Growth suppressor lingerer regulates bantam microRNA to restrict organ size

被引:8
作者
Dong, Liang [1 ]
Li, Jinhui [1 ]
Huang, Hongling [1 ]
Yin, Meng-Xin [1 ]
Xu, Jinjin [1 ]
Li, Peixue [1 ]
Lu, Yi [1 ]
Wu, Wenqing [1 ]
Yang, Hang [2 ]
Zhao, Yun [1 ,3 ]
Zhang, Lei [1 ,3 ]
机构
[1] Chinese Acad Sci, State Key Lab Cell Biol, Innovat Ctr Cell Signaling Network, Inst Biochem & Cell Biol,Shanghai Inst Biol Sci, Shanghai 200031, Peoples R China
[2] Dept Biochem & Mol Biol, Los Angeles, CA 90033 USA
[3] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
基金
中国国家自然科学基金;
关键词
lingerer; Hippo; Salvador; Yorkie; Mad; organ size control; bantam; HIPPO SIGNALING PATHWAY; CONTROLS TISSUE-GROWTH; CELL-CYCLE EXIT; TUMOR-SUPPRESSOR; PROMOTES APOPTOSIS; TEAD/TEF FAMILY; PROTEIN-KINASE; HUMAN CANCER; YAP PATHWAY; DROSOPHILA;
D O I
10.1093/jmcb/mjv045
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The evolutionarily conserved Hippo signaling pathway plays an important role in organ size control by regulating cell proliferation and apoptosis. Here, we identify Lingerer (Lig) as a growth suppressor using RNAi modifying screen in Drosophila melanogaster. Loss of lig increases organ size and upregulates bantam (ban) and the expression of the Hippo pathway target genes, while overexpression of lig results in diminished ban expression and organ size reduction. We demonstrate that Lig C-terminal exhibits dominant-negative function on growth and ban expression, and thus plays an important role in organ size control and ban regulation. In addition, we provide evidence that both Yki and Mad are essential for Lig-induced ban expression. We also show that Lig regulates the expression of the Hippo pathway target genes partially via Yorkie. Moreover, we find that Lig physically interacts with and requires Salvador to restrict cell growth. Taken together, we demonstrate that Lig functions as a critical growth suppressor to control organ size via ban and Hippo signaling.
引用
收藏
页码:415 / 428
页数:14
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