A peptide aptamer to antagonize BCL-6 function

被引:40
作者
Chattopadhyay, A
Tate, SA
Beswick, RW
Wagner, SD
Ferrigno, PK
机构
[1] Hammersmith Hosp, Imperial Coll London, Div Invest Sci, Dept Haematol, London W12 0NN, England
[2] MRC, Canc Cell Unit, Hutchison MRC Res Ctr, Cambridge, England
[3] Univ Cambridge, Canc Res UK, Dept Oncol, Hutchison MRC Res Ctr, Cambridge, England
基金
英国医学研究理事会;
关键词
peptide aptamer; BCL-6; B-cell lymphoma;
D O I
10.1038/sj.onc.1209252
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
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. Apt 48 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. Not ably, expression of the differentiation markers CD69, Blimp-1 and cyclin D2 was increased in B-cell lines when Apt48 was expressed. W e also show that expression of Apt48 restores cytokine-mediated growth arrest to BCL-6 over-expressing 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.
引用
收藏
页码:2223 / 2233
页数:11
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