Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization

Author:

West Jason A.12ORCID,Mito Mari3,Kurosaka Satoshi4ORCID,Takumi Toru4ORCID,Tanegashima Chiharu5ORCID,Chujo Takeshi6ORCID,Yanaka Kaori3,Kingston Robert E.12,Hirose Tetsuro6ORCID,Bond Charles7ORCID,Fox Archa89ORCID,Nakagawa Shinichi310ORCID

Affiliation:

1. Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114

2. Department of Genetics, Harvard Medical School, Boston, MA 02115

3. RNA Biology Laboratory, RIKEN, Wako 351-0198, Japan

4. RIKEN Brain Science Institute, Wako, Saitama 351-0198, Japan

5. Phyloinformatics Unit, RIKEN Center for Life Science Technologies, Chuo-ku, Kobe, Hyogo 650-0047, Japan

6. Institute for Genetic Medicine, Hokkaido University, Sapporo 060-0815, Japan

7. School of Chemistry and Biochemistry, The University of Western Australia, Crawley, Western Australia 6009, Australia

8. School of Anatomy, Physiology and Human Biology, The University of Western Australia, Crawley, Western Australia 6009, Australia

9. Harry Perkins Institute of Medical Research, Queen Elizabeth II Medical Centre, Nedlands, Western Australia 6009, Australia

10. RNA Biology Laboratory, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan

Abstract

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.

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Publisher

Rockefeller University Press

Subject

Cell Biology

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