Phylogeny and Function of the Invertebrate p53 Superfamily

被引:80
作者
Rutkowski, Rachael [1 ]
Hofmann, Kay [2 ]
Gartner, Anton [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Wellcome Trust Ctr Gene Regulat & Express, Dundee DD1 5EH, Scotland
[2] Miltenyi Biotec GmbH, Bioinformat Grp, D-51429 Bergisch Gladbach, Germany
关键词
DAMAGE-INDUCED APOPTOSIS; NUCLEOTIDE EXCISION-REPAIR; CAENORHABDITIS-ELEGANS P53; PRIMORDIAL GERM-CELLS; TUMOR-SUPPRESSOR P53; DNA-DAMAGE; C-ELEGANS; DROSOPHILA-MELANOGASTER; LIFE-SPAN; P53-DEPENDENT APOPTOSIS;
D O I
10.1101/cshperspect.a001131
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The origin of the p53 superfamily predates animal evolution and first appears in unicellular Flagellates. Invertebrate p53 superfamily members appear to have a p63-like domain structure, which seems to be evolutionarily ancient. The radiation into p53, p63, and p73 proteins is a vertebrate invention. In invertebrate models amenable to genetic analysis p53 superfamily members mainly act in apoptosis regulation in response to genotoxic agents and do not have overt developmental functions. We summarize the literature on cnidarian and mollusc p53 superfamily members and focus on the function and regulation of Drosophila melanogaster and Caenorhabditis elegans p53 superfamily members in triggering apoptosis. Furthermore, we examine the emerging evidence showing that invertebrate p53 superfamily proteins also have functions unrelated to apoptosis, such as DNA repair, cell cycle checkpoint responses, compensatory proliferation, aging, autophagy, and innate immunity.
引用
收藏
页数:13
相关论文
共 78 条
[41]   A Novel Role for the SMG-1 Kinase in Lifespan and Oxidative Stress Resistance in Caenorhabditis elegans [J].
Masse, Ingrid ;
Molin, Laurent ;
Mouchiroud, Laurent ;
Vanhems, Philippe ;
Palladino, Francesca ;
Billaud, Marc ;
Solari, Florence .
PLOS ONE, 2008, 3 (10)
[42]   Modification of Drosophila p53 by SUMO modulates its transactivation and pro-apoptotic functions [J].
Mauri, Federico ;
McNamee, Laura M. ;
Lunardi, Andrea ;
Chiacchiera, Fulvio ;
Del Sal, Giannino ;
Brodsky, Michael H. ;
Collavin, Licio .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (30) :20848-20856
[43]   Endocycling cells do not apoptose in response to DNA rereplication genotoxic stress [J].
Mehrotra, Sonam ;
Maqbool, Shahina B. ;
Kolpakas, Alexis ;
Murnen, Katherine ;
Calvi, Brian R. .
GENES & DEVELOPMENT, 2008, 22 (22) :3158-3171
[44]   Ehp53, an Entamoeba histolytica protein, ancestor of the mammalian tumour suppressor p53 [J].
Mendoza, L ;
Orozco, E ;
Rodríguez, MA ;
García-Rivera, G ;
Sánchez, T ;
García, E ;
Gariglio, P .
MICROBIOLOGY-SGM, 2003, 149 :885-893
[45]   Functional Dissection of Caenorhabditis elegans CLK-2/TEL2 Cell Cycle Defects during Embryogenesis and Germline Development [J].
Moser, Sandra C. ;
von Elsner, Sophie ;
Buessing, Ingo ;
Alpi, Arno ;
Schnabel, Ralf ;
Gartner, Anton .
PLOS GENETICS, 2009, 5 (04)
[46]   Identification and phylogenetic comparison of p53 in two distinct mussel species (Mytilus) [J].
Muttray, AF ;
Cox, RL ;
St-Jean, S ;
van Poppelen, P ;
Reinisch, CL ;
Baldwin, SA .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2005, 140 (02) :237-250
[47]   Invertebrate p53-like mRNA isoforms are differentially expressed in mussel haemic neoplasia [J].
Muttray, Annette F. ;
Schulte, Patricia M. ;
Baldwin, Susan A. .
MARINE ENVIRONMENTAL RESEARCH, 2008, 66 (04) :412-421
[48]   Identification of DeltaN isoform and polyadenylation site choice variants in molluscan p63/p73-like homologues [J].
Muttray, Annette F. ;
Cox, Rachel L. ;
Reinisch, Carol L. ;
Baldwin, Susan A. .
MARINE BIOTECHNOLOGY, 2007, 9 (02) :217-230
[49]   Early diversification and complex evolutionary history of the p53 tumor suppressor gene family [J].
Nedelcu, Aurora M. ;
Tan, Christopher .
DEVELOPMENT GENES AND EVOLUTION, 2007, 217 (11-12) :801-806
[50]   Drosophila p53 is a structural and functional homolog of the tumor suppressor p53 [J].
Ollmann, M ;
Young, LM ;
Di Como, CJ ;
Karim, F ;
Belvin, M ;
Robertson, S ;
Whittaker, K ;
Demsky, M ;
Fisher, WW ;
Buchman, A ;
Duyk, G ;
Friedman, L ;
Prives, C ;
Kopczynski, C .
CELL, 2000, 101 (01) :91-101