TY  - JOUR
A1  - Sunwoo, Hongjae
A1  - Dinger, Marcel E.
A1  - Wilusz, Jeremy E.
A1  - Amaral, Paulo P.
A1  - Mattick, John S.
A1  - Spector, David L.
T1  - MEN ε/β nuclear-retained non-coding RNAs are up-regulated upon muscle differentiation and are essential components of paraspeckles
Y1  - 2009/03/01 
JF  - Genome Research 
JO  - Genome Research 
SP  - 347 
EP  - 359 
DO  - 10.1101/gr.087775.108 
VL  - 19 
IS  - 3 
UR  - http://genome.cshlp.org/content/19/3/347.abstract 
N2  - Studies of the transcriptional output of the human and mouse genomes have revealed that there are many more transcripts produced than can be accounted for by predicted protein-coding genes. Using a custom microarray, we have identified 184 non-coding RNAs that exhibit more than twofold up- or down-regulation upon differentiation of C2C12 myoblasts into myotubes. Here, we focus on the Men ε/β locus, which is up-regulated 3.3-fold during differentiation. Two non-coding RNA isoforms are produced from a single RNA polymerase II promoter, differing in the location of their 3′ ends. Men ε is a 3.2-kb polyadenylated RNA, whereas Men β is an ∼20-kb transcript containing a genomically encoded poly(A)-rich tract at its 3′-end. The 3′-end of Men β is generated by RNase P cleavage. The Men ε/β transcripts are localized to nuclear paraspeckles and directly interact with NONO. Knockdown of MEN ε/β expression results in the disruption of nuclear paraspeckles. Furthermore, the formation of paraspeckles, after release from transcriptional inhibition by DRB treatment, was suppressed in MEN ε/β-depleted cells. Our findings indicate that the MEN ε/β non-coding RNAs are essential structural/organizational components of paraspeckles. 
ER  -