kep1 interacts genetically with dredd/caspase-8, and kep1 mutants alter the balance of dredd isoforms

被引:18
作者
Di Fruscio, M
Styhler, S
Wikholm, E
Boulanger, MC
Lasko, P
Richard, S
机构
[1] McGill Univ, Dept Biol, Montreal, PQ H3A 1B1, Canada
[2] Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, Terry Fox Mol Oncol Grp, Montreal, PQ H3T 1E2, Canada
[3] Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, Bloomfield Ctr Res Aging, Montreal, PQ H3T 1E2, Canada
[4] McGill Univ, Dept Oncol, Montreal, PQ H3T 1E2, Canada
[5] McGill Univ, Dept Med, Montreal, PQ H3T 1E2, Canada
[6] McGill Univ, Dept Microbiol, Montreal, PQ H3T 1E2, Canada
[7] McGill Univ, Dept Immunol, Montreal, PQ H3T 1E2, Canada
关键词
KH domain; apoptosis; Drosophila; caspases;
D O I
10.1073/pnas.0236048100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Drosophila kepi gene encodes an RNA binding protein related to the murine QUAKING apoptotic inducer. We have previously shown that kepi can induce apoptosis when transfected into different cell lines. To better define the role of Kep1 in apoptosis, we generated kep1 null flies. These flies were viable, but females displayed reduced fertility, with approximately half of the eggs laid from kep1- homozygotes failing to hatch. In addition, loss of kep1 suppressed GMR-rpr-mediated apoptosis in the Drosophila eye, and kep1 mutant flies had increased susceptibility to Escherichia coli infection. We found that Kep1 bound dredd RNA in vitro, and that extracts prepared from kep1 mutant ovaries had markedly reduced proteolytic cleavage activity toward the caspase-8 target substrate IETD-7-amino-4-trifluoromethyl coumarin. We observed increased levels of the beta isoform of dredd mRNA in kep1 mutants as compared with wild-type. Taken together, our results suggest that Kep1 regulates apoptosis by influencing the processing of dredd RNA.
引用
收藏
页码:1814 / 1819
页数:6
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