RNA buffers the phase separation behavior of prion-like RNA binding proteins

<jats:title>RNA and membraneless organelles</jats:title> <jats:p> Membraneless compartments can form in cells through liquidliquid phase separation (see the Perspective by Polymenidou). But what prevents these cellular condensates from randomly fusing together? Using the RNA-binding protein (RBP) Whi3, Langdon <jats:italic>et al.</jats:italic> demonstrated that the secondary structure of different RNA components determines the distinct biophysical and biological properties of the two types of condensates that Whi3 forms. Several RBPs, such as FUS and TDP43, contain prion-like domains and are linked to neurodegenerative diseases. These RBPs are usually soluble in the nucleus but can form pathological aggregates in the cytoplasm. Maharana <jats:italic>et al.</jats:italic> showed that local RNA concentrations determine distinct phase separation behaviors in different subcellular locations. The higher RNA concentrations in the nucleus act as a buffer to prevent phase separation of RBPs; when mislocalized to the cytoplasm, lower RNA concentrations trigger aggregation. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6391" page="922" related-article-type="in-this-issue" vol="360" xlink:href="10.1126/science.aar7432">922</jats:related-article> , p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6391" page="918" related-article-type="in-this-issue" vol="360" xlink:href="10.1126/science.aar7366">918</jats:related-article> ; see also p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6391" page="859" related-article-type="in-this-issue" vol="360" xlink:href="10.1126/science.aat8028">859</jats:related-article> </jats:p>