DECAY, a novel Drosophila caspase related to mammalian caspase-3 and caspase-7

被引:105
|
作者
Dorstyn, L
Read, SH
Quinn, LM
Richardson, H
Kumar, S
机构
[1] Inst Med & Vet Sci, Hanson Ctr Canc Res, Adelaide, SA 5000, Australia
[2] Univ Adelaide, Dept Genet, Adelaide, SA 5001, Australia
[3] Univ Adelaide, Dept Med, Adelaide, SA 5001, Australia
关键词
D O I
10.1074/jbc.274.43.30778
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Caspases are key effecters of programmed cell death in metazoans. In Drosophila, four caspases have been described so far. Here we describe the identification and characterization of the fifth Drosophila caspase, DECAY. DECAY shares a high degree of homology with the members of the mammalian caspase-3 subfamily, particularly caspase-3 and caspase-7, DECAY lacks a long prodomain and thus appears to be a class II effector caspase;Ectopic expression of DECAY in cultured cells induces apoptosis. Recombinant DECAY exhibited substrate specificity similar to the mammalian caspase-3 subfamily. Low levels of decay mRNA are ubiquitously expressed in Drosophila embryos during early stages of development but its expression becomes somewhat spatially restricted in some tissues. During oogenesis decay mRNA was detected in egg chambers of all stages consistent with a rob for DECAY in apoptosis of nurse cells, Relatively high levels of decay mRNA are expressed in larval salivary glands and midgut, two tissues which undergo histolysis during larval/pupal metamorphosis, suggesting that DECAY may play a role in developmentally programmed cell death in Drosophila.
引用
收藏
页码:30778 / 30783
页数:6
相关论文
共 50 条
  • [1] DECAY, a novel Drosophila caspase related to mammalian caspase-3 and caspase-7 (vol 274, pg 30778, 1999)
    Dorstyn, L
    Read, SH
    Quinn, LM
    Richardson, H
    Kumar, S
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (20) : 15600 - 15600
  • [3] Executioner caspase-3 and caspase-7 are functionally distinct proteases
    Walsh, John G.
    Cullen, Sean P.
    Sheridan, Clare
    Luethi, Alexander U.
    Gerner, Christopher
    Martin, Seamus J.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (35) : 12815 - 12819
  • [4] Vasculogenic mimicry: Possible role of effector caspase-3, caspase-6 and caspase-7
    Linder, Manuel
    Tschernig, Thomas
    [J]. ANNALS OF ANATOMY-ANATOMISCHER ANZEIGER, 2016, 204 : 114 - 117
  • [5] Caspase-9, caspase-3 and caspase-7 have distinct roles during intrinsic apoptosis
    Brentnall, Matthew
    Rodriguez-Menocal, Luis
    De Guevara, Rebeka Ladron
    Cepero, Enrique
    Boise, Lawrence H.
    [J]. BMC CELL BIOLOGY, 2013, 14
  • [6] Caspase-9, caspase-3 and caspase-7 have distinct roles during intrinsic apoptosis
    Matthew Brentnall
    Luis Rodriguez-Menocal
    Rebeka Ladron De Guevara
    Enrique Cepero
    Lawrence H Boise
    [J]. BMC Cell Biology, 14
  • [7] Conformational similarity in the activation of caspase-3 and -7 revealed by the unliganded and inhibited structures of caspase-7
    Johnson Agniswamy
    Bin Fang
    Irene T. Weber
    [J]. Apoptosis, 2009, 14 : 1135 - 1144
  • [8] Immunoreactivity to caspase-3, caspase-7, caspase-8, and caspase-9 forms is frequently lost in human prostate tumors
    Rodriguez-Berriguete, Gonzalo
    Galvis, Laura
    Fraile, Benito
    de Bethencourt, Fermin R.
    Martinez-Onsurbe, Pilar
    Olmedilla, Gabriel
    Paniagua, Ricardo
    Royuela, Mar
    [J]. HUMAN PATHOLOGY, 2012, 43 (02) : 229 - 237
  • [9] Conformational similarity in the activation of caspase-3 and-7 revealed by the unliganded and inhibited structures of caspase-7
    Agniswamy, Johnson
    Fang, Bin
    Weber, Irene T.
    [J]. APOPTOSIS, 2009, 14 (10) : 1135 - 1144
  • [10] Eliminating caspase-7 and cathepsin B cross-reactivity on fluorogenic caspase-3 substrates
    Mackay, Martha
    Perez-Lopez, Ana M.
    Bradley, Mark
    Lilienkampf, Annamaria
    [J]. MOLECULAR BIOSYSTEMS, 2016, 12 (03) : 693 - 696