TY - JOUR
T1 - Establishment of a tissue-specific RNAi system in C. elegans
AU - Qadota, Hiroshi
AU - Inoue, Makiko
AU - Hikita, Takao
AU - Köppen, Mathias
AU - Hardin, Jeffrey D.
AU - Amano, Mutsuki
AU - Moerman, Donald G.
AU - Kaibuchi, Kozo
N1 - Funding Information:
We thank Dr. Alan Coulson for cosmids and YAC clones; Dr. Yuji Kohara for cDNA clones; Dr. Andy Fire for vectors; Dr. Robert H. Waterston for MH27 antibody; Drs. Hiroaki Tabara and Craig Mello for the rde-1 strain and cDNA; Fumie Nishimura for technical assistance; Katsuhisa Kasuya for discussions; Dr. Shinya Kuroda and THE TEAM for helpful discussion. We also thank Dr. Ken Norman and Dr. Guy Benian for critical reading of this manuscript. Some of the strains used in this work were provided by the Caenorhabditis elegans Genetics Center, which is funded by the National Institutes of Health (NIH) Center for Research Resources. H. Q., M. A., and K. K. were supported by grants-in-aid for Scientific Research from the Ministry of Education, Science, and Culture, Japan, by the Japan Society of the Promotion of Science Research for the Future, by the Human Frontier Science Program. M.K and J.H. were supported by NIH grant GM058038.
PY - 2007/10/1
Y1 - 2007/10/1
N2 - In C. elegans, mosaic analysis is a powerful genetic tool for determining in which tissue or specific cells a gene of interest is required. For traditional mosaic analysis, a loss-of-function mutant and a genomic fragment that can rescue the mutant phenotype are required. Here we establish an easy and rapid mosaic system using RNAi (RNA mediated interference), using a rde-1 mutant that is resistant to RNAi. Tissue-specific expression of the wild type rde-1 cDNA in rde-1 mutants limits RNAi sensitivity to a specific tissue. We established hypodermal-and muscle-specific RNAi systems by expressing rde-1 cDNA under the control of the lin-26 and hlh-1 promoters, respectively. We confirmed tissue-specific RNAi using two assays: (1) tissue-specific knockdown of GFP expression, and (2) phenocopy of mutations in essential genes that were previously known to function in a tissue-specific manner. We also applied this system to an essential gene, ajm-1, expressed in hypodermis and gut, and show that lethality in ajm-1 mutants is due to loss of expression in hypodermal cells. Although we demonstrate tissue-specific RNAi in hypodermis and muscle, this method could be easily applied to other tissues.
AB - In C. elegans, mosaic analysis is a powerful genetic tool for determining in which tissue or specific cells a gene of interest is required. For traditional mosaic analysis, a loss-of-function mutant and a genomic fragment that can rescue the mutant phenotype are required. Here we establish an easy and rapid mosaic system using RNAi (RNA mediated interference), using a rde-1 mutant that is resistant to RNAi. Tissue-specific expression of the wild type rde-1 cDNA in rde-1 mutants limits RNAi sensitivity to a specific tissue. We established hypodermal-and muscle-specific RNAi systems by expressing rde-1 cDNA under the control of the lin-26 and hlh-1 promoters, respectively. We confirmed tissue-specific RNAi using two assays: (1) tissue-specific knockdown of GFP expression, and (2) phenocopy of mutations in essential genes that were previously known to function in a tissue-specific manner. We also applied this system to an essential gene, ajm-1, expressed in hypodermis and gut, and show that lethality in ajm-1 mutants is due to loss of expression in hypodermal cells. Although we demonstrate tissue-specific RNAi in hypodermis and muscle, this method could be easily applied to other tissues.
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U2 - 10.1016/j.gene.2007.06.020
DO - 10.1016/j.gene.2007.06.020
M3 - Article
C2 - 17681718
AN - SCOPUS:34548013965
SN - 0378-1119
VL - 400
SP - 166
EP - 173
JO - Gene
JF - Gene
IS - 1-2
ER -