Developmental cell death in Dictyostelium does not require paracaspase

被引:61
作者
Roisin-Bouffay, C
Luciani, MF
Klein, G
Levraud, JP
Adam, M
Golstein, P
机构
[1] Univ Mediterranie, Ctr Immunol Marseille Luminy, CNRS, INSERM, F-13288 Marseille 9, France
[2] Comm Energie Atom Grenobel, Lab Biochim & Biophys Syst Integres, F-38054 Grenoble 9, France
[3] Inst Pasteur, Unite Postulante Macrophages & Dev Immun, F-75724 Paris 15, France
关键词
D O I
10.1074/jbc.M312741200
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
Apoptotic cell death often requires caspases. Caspases are part of a family of related molecules including also paracaspases and metacaspases. Are molecules of this family generally involved in cell death? More specifically, do non-apoptotic caspase-independent types of cell death require paracaspases or metacaspases? Dictyostelium discoideum lends itself well to answering these questions because 1) it undergoes non-apoptotic developmental cell death of a vacuolar autophagic type and 2) it bears neither caspase nor metacaspase genes and apparently only one paracaspase gene. This only paracaspase gene can be inactivated by homologous recombination. Paracaspase-null clones were thus obtained in each of four distinct Dictyostelium strains. These clones were tested in two systems, developmental stalk cell death in vivo and vacuolar autophagic cell death in a monolayer system mimicking developmental cell death. Compared with parent cells, all of the paracaspase-null cells showed unaltered cell death in both test systems. In addition, paracaspase inactivation led to no alteration in development or interaction with a range of bacteria. Thus, in Dictyostelium, vacuolar programmed cell death in development and in a monolayer model in vitro would seem not to require paracaspase. To our knowledge, this is the first instance of developmental programmed cell death shown to be independent of any caspase, paracaspase or metacaspase. These results have implications as to the relationship in evolution between cell death and the caspase family.
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页码:11489 / 11494
页数:6
相关论文
共 28 条
[1]   Ways of dying: multiple pathways to apoptosis [J].
Adams, JM .
GENES & DEVELOPMENT, 2003, 17 (20) :2481-2495
[2]   Classification of the caspase-hemoglobinase fold: Detection of new families and implications for the origin of the eukaryotic separins [J].
Aravind, L ;
Koonin, EV .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2002, 46 (04) :355-367
[3]   A kingdom-level phylogeny of eukaryotes based on combined protein data [J].
Baldauf, SL ;
Roger, AJ ;
Wenk-Siefert, I ;
Doolittle, WF .
SCIENCE, 2000, 290 (5493) :972-977
[4]  
CORNILLON S, 1994, J CELL SCI, V107, P2691
[5]   MOLECULAR COMPLEMENTATION OF A GENETIC-MARKER IN DICTYOSTELIUM USING A GENOMIC DNA LIBRARY [J].
DYNES, JL ;
FIRTEL, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (20) :7966-7970
[6]   Crawling into a new era -: the Dictyostelium genome project [J].
Eichinger, L ;
Noegel, AA .
EMBO JOURNAL, 2003, 22 (09) :1941-1946
[7]   GENETIC-CONTROL OF PROGRAMMED CELL-DEATH IN THE NEMATODE C-ELEGANS [J].
ELLIS, HM ;
HORVITZ, HR .
CELL, 1986, 44 (06) :817-829
[8]   PROTEASE ACTIVITY DURING CELL-DIFFERENTIATION OF CELLULAR SLIME-MOLD DICTYOSTELIUM-DISCOIDEUM [J].
FONG, D ;
RUTHERFORD, CL .
JOURNAL OF BACTERIOLOGY, 1978, 134 (02) :521-527
[9]   Cell-death alternative model organisms: Why and which? [J].
Golstein, P ;
Aubry, L ;
Levraud, JP .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (10) :798-807
[10]   ANALYSIS OF G-ALPHA-4, A G-PROTEIN SUBUNIT REQUIRED FOR MULTICELLULAR DEVELOPMENT IN DICTYOSTELIUM [J].
HADWIGER, JA ;
FIRTEL, RA .
GENES & DEVELOPMENT, 1992, 6 (01) :38-49