Ling Xuemei, Huang Qinzhu, Xu Yanqin, Jin Yuxiao, Feng Ying, Shi Weijie, Ye Xiaolei, Lin Yi, Hou Ling, Lin Xinhua
School of Optometry and Ophthalmology and Eye Hospital, Wenzhou Medical University, Zhejiang, China.
Taizhou Hospital of Zhejiang Province, Wenzhou Medical University, Linhai, Zhejiang, China.
FEBS Lett. 2017 Mar;591(6):875-888. doi: 10.1002/1873-3468.12580. Epub 2017 Mar 6.
Usp5 belongs to the USP family of deubiquitinating enzymes (DUBs), which comprises the largest class of DUBs. We previously reported that loss of Usp5 impairs development of photoreceptors in Drosophila eyes, although the detailed mechanism remained unclear. In the present study, we demonstrate that Usp5 regulates both Notch and receptor tyrosine kinase (RTK) signaling. Loss of Usp5 results in upregulation of Notch signaling and downregulation of RTK signaling, leading to impaired photoreceptor development. Moreover, genetic rescue experiments with the DNA binding protein Suppressor of Hairless or Notch RNAi indicate that they mediate the regulation of RTK signaling by Usp5. The present study provides mechanistic insight into how Usp5 regulates photoreceptor differentiation by Notch and RTK signaling in the Drosophila eye.
Usp5属于去泛素化酶(DUBs)的USP家族,该家族是最大的DUBs类别。我们之前报道过,Usp5的缺失会损害果蝇眼睛中光感受器的发育,尽管具体机制仍不清楚。在本研究中,我们证明Usp5调节Notch和受体酪氨酸激酶(RTK)信号通路。Usp5的缺失导致Notch信号通路上调和RTK信号通路下调,从而导致光感受器发育受损。此外,用DNA结合蛋白无毛抑制因子或Notch RNA干扰进行的基因拯救实验表明,它们介导了Usp5对RTK信号通路的调节。本研究为Usp5如何通过Notch和RTK信号通路调节果蝇眼睛中的光感受器分化提供了机制上的见解。