TY - JOUR
T1 - A large-scale screen reveals genes that mediate electrotaxis in Dictyostelium discoideum
AU - Gao, Runchi
AU - Zhao, Siwei
AU - Jiang, Xupin
AU - Sun, Yaohui
AU - Zhao, Sanjun
AU - Gao, Jing
AU - Borleis, Jane
AU - Willard, Stacey
AU - Tang, Ming
AU - Cai, Huaqing
AU - Kamimura, Yoichiro
AU - Huang, Yuesheng
AU - Jiang, Jianxin
AU - Huang, Zunxi
AU - Mogilner, Alex
AU - Pan, Tingrui
AU - Devreotes, Peter N.
AU - Zhao, Min
N1 - Publisher Copyright:
Copyright © 2015 by the American Association for the Advancement of Science.
PY - 2015/5/26
Y1 - 2015/5/26
N2 - Directional cell migration in an electric field, a phenomenon called galvanotaxis or electrotaxis, occurs in many types of cells, and may play an important role in wound healing and development. Small extracellular electric fields can guide the migration of amoeboid cells, and we established a large-scale screening approach to search for mutants with electrotaxis phenotypes from a collection of 563 Dictyostelium discoideum strains with morphological defects. We identified 28 strains that were defective in electrotaxis and 10 strains with a slightly higher directional response. Using plasmid rescue followed by gene disruption, we identified some of the mutated genes, including some previously implicated in chemotaxis. Among these, we studied PiaA, which encodes a critical component of TORC2, a kinase protein complex that transduces changes in motility by activating the kinase PKB (also known as Akt). Furthermore, we found that electrotaxis was decreased in mutants lacking gefA, rasC, rip3, lst8, or pkbR1, genes that encode other components of the TORC2-PKB pathway. Thus, we have developed a high-throughput screening technique that will be a useful tool to elucidate the molecular mechanisms of electrotaxis.
AB - Directional cell migration in an electric field, a phenomenon called galvanotaxis or electrotaxis, occurs in many types of cells, and may play an important role in wound healing and development. Small extracellular electric fields can guide the migration of amoeboid cells, and we established a large-scale screening approach to search for mutants with electrotaxis phenotypes from a collection of 563 Dictyostelium discoideum strains with morphological defects. We identified 28 strains that were defective in electrotaxis and 10 strains with a slightly higher directional response. Using plasmid rescue followed by gene disruption, we identified some of the mutated genes, including some previously implicated in chemotaxis. Among these, we studied PiaA, which encodes a critical component of TORC2, a kinase protein complex that transduces changes in motility by activating the kinase PKB (also known as Akt). Furthermore, we found that electrotaxis was decreased in mutants lacking gefA, rasC, rip3, lst8, or pkbR1, genes that encode other components of the TORC2-PKB pathway. Thus, we have developed a high-throughput screening technique that will be a useful tool to elucidate the molecular mechanisms of electrotaxis.
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U2 - 10.1126/scisignal.aab0562
DO - 10.1126/scisignal.aab0562
M3 - Article
C2 - 26012633
AN - SCOPUS:84929901375
SN - 1945-0877
VL - 8
JO - Science signaling
JF - Science signaling
IS - 378
ER -