Spermatogenesis |
Decrease of spermatocytes |
The reduction of histone H3K4 methyltransferase MII2 activity |
Mouse |
Glaser et al.[69] |
Sperm apoptosis and sterility |
The loss of LSD1/KDM1 |
Human |
Shi et al.[70] |
Impaired post meiotic chromatin condensation |
Deficiency of the JHMD2A can down regulate the expression of two genes, the P1 and TNP1, leading to the condensation and proper packaging of the chromatin failure in sperms |
Mouse |
Najafipour et al.[71] |
Inhibit the process of spermatogenesis |
Altered dimethylation states of the H3K9 |
Mouse |
Xiong et al.[74] |
Nucleosome removal abnormality |
Deficiency of the RNF8, a ubiquitin ligase, could lead to the abnormal H4K16 acetylation that significantly suppresses the histone removal and results in the incorporation of the transition protein |
Mouse |
Lu et al.[72] |
Partial failure in chromatin condensation, abnormal sperm head morphology, immotility of epididymal sperm, and male infertility |
Knockout Chd5, a gene encoding chromatin-remodeling nuclear protein, decreases the H4 hyperacetylation in elongating spermatids |
Mouse |
Zhuang et al.[73] |
Embryogenesis |
Insufficient sperm chromatin compaction that persists in the zygote |
Aberrant acetylation of the H4K12 in promoters of the development of important genes |
Human |
Paradowska et al.[75] |
Less developmentally competent embryos |
abnormal expression of BRG1 and KDM1A around the period of embryonic genome activation could alter the H3K4 methylation |
Porcine |
Glanzneret al.[76] |
Peri-implantation lethality |
Absence of the ERG-associated protein with the SET domain, a histone methyltransferase that specifically trimethylates the H3K9 residue |
Mouse |
Dodge et al.[77] |
Birth |
Rubinstein-Taybi syndrome |
Acetylation of histones alters the folding of the chromatin nucleoprotein complex |
Human |
Ausio et al.[78] |