TUCAN/CARDINAL and DRAL participate in a common pathway for modulation of NF-κB activation

被引:57
作者
Stilo, R
Leonardi, A
Formisano, L
Di Jeso, B
Vito, P [1 ]
Liguoro, D
机构
[1] BioGeM Consortium, Naples, Italy
[2] Univ Naples Federico II, Dipartimento Biol & Patol Cellulare & Mol, I-80131 Naples, Italy
[3] Univ Naples Federico II, Dipartimento Neurosci, I-80131 Naples, Italy
[4] Univ Lecce, Fac Sci MFN, Dipartimento Sci & Tecnol Biol Ambientali, I-73100 Lecce, Italy
[5] Ctr Endocrinol & Oncol Sperimentale, Naples, Italy
关键词
caspase recruitment domain; protein; nuclear factor-kappa B; apoptosis; p53; DRAL;
D O I
10.1016/S0014-5793(02)02869-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteins containing the caspase recruiting domain (CARD) have emerged as critical regulators of different signal transduction pathways, including those controlling apoptosis and activation of necrosis factor (NF)-kappaB transcription factor. TUCAN/CARDINAL is a recently identified CARD-containing protein involved in regulation of caspases and NF-kappaB activation. We rind that TUCAN/CARDINAL associates with DRAL, a p53-responsive gene implicated in induction of apoptosis. We also show that, whereas TUCAN/CARDINAL exerts a suppressive effect on NF-kappaB activity, expression of DRAL results in enhancement of NF-kappaB activation. Thus, our observations suggest that DRAL and TUCAN/CARDINAL may participate in a regulatory mechanism that coordinates cellular responses controlled by NF-kappaB transcription factor. (C) 2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:165 / 169
页数:5
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