Noncoding Transcripts in Sense and Antisense Orientation Regulate the Epigenetic State of Ribosomal RNA Genes

被引:82
作者
Bierhoff, H. [1 ]
Schmitz, K. [1 ]
Maass, F. [1 ]
Ye, J. [1 ]
Grummt, I. [1 ]
机构
[1] DKFZ ZMBH Alliance, German Canc Res Ctr, Div Mol Biol Cell 2, D-69120 Heidelberg, Germany
来源
NUCLEAR ORGANIZATION AND FUNCTION | 2010年 / 75卷
关键词
REMODELING COMPLEX NORC; X-CHROMOSOME; PROMOTER; METHYLATION; SPACER; RECRUITMENT; MECHANISMS; SEQUENCES; REPEATS; DOMAIN;
D O I
10.1101/sqb.2010.75.060
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
Alternative transcription of the same gene in sense and antisense orientation regulates expression of protein-coding genes. Here we show that noncoding RNA (ncRNA) in sense and antisense orientation also controls transcription of rRNA genes (rDNA). rDNA exists in two types of chromatin-a euchromatic conformation that is permissive to transcription and a heterochromatic conformation that is transcriptionally silent. Silencing of rDNA is mediated by NoRC, a chromatin-remodeling complex that triggers heterochromatin formation. NoRC function requires RNA that is complementary to the rDNA promoter (pRNA). pRNA forms a DNA:RNA triplex with a regulatory element in the rDNA promoter, and this triplex structure is recognized by DNMT3b. The results imply that triplex-mediated targeting of DNMT3b to specific sequences may be a common pathway in epigenetic regulation. We also show that rDNA is transcribed in antisense orientation. The level of antisense RNA (asRNA) is down-regulated in cancer cells and up-regulated in senescent cells. Ectopic asRNA triggers trimethylation of histone H4 at lysine 20 (H4K20me3), suggesting that antisense transcripts guide the histone methyltransferase Suv4-20 to rDNA. The results reveal that noncoding RNAs in sense and antisense orientation are important determinants of the epigenetic state of rDNA.
引用
收藏
页码:357 / 364
页数:8
相关论文
共 41 条
[1]   X-chromosome inactivation: Counting, choice and initiation [J].
Avner, P ;
Heard, E .
NATURE REVIEWS GENETICS, 2001, 2 (01) :59-67
[2]   A triplex-forming sequence from the human c-MYC promoter interferes with DNA transcription [J].
Belotserkovskii, Boris P. ;
De Silva, Erandi ;
Tornaletti, Silvia ;
Wang, Guliang ;
Vasquez, Karen M. ;
Hanawalt, Philip C. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (44) :32433-32441
[3]   Phosphorylation by casein kinase 2 facilitates rRNA gene transcription by promoting dissociation of TIF-IA from elongating RNA polymerase I [J].
Bierhoff, Holger ;
Dundr, Miroslav ;
MichelS, Annernieke A. ;
Grummt, Ingrid .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (16) :4988-4998
[4]   DNA methylation and methyl-CpG binding proteins: developmental requirements and function [J].
Bogdanovic, Ozren ;
Veenstra, Gert Jan C. .
CHROMOSOMA, 2009, 118 (05) :549-565
[5]  
BOUKAMP P, 1990, CANCER RES, V50, P2840
[6]   NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE [J].
BOUKAMP, P ;
PETRUSSEVSKA, RT ;
BREITKREUTZ, D ;
HORNUNG, J ;
MARKHAM, A ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :761-771
[7]   ADDITIONAL RNA POLYMERASE-I INITIATION SITE WITHIN THE NONTRANSCRIBED SPACER REGION OF THE RAT RIBOSOMAL-RNA GENE [J].
CASSIDY, BG ;
YANGYEN, HF ;
ROTHBLUM, LI .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (07) :2388-2396
[8]   Role of the mammalian RNA polymerase IIC-terminal domain (CTD) nonconsensus repeats in CTD stability and cell proliferation [J].
Chapman, RD ;
Conrad, M ;
Eick, D .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (17) :7665-7674
[9]   Targeting RNA Polymerase I with an Oral Small Molecule CX-5461 Inhibits Ribosomal RNA Synthesis and Solid Tumor Growth [J].
Drygin, Denis ;
Lin, Amy ;
Bliesath, Josh ;
Ho, Caroline B. ;
O'Brien, Sean E. ;
Proffitt, Chris ;
Omori, Mayuko ;
Haddach, Mustapha ;
Schwaebe, Michael K. ;
Siddiqui-Jain, Adam ;
Streiner, Nicole ;
Quin, Jaclyn E. ;
Sanij, Elaine ;
Bywater, Megan J. ;
Hannan, Ross D. ;
Ryckman, David ;
Anderes, Kenna ;
Rice, William G. .
CANCER RESEARCH, 2011, 71 (04) :1418-1430
[10]   DIFFERENT DOMAINS OF THE MURINE RNA-POLYMERASE I-SPECIFIC TERMINATION FACTOR MTTF-I SERVE DISTINCT FUNCTIONS IN TRANSCRIPTION TERMINATION [J].
EVERS, R ;
SMID, A ;
RUDLOFF, U ;
LOTTSPEICH, F ;
GRUMMT, I .
EMBO JOURNAL, 1995, 14 (06) :1248-1256