H3.3 kinetics predicts chromatin compaction status of parental genomes in early embryos

• Main Authors: Shi-meng Guo, Xing-ping Liu, Li-quan Zhou
• Format: Article
• Language: English
• Published: BMC 2021-06-01
• Series: Reproductive Biology and Endocrinology
• Subjects: H3.3; Chromatin mobility; Totipotency
• Online Access: https://doi.org/10.1186/s12958-021-00776-3

Abstract Background After fertilization, the fusion of gametes results in the formation of totipotent zygote. During sperm-egg fusion, maternal factors participate in parental chromatin remodeling. H3.3 is a histone H3 variant that plays essential roles in mouse embryogenesis. Methods Here, we used transgenic early embryos expressing H3.3-eGFP or H2B-mCherry to elucidate changes of histone mobility. Results We used FRAP analysis to identify that maternally stored H3.3 has a more significant change than H2B during maternal-to-embryonic transition. We also found that H3.3 mobile fraction, which may be regulated by de novo H3.3 incorporation, reflects chromatin compaction of parental genomes in GV oocytes and early embryos. Conclusions Our results show that H3.3 kinetics in GV oocytes and early embryos is highly correlated with chromatin compaction status of parental genomes, indicating critical roles of H3.3 in higher-order chromatin organization.