Summary: Study reveals the critical and novel roles Integrator complex proteins play in promoting healthy brain development in flies.
Source: Duke-NUS Medical School
A study by Duke-NUS Medical School has found that members of the multiprotein ‘Integrator complex’, known for its role in gene regulation, are crucial for healthy brain development in fruit flies. The findings have implications for further understanding and treating neurodevelopmental disorders in humans.
Mutations in human Integrator genes intS1 and intS8 were associated with neurodevelopmental syndrome, which is characterized by profound intellectual disability, epilepsy and subtle structural brain abnormalities. However, the role of the Integrator complex during brain development has not been well understood. Associate Professor Wang Hongyan, Deputy Director of Duke-NUS’ Neuroscience and Behavioural Disorders Programme and lead author of the study, said, “We examined members of the Integrator complex in fruit fly brains to understand their roles in the development of the nervous system.”
Normally, neural stem cells in larval brains differentiate into intermediate neural progenitors, which ultimately form into nerve cells. Several factors are understood to prevent intermediate neural progenitor cells from turning back into neural stem cells, a process called dedifferentiation. Assoc Prof Wang and her team previously showed that when dedifferentiation occurs, abnormal neural stem cell-derived tumours can form in fruit fly brains. Nerve cell generation also becomes insufficient.
Assoc Prof Wang and her team mutated and turned off members of the Integrator complex in the fruit fly brains. Abnormal neural stem cells were formed when Integrator proteins were absent in brain cells. Turning off several Integrator genes in intermediate neural progenitor cells led to excessive formation of neural stem cells. Their investigations provided evidence that Integrator proteins help prevent intermediate neural progenitors from dedifferentiating into neural stem cells. A transcription factor called Earmuff, which is needed for the prevention of dedifferentiation, was identified as the primary target of Integrator complex proteins in the brain cells.
The findings highlight the critical and novel roles played by Integrator complex proteins in preventing dedifferentiation, and thus in promoting brain development in fruit flies. They also show that Integrator complex proteins regulate Earmuff, which is a known dedifferentiation suppressor. “Given that Integrator and Earmuff are highly conserved in flies and humans, our study will facilitate understanding the function of their mammalian and human counterparts during brain development, in addition to understanding potential disease mechanisms,” says Assoc Prof Wang.
Professor Patrick Casey, Senior Vice Dean of Research, Duke-NUS Medical School, commented, “The study of the Integrator complex in neurodevelopment has been largely unexplored, and these findings provide valuable insights to better understand and treat neurodegenerative diseases in the future.”
About this neuroscience research article
Source: Duke-NUS Medical School Media Contacts: Federico Graciano – Duke-NUS Medical School Image Source: The image is credited to Yingjie Zhang and Chwee Tat Koe.
The Integrator Complex Prevents Dedifferentiation of Intermediate Neural Progenitors back into Neural Stem Cells
Highlights • Drosophila Integrator complex is important for larval brain development • Neural-progenitor-specific depletion of integrator induces ectopic type II neuroblasts • DamID analysis identifies earmuff as an IntS5-binding site in INPs • Integrator promotes the expression of erm and brm in type II neuroblast lineages
Summary 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.