scholarly journals Homeodomain protein Six4 prevents the generation of supernumerary Drosophila type II neuroblasts and premature differentiation of intermediate neural progenitors

PLoS Genetics ◽  
2021 ◽  
Vol 17 (2) ◽  
pp. e1009371
Author(s):  
Rui Chen ◽  
Yanjun Hou ◽  
Marisa Connell ◽  
Sijun Zhu

In order to boost the number and diversity of neurons generated from neural stem cells, intermediate neural progenitors (INPs) need to maintain their homeostasis by avoiding both dedifferentiation and premature differentiation. Elucidating how INPs maintain homeostasis is critical for understanding the generation of brain complexity and various neurological diseases resulting from defects in INP development. Here we report that Six4 expressed in Drosophila type II neuroblast (NB) lineages prevents the generation of supernumerary type II NBs and premature differentiation of INPs. We show that loss of Six4 leads to supernumerary type II NBs likely due to dedifferentiation of immature INPs (imINPs). We provide data to further demonstrate that Six4 inhibits the expression and activity of PntP1 in imINPs in part by forming a trimeric complex with Earmuff and PntP1. Furthermore, knockdown of Six4 exacerbates the loss of INPs resulting from the loss of PntP1 by enhancing ectopic Prospero expression in imINPs, suggesting that Six4 is also required for preventing premature differentiation of INPs. Taken together, our work identified a novel transcription factor that likely plays important roles in maintaining INP homeostasis.

2009 ◽  
Vol 40 (4) ◽  
pp. 442-450 ◽  
Author(s):  
Fang Gao ◽  
Qi Zhang ◽  
Min-Hua Zheng ◽  
Hui-Ling Liu ◽  
Yi-Yang Hu ◽  
...  

Author(s):  
Srivathsa S. Magadi ◽  
Chrysanthi Voutyraki ◽  
Gerasimos Anagnostopoulos ◽  
Evanthia Zacharioudaki ◽  
Ioanna K. Poutakidou ◽  
...  

ABSTRACTNeural stem cells divide during embryogenesis and post embryonic development to generate the entire complement of neurons and glia in the nervous system of vertebrates and invertebrates. Studies of the mechanisms controlling the fine balance between neural stem cells and more differentiated progenitors have shown that in every asymmetric cell division progenitors send a Delta-Notch signal back to their sibling stem cells. Here we show that excessive activation of Notch or overexpression of its direct targets of the Hes family causes stem-cell hyperplasias in the Drosophila larval central nervous system, which can progress to malignant tumours after allografting to adult hosts. We combined transcriptomic data from these hyperplasias with chromatin occupancy data for Dpn, a Hes transcription factor, to identify genes regulated by Hes factors in this process. We show that the Notch/Hes axis represses a cohort of transcription factor genes. These are excluded from the stem cells and promote early differentiation steps, most likely by preventing the reversion of immature progenitors to a stem-cell fate. Our results suggest that Notch signalling sets up a network of mutually repressing stemness and anti-stemness transcription factors, which include Hes proteins and Zfh1, respectively. This mutual repression ensures robust transition to neuronal and glial differentiation and its perturbation can lead to malignant transformation.


Cell Reports ◽  
2020 ◽  
Vol 33 (7) ◽  
pp. 108394
Author(s):  
Suihong Huang ◽  
Ming Ho Choi ◽  
Hao Huang ◽  
Xin Wang ◽  
Yu Chen Chang ◽  
...  

2002 ◽  
Vol 333 (1) ◽  
pp. 74-78 ◽  
Author(s):  
Myung Ae Lee ◽  
Hye-Souk Lee ◽  
Hyun Soo Lee ◽  
Kyung G. Cho ◽  
Byung Kwan Jin ◽  
...  

2015 ◽  
Vol 29 (2) ◽  
pp. 129-143 ◽  
Author(s):  
Francesca Froldi ◽  
Milan Szuperak ◽  
Chen-Fang Weng ◽  
Wei Shi ◽  
Anthony T. Papenfuss ◽  
...  

EMBO Reports ◽  
2015 ◽  
Vol 16 (9) ◽  
pp. 1177-1191 ◽  
Author(s):  
Tapan Kumar Mistri ◽  
Arun George Devasia ◽  
Lee Thean Chu ◽  
Wei Ping Ng ◽  
Florian Halbritter ◽  
...  

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