Topic Highlight
Copyright ©2011 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Biol Chem. Jun 26, 2011; 2(6): 161-166
Published online Jun 26, 2011. doi: 10.4331/wjbc.v2.i6.161
Zinc finger structure-function in Ikaros Marvin A Payne
Marvin A Payne, Department of Chemistry and Biochemistry, La Sierra University, 4500 Riverwalk Parkway, Riverside, CA 92515, United States
Author contributions: Payne MA contributed solely to the manuscript.
Supported by NIH P41 RR-01081
Correspondence to: Marvin A Payne, PhD, Associate Professor, Department of Chemistry and Biochemistry, 4500 Riverwalk Parkway, Riverside, CA 92515, United States. mpayne@lasierra.edu
Telephone: +1-951-7852148 Fax: +1-951-7852901
Received: March 22, 2011
Revised: May 6, 2011
Accepted: May 13, 2011
Published online: June 26, 2011
Abstract

The zinc finger motif was used as a vehicle for the initial discovery of Ikaros in the context of T-cell differentiation and has been central to all subsequent analyses of Ikaros function. The Ikaros gene is alternately spliced to produce several isoforms that confer diversity of function and consequently have complicated analysis of the function of Ikaros in vivo. Key features of Ikaros in vivo function are associated with six C2H2 zinc fingers; four of which are alternately incorporated in the production of the various Ikaros isoforms. Although no complete structures are available for the Ikaros protein or any of its family members, considerable evidence has accumulated about the structure of zinc fingers and the role that this structure plays in the functions of the Ikaros family of proteins. This review summarizes the structural aspects of Ikaros zinc fingers, individually, and in tandem to provide a structural context for Ikaros function and to provide a structural basis to inform the design of future experiments with Ikaros and its family members.

Keywords: Ikaros; Zinc finger; DNA binding protein; Transcription factor IIIA; C2H2; Tandem