Fleming JA, et al. (2002) Complementary whole-genome technologies reveal the cellular response to proteasome inhibition by PS-341. Proc Natl Acad Sci U S A 99(3):1461-6
Abstract: Although the biochemical targets of most drugs are known, the biological consequences of their actions are typically less well understood. In this study, we have used two whole-genome technologies in Saccharomyces cerevisiae to determine the cellular impact of the proteasome inhibitor PS-341. By combining population genomics, the screening of a comprehensive panel of bar-coded mutant strains, and transcript profiling, we have identified the genes and pathways most affected by proteasome inhibition. Many of these function in regulated protein degradation or a subset of mitotic activities. In addition, we identified Rpn4p as the transcription factor most responsible for the cell's ability to compensate for proteasome inhibition. Used together, these complementary technologies provide a general and powerful means to elucidate the cellular ramifications of drug treatment.
| Status: Published | Type: Journal Article | PubMed ID: 11830665 |
Topics addressed in this paper
Number of different genes curated to this paper: 61
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| APN1 | ATG17 | BEM4 | BIK1 | CCR4 | CDC26 | CHL1 | CHL4 | CLB2 | CLB5 | ||
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| CSM3 | CTF19 | CTF8 | DCC1 | DOA4 | ERG2 | ERG3 | ERG4 | FYV7 | GET2 | |
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| HNT3 | HTA1 | IDP1 | IML3 | IRC15 | LTE1 | MCM21 | NEM1 | NUP2 | PDR5 | |
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| Topics | Genes linked to topics (#31 - 40 ) | |||||||||
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| PFD1 | PRE9 | PRO1 | RAD50 | RAD51 | RIC1 | RPN10 | RPN4 | RTT107 | SAP30 | |
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| SCP160 | SHE1 | SIC1 | SIN3 | SNF2 | SNQ2 | SPO7 | SRC1 | SWI3 | SWM1 | |
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| TOF1 | TUB3 | UBX2 | VAC14 | VAM3 | VIK1 | VPS61 | WHI3 | YAP1 | YME1 | |
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| Topics | Genes linked to topics (#61 ) |
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| YPT6 | |
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