The Airn lncRNA does not require any DNA elements within its locus to silence distant imprinted genes

被引:41
作者
Andergassen, Daniel [1 ,6 ]
Muckenhuber, Markus [1 ,7 ]
Bammer, Philipp C. [1 ,8 ]
Kulinski, Tomasz M. [1 ,9 ]
Theussl, Hans-Christian [2 ]
Shimizu, Takahiko [3 ]
Penninger, Josef M. [4 ]
Pauler, Florian M. [1 ,10 ]
Hudson, Quanah J. [1 ,4 ,5 ]
机构
[1] Austrian Acad Sci, CeMM, Res Ctr Mol Med, Vienna, Austria
[2] Inst Mol Pathol, IMP IMBA Transgen Serv, Vienna, Austria
[3] Natl Ctr Geriatr & Gerontol, Obu, Aichi, Japan
[4] Austrian Acad Sci, IMBA, Inst Mol Biotechnol, Vienna, Austria
[5] Med Univ Vienna, Dept Obstet & Gynecol, Vienna, Austria
[6] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[7] German Canc Res Ctr, DKFZ, Heidelberg, Germany
[8] Friedrich Miescher Inst Biomed Res, FMI, Basel, Switzerland
[9] Polish Acad Sci, IBB, Warsaw, Poland
[10] IST Austria, Klosterneuburg, Austria
基金
奥地利科学基金会;
关键词
REPRESSIVE HISTONE METHYLATION; RNA; EXPRESSION; IGF2R; TRANSCRIPTION; MECHANISMS; PROMOTERS; CHROMATIN; GROWTH; NCRNA;
D O I
10.1371/journal.pgen.1008268
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Long non-coding (lnc) RNAs are numerous and found throughout the mammalian genome, and many are thought to be involved in the regulation of gene expression. However, the majority remain relatively uncharacterised and of uncertain function making the use of model systems to uncover their mode of action valuable. Imprinted lncRNAs target and recruit epigenetic silencing factors to a cluster of imprinted genes on the same chromosome, making them one of the best characterized lncRNAs for silencing distant genes in cis. In this study we examined silencing of the distant imprinted gene Slc22a3 by the lncRNA Airn in the Igf2r imprinted cluster in mouse. Previously we proposed that imprinted lncRNAs may silence distant imprinted genes by disrupting promoter-enhancer interactions by being transcribed through the enhancer, which we called the enhancer interference hypothesis. Here we tested this hypothesis by first using allele-specific chromosome conformation capture (3C) to detect interactions between the Slc22a3 promoter and the locus of the Airn lncRNA that silences it on the paternal chromosome. In agreement with the model, we found interactions enriched on the maternal allele across the entire Airn gene consistent with multiple enhancer-promoter interactions. Therefore, to test the enhancer interference hypothesis we devised an approach to delete the entire Airn gene. However, the deletion showed that there are no essential enhancers for Slc22a2, Pde10a and Slc22a3 within the Airn gene, strongly indicating that the Airn RNA rather than its transcription is responsible for silencing distant imprinted genes. Furthermore, we found that silent imprinted genes were covered with large blocks of H3K27me3 on the repressed paternal allele. Therefore we propose an alternative hypothesis whereby the chromosome interactions may initially guide the lncRNA to target imprinted promoters and recruit repressive chromatin, and that these interactions are lost once silencing is established.
引用
收藏
页数:18
相关论文
共 52 条
[1]   Mapping the mouse Allelome reveals tissue-specific regulation of allelic expression [J].
Andergassen, Daniel ;
Dotter, Christoph P. ;
Wenzel, Daniel ;
Sigl, Verena ;
Bammer, Philipp C. ;
Muckenhuber, Markus ;
Mayer, Daniela ;
Kulinski, Tomasz M. ;
Theussl, Hans-Christian ;
Penninger, Josef M. ;
Bock, Christoph ;
Barlow, Denise P. ;
Pauler, Florian M. ;
Hudson, Quanah J. .
ELIFE, 2017, 6
[2]   Allelome.PRO, a pipeline to define allele-specific genomic features from high-throughput sequencing data [J].
Andergassen, Daniel ;
Dotter, Christoph P. ;
Kulinski, Tomasz M. ;
Guenzl, Philipp M. ;
Bammer, Philipp C. ;
Barlow, Denise P. ;
Pauler, Florian M. ;
Hudson, Quanah J. .
NUCLEIC ACIDS RESEARCH, 2015, 43 (21)
[3]  
Balas Maggie M, 2018, Noncoding RNA Res, V3, P108, DOI 10.1016/j.ncrna.2018.03.001
[4]  
Barlow D.P., 2014, Cold Spring Harb Perspect Biol, V6
[5]   Genomic Imprinting: A Mammalian Epigenetic Discovery Model [J].
Barlow, Denise P. .
ANNUAL REVIEW OF GENETICS, VOL 45, 2011, 45 :379-403
[6]   THE MOUSE INSULIN-LIKE GROWTH-FACTOR TYPE-2 RECEPTOR IS IMPRINTED AND CLOSELY LINKED TO THE TME LOCUS [J].
BARLOW, DP ;
STOGER, R ;
HERRMANN, BG ;
SAITO, K ;
SCHWEIFER, N .
NATURE, 1991, 349 (6304) :84-87
[7]   Assessing sufficiency and necessity of enhancer activities for gene expression and the mechanisms of transcription activation [J].
Catarino, Rui R. ;
Stark, Alexander .
GENES & DEVELOPMENT, 2018, 32 (3-4) :202-223
[8]   Topology of mammalian developmental enhancers and their regulatory landscapes [J].
de Laat, Wouter ;
Duboule, Denis .
NATURE, 2013, 502 (7472) :499-506
[9]   IncRNAs in development and disease: from functions to mechanisms [J].
Delas, M. Joaquina ;
Hannon, Gregory J. .
OPEN BIOLOGY, 2017, 7 (07)
[10]   Chromosome Conformation Capture Carbon Copy (5C): A massively parallel solution for mapping interactions between genomic elements [J].
Dostie, Josee ;
Richmond, Todd A. ;
Arnaout, Ramy A. ;
Selzer, Rebecca R. ;
Lee, William L. ;
Honan, Tracey A. ;
Rubio, Eric D. ;
Krumm, Anton ;
Lamb, Justin ;
Nusbaum, Chad ;
Green, Roland D. ;
Dekker, Job .
GENOME RESEARCH, 2006, 16 (10) :1299-1309