Dictyostelium discoideum-a model for many reasons

被引:111
作者
Annesley, Sarah J. [1 ]
Fisher, Paul R. [1 ]
机构
[1] La Trobe Univ, Dept Microbiol, Bundoora, Vic 3086, Australia
关键词
Dictyostelium; Chemotaxis; Actin cytoskeleton; Legionella; Intracellular pathogen; Mitochondrial disease; Neurological disease; NDPK; NUCLEOSIDE DIPHOSPHATE KINASE; ACTIVATED PROTEIN-KINASE; PATHWAYS MEDIATING CHEMOTAXIS; FREE POLYUBIQUITIN CHAINS; X-RAY-STRUCTURE; MITOCHONDRIAL DISEASE; SIGNAL-TRANSDUCTION; CELL MOTILITY; SOCIAL AMEBA; SWISS-MODEL;
D O I
10.1007/s11010-009-0111-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The social amoeba or cellular slime mould Dictyostelium discoideum is a "professional" phagocyte that has long been recognized for its value as a biomedical model organism, particularly in studying the actomyosin cytoskeleton and chemotactic motility in non-muscle cells. The complete genome sequence of D. discoideum is known, it is genetically tractable, readily grown clonally as a eukaryotic microorganism and is highly accessible for biochemical, cell biological and physiological studies. These are the properties it shares with other microbial model organisms. However, Dictyostelium combines these with a unique life style, with motile unicellular and multicellular stages, and multiple cell types that offer for study an unparalleled variety of phenotypes and associated signalling pathways. These advantages have led to its recent emergence as a valuable model organism for studying the molecular pathogenesis and treatment of human disease, including a variety of infectious diseases caused by bacterial and fungal pathogens. Perhaps surprisingly, this organism, without neurons or brain, has begun to yield novel insights into the cytopathology of mitochondrial diseases as well as other genetic and idiopathic disorders affecting the central nervous system. Dictyostelium has also contributed significantly to our understanding of NDP kinase, as it was the Dictyostelium enzyme whose structure was first determined and related to enzymatic activity. The phenotypic richness and tractability of Dictyostelium should provide a fertile arena for future exploration of NDPK's cellular roles.
引用
收藏
页码:73 / 91
页数:19
相关论文
共 158 条
[51]   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
[52]   SWISS-MODEL and the Swiss-PdbViewer: An environment for comparative protein modeling [J].
Guex, N ;
Peitsch, MC .
ELECTROPHORESIS, 1997, 18 (15) :2714-2723
[53]   Dictyostelium discoideum:: a new host model system for intracellular pathogens of the genus Legionella [J].
Hägele, S ;
Köhler, R ;
Merkert, H ;
Schleicher, M ;
Hacker, J ;
Steinert, M .
CELLULAR MICROBIOLOGY, 2000, 2 (02) :165-171
[54]   AMP-activated protein kinase: the energy charge hypothesis revisited [J].
Hardie, DG ;
Hawley, SA .
BIOESSAYS, 2001, 23 (12) :1112-1119
[55]   The AMP-activated protein kinase pathway - new players upstream and downstream [J].
Hardie, DG .
JOURNAL OF CELL SCIENCE, 2004, 117 (23) :5479-5487
[56]   AMPK: A key sensor of fuel and energy status in skeletal muscle [J].
Hardie, DG ;
Sakamoto, K .
PHYSIOLOGY, 2006, 21 :48-60
[57]   Search for a common mechanism of mood stabilizers [J].
Harwood, AJ ;
Agam, G .
BIOCHEMICAL PHARMACOLOGY, 2003, 66 (02) :179-189
[58]  
HAYASHI T, 2000, DIABETES, V49, P1
[59]   Chemotaxis in the absence of PIP3 gradients [J].
Hoeller, Oliver ;
Kay, Robert R. .
CURRENT BIOLOGY, 2007, 17 (09) :813-817
[60]   ULTRASTRUCTURE OF SPORE DIFFERENTIATION IN DICTYOSTELIUM - PRESPORE VACUOLE [J].
HOHL, HR ;
HAMAMOTO, ST .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1969, 26 (5-6) :442-&