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
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