The N-terminus of a novel isoform of human iASPP is required for its cytoplasmic localization

ASPP1 and ASPP2 are both proteins that interact with p53 and enhance its ability to induce apoptosis by selectively elevating the expression of proapoptotic p53-responsive genes. iASPP(RAI) is a third member of the family that is the most conserved inhibitor of p53-mediated apoptosis. Here, we have...

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Published inOncogene Vol. 23; no. 56; pp. 9007 - 9016
Main Authors Slee, Elizabeth A, Gillotin, Sébastien, Bergamaschi, Daniele, Royer, Christophe, Llanos, Susana, Ali, Safia, Jin, Boquan, Trigiante, Giuseppe, Lu, Xin
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 02.12.2004
Nature Publishing
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Abstract ASPP1 and ASPP2 are both proteins that interact with p53 and enhance its ability to induce apoptosis by selectively elevating the expression of proapoptotic p53-responsive genes. iASPP(RAI) is a third member of the family that is the most conserved inhibitor of p53-mediated apoptosis. Here, we have described iASPP, a longer form of iASPP(RAI), which at 828 amino acids is more than twice the size of iASPP(RAI). Using two antibodies that recognize both iASPP and iASPP(RAI), we report that this longer form of iASPP is the predominant form of the molecule expressed in cells. Like iASPP(RAI), iASPP also binds to p53 and inhibits apoptosis induced by p53 overexpression. However, whereas iASPP(RAI) is predominantly nuclear, the N-terminus of iASPP is entirely cytoplasmic, and the longer iASPP is located in both the cytoplasm and the nucleus. The effect upon subcellular localization of the longer N-terminus of iASPP means that this new, longer form of the molecule may be subject to greater regulation and provides another layer in the control of p53-induced apoptosis.
AbstractList ASPP1 and ASPP2 are both proteins that interact with p53 and enhance its ability to induce apoptosis by selectively elevating the expression of proapoptotic p53-responsive genes. iASPP(RAI) is a third member of the family that is the most conserved inhibitor of p53-mediated apoptosis. Here, we have described iASPP, a longer form of iASPP(RAI), which at 828 amino acids is more than twice the size of iASPP(RAI). Using two antibodies that recognize both iASPP and iASPP(RAI), we report that this longer form of iASPP is the predominant form of the molecule expressed in cells. Like iASPP(RAI), iASPP also binds to p53 and inhibits apoptosis induced by p53 overexpression. However, whereas iASPP(RAI) is predominantly nuclear, the N-terminus of iASPP is entirely cytoplasmic, and the longer iASPP is located in both the cytoplasm and the nucleus. The effect upon subcellular localization of the longer N-terminus of iASPP means that this new, longer form of the molecule may be subject to greater regulation and provides another layer in the control of p53-induced apoptosis.
Audience Academic
Author Slee, Elizabeth A
Ali, Safia
Llanos, Susana
Royer, Christophe
Bergamaschi, Daniele
Trigiante, Giuseppe
Lu, Xin
Gillotin, Sébastien
Jin, Boquan
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  surname: Slee
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  organization: Ludwig Institute for Cancer Research, Imperial College School of Medicine, Ludwig Institute for Cancer Research, University College London
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  surname: Gillotin
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  organization: Ludwig Institute for Cancer Research, Imperial College School of Medicine, Ludwig Institute for Cancer Research, University College London
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  fullname: Lu, Xin
  email: x.lu@imperial.ac.uk
  organization: Ludwig Institute for Cancer Research, Imperial College School of Medicine, Ludwig Institute for Cancer Research, University College London
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Issue 56
Keywords apoptosis
iASPP
p53
Human
Molecular form
TP53 Gene
Localization
Carcinogenesis
Apoptosis
Tumor suppressor gene
Language English
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Snippet ASPP1 and ASPP2 are both proteins that interact with p53 and enhance its ability to induce apoptosis by selectively elevating the expression of proapoptotic...
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SubjectTerms Adaptor Proteins, Signal Transducing
Ageing, cell death
Amino Acid Sequence
Amino acids
Apoptosis
Apoptosis - physiology
Apoptosis Regulatory Proteins
Base Sequence
Biological and medical sciences
Cancer research
Carrier Proteins - chemistry
Carrier Proteins - metabolism
Cell Biology
Cell cycle
Cell death
Cell division
Cell Line, Tumor
Cell physiology
Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes
Cytoplasm
Cytoplasm - metabolism
DNA damage
DNA Primers
Fundamental and applied biological sciences. Psychology
Human Genetics
Humans
Internal Medicine
Localization
Medical research
Medicine
Medicine & Public Health
Molecular and cellular biology
Molecular Sequence Data
N-Terminus
Nematodes
Oncology
original-paper
p53 Protein
Protein Isoforms - chemistry
Protein Isoforms - metabolism
Proteins
Sequence Homology, Amino Acid
Tumor Suppressor Protein p53 - metabolism
Tumor Suppressor Protein p53 - physiology
Title The N-terminus of a novel isoform of human iASPP is required for its cytoplasmic localization
URI http://dx.doi.org/10.1038/sj.onc.1208088
https://link.springer.com/article/10.1038/sj.onc.1208088
https://www.ncbi.nlm.nih.gov/pubmed/15489900
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Volume 23
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