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Landscape of semi-extractable RNAs across five human cell lines.
Zeng, Chao; Chujo, Takeshi; Hirose, Tetsuro; Hamada, Michiaki.
Afiliación
  • Zeng C; Faculty of Science and Engineering, Waseda University, Tokyo 1698555, Japan.
  • Chujo T; Faculty of Life Sciences, Kumamoto University, Kumamoto 8608556, Japan.
  • Hirose T; Graduate School of Frontier Biosciences, Osaka University, Suita 5650871, Japan.
  • Hamada M; Institute for Open and Transdisciplinary Research Initiatives (OTRI), Osaka University, Suita 5650871, Japan.
Nucleic Acids Res ; 51(15): 7820-7831, 2023 08 25.
Article en En | MEDLINE | ID: mdl-37463833
ABSTRACT
Phase-separated membraneless organelles often contain RNAs that exhibit unusual semi-extractability using the conventional RNA extraction method, and can be efficiently retrieved by needle shearing or heating during RNA extraction. Semi-extractable RNAs are promising resources for understanding RNA-centric phase separation. However, limited assessments have been performed to systematically identify and characterize semi-extractable RNAs. In this study, 1074 semi-extractable RNAs, including ASAP1, DANT2, EXT1, FTX, IGF1R, LIMS1, NEAT1, PHF21A, PVT1, SCMH1, STRG.3024.1, TBL1X, TCF7L2, TVP23C-CDRT4, UBE2E2, ZCCHC7, ZFAND3 and ZSWIM6, which exhibited consistent semi-extractability were identified across five human cell lines. By integrating publicly available datasets, we found that semi-extractable RNAs tend to be distributed in the nuclear compartments but are dissociated from the chromatin. Long and repeat-containing semi-extractable RNAs act as hubs to provide global RNA-RNA interactions. Semi-extractable RNAs were divided into four groups based on their k-mer content. The NEAT1 group preferred to interact with paraspeckle proteins, such as FUS and NONO, implying that RNAs in this group are potential candidates of architectural RNAs that constitute nuclear bodies.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: ARN / ARN Largo no Codificante Límite: Humans Idioma: En Revista: Nucleic Acids Res Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: ARN / ARN Largo no Codificante Límite: Humans Idioma: En Revista: Nucleic Acids Res Año: 2023 Tipo del documento: Article País de afiliación: Japón