Identification of apoptosis-related PLZF target genes

被引:35
作者
Bernardo, Maria Victoria [1 ]
Yelo, Estefania [1 ]
Gimeno, Lourdes [1 ]
Campillo, Jose Antonio [1 ]
Parrado, Antonio [1 ]
机构
[1] Hosp Univ Virgen Arrixaca, Serv Immunol, Murcia 30120, Spain
关键词
PLZF; ZBTB16; apoptosis; Jurkat; TP53INP1; ID1; ID3; TERT; nuclear speckles;
D O I
10.1016/j.bbrc.2007.05.085
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 PLZF gene encodes a BTB/POZ-zinc finger-type transcription factor, involved in physiological development,, proliferation, differentiation, and apoptosis. In this paper, we investigate proliferation, survival, and gene expression regulation in stable clones from the human haematopoietic K562, DG75, and Jurkat cell lines with inducible expression of PLZF. In Jurkat cells, but not in K562 and DG75 cells, PLZF induced growth suppression and apoptosis in a cell density-dependent manner. Deletion of the BTB/POZ domain of PLZF abrogated growth suppression and apoptosis. PLZF was expressed with a nuclear speckled pattern distinctively in the full-length PLZF-expressing Jurkat clones, suggesting that the nuclear speckled localization is required for PLZF-induced apoptosis. By microarray analysis, we identified that the apoptosis-inducer TP53INP1, ID 1, and ID3 genes were upregulated, and the apoptosis-inhibitor TERT gene was downregulated. The identification of apoptosis-related PLZF target genes may have biological and clinical relevance in cancer typified by altered PLZF expression. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:317 / 322
页数:6
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