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Mapping RNA-RNA interactome and RNA structure in vivo by MARIO
被引:122
作者:
Nguyen, Tri C.
[1
]
Cao, Xiaoyi
[1
]
Yu, Pengfei
[1
]
Xiao, Shu
[1
]
Lu, Jia
[1
]
Biase, Fernando H.
[1
]
Sridhar, Bharat
[1
]
Huang, Norman
[1
]
Zhang, Kang
[2
]
Zhong, Sheng
[1
]
机构:
[1] Univ Calif San Diego, Dept Bioengn, Powell Focht Bioengn Hall 384,9500 Gilman Dr, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Ophthalmol, La Jolla, CA 92093 USA
关键词:
CROSS-LINKING;
MESSENGER-RNA;
NUCLEOTIDE-RESOLUTION;
QUANTUM DOTS;
CHROMATIN IMMUNOPRECIPITATION;
WIDE IDENTIFICATION;
RIBONUCLEIC-ACID;
BINDING PROTEINS;
GENE-REGULATION;
NONCODING RNAS;
D O I:
10.1038/ncomms12023
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
The pervasive transcription of our genome presents a possibility of revealing new genomic functions by investigating RNA interactions. Current methods for mapping RNA-RNA interactions have to rely on an 'anchor' protein or RNA and often require molecular perturbations. Here we present the MARIO (Mapping RNA interactome in vivo) technology to massively reveal RNA-RNA interactions from unperturbed cells. We mapped tens of thousands of endogenous RNA-RNA interactions from mouse embryonic stem cells and brain. We validated seven interactions by RNA antisense purification and one interaction using single-molecule RNA-FISH. The experimentally derived RNA interactome is a scale-free network, which is not expected from currently perceived promiscuity in RNA-RNA interactions. Base pairing is observed at the interacting regions between long RNAs, including transposon transcripts, suggesting a class of regulatory sequences acting in trans. In addition, MARIO data reveal thousands of intra-molecule interactions, providing in vivo data on high-order RNA structures.
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页数:12
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