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Stoichiometry of long noncoding RNA interactions with other RNAs: Insights from OIP5-AS1
被引:2
|作者:
Yang, Jen-Hao
[1
,2
,3
]
Tsitsipatis, Dimitrios
[2
]
Gorospe, Myriam
[2
,4
]
机构:
[1] Natl Sun Yat Sen Univ, Inst Biomed Sci, Kaohsiung, Taiwan
[2] NIH, Lab Genet & Genom, Natl Inst Aging Intramural Res Program, Baltimore, MD USA
[3] Natl Sun Yat set Univ, Inst Biomed Sci, Kaohsiung 804, Taiwan
[4] NIA IRP, Lab Genet & Genom, NIH, Baltimore, MD 21224 USA
基金:
美国国家卫生研究院;
关键词:
lncRNA;
OIP5-AS1;
RNA copy number;
RNA-RNA interaction;
target RNA-directed microRNA degradation (TDMD);
COMPETING ENDOGENOUS RNA;
MUSCLE DIFFERENTIATION;
MESSENGER-RNA;
MIRNA;
D O I:
10.1002/wrna.1841
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Long noncoding (lnc)RNAs modulate gene expression programs in a range of developmental processes in different organs. In skeletal muscle, lncRNAs have been implicated in myogenesis, the process whereby muscle precursor cells form muscle fibers during embryonic development and regenerate muscle fibers in the adult. Here, we discuss OIP5-AS1, a lncRNA that is highly expressed in skeletal muscle and is capable of coordinating protein expression programs during myogenesis. Given that several myogenic functions of OIP5-AS1 involve interactions with MEF2C mRNA and with the microRNA miR-7, it was critical to carefully evaluate the precise levels of OIP5-AS1 during myogenesis. We discuss the approaches used to examine lncRNA copy number using OIP5-AS1 as an example, focusing on quantification by quantitative PCR analysis with reference to nucleic acids of known abundance, by droplet digital (dd)PCR measurement, and by microscopic visualization of individual lncRNAs in cells. We discuss considerations of RNA stoichiometry in light of developmental processes in which lncRNAs are implicated. This article is categorized under: Regulatory RNAs/RNAi/Riboswitches > Regulatory RNAs
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页数:8
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