCAN domain protein family;intrinsically disordered protein;zinc finger protein;circular dichroism;mass spectrometry;yeast two-hybrid system