生物
加压器
心理压抑
转录因子
周期素D2抗原
抑制因子
细胞生物学
分子生物学
癌症研究
基因
基因表达
遗传学
细胞周期
细胞周期蛋白
作者
Anasuya Chattopadhyay,Sharon Tate,Richard Beswick,Simon D. Wagner,Paul Ko Ferrigno
出处
期刊:Oncogene
[Springer Nature]
日期:2005-12-05
卷期号:25 (15): 2223-2233
被引量:50
标识
DOI:10.1038/sj.onc.1209252
摘要
BCL-6 is a transcription factor essential for germinal centre B-cell development. The BCL-6 gene is involved in diffuse large-cell lymphoma and overexpressed in other types of non-Hodgkin's lymphoma and in high-grade breast cancer. BCL-6 is a transcriptional repressor whose N-terminal POZ domain mediates protein-protein interactions to exert its effects. Reasoning that disruption of POZ domain-mediated interactions may be an effective route to antagonizing the effects of BCL-6 in lymphoma, we screened a library for peptide aptamers that specifically bind to BCL-6 POZ and not the POZ domains of related proteins and describe here the first of these reagents, Apt48. Apt48 binds BCL-6 POZ in a manner distinct from the transcriptional corepressor SMRT, yet was found to prevent BCL-6-mediated repression of a luciferase reporter gene. Apt48 also reproduced several previously validated effects of BCL-6 inhibition. Notably, expression of the differentiation markers CD69, Blimp-1 and cyclin D2 was increased in B-cell lines when Apt48 was expressed. We also show that expression of Apt48 restores cytokine-mediated growth arrest to BCL-6 overexpressing cells. Thus, we have identified a peptide aptamer that affects a function of BCL-6 that is required to prevent differentiation of proliferating B cells.
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