| First Author | Quan Y | Year | 2022 |
| Journal | Nucleic Acids Res | Volume | 50 |
| Issue | 8 | Pages | 4414-4435 |
| PubMed ID | 35390160 | Mgi Jnum | J:324247 |
| Mgi Id | MGI:7275795 | Doi | 10.1093/nar/gkac236 |
| Citation | Quan Y, et al. (2022) Cnot8 eliminates naive regulation networks and is essential for naive-to-formative pluripotency transition. Nucleic Acids Res 50(8):4414-4435 |
| abstractText | Mammalian early epiblasts at different phases are characterized by naive, formative, and primed pluripotency states, involving extensive transcriptome changes. Here, we report that deadenylase Cnot8 of Ccr4-Not complex plays essential roles during the transition from naive to formative state. Knock out (KO) Cnot8 resulted in early embryonic lethality in mice, but Cnot8 KO embryonic stem cells (ESCs) could be established. Compared with the cells differentiated from normal ESCs, Cnot8 KO cells highly expressed a great many genes during their differentiation into the formative state, including several hundred naive-like genes enriched in lipid metabolic process and gene expression regulation that may form the naive regulation networks. Knockdown expression of the selected genes of naive regulation networks partially rescued the differentiation defects of Cnot8 KO ESCs. Cnot8 depletion led to the deadenylation defects of its targets, increasing their poly(A) tail lengths and half-life, eventually elevating their expression levels. We further found that Cnot8 was involved in the clearance of targets through its deadenylase activity and the binding of Ccr4-Not complex, as well as the interacting with Tob1 and Pabpc1. Our results suggest that Cnot8 eliminates naive regulation networks through mRNA clearance, and is essential for naive-to-formative pluripotency transition. |
