Other

Dataset Information

0

Genomic RNA elements drive phase separation of the SARS-CoV-2 nucleocapsid


ABSTRACT: We report that the SARS-CoV-2 nucleocapsid protein (N-protein) undergoes liquid-liquid phase separation (LLPS) with viral RNA. N-protein condenses with specific RNA genomic elements under physiological buffer conditions and condensation is enhanced at human body temperatures (33°C and 37°C) and reduced at room temperature (22°C). RNA sequence and structure in specific genomic regions regulate N-protein condensation while other genomic regions promote condensate dissolution, potentially preventing aggregation of the large genome. At low concentrations, N-protein preferentially crosslinks to specific regions characterized by single-stranded RNA flanked by structured elements and these features specify the location, number, and strength of N-protein binding sites (valency). Liquid-like N-protein condensates form in mammalian cells in a concentration-dependent manner and can be altered by small molecules. Condensation of N-protein is RNA sequence and structure specific, sensitive to human body temperature, and manipulatable with small molecules, and presents a screenable process for identifying antiviral compounds effective against SARS-CoV-2.

ORGANISM(S): Severe acute respiratory syndrome coronavirus 2

PROVIDER: GSE162569 | GEO | 2020/12/17

REPOSITORIES: GEO

Dataset's files

Source:
Action DRS
Other
Items per page:
1 - 1 of 1

Similar Datasets

2020-11-27 | E-MTAB-9781 | biostudies-arrayexpress
2014-10-31 | E-GEOD-52920 | biostudies-arrayexpress
2023-08-31 | E-MTAB-13040 | biostudies-arrayexpress
2022-02-04 | GSE84081 | GEO
2022-06-03 | E-MTAB-11261 | biostudies-arrayexpress
2024-09-16 | E-MTAB-14342 | biostudies-arrayexpress
2015-05-19 | E-GEOD-59185 | biostudies-arrayexpress
2023-04-26 | GSE201626 | GEO
2007-04-25 | E-MEXP-510 | biostudies-arrayexpress
2007-10-30 | E-MEXP-511 | biostudies-arrayexpress