BCL6 positively regulates AID and germinal center gene expression via repression of miR-155

被引:97
作者
Basso, Katia [1 ,2 ,3 ]
Schneider, Christof [1 ]
Shen, Qiong [1 ]
Holmes, Antony B. [1 ]
Setty, Manu [6 ]
Leslie, Christina [6 ]
Dalla-Favera, Riccardo [1 ,2 ,3 ,4 ,5 ]
机构
[1] Columbia Univ, Inst Canc Genet, New York, NY 10027 USA
[2] Columbia Univ, Herbert Irving Comprehens Canc Ctr, New York, NY 10027 USA
[3] Columbia Univ, Dept Pathol & Cell Biol, New York, NY 10027 USA
[4] Columbia Univ, Dept Genet & Dev, New York, NY 10027 USA
[5] Columbia Univ, Dept Microbiol & Immunol, New York, NY 10027 USA
[6] Mem Sloan Kettering Canc Ctr, New York, NY 10065 USA
关键词
VIRUS-INDUCED LYMPHOMAS; B-CELLS; MICRORNA-155; IDENTIFICATION; MUTATIONS; PROGRAM; PATHWAY; PROTEIN; ROLES; BETA;
D O I
10.1084/jem.20121387
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The BCL6 proto-oncogene encodes a transcriptional repressor that is required for germinal center (GC) formation and whose de-regulation is involved in lymphomagenesis. Although substantial evidence indicates that BCL6 exerts its function by repressing the transcription of hundreds of protein-coding genes, its potential role in regulating gene expression via microRNAs (miRNAs) is not known. We have identified a core of 15 miRNAs that show binding of BCL6 in their genomic loci and are down-regulated in GC B cells. Among BCL6 validated targets, miR-155 and miR-361 directly modulate AID expression, indicating that via repression of these miRNAs, BCL6 up-regulates AID. Similarly, the expression of additional genes relevant for the GC phenotype, including SPI1, IRF8, and MYB, appears to be sustained via BCL6-mediated repression of miR-155. These findings identify a novel mechanism by which BCL6, in addition to repressing protein coding genes, promotes the expression of important GC functions by repressing specific miRNAs.
引用
收藏
页码:2455 / 2465
页数:11
相关论文
共 47 条
[1]   Tracking CD40 signaling during germinal center development [J].
Basso, K ;
Klein, U ;
Niu, HF ;
Stolovitzky, GA ;
Tu, YH ;
Califano, A ;
Cattoretti, G ;
Dalla-Favera, R .
BLOOD, 2004, 104 (13) :4088-4096
[2]   Roles of BCL6 in normal and transformed germinal center B cells [J].
Basso, Katia ;
Dalla-Favera, Riccardo .
IMMUNOLOGICAL REVIEWS, 2012, 247 :172-183
[3]   Integrated biochemical and computational approach identifies BCL6 direct target genes controlling multiple pathways in normal germinal center B cells [J].
Basso, Katia ;
Saito, Masumichi ;
Sumazin, Pavel ;
Margolin, Adam A. ;
Wang, Kai ;
Lim, Wei-Keat ;
Kitagawa, Yukiko ;
Schneider, Christof ;
Alvarez, Mariano J. ;
Califano, Andrea ;
Dalla-Favera, Riccardo .
BLOOD, 2010, 115 (05) :975-984
[4]   Identification of the Human Mature B Cell miRNome [J].
Basso, Katia ;
Sumazin, Pavel ;
Morozov, Pavel ;
Schneider, Christof ;
Maute, Roy L. ;
Kitagawa, Yukiko ;
Mandelbaum, Jonathan ;
Haddad, Joseph, Jr. ;
Chen, Chang-Zheng ;
Califano, Andrea ;
Dalla-Favera, Riccardo .
IMMUNITY, 2009, 30 (05) :744-752
[5]   Comprehensive modeling of microRNA targets predicts functional non-conserved and non-canonical sites [J].
Betel, Doron ;
Koppal, Anjali ;
Agius, Phaedra ;
Sander, Chris ;
Leslie, Christina .
GENOME BIOLOGY, 2010, 11 (08)
[6]   Stringent doxycycline-dependent control of gene activities using an episomal one-vector system -: art. no. e137 [J].
Bornkamm, GW ;
Berens, C ;
Kuklik-Roos, C ;
Bechet, JM ;
Laux, G ;
Bachl, J ;
Korndoerfer, M ;
Schlee, M ;
Hölzel, M ;
Malamoussi, A ;
Chapman, RD ;
Nimmerjahn, F ;
Mautner, J ;
Hillen, W ;
Bujard, H ;
Feuillard, J .
NUCLEIC ACIDS RESEARCH, 2005, 33 (16) :1-11
[7]   Surprising new roles for PU.1 in the adaptive immune response [J].
Carotta, Sebastian ;
Wu, Li ;
Nutt, Stephen L. .
IMMUNOLOGICAL REVIEWS, 2010, 238 :63-75
[8]   Deregulated BCL6 expression recapitulates the pathogenesis of human diffuse large B cell lymphomas in mice [J].
Cattoretti, G ;
Pasqualucci, L ;
Ballon, G ;
Tam, W ;
Nandula, SV ;
Shen, Q ;
Mo, TW ;
Murty, VV ;
Dalla-Favera, R .
CANCER CELL, 2005, 7 (05) :445-455
[9]   Nuclear and cytoplasmic AID in extrafollicular and germinal center B cells [J].
Cattoretti, Giorgio ;
Buettner, Maike ;
Shaknovich, Rita ;
Kremmer, Elisabeth ;
Alobeid, Bachir ;
Niedobitek, Gerald .
BLOOD, 2006, 107 (10) :3967-3975
[10]   BCL-6, a POZ/zinc-finger protein, is a sequence-specific transcriptional repressor [J].
Chang, CC ;
Ye, BH ;
Chaganti, RSK ;
DallaFavera, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) :6947-6952