The CASBAH:: a searchable database of caspase substrates

被引:306
作者
Luthi, A. U. [1 ]
Martin, S. J. [1 ]
机构
[1] Trinity Coll Dublin, Mol Cell Biol Lab, Smurfit Inst Genet, Dept Genet, Dublin 2, Ireland
基金
爱尔兰科学基金会;
关键词
apoptosis; caspases; caspase substrates; degradome; proteome;
D O I
10.1038/sj.cdd.4402103
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
Apoptosis is coordinated by members of the caspase family of aspartic acid-specific proteases. Other members of this protease family also play essential roles in inflammation where they participate in the maturation of pro-inflammatory cytokines. To date, almost 400 substrates for the apoptosis-associated caspases have been reported and there are likely to be hundreds more yet to be discovered. Thus, the fraction of the proteome that is degraded (the degradome) by caspases during the demolition phase of apoptosis appears to be quite substantial. Despite this, we still know surprisingly little concerning how caspases provoke some of the signature events in apoptosis, such as membrane phosphatidylserine externalization, cellular retraction, chromatin condensation and apoptotic body production. The inflammatory caspases appear to be much more specific proteases than those involved in apoptosis and only two confirmed substrates for these proteases have been described to date. Here, we have compiled a comprehensive list of caspase substrates and describe a searchable web resource (The Casbah; www.casbah.ie) which contains information pertaining to all currently known caspase substrates. We also discuss some of the unresolved issues relating to caspase-dependent events in apoptosis and inflammation.
引用
收藏
页码:641 / 650
页数:10
相关论文
共 57 条
[1]   The mitochondrial apoptosome: a killer unleashed by the cytochrome seas [J].
Adrain, C ;
Martin, SJ .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (06) :390-397
[2]   Apoptosomes: protease activation platforms to die from [J].
Adrain, Colin ;
Brumatti, Gabriela ;
Martin, Seamus J. .
TRENDS IN BIOCHEMICAL SCIENCES, 2006, 31 (05) :243-247
[3]   Apaf1 (CED-4 homolog) regulates programmed cell death in mammalian development [J].
Cecconi, F ;
Alvarez-Bolado, G ;
Meyer, BI ;
Roth, KA ;
Gruss, P .
CELL, 1998, 94 (06) :727-737
[4]   The apical caspase dronc governs programmed and unprogrammed cell death in Drosophila [J].
Chew, SK ;
Akdemir, F ;
Chen, P ;
Lu, WJ ;
Mills, K ;
Daish, T ;
Kumar, S ;
Rodriguez, A ;
Abrams, JM .
DEVELOPMENTAL CELL, 2004, 7 (06) :897-907
[5]  
Chipuk JE, 2005, NAT REV MOL CELL BIO, V6, P268, DOI [10.1038/nrm1573, 10.1038/nrm2239]
[6]   Membrane blebbing during apoptosis results from caspase-mediated activation of ROCK I [J].
Coleman, ML ;
Sahai, EA ;
Yeo, M ;
Bosch, M ;
Dewar, A ;
Olson, MF .
NATURE CELL BIOLOGY, 2001, 3 (04) :339-345
[7]  
COTTER TG, 1992, CANCER RES, V52, P997
[8]   Caspase-6 is the direct activator of caspase-8 in the cytochrome c-induced apoptosis pathway:: Absolute requirement for removal of caspase-6 prodomain [J].
Cowling, V ;
Downward, J .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (10) :1046-1056
[9]   Actin-myosin-based contraction is responsible for apoptotic nuclear disintegration [J].
Croft, DR ;
Coleman, ML ;
Li, SX ;
Robertson, D ;
Sullivan, T ;
Stewart, CL ;
Olson, MF .
JOURNAL OF CELL BIOLOGY, 2005, 168 (02) :245-255
[10]   Drosophila caspase DRONC is required for specific developmental cell death pathways and stress-induced apoptosis [J].
Daish, TJ ;
Mills, K ;
Kumar, S .
DEVELOPMENTAL CELL, 2004, 7 (06) :909-915