Unique Residues on the H2A.Z Containing Nucleosome Surface Are Important for Xenopus laevis Development

• Published in: The Journal of biological chemistry Vol. 279; no. 42; pp. 43815 - 43820
• Main Authors: Ridgway, Patricia, Brown, Karl D, Rangasamy, Danny, Svensson, Ulrica, Tremethick, David J
• Format: Journal Article
• Language: English
• Published: United States American Society for Biochemistry and Molecular Biology 15.10.2004
• Subjects: Amino Acid Sequence; Animals; Conserved Sequence; Freshwater; Histones - genetics; Histones - metabolism; Mice; Molecular Sequence Data; Morphogenesis; Sequence Alignment; Sequence Homology, Amino Acid; Xenopus laevis - embryology; Xenopus Proteins - genetics; Xenopus Proteins - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M408409200

Critical to vertebrate development is a complex program of events that establishes specialized tissues and organs from a single fertilized cell. Transitions in chromatin architecture, through alterations in its composition and modification markings, characterize early development. A variant of the H2A core histone, H2A.Z, is essential for development of both Drosophila and mice. We recently showed that H2A.Z is required for proper chromosome segregation. Whether H2A.Z has additional specific functions during early development remains unknown. Here we demonstrate that depletion of H2A.Z by RNA interference perturbs Xenopus laevis development at gastrulation leading to embryos with malformed, shortened trunks. Consistent with this result, whole embryo in situ hybridization indicates that endogenous expression of H2A.Z is highly enriched in the notochord. H2A.Z modifies the surface of a canonical nucleosome by creating an extended acidic patch and a metal ion-binding site stabilized by two histidine residues. To examine the significance of these specific surface regions in vivo , we investigated the consequences of overexpressing H2A.Z and mutant proteins during X. laevis development. Overexpression of H2A.Z slowed development following gastrulation. Altering the extended acidic patch of H2A.Z reversed this effect. Remarkably, modification of a single stabilizing histidine residue located on the exposed surface of an H2A.Z containing nucleosome was sufficient to disrupt normal trunk formation mimicking the effect observed by RNA interference. Taken together, these results argue that key determinants located on the surface of an H2A.Z nucleosome play an important specific role during embryonic patterning and provide a link between a chromatin structural modification and normal vertebrate development.