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Mariasina, S.

Publications and source records attributed to Mariasina, S..

2 recordsLinked to original sources

Beyond DNA Binding: single C2H2 zinc fingers with adjacent β-strands mediate dimerization in Drosophila transcription factors

C2H2 proteins, characterized by DNA-binding C2H2-type zinc finger domains, constitute the largest group of transcription factors. In addition to binding DNA, C2H2 domains can mediate protein-protein interactions, facilitating oligomerization of C2H2 proteins. In this study, we identified eight C2H2 proteins in the Drosophila genome that feature a unique single C2H2 domain containing a conservedCGEx motif. Yeast two-hybrid assays, SEC-MALS, and chemical cross-linking experiments revealed a strong propensity of these domains to form dimers. Using NMR spectroscopy, we determined the solution structure of the dimeric C2H2 domain from IMZF (Immune-mediated Zinc Finger) protein, providing structural evidence towards the dimerization of C2H2 domains. The structure revealed that dimerization is mediated by the interface between the core C2H2 fold and the adjacent {beta}-strand containingCGEx motif, which was further validated by structure-guided mutagenesis. A bioinformatic survey showed thatCGEx-type C2H2 domains are specific to Diptera. Finally, we demonstrate that putatively dimerizing C2H2 domains containing additional structural elements beyond the canonical fold are widespread among diverse eukaryotic taxa, with the highest prevalence observed in insects. These findings establish that single C2H2 domains can mediate self-association and identify theCGEx-type C2H2 domain as a distinct structural subclass specific to Dipteran insects.

molecular biology↗

Structural basis for interaction between CLAMP and MSL2 proteins involved in the specific recruitment of the dosage compensation complex in Drosophila

Transcriptional regulators select their targets from a large pool of similar genomic sites. The binding of the Drosophila dosage compensation complex (DCC) exclusively to the male X chromosome provides insight into binding site selectivity rules. Previous studies showed that the male-specific organizer of the complex, MSL2, and ubiquitous DNA-binding protein CLAMP directly interact and play an important role in the specificity of X chromosome binding. Here we studied the highly specific interaction between the intrinsically disordered region of MSL2 and the N-terminal zinc-finger C2H2-type (C2H2) domain of CLAMP. We obtained the NMR structure of the CLAMP N-terminal C2H2 zinc finger, which has a classic C2H2 zinc-finger fold with a rather unusual distribution of residues typically used in DNA recognition. Substitutions of residues in this C2H2 domain had the same effect on the viability of males and females, suggesting that it plays a general role in CLAMP activity. The N-terminal C2H2 domain of CLAMP is highly conserved in insects. However, the MSL2 region involved in the interaction is conserved only within the Drosophila genus, suggesting that this interaction emerged during the evolution of a mechanism for the specific recruitment of the DCC on the male X chromosome in Drosophilidae.

molecular biology↗