The histone H3.3 chaperone HIRA is essential for chromatin assembly in the male pronucleus
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 m...
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Veröffentlicht in: | Nature (London) 2005-10, Vol.437 (7063), p.1386-1390 |
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Sprache: | eng |
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Zusammenfassung: | 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 histones
1
,
2
. This fundamental process is specifically impaired in
sésame
(
ssm
), a unique
Drosophila
maternal effect mutant that prevents male pronucleus formation
3
. 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 variant
4
,
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. |
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ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/nature04059 |