TY - JOUR
T1 - Highly ordered spatial organization of the structural long noncoding NEAT1 RNAs within paraspeckle nuclear bodies
AU - Souquere, Sylvie
AU - Beauclair, Guillaume
AU - Harper, Francis
AU - Fox, Archa
AU - Pierron, Gérard
PY - 2010/11/15
Y1 - 2010/11/15
N2 - Paraspeckles (PSPs) are nuclear bodies associated with the retention in the nucleus of specific mRNAs. Two isoforms of a long noncoding RNA (NEAT1-v1/Menε and NEAT1-v2/Menβ) are required for the integrity of PSPs. Here, we analyzed the molecular organization of PSPs by immuno- and in situ hybridization electron microscopy. Detection of the paraspeckle markers PSPC1 and P54NRB/NONO confirm the identity between PSPs and the previously described interchromatin granule-associated zones (IGAZs). High-resolution in situ hybridization of NEAT1 transcripts revealed a highly ordered organization of IGAZ/PSPs. Although the 3.7-kb NEAT1-v1 and the identical 5′ end of the 22.7-kb NEAT1-v2 transcripts are confined to the periphery, central sequences of NEAT1-v2 are found within the electron-dense core of the bodies. Moreover, the 3′ end of NEAT1-v2 also localize to the periphery, indicating possible architectures for IGAZ/PSPs. These results further suggest that the organization of NEAT1 transcripts constrains the geometry of these bodies. Accordingly, we observed in HeLa and NIH 3T3 cells that IGAZ/PSPs are elongated structures with a well-defined diameter. Our results provide new insight on the ability of noncoding RNAs to form subcellular structures.
AB - Paraspeckles (PSPs) are nuclear bodies associated with the retention in the nucleus of specific mRNAs. Two isoforms of a long noncoding RNA (NEAT1-v1/Menε and NEAT1-v2/Menβ) are required for the integrity of PSPs. Here, we analyzed the molecular organization of PSPs by immuno- and in situ hybridization electron microscopy. Detection of the paraspeckle markers PSPC1 and P54NRB/NONO confirm the identity between PSPs and the previously described interchromatin granule-associated zones (IGAZs). High-resolution in situ hybridization of NEAT1 transcripts revealed a highly ordered organization of IGAZ/PSPs. Although the 3.7-kb NEAT1-v1 and the identical 5′ end of the 22.7-kb NEAT1-v2 transcripts are confined to the periphery, central sequences of NEAT1-v2 are found within the electron-dense core of the bodies. Moreover, the 3′ end of NEAT1-v2 also localize to the periphery, indicating possible architectures for IGAZ/PSPs. These results further suggest that the organization of NEAT1 transcripts constrains the geometry of these bodies. Accordingly, we observed in HeLa and NIH 3T3 cells that IGAZ/PSPs are elongated structures with a well-defined diameter. Our results provide new insight on the ability of noncoding RNAs to form subcellular structures.
UR - http://www.scopus.com/inward/record.url?scp=78649637489&partnerID=8YFLogxK
U2 - 10.1091/mbc.E10-08-0690
DO - 10.1091/mbc.E10-08-0690
M3 - Article
C2 - 20881053
AN - SCOPUS:78649637489
SN - 1059-1524
VL - 21
SP - 4020
EP - 4027
JO - Molecular Biology of the Cell
JF - Molecular Biology of the Cell
IS - 22
ER -