TY - JOUR
T1 - Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization
AU - West, Jason A.
AU - Mito, Mari
AU - Kurosaka, Satoshi
AU - Takumi, Toru
AU - Tanegashima, Chiharu
AU - Chujo, Takeshi
AU - Yanaka, Kaori
AU - Kingston, Robert E.
AU - Hirose, Tetsuro
AU - Bond, Charles S.
AU - Fox, Archa
AU - Nakagawa, Shinichi
PY - 2016
Y1 - 2016
N2 - Paraspeckles are nuclear bodies built on the long noncoding RNA Neat1, which regulates a variety of physiological processes including cancer progression and corpus luteum formation. To obtain further insight into the molecular basis of the function of paraspeckles, we performed fine structural analyses of these nuclear bodies using structural illumination microscopy. Notably, paraspeckle proteins are found within different layers along the radially arranged bundles of Neat1 transcripts, forming a characteristic core-shell spheroidal structure. In cells lacking the RNA binding protein Fus, paraspeckle spheroids are disassembled into smaller particles containing Neat1, which are diffusely distributed in the nucleoplasm. Sequencing analysis of RNAs purified from paraspeckles revealed that AG-rich transcripts associate with Neat1, which are distributed along the shell of the paraspeckle spheroids. We propose that paraspeckles sequester core components inside the spheroids, whereas the outer surface associates with other components in the nucleoplasm to fulfill their function.
AB - Paraspeckles are nuclear bodies built on the long noncoding RNA Neat1, which regulates a variety of physiological processes including cancer progression and corpus luteum formation. To obtain further insight into the molecular basis of the function of paraspeckles, we performed fine structural analyses of these nuclear bodies using structural illumination microscopy. Notably, paraspeckle proteins are found within different layers along the radially arranged bundles of Neat1 transcripts, forming a characteristic core-shell spheroidal structure. In cells lacking the RNA binding protein Fus, paraspeckle spheroids are disassembled into smaller particles containing Neat1, which are diffusely distributed in the nucleoplasm. Sequencing analysis of RNAs purified from paraspeckles revealed that AG-rich transcripts associate with Neat1, which are distributed along the shell of the paraspeckle spheroids. We propose that paraspeckles sequester core components inside the spheroids, whereas the outer surface associates with other components in the nucleoplasm to fulfill their function.
UR - http://www.scopus.com/inward/record.url?scp=84991256820&partnerID=8YFLogxK
U2 - 10.1083/jcb.201601071
DO - 10.1083/jcb.201601071
M3 - Article
C2 - 27646274
AN - SCOPUS:84991256820
SN - 0021-9525
VL - 214
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 7
M1 - 817
ER -