SLUG, a ces-1-related zinc finger transcription factor gene with antiapoptotic activity, is a downstream target of the E2A-HLF oncoprotein

被引:171
作者
Inukai, T
Inoue, A
Kurosawa, H
Goi, K
Shinjyo, T
Ozawa, K
Mao, M
Inaba, T
Look, AT
机构
[1] St Jude Childrens Res Hosp, Dept Expt Oncol, Memphis, TN 38105 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[3] Jichi Med Sch, Dept Mol Biol, Minami Kawachi, Tochigi 32904, Japan
[4] Jichi Med Sch, Dept Hematol, Minami Kawachi, Tochigi 32904, Japan
[5] Shanghai Second Med Univ, Rui Jin Hosp, Shanghai Inst Hematol, Shanghai 200025, Peoples R China
关键词
D O I
10.1016/S1097-2765(00)80336-6
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
The E2A-HLF fusion gene transforms human pro-B lymphocytes by interfering with an early step in apoptotic signaling. In a search for E2A-HLF-responsive genes, we identified a zinc finger transcription factor, SLUG, whose product belongs to the Snail family of developmental regulatory proteins. Importantly, SLUG bears close homology to the CES-1 protein of C. elegans, which acts downstream of CES-2 in a neuron-specific cell death pathway. Consistent with the postulated role of CES-1 as an antiapoptotic transcription factor, SLUG was nearly as active as Bcl-2 or Bcl-x(L) in promoting the survival of IL-3-dependent murine pro-B cells deprived of the cytokine. We conclude that SLUG is an evolutionarily conserved transcriptional repressor whose activation by E2A-HLF promotes the aberrant survival and eventual malignant transformation of mammalian pro-B cells otherwise slated for apoptotic death.
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收藏
页码:343 / 352
页数:10
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