Abstract

BackgroundThe C2H2 zinc finger (ZF) domain is widely conserved among eukaryotic proteins. In Zic/Gli/Zap1 C2H2 ZF proteins, the two N-terminal ZFs form a single structural unit by sharing a hydrophobic core. This structural unit defines a new motif comprised of two tryptophan side chains at the center of the hydrophobic core. Because each tryptophan residue is located between the two cysteine residues of the C2H2 motif, we have named this structure the tandem CWCH2 (tCWCH2) motif.ResultsHere, we characterized 587 tCWCH2-containing genes using data derived from public databases. We categorized genes into 11 classes including Zic/Gli/Glis, Arid2/Rsc9, PacC, Mizf, Aebp2, Zap1/ZafA, Fungl, Zfp106, Twincl, Clr1, and Fungl-4ZF, based on sequence similarity, domain organization, and functional similarities. tCWCH2 motifs are mostly found in organisms belonging to the Opisthokonta (metazoa, fungi, and choanoflagellates) and Amoebozoa (amoeba, Dictyostelium discoideum). By comparison, the C2H2 ZF motif is distributed widely among the eukaryotes. The structure and organization of the tCWCH2 motif, its phylogenetic distribution, and molecular phylogenetic analysis suggest that prototypical tCWCH2 genes existed in the Opisthokonta ancestor. Within-group or between-group comparisons of the tCWCH2 amino acid sequence identified three additional sequence features (site-specific amino acid frequencies, longer linker sequence between two C2H2 ZFs, and frequent extra-sequences within C2H2 ZF motifs).ConclusionThese features suggest that the tCWCH2 motif is a specialized motif involved in inter-zinc finger interactions.

Highlights

  • The C2H2 zinc finger (ZF) domain is widely conserved among eukaryotic proteins

  • ZFDs were originally identified as the DNA-binding domain of transcription factor IIIA (TFIIIa) and other transcription factors, but accumulating evidence suggests that ZFDs bind RNA and

  • This result suggested that the tryptophans play a role in both the stabilization of their own ZFs and the formation of a hydrophobic core between the two adjacent ZFs

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Summary

Introduction

The C2H2 zinc finger (ZF) domain is widely conserved among eukaryotic proteins. In Zic/Gli/Zap C2H2 ZF proteins, the two N-terminal ZFs form a single structural unit by sharing a hydrophobic core. This structural unit defines a new motif comprised of two tryptophan side chains at the center of the hydrophobic core. Zinc finger (ZF) domains (ZFDs) are found in a large number of eukaryotic proteins [1,2,3]. The two N-terminal ZFs (ZF1 and ZF2) of human ZIC3, which has a ZFD composed of five ZFs (ZF1-ZF5), form a single structural unit through a common hydrophobic core

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