Drug-Induced Haploinsufficiency of Fission Yeast Provides a powerful Tool for Identification of Drug Targets

Genome-wide systematic deletion mutants were generated using a PCR-based targeted mutgenesis of Schizosaccharomyces pombe. In a drug-sensitivity assay using thiabendazole, an inhibitor of microutubule assembly, a heterozygous nda2 mutant, deleting one copy of nda2 encoding the microtubule subunit al...

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Veröffentlicht in:Journal of microbiology and biotechnology 2003, 13(2), , pp.317-320
Hauptverfasser: Park, J.Y, Jang, Y.J, You, S.J, Kil, Y.S, Kang, E.J, Ahn, J.H, Ryoo, Y.K, Lee, M.Y, Song, K.B, Hoe, K.L, Chung, K.S, Kim, D.U, Yoo, H.S, Won, M.S. (KRIBB, Daejeon, Republic of Korea), Park, S.Y., Lee, H.J, Kim, J.Y, Kim, S.H. (DNA Chip Team, Daejon, Republic of Korea), Yang, W.S., Park, H.M, Chung, Y.I. (Chungnam National University, Daejeon, Republic of Korea), Kim, H.B. (Korea University, Seoul, Republic of Korea)
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Sprache:eng
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Zusammenfassung:Genome-wide systematic deletion mutants were generated using a PCR-based targeted mutgenesis of Schizosaccharomyces pombe. In a drug-sensitivity assay using thiabendazole, an inhibitor of microutubule assembly, a heterozygous nda2 mutant, deleting one copy of nda2 encoding the microtubule subunit alpha1 demonstrated a distinct sensitivity to TBZ, indicating TBZ- induced haploinsufficiency. This result suggests that profiling drug-induced haploinsufficiency can be exploited to identify target genes for drugs and discover new drugs
ISSN:1017-7825