Death Effector Domain-Containing Proteins

被引:90
作者
Valmiki, M. Gudur [1 ,2 ]
Ramos, J. W. [1 ]
机构
[1] Univ Hawaii Manoa, Dept Nat Prod & Canc Biol, Canc Res Ctr Hawaii, Honolulu, HI 96813 USA
[2] Univ Hawaii Manoa, Dept Mol Biosci & Bioengn, Honolulu, HI 96822 USA
基金
美国国家卫生研究院;
关键词
Death effector domain; apoptosis; proliferation; signal transduction; migration; caspase; FADD; NF-KAPPA-B; FLICE-INHIBITORY PROTEIN; AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; RECEPTOR-INDUCED APOPTOSIS; ERK MAP KINASE; RHEUMATOID-ARTHRITIS SYNOVIUM; CELL-CYCLE PROGRESSION; FAS-SIGNALING PATHWAY; BREAST-CANCER CELLS; KAPOSIS-SARCOMA;
D O I
10.1007/s00018-008-8489-0
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
Death effector domains (DEDs) are protein-protein interaction structures that are found in proteins that regulate a variety of signal transduction pathways. DEDs are a part of the larger family of Death Domain structures that have been primarily described in the control of programmed cell death. The seven standard DED-containing proteins are fas associated death domain protein (FADD), Caspase-8 and 10, cellular FLICE-like inhibitory protein (c-FLIP), death effector domain containing DNA binding (DEDD), DEDD2 and phosphoprotein enriched in astrocytes 15-Kda (PEA-15). These proteins are particularly associated with the regulation of apoptosis and proliferation mediated by the tumor necrosis factor alpha (TNF alpha) receptor family. Consequently DED-containing proteins are reported to regulate transcription, migration, and proliferation, in addition to both pro and anti-apoptotic functions. Moreover, DED proteins are essential in embryonic development and homeostasis of the immune system. Here we focus on the role of DED-containing proteins in development and the pathologies arising from abnormal expression of these proteins.
引用
收藏
页码:814 / 830
页数:17
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