scholarly journals Silver nanoparticles disrupt germline stem cell maintenance in the Drosophila testis

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Cynthia Ong ◽  
Qian Ying Lee ◽  
Yu Cai ◽  
Xiaoli Liu ◽  
Jun Ding ◽  
...  
Development ◽  
2013 ◽  
Vol 141 (1) ◽  
pp. 73-82 ◽  
Author(s):  
A. R. Shields ◽  
A. C. Spence ◽  
Y. M. Yamashita ◽  
E. L. Davies ◽  
M. T. Fuller

Development ◽  
2018 ◽  
Vol 145 (23) ◽  
pp. dev170639 ◽  
Author(s):  
Ferenc Jankovics ◽  
Melinda Bence ◽  
Rita Sinka ◽  
Anikó Faragó ◽  
László Bodai ◽  
...  

PLoS ONE ◽  
2020 ◽  
Vol 15 (12) ◽  
pp. e0243756
Author(s):  
Tianlu Ma ◽  
Shinya Matsuoka ◽  
Daniela Drummond-Barbosa

Reproduction is highly sensitive to changes in physiology and the external environment. Neuropeptides are evolutionarily conserved signaling molecules that regulate multiple physiological processes. However, the potential reproductive roles of many neuropeptide signaling pathways remain underexplored. Here, we describe the results of RNAi-based screens in Drosophila melanogaster to identify neuropeptides/neuropeptide receptors with potential roles in oogenesis. The screen read-outs were either the number of eggs laid per female per day over time or fluorescence microscopy analysis of dissected ovaries. We found that the orphan neuropeptide receptor encoded by moody (homologous to mammalian melatonin receptors) is likely required in somatic cells for normal egg production and proper germline stem cell maintenance. However, the egg laying screens had low signal-to-noise ratio and did not lead to the identification of additional candidates. Thus, although egg count assays might be useful for large-scale screens to identify oogenesis regulators that result in dramatic changes in oogenesis, more labor-intensive microscopy-based screen are better applicable for identifying new physiological regulators of oogenesis with more subtle phenotypes.


PLoS Genetics ◽  
2013 ◽  
Vol 9 (11) ◽  
pp. e1003903 ◽  
Author(s):  
Jose Rafael Morillo Prado ◽  
Shrividhya Srinivasan ◽  
Margaret T. Fuller

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