Regulation of Bcl-2 expression by C/EBP in t(14;18) lymphoma cells

被引:36
作者
Heckman, CA
Wheeler, MA
Boxer, LM
机构
[1] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[2] Vet Affairs Palo Alto Hlth Care Syst, Ctr Mol Biol Med, Palo Alto, CA 94304 USA
关键词
bcl-2; lymphoma; transcription; C/EBP;
D O I
10.1038/sj.onc.1206639
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
In follicular lymphomas with the t(14;18) translocation, there is increased expression of the bcl-2 gene, which is dependent upon regulatory elements within the bcl-2 5' flanking region and the immunoglobulin heavy-chain gene enhancers. We found that t(14;18) lymphomas expressed C/EBPalpha, which is not normally expressed in B lymphocytes. Expression of C/EBPalpha increased bcl-2 expression, and two regions of the bcl-2 P2 promoter that mediated this effect were identified. C/EBPbeta was also able to increase bcl-2 promoter activity through these sites. The 5' site was GC-rich and did not contain a C/EBP consensus sequence; however, C/EBP was observed to interact with this site both in vitro by EMSA and in vivo by chromatin immunoprecipitation assay. The 3' region contained the Cdx site, which mediates the effect of A-Myb on the bcl-2 promoter. In vivo binding studies revealed that C/EBP interacted with this region of the bcl-2 promoter as well. Decreased expression of C/EBP factors due to targeting of their transcripts by siRNA molecules resulted in downregulation of Bcl-2 protein. We conclude that C/EBPalpha and C/EBPbeta contribute to the deregulated expression of Bcl-2 in t(14;18) lymphoma cells.
引用
收藏
页码:7891 / 7899
页数:9
相关论文
共 33 条
[1]   Ras signaling enhances the activity of C/EBPα to induce granulocytic differentiation by phosphorylation of serine 248 [J].
Behre, G ;
Singh, SM ;
Liu, HT ;
Bortolin, LT ;
Christopeit, M ;
Radomska, HS ;
Rangatia, J ;
Hiddemann, W ;
Friedman, AD ;
Tenen, DG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (29) :26293-26299
[2]  
Boyd KE, 1999, MOL CELL BIOL, V19, P8393
[3]   Dichotomy of AML1-ETO functions: Growth arrest versus block of differentiation [J].
Burel, SA ;
Harakawa, N ;
Zhou, LM ;
Pabst, T ;
Tenen, DG ;
Zhang, DE .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (16) :5577-5590
[4]  
CHEN HM, 1995, MOL CELL BIOL, V15, P3840
[5]  
Chen XN, 1997, BLOOD, V90, P156
[6]   CCAAT ENHANCER BINDING-PROTEIN GENE PROMOTER - BINDING OF NUCLEAR FACTORS DURING DIFFERENTIATION OF 3T3-L1 PREADIPOCYTES [J].
CHRISTY, RJ ;
KAESTNER, KH ;
GEIMAN, DE ;
LANE, MD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (06) :2593-2597
[7]   CLONING AND STRUCTURAL-ANALYSIS OF CDNAS FOR BCL-2 AND A HYBRID BCL-2/IMMUNOGLOBULIN TRANSCRIPT RESULTING FROM THE T(14-18) TRANSLOCATION [J].
CLEARY, ML ;
SMITH, SD ;
SKLAR, J .
CELL, 1986, 47 (01) :19-28
[8]  
COOPER CL, 1994, J IMMUNOL, V153, P5049
[9]   Expression and function of CCAAT/enhancer binding proteinβ (C/EBPβ) LAP and LIP isoforms in mouse mammary gland, tumors and cultured mammary epithelial cells [J].
Dearth, LR ;
Hutt, J ;
Sattler, A ;
Gigliotti, A ;
DeWille, J .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2001, 82 (03) :357-370
[10]   EXPRESSION OF BCL-2 AND BCL-2-IG FUSION TRANSCRIPTS IN NORMAL AND NEOPLASTIC-CELLS [J].
GRANINGER, WB ;
SETO, M ;
BOUTAIN, B ;
GOLDMAN, P ;
KORSMEYER, SJ .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (05) :1512-1515