C. elegansestablishes germline versus soma by balancing inherited histone methylation

Embryos undergo extensive reprogramming at fertilization to prevent the inappropriate inheritance of histone methylation. InC. elegans,this reprogramming is mediated by the H3K4me2 demethylase, SPR-5, and the H3K9 methyltransferase, MET-2. In contrast to this reprogramming, the H3K36 methyltransferase, MES-4, maintains H3K36me2/3 at germline genes between generations to help re-establish the germline. To determine whether the MES-4 germline inheritance system antagonizesspr-5; met-2reprogramming, we examined the interaction between these two systems. We find that the developmental delay ofspr-5; met-2mutant progeny is associated with ectopic H3K36me2/3 and the ectopic expression of MES-4 targeted germline genes in somatic tissues. Furthermore, the developmental delay is dependent upon MES-4 and the H3K4 methyltransferase, SET-2. We propose that the MES-4 inheritance system prevents critical germline genes from being repressed by maternalspr-5; met-2reprogramming. Thus, the balance of inherited histone modifications is necessary to distinguish germline versus soma and prevent developmental delay.