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
相关论文
共 35 条
[21]   BCL-6 is expressed in breast cancer and prevents mammary epithelial differentiation [J].
Logarajah, S ;
Hunter, P ;
Kraman, M ;
Steele, D ;
Lakhani, S ;
Bobrow, L ;
Venkitaraman, A ;
Wagner, S .
ONCOGENE, 2003, 22 (36) :5572-5578
[22]   In-depth mutational analysis of the promyelocytic leukemia zinc finger BTB/POZ domain reveals motifs and residues required for biological and transcriptional functions [J].
Melnick, A ;
Ahmad, KF ;
Arai, S ;
Polinger, A ;
Ball, H ;
Borden, KL ;
Carlile, GW ;
Prive, GG ;
Licht, JD .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (17) :6550-6567
[23]   Critical residues within the BTB domain of PLZF and bcl-6 modulate interaction with corepressors [J].
Melnick, A ;
Carlile, G ;
Ahmad, KF ;
Kiang, CL ;
Corcoran, C ;
Bardwell, V ;
Prive, GG ;
Licht, JD .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (06) :1804-1818
[24]   Identification of Bach2 as a B-cell-specific partner for small Maf proteins that negatively regulate the immunoglobulin heavy chain gene 3′ enhancer [J].
Muto, A ;
Hoshino, H ;
Madisen, L ;
Yanai, N ;
Obinata, M ;
Karasuyama, H ;
Hayashi, M ;
Nakauchi, H ;
Yamamoto, M ;
Groudine, M ;
Igarashi, K .
EMBO JOURNAL, 1998, 17 (19) :5734-5743
[25]   Antigen receptor signaling induces MAP kinase-mediated phosphorylation and degradation of the BCL-6 transcription factor [J].
Niu, HF ;
Ye, BHH ;
Dalla-Favera, R .
GENES & DEVELOPMENT, 1998, 12 (13) :1953-1961
[26]   BAZF, a novel Bcl6 homolog, functions as a transcriptional repressor [J].
Okabe, S ;
Fukuda, T ;
Ishibashi, K ;
Kojima, S ;
Okada, S ;
Hatano, M ;
Ebara, M ;
Saisho, H ;
Tokuhisa, T .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (07) :4235-4244
[27]   BCL-6 GENE-PRODUCT, A 92-KD TO 98-KD NUCLEAR PHOSPHOPROTEIN, IS HIGHLY EXPRESSED IN GERMINAL CENTER B-CELLS AND THEIR NEOPLASTIC COUNTERPARTS [J].
ONIZUKA, T ;
MORIYAMA, M ;
YAMOCHI, T ;
KURODA, T ;
KAZAMA, A ;
KANAZAWA, N ;
SATO, K ;
KATO, T ;
OTA, H ;
MORI, S .
BLOOD, 1995, 86 (01) :28-37
[28]   Specific peptide interference reveals BCL6 transcriptional and oncogenic mechanisms in B-cell lymphoma cells [J].
Polo, JM ;
Dell'Oso, T ;
Ranuncolo, SM ;
Cerchietti, L ;
Beck, D ;
Da Silva, GF ;
Prive, GG ;
Licht, JD ;
Melnick, A .
NATURE MEDICINE, 2004, 10 (12) :1329-1335
[29]   Suppression of signal transducer and activator of transcription 3-dependent B lymphocyte terminal differentiation by BCL-6 [J].
Reljic, R ;
Wagner, SD ;
Peakman, LJ ;
Fearon, DT .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (12) :1841-1847
[30]  
Rose MD, 1990, Methods in Yeast Genetics: A Laboratory Course Manual