TY - JOUR
T1 - Hippo activation through homodimerization and membrane association for growth inhibition and organ size control
AU - Deng, Yaoting
AU - Matsui, Yurika
AU - Zhang, Yifan
AU - Lai, Zhi Chun
N1 - Funding Information:
We would like to thank the Bloomington Drosophila Stock Center (BDSC) and the Vienna Drosophila RNAi Center (VDRC) for fly strains, Dr. Avery August, Dr. George Halder, Dr. Ken Irvine, Dr. Nicolas Tapon, Dr. Helen McNeill for reagents, and the National Science Foundation for Grant support to (Z.-C.L.).
PY - 2013/3/15
Y1 - 2013/3/15
N2 - Hippo (Hpo) signaling plays a critical role in restricting tissue growth and organ size in both invertebrate and vertebrate animals. However, how the Hpo kinase is regulated during development has not been clearly understood. Using a Bimolecular Fluorescence Complementation assay, we have investigated the functional significance of Hpo homo-dimer formation and subcellular localization in living cells. We found that Hpo dimerization and membrane association are critical for its activation in growth inhibition. As dimerization facilitates Hpo to access its binding partner, Hpo kinases in the homo-dimer trans-phosphorylate each other to increase their enzymatic activity. Moreover, loss- and gain-of-function studies indicate that upstream regulators, Expanded, Merlin and Kibra, play a critical role in promoting Hpo dimerization as well as association to the cortical F-actin beneath the plasma membrane. Enforced Hpo localization to the plasma membrane increases Hpo dimerization and activity. Therefore, homo-dimerization and plasma membrane association are two important mechanisms for Hpo activation in growth control during animal development.
AB - Hippo (Hpo) signaling plays a critical role in restricting tissue growth and organ size in both invertebrate and vertebrate animals. However, how the Hpo kinase is regulated during development has not been clearly understood. Using a Bimolecular Fluorescence Complementation assay, we have investigated the functional significance of Hpo homo-dimer formation and subcellular localization in living cells. We found that Hpo dimerization and membrane association are critical for its activation in growth inhibition. As dimerization facilitates Hpo to access its binding partner, Hpo kinases in the homo-dimer trans-phosphorylate each other to increase their enzymatic activity. Moreover, loss- and gain-of-function studies indicate that upstream regulators, Expanded, Merlin and Kibra, play a critical role in promoting Hpo dimerization as well as association to the cortical F-actin beneath the plasma membrane. Enforced Hpo localization to the plasma membrane increases Hpo dimerization and activity. Therefore, homo-dimerization and plasma membrane association are two important mechanisms for Hpo activation in growth control during animal development.
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U2 - 10.1016/j.ydbio.2012.12.017
DO - 10.1016/j.ydbio.2012.12.017
M3 - Article
C2 - 23298890
AN - SCOPUS:84874237773
SN - 0012-1606
VL - 375
SP - 152
EP - 159
JO - Developmental biology
JF - Developmental biology
IS - 2
ER -