“…La Spina and colleagues evaluated the methylation of H3K4Me, H3K4Me3, H3K9Me2, H3K79Me2, H3K36Me3, and acetylation of H3K4Ac and H4K5Ac in normal and abnormal human sperm. They reported the presence of heterogeneous histone modifications, and the presence of H3K4Me1, H3K9Me2, H3K4Me3, H3K79Me2, and H3K36Me3 marks in poorly functional human sperm [79]. Yuen and colleagues made a knockout mouse model for the histone variant H3.3, H3f3b, which is involved in various biological processes including development, transcriptional memory, and transcriptional reprogramming.…”