| Literature DB >> 31018143 |
Yingjie Zhang1, Chwee Tat Koe2, Ye Sing Tan3, Joses Ho4, Patrick Tan5, Fengwei Yu6, Wing-Kin Sung7, Hongyan Wang8.
Abstract
Mutations of the Integrator subunits are associated with neurodevelopmental disorders and cancers. However, their role during neural development is poorly understood. Here, we demonstrate that the Drosophila Integrator complex prevents dedifferentiation of intermediate neural progenitors (INPs) during neural stem cell (neuroblast) lineage development. Loss of intS5, intS8, and intS1 generated ectopic type II neuroblasts. INP-specific knockdown of intS8, intS1, and intS2 resulted in the formation of excess type II neuroblasts, indicating that Integrator prevents INP dedifferentiation. Cell-type-specific DamID analysis identified 1413 IntS5-binding sites in INPs, including zinc-finger transcription factor earmuff (erm). Furthermore, erm expression is lost in intS5 and intS8 mutant neuroblast lineages, and intS8 genetically interacts with erm to suppress the formation of ectopic neuroblasts. Taken together, our data demonstrate that the Drosophila Integrator complex plays a critical role in preventing INP dedifferentiation primarily by regulating a key transcription factor Erm that also suppresses INP dedifferentiation.Entities:
Keywords: Drosophila; dedifferentiation; intermediate neural progenitors; neural stem cells; neuroblasts
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Year: 2019 PMID: 31018143 DOI: 10.1016/j.celrep.2019.03.089
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423