Safeguarding Drosophila female germ cell identity depends on an H3K9me3 mini domain guided by a ZAD zinc finger protein

• Published in: PLoS genetics 2022-12, Vol.18 (12), p.e1010568
• Main Authors: Shapiro-Kulnane, Laura, Selengut, Micah, Salz, Helen K
• Format: Article
• Language: English
• Subjects: Animals; Biology and Life Sciences; Cell fate; DNA binding proteins; DNA methylation; Drosophila; Drosophila - metabolism; Drosophila melanogaster - genetics; Drosophila melanogaster - metabolism; Drosophila Proteins - genetics; Drosophila Proteins - metabolism; Epigenetic inheritance; Epigenetics; Female; Gene expression; Gene regulation; Gene silencing; Genes; Genetic aspects; Genetic engineering; Genetic research; Germ cells; Germ Cells - metabolism; Homeodomain Proteins - metabolism; Insects; Male; Mammals; Medicine and Health Sciences; Methylation; Ovaries; Physiological aspects; Proteins; Regulatory sequences; Research and Analysis Methods; Transposons; Wildlife conservation; Zinc finger proteins; Zinc Fingers - genetics
• ISSN: 1553-7404; 1553-7390; 1553-7404
• DOI: 10.1371/journal.pgen.1010568

H3K9me3-based gene silencing is a conserved strategy for securing cell fate, but the mechanisms controlling lineage-specific installation of this epigenetic mark remain unclear. In Drosophila, H3K9 methylation plays an essential role in securing female germ cell fate by silencing lineage inappropriate phf7 transcription. Thus, phf7 regulation in the female germline provides a powerful system to dissect the molecular mechanism underlying H3K9me3 deposition onto protein coding genes. Here we used genetic studies to identify the essential cis-regulatory elements, finding that the sequences required for H3K9me3 deposition are conserved across Drosophila species. Transposable elements are also silenced by an H3K9me3-mediated mechanism. But our finding that phf7 regulation does not require the dedicated piRNA pathway components, piwi, aub, rhino, panx, and nxf2, indicates that the mechanisms of H3K9me3 recruitment are distinct. Lastly, we discovered that an uncharacterized member of the zinc finger associated domain (ZAD) containing C2H2 zinc finger protein family, IDENTITY CRISIS (IDC; CG4936), is necessary for H3K9me3 deposition onto phf7. Loss of idc in germ cells interferes with phf7 transcriptional regulation and H3K9me3 deposition, resulting in ectopic PHF7 protein expression. IDC's role is likely to be direct, as it localizes to a conserved domain within the phf7 gene. Collectively, our findings support a model in which IDC guides sequence-specific establishment of an H3K9me3 mini domain, thereby preventing accidental female-to-male programming.