The histone H3.3 chaperone HIRA is essential for chromatin assembly in the male pronucleus

Benjamin Loppin (), Emilie Bonnefoy, Caroline Anselme, Anne Laurençon, Timothy L. Karr and Pierre Couble
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Benjamin Loppin: U.M.R. 5534, C.N.R.S. – Université Claude Bernard, Lyon-1
Emilie Bonnefoy: U.M.R. 5534, C.N.R.S. – Université Claude Bernard, Lyon-1
Caroline Anselme: U.M.R. INRA/INSA BF2I
Anne Laurençon: U.M.R. 5534, C.N.R.S. – Université Claude Bernard, Lyon-1
Timothy L. Karr: University of Bath
Pierre Couble: U.M.R. 5534, C.N.R.S. – Université Claude Bernard, Lyon-1

Nature, 2005, vol. 437, issue 7063, 1386-1390

Abstract: Abstract In sexually reproducing animals, a crucial step in zygote formation is the decondensation of the fertilizing sperm nucleus into a DNA replication-competent male pronucleus. Genome-wide nucleosome assembly on paternal DNA implies the replacement of sperm chromosomal proteins, such as protamines, by maternally provided histones1,2. This fundamental process is specifically impaired in sésame (ssm), a unique Drosophila maternal effect mutant that prevents male pronucleus formation3. Here we show that ssm is a point mutation in the Hira gene, thus demonstrating that the histone chaperone protein HIRA is required for nucleosome assembly during sperm nucleus decondensation. In vertebrates, HIRA has recently been shown to be critical for a nucleosome assembly pathway independent of DNA synthesis that specifically involves the H3.3 histone variant4,5. We also show that nucleosomes containing H3.3, and not H3, are specifically assembled in paternal Drosophila chromatin before the first round of DNA replication. The exclusive marking of paternal chromosomes with H3.3 represents a primary epigenetic distinction between parental genomes in the zygote, and underlines an important consequence of the critical and highly specialized function of HIRA at fertilization.

Date: 2005
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DOI: 10.1038/nature04059

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