Molecular cloning and characterization of a novel inhibitor of apoptosis protein from Xenopus laevis
A novel inhibitor of apoptosis protein family member termed SIX was identified in Xenopus containing a single baculoviral IAP repeat (BIR) domain and no COOH-terminal RING finger domain. It exhibited striking amino acid sequence similarity with human survivin, mouse TIAP, and recently found Xenopus...
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Published in | Biochemical and biophysical research communications Vol. 301; no. 1; pp. 236 - 242 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
31.01.2003
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Subjects | |
Online Access | Get full text |
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Summary: | A novel inhibitor of apoptosis protein family member termed SIX was identified in
Xenopus containing a single baculoviral IAP repeat (BIR) domain and no COOH-terminal RING finger domain. It exhibited striking amino acid sequence similarity with human
survivin, mouse
TIAP, and recently found
Xenopus survivin, especially a part of BIR domain was highly conserved. Interestingly,
SIX interacted with RXRα through the AF2 domain in the absence of ligand, which was weakened when the ligand was present. Northern blot analysis demonstrated that
SIX mRNA was not detectable in adult with exception of the ovary and testis, and
whole-mount in situ hybridization and Northern blot analyses revealed strong and homogeneous expression of SIX in the developing oocytes. In the embryos, the expression of
SIX was observed in the animal hemisphere from one-cell to yolk plug stages and high level of expression was detected in the future brain and dorsal region of the neural tube at the neurula stage and early tail-bud stage. These results strongly support the fact that survivin is evolutionarily conserved in structure and
SIX is likely to be the
Xenopus counterpart of human and mouse survivin. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1016/S0006-291X(02)03013-9 |