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 inBiochemical and biophysical research communications Vol. 301; no. 1; pp. 236 - 242
Main Authors Song, Kwang-Hoon, Kim, Tae-Moon, Kim, Han-Jong, Kim, Jung Woo, Kim, Hong-Hee, Kwon, Hyuk-Bang, Kim, Won Sun, Choi, Hueng-Sik
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 31.01.2003
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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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ISSN:0006-291X
1090-2104
DOI:10.1016/S0006-291X(02)03013-9