Cloning of AIP1, a Novel Protein That Associates with the Apoptosis-linked Gene ALG-2 in a Ca2+-dependent Reaction*

ALG-2 is a 22-kDa calcium-binding protein necessary for cell death induced by different stimuli in 3DO T-cell hybridoma. 3DO cell clones depleted of ALG-2 protein exhibit normal caspases activation, suggesting that ALG-2 function is required downstream or is independent of caspase proteases activity for apoptosis to occur. Using the yeast two-hybrid screening system, we have isolated and characterized the mouse cDNA encoding for ALG-2 interacting protein 1 (AIP1), a novel protein that interacts with ALG-2. ALG-2 and AIP1 colocalize in the cytosol and the presence of calcium is an indispensable requisite for their association. Sequence alignment shows that AIP1 is highly similar to BRO1, a yeast protein related to components of the Pkc1p-MAP kinase cascade. Overexpression of a truncated form of AIP1 protects two different cell types from death induced by trophic factors withdrawal; thus, our data indicate that AIP1 cooperates with ALG-2 in executing the calcium-dependent requirements along the cell death pathway.

[1]  M. Moskowitz,et al.  Defects in regulation of apoptosis in caspase-2-deficient mice. , 1998, Genes & development.

[2]  G. Häcker,et al.  Activation of caspase‐3‐like enzymes in non‐apoptotic T cells , 1998, European journal of immunology.

[3]  M. Weil,et al.  Molecular cloning of a splice variant of Caenorhabditis elegans YNK1, a putative element in signal transduction. , 1997, Biochimica et biophysica acta.

[4]  K. Heidenreich,et al.  Apoptosis Induced by Withdrawal of Trophic Factors Is Mediated by p38 Mitogen-activated Protein Kinase* , 1997, The Journal of Biological Chemistry.

[5]  G M Cohen,et al.  Caspases: the executioners of apoptosis. , 1997, The Biochemical journal.

[6]  A. Marks,et al.  T cells deficient in inositol 1,4,5-trisphosphate receptor are resistant to apoptosis , 1997, Molecular and cellular biology.

[7]  P. Vito,et al.  Dissociation of apoptosis and activation of IL-1beta-converting enzyme/Ced-3 proteases by ALG-2 and the truncated Alzheimer's gene ALG-3. , 1997, Journal of immunology.

[8]  F. Fassy,et al.  Evidence for CPP32 Activation in the Absence of Apoptosis during T Lymphocyte Stimulation* , 1997, The Journal of Biological Chemistry.

[9]  F. Shibasaki,et al.  Suppression of signalling through transcription factor NF-AT by interactions between calcineurin and Bcl-2 , 1997, Nature.

[10]  H. Arst,et al.  Characterization of the pH signal transduction pathway gene palA of Aspergillus nidulans and identification of possible homologs , 1997, Journal of bacteriology.

[11]  M. Raff,et al.  Programmed Cell Death in Animal Development , 1997, Cell.

[12]  A. Chinnaiyan,et al.  Portrait of an executioner: the molecular mechanism of FAS/APO-1-induced apoptosis. , 1997, Seminars in immunology.

[13]  P. Vito,et al.  Functional cloning of genes involved in T-cell receptor-induced programmed cell death. , 1997, Seminars in immunology.

[14]  E. Pennisi Linker Histones, DNA's Protein Custodians, Gain New Respect , 1996, Science.

[15]  Merle Goldman Conditions of Science. (Book Reviews: Science and Dissent in Post-Mao China. The Politics of Knowledge.) , 1996 .

[16]  M. Nickas,et al.  BRO1, a novel gene that interacts with components of the Pkc1p-mitogen-activated protein kinase pathway in Saccharomyces cerevisiae , 1996, Molecular and cellular biology.

[17]  F. Shibasaki,et al.  Calcineurin functions in Ca(2+)-activated cell death in mammalian cells , 1995, The Journal of cell biology.

[18]  W. Fiers,et al.  Requirement of an ICE/CED-3 protease for Fas/APO-1-mediated apoptosis , 1995, Nature.

[19]  S. Nagata,et al.  Involvement of an ICE-like protease in Fas-mediated apoptosis , 1995, Nature.

[20]  S. Miyazaki,et al.  Fas antigen-mediated DNA fragmentation and apoptotic morphologic changes are regulated by elevated cytosolic Ca2+ level. , 1995, Journal of immunology.

[21]  N. Copeland,et al.  Induction of apoptosis by the mouse Nedd2 gene, which encodes a protein similar to the product of the Caenorhabditis elegans cell death gene ced-3 and the mammalian IL-1 beta-converting enzyme. , 1994, Genes & development.

[22]  G. Dubyak,et al.  Evidence that BCL-2 represses apoptosis by regulating endoplasmic reticulum-associated Ca2+ fluxes. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[23]  Junying Yuan,et al.  Induction of apoptosis in fibroblasts by IL-1β-converting enzyme, a mammalian homolog of the C. elegans cell death gene ced-3 , 1993, Cell.

[24]  J. Tschopp,et al.  Characterization of the endogenous deoxyribonuclease involved in nuclear DNA degradation during apoptosis (programmed cell death). , 1993, The EMBO journal.

[25]  C. June,et al.  In vivo calcium elevations in thymocytes with T cell receptors that are specific for self ligands. , 1992, Science.

[26]  S. Orrenius,et al.  Calcium-dependent killing of immature thymocytes by stimulation via the CD3/T cell receptor complex. , 1989, Journal of immunology.

[27]  J. Cohen,et al.  Glucocorticoid activation of a calcium-dependent endonuclease in thymocyte nuclei leads to cell death. , 1984, Journal of immunology.

[28]  A. Wyllie,et al.  Chromatin cleavage in apoptosis: Association with condensed chromatin morphology and dependence on macromolecular synthesis , 1984, The Journal of pathology.

[29]  A. Wyllie,et al.  Apoptosis: mechanisms and roles in pathology. , 1991, International review of experimental pathology.

[30]  A. Fabiato,et al.  Computer programs for calculating total from specified free or free from specified total ionic concentrations in aqueous solutions containing multiple metals and ligands. , 1988, Methods in enzymology.