Epigenetic marks in zebrafish sperm: insights into chromatin compaction, maintenance of pluripotency, and the role of the paternal genome after fertilization.

H uman sperm chromatin, and the sperm of most mammals, undergoes extensive remodeling during spermiogenesis during which 85%–95% of the histones are removed and replaced with protamines. The replacement of most histones with protamines facilitates a tighter packaging of the chromatin that is necessary for normal sperm function, and may help protect sperm DNA from damage during transport. An intriguing question has been why the replacement of histones with protamines is not complete, and if the histones that remain in human sperm chromatin could have a programmatic role in regulating gene expression postfertilization? Recently, genome-wide studies of human and mouse sperm have demonstrated that most key developmental gene promoters are uniquely packaged with nucleosomes containing bivalent marks, defined as the presence of both activating histone modifications and deactivating histone modifications at the same location, and the DNA is profoundly demethylated. The bivalent marks and demethylation are similar to the bivalent poising of promoters of regulator genes seen in embryonic stem (ES) cells, and may have important ramifications and insights into embryonic gene expression and the establishment of totipotency in germ cells and/or the maintenance of pluripotency in ES cells. In an exciting paper recently published in Genome Research, Wu et al. evaluated the epigenetic marks of chromatin from zebrafish sperm, a vertebrate species that does not have any protamines involved in sperm chromatin packaging, and report that while interesting differences exist between zebrafish and human or mouse sperm chromatin packaging, the underlying pattern of bivalent packaging of developmental genes exists in zebrafish sperm. An initial aim of Wu et al. was to understand the condensation of protamine-free zebrafish sperm chromatin. Chromatin preparations from the zebrafish sperm confirmed that no protamines or transition proteins were present in the preparations. Canonical histones H2A, H2B, H3, histone variants H2AFX and H2AFV, and linker histone H1 and related variants were all identified from the chromatin preparations, and linker histone H1 was found at fourfold levels compared to fibroblasts. Linker histones facilitate development of chromatosomes that have an increase in the average nucleosome repeat length, which indeed was confirmed in the zebrafish sperm nucleosomes. Therefore, it appears that chromatin condensation is partially facilitated by an increased level of linker histone H1. Secondly, Wu et al. found that histone H4K16ac, which inhibits transition of 10-nm chromatin fibers into more dense 30-nm fibers, was virtually absent in the chromatin. It appears that these two mechanisms are largely responsible for the protamine-free compaction of zebrafish sperm chromatin. As was reported previously for human sperm, the genome-wide location of histones with specific activating or repressing modifications and the status of DNA methylation were determined using chromatin immunoprecipitation and methylated DNA immunoprecipitation, respectively. The zebrafish sperm chromatin contained both ‘repressive or silencing’ histone modifications (H3K27me3 and H3K9me3) and ‘activating or positive’ histone modifications (H3K4me3, H3K4me2 and H3K14ac) in bulk levels comparable to zebrafish fibroblasts. As mentioned above, no H4K16ac was detected in the sperm chromatin. Sperm DNA was generally hypermethylated, although hypomethylation was observed in regions of developmental regulators, transcription factors and metabolism/ biosynthesis loci. Similar to the human, the zebrafish chromatin appears to contain activating histone modifications (H3K4me3, H3K4 me2 and H3K14ac) at sets of genes that may reflect a historical record of gene activation during spermatogenesis. The spermatogenesis-related genes include genes involved in processes such as flagella/microtubule development, DNA repair and meiosis-related genes. The repressive mark H3K27me3 was seen mostly in developmentally important gene regions at high density. The activating marks H3K4me3 and H3K4me2 were also seen in more moderate levels at the same groups of developmental loci. Importantly, the large sections of ‘multivalent’ or ‘bivalent’ chromatin described above were seen at key developmental transcription factors involved in embryonic development and similar to bivalency observed in ES cells. Similar to the human and mouse, the large bivalent and multivalent loci were hypomethylated. Human and mouse sperm display a ‘bivalent poising’ of H3K4me3/ H3K27me3 with concurrent hyomethylation near the transcription start sites of key developmental genes. Interesting, Wu et al. found that the bivalency was present in larger blocks of DNA in zebrafish sperm, up to tens of kilobases at clustered gene loci and often extending throughout the entire locus. Andrology and IVF Laboratories, Departments of Surgery (Urology), Obstetrics and Gynecology, and Physiology, University of Utah School of Medicine, Salt Lake City, UT 84108, USA Correspondence: Professor DT Carrell (douglas.carrell@ hsc.utah.edu) Asian Journal of Andrology (2011) 13, 620–621 2011 AJA, SIMM & SJTU. All rights reserved 1008-682X/11 $32.00