PUBLICATION
Genes for embryo development are packaged in blocks of multivalent chromatin in zebrafish sperm
- Authors
- Wu, S.F., Zhang, H., and Cairns, B.R.
- ID
- ZDB-PUB-110317-42
- Date
- 2011
- Source
- Genome research 21(4): 578-89 (Journal)
- Registered Authors
- Wu, Shan-Fu
- Keywords
- none
- Datasets
- GEO:GSE26609
- MeSH Terms
-
- Animals
- Chromatin/genetics*
- Chromatin/metabolism*
- DNA Methylation/genetics
- Embryonic Development/genetics*
- Gene Expression Regulation, Developmental
- Genome/genetics
- Histones/metabolism
- Male
- RNA, Untranslated/genetics
- RNA, Untranslated/metabolism
- Repetitive Sequences, Nucleic Acid/genetics
- Spermatozoa/cytology
- Spermatozoa/metabolism*
- Time Factors
- Zebrafish/embryology*
- Zebrafish/genetics*
- PubMed
- 21383318 Full text @ Genome Res.
Citation
Wu, S.F., Zhang, H., and Cairns, B.R. (2011) Genes for embryo development are packaged in blocks of multivalent chromatin in zebrafish sperm. Genome research. 21(4):578-89.
Abstract
In mature human sperm, genes of importance for embryo development (i.e., transcription factors) lack DNA methylation and bear nucleosomes with distinctive histone modifications, suggesting the specialized packaging of these developmental genes in the germline. Here, we explored the tractable zebrafish model and found conceptual conservation as well as several new features. Biochemical and mass spectrometric approaches reveal the zebrafish sperm genome packaged in nucleosomes and histone variants (and not protamine), and we find linker histones high and H4K16ac absent, key factors that may contribute to genome condensation. We examined several activating (H3K4me2/3, H3K14ac, H2AFV) and repressing (H3K27me3, H3K36me3, H3K9me3, hypoacetylation) modifications/compositions genome-wide and find developmental genes packaged in large blocks of chromatin with coincident activating and repressing marks and DNA hypomethylation, revealing complex "multivalent" chromatin. Notably, genes that acquire DNA methylation in the soma (muscle) are enriched in transcription factors for alternative cell fates. Remarkably, whereas H3K36me is located in the 3' coding region of heavily transcribed genes in somatic cells, H3K36me is present in the promoters of "silent" developmental regulators in sperm, suggesting different rules for H3K36me3 in the germline and soma. We also reveal the chromatin patterns of transposons, rDNA, and tDNAs. Finally, high levels of H3K4me3 and H3K14ac in sperm are correlated with genes activated in embryos prior to the mid-blastula transition (MBT), whereas multivalent genes are correlated with activation at or after MBT. Taken together, gene sets with particular functions in the embryo are packaged by distinctive types of complex and often atypical chromatin in sperm.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping