scholarly journals Drosophila microRNA-34 Impairs Axon Pruning of Mushroom Body γ Neurons by Downregulating the Expression of Ecdysone Receptor

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Yen-Wei Lai ◽  
Sao-Yu Chu ◽  
Jia-Yi Wei ◽  
Chu-Ya Cheng ◽  
Jian-Chiuan Li ◽  
...  
Neuron ◽  
2000 ◽  
Vol 28 (3) ◽  
pp. 807-818 ◽  
Author(s):  
Tzumin Lee ◽  
Simone Marticke ◽  
Carl Sung ◽  
Steven Robinow ◽  
Liqun Luo

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Ana Boulanger ◽  
Camille Thinat ◽  
Stephan Züchner ◽  
Lee G. Fradkin ◽  
Hugues Lortat-Jacob ◽  
...  

AbstractThe remodeling of neurons is a conserved fundamental mechanism underlying nervous system maturation and function. Astrocytes can clear neuronal debris and they have an active role in neuronal remodeling. Developmental axon pruning ofDrosophilamemory center neurons occurs via a degenerative process mediated by infiltrating astrocytes. However, how astrocytes are recruited to the axons during brain development is unclear. Using an unbiased screen, we identify the gene requirement oforion, encoding for a chemokine-like protein, in the developing mushroom bodies. Functional analysis shows that Orion is necessary for both axonal pruning and removal of axonal debris. Orion performs its functions extracellularly and bears some features common to chemokines, a family of chemoattractant cytokines. We propose that Orion is a neuronal signal that elicits astrocyte infiltration and astrocyte-driven axonal engulfment required during neuronal remodeling in theDrosophiladeveloping brain.


2021 ◽  
Author(s):  
Oded Mayseless ◽  
El-Yazid Rachad ◽  
Gal Shapira ◽  
Andre Fiala ◽  
Oren Schuldiner

Postnatal refinement of neuronal connectivity shapes the mature nervous system. Pruning of exuberant connections involves both cell autonomous and non-cell autonomous mechanisms, such as neuronal activity. While the role of neuronal activity in the plasticity of excitatory synapses has been extensively studied, the involvement of inhibition is less clear. Furthermore, the role of activity during stereotypic developmental remodeling, where competition is not as apparent, is not well understood. Here we use the Drosophila mushroom body as a model to show that regulated silencing of neuronal activity is required for developmental axon pruning of the γ-Kenyon cells. We demonstrate that silencing neuronal activity is mechanistically achieved by cell autonomous expression of the inward rectifying potassium channel (irk1) combined with inhibition by the GABAergic APL neuron. These results support the Hebbian-like rule 'use it or lose it', where inhibition can destabilize connectivity and promote pruning while excitability stabilizes existing connections.


2017 ◽  
Author(s):  
Ching-Po Yang ◽  
Tamsin J. Samuels ◽  
Yaling Huang ◽  
Lu Yang ◽  
David Ish-Horowicz ◽  
...  

AbstractTiming of Drosophila neuroblast decommissioning is controlled in a lineage-specific manner. Following a prepupal ecdysone pulse, the ecdysone receptor and mediator complex cause neuroblasts to shrink. Shrinking is followed by nuclear accumulation of Prospero and cell cycle exit. Only mushroom body (MB) neuroblasts escape early pupal termination. Here, we demonstrate that the opposing temporal gradients of Imp and Syp RNA-binding proteins that govern temporal fate also regulate neuroblast decommissioning. The Imp gradient declines slower in MB neuroblasts so they still express Imp when it is absent from others. The presence of Imp in MB neuroblasts prevents decommissioning partly through inhibiting the mediator complex. Moreover, a timely induction of Imp can protect many non-MB neuroblasts from aging. We also show that the increasing Syp gradient permits Prospero accumulation and neuroblast termination. Together our results reveal that progeny temporal fate and progenitor decommissioning are co-regulated in protracted neuronal lineages.


Development ◽  
2012 ◽  
Vol 139 (18) ◽  
pp. 3392-3401 ◽  
Author(s):  
N. T. Takaesu ◽  
M. J. Stinchfield ◽  
K. Shimizu ◽  
M. Arase ◽  
J. C. Quijano ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (1) ◽  
pp. e86178 ◽  
Author(s):  
Yaniv Hakim ◽  
Shiri P. Yaniv ◽  
Oren Schuldiner
Keyword(s):  

2021 ◽  
Vol 14 ◽  
Author(s):  
Mengying Yang ◽  
Yige Guo ◽  
Shuran Wang ◽  
Changyan Chen ◽  
Yung-Heng Chang ◽  
...  

Protein homeostasis serves as an important step in regulating diverse cellular processes underlying the function and development of the nervous system. In particular, the ubiquitination proteasome system (UPS), a universal pathway mediating protein degradation, contributes to the development of numerous synaptic structures, including the Drosophila olfactory-associative learning center mushroom body (MB), thereby affecting associated function. Here, we describe the function of a newly characterized Drosophila F-box protein CG5003, an adaptor for the RING-domain type E3 ligase (SCF complex), in MB development. Lacking CG5003 ubiquitously causes MB γ axon pruning defects and selective CG5003 expression in pan-neurons leads to both γ axon and α/β lobe abnormalities. Interestingly, change in CG5003 expression in MB neurons does not cause any abnormalities in axons, suggesting that CG5003 functions in cells extrinsic to MB to regulate its development. Mass spectrum analysis indicates that silencing CG5003 expression in all neurons affects expression levels of proteins in the cell and structural morphogenesis, transcription regulator activity, and catalytic activity. Our findings reinforce the importance of UPS and identify a new factor in regulating neuronal development as exemplified by the synaptic structure MB.


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