Cut homeodomain transcription factor is a novel regulator of cortex glia morphogenesis and maintenance of neural niche

Abstract

Cortical glia in Drosophila central nervous system forms a niche around neural stem cells (NSCs) and their progeny for necessary signals to establish cross-talk with their surroundings. These cells grow and expand their thin cytoplasmic extensions around neural cell bodies in the nervous system. Although essential for the development and function of the nervous system, how these cells make extensive and intricate membrane networks remain largely unknown. Here we show that Cut, a homeodomain transcription factor, directly regulates the fate of the cortical glial cells impacting NSC homeostasis. Focusing on the thoracic ventral nerve cord (tVNC), we found that Cut is required for normal growth and development of cortical glial cells. We also highlight that levels of Cut expression play an essential role in the cytoplasmic membrane network growth around the neural cells. Loss of Cut in cortical glia results in a substantial reduction in their cytoplasmic extensions and network around cell bodies of NSCs and their progeny, whereas its overexpression induces the overall growth of cortical glia main branches at the expense of side ones. We also note a striking gain in the nuclear size and volume of cortical glial cells upon Cut overexpression. Furthermore, constitutively high Cut levels increase DNA content in these cells more than threefold, indicating an interference with the splitting of nuclei during endomitosis. Since cortical glia makes syncytial membrane networks around neural cells, the finding identifies Cut as a regulator of glial growth and endomitosis to support a functional nervous system. It is the first report that highlights a novel function of Cut in regulating the growth and branching of cortical glial cells and control over endomitosis.

The multiple lncRNAs encodinghsrω gene is essential for oogenesis inDrosophila

“…55851), a ubiquitous GAL4 driver (Chaturvedi et al, 2016), 6) w* ; tjGAL4/CyO, a follicle cell specific driver (Weaver et al, 2020) received from Dr. Pralay Majumder (Presidency University, India), 7) w * ; Act5CGAL4/CyO-GFP (BDSC no. 4414), a ubiquitous driver (Hongay and Orr-Weaver, 2011) referred to here as ActGAL4, 8) w 1118 ; UAShsrω-RH, carrying the UAS-hsrω-RH transgene (Sahu et al, 2021) insertion on chromosome 3 (referred to here as UAS-hsrωRH), permitting targeted expression of the hsrω-RH transcript, 9) w 1118 ; UAS-hsrωRH hsrω 66 /TM6B, 10) w * ; ), referred to here as cutRNAi, 11) w * ; UAS-cut/CyO (Yadav et al, 2022), referred to here as UAS-cut, 12) UAS-Notch act, for targeted expression of active Notch (Arya et al, 2015), 13) y 1 sc* 1 v 1 sev 21 ; +/+; UAS-cazRNAi (dFus) (BDSC no. 34839), referred to here as cazRNAi, and 14) y 1 sc* 1 v 1 sev 21 ; UAS-TBPH-RNAi/CyO; +/+ (BDSC no.…”