4.7 Article

The effector caspases drICE and dcp-1 have partially overlapping functions in the apoptotic pathway in Drosophila

期刊

CELL DEATH AND DIFFERENTIATION
卷 13, 期 10, 页码 1697-1706

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/sj.cdd.4401920

关键词

DrICE; Dcp-1; Drosophila; programmed cell death; Diap1; Dronc

资金

  1. NCI NIH HHS [CA16672, P30 CA016672] Funding Source: Medline
  2. NIGMS NIH HHS [R01 GM068016-03, R01 GM068016, GM068016] Funding Source: Medline

向作者/读者索取更多资源

Caspases are essential components of the apoptotic machinery in both vertebrates and invertebrates. Here, we report the isolation of a mutant allele of the Drosophila effector caspase drICE as a strong suppressor of hid- (head involution defective-) induced apoptosis. This mutant was used to determine the apoptotic role of drICE. Our data are consistent with an important function of drICE for developmental and irradiation-induced cell death. Epistatic analysis suggests that drICE acts genetically downstream of Drosophila inhibitor of apoptosis protein 1 (Diap1). However, although cell death is significantly reduced in drICE mutants in all assays, it is not completely blocked. A double-mutant analysis between drICE and death caspase-1 (dcp-1), another effector caspase, reveals that some cells (type I) strictly require drICE for apoptosis, whereas other cells (type II) require either drICE or dcp-1. Thus, these data demonstrate a barely appreciated complexity in the apoptotic pathway, and are consistent with current models about effector caspase regulation in both vertebrates and invertebrates.

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