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As one of the most abundant modifications on mRNA in mammal, N6-methyladenosine (m6A) has been demonstrated to play important roles in various biological processes including nuclear RNA export, mRNA splicing, miRNA processing, mRNA degradation and translation (Shi et al., 2019). Importantly, different m6A reader proteins have been shown to play central roles in these processes.
YTH (YT521-B homology)-domain containing proteins are members of the conserved m6A reader family, which recognize m6A via the YTH domain (Hazra et al., 2019). Members of this family have been shown to play a role in mRNA translation and mRNA decay (Wang et al., 2014; Wang et al., 2015; Li et al., 2017; Shi et al.,2017). However, mechanisms by which these readers impact various biological processes are still elusive. For instance, YTHDF2 has been shown to regulate mRNA decay and is localized to the membrane-less cytoplasmic P granules (Wang et al., 2014), where mRNA decay occurs. But how YTHDF2 and its associated m6A RNAs are localized to this phase-separated granule (Standart and Weil, 2018) remains largely unknown.
As P bodies are liquid-like droplets in cytoplasm (Standart and Weil, 2018), we speculated that YTHDF2 may share liquid-like phase separation (LLPS) features. As with many LLPS proteins, YTHDF2 contains a low complexity (LC) domain (aa 230–383), which includes a glutamine (Q) rich domain (aa 288–383) (Fig. 1A). Interestingly, recombinant YTHDF2 protein containing the LC domain (YTHDF2aa 230−383) forms liquid droplets (23 μmol/L protein in 37 mmol/L NaCl, 10% PEG8000), which are sensitive to 1,6-hexanediol (previously shown to specifically disrupt liquid-like assemblies) (Kroschwald et al., 2017) (Fig. 1B), suggesting phase separation. This phase separation ability is dependent on NaCl concentration (Fig. S1A), which is consistent with another report (Ries et al., 2019). Moreover, we found these droplets fuse with each other to form bigger droplets, which further suggests a liquid like phase separation feature of YTHDF2aa 230−383 (Fig. S1B, and Video S1). Other members of this family, YTHDF1 and YTHDF3, also contain glutamine (Q) rich domain (Fig. S1C), and also have phase separation ability (Fig. S1D). As YTHDF2 glutamine compositional bias is conserved among vertebrates, to determine whether glutamine richness within the LC domain is important for LLPS of YTHDF2, we changed all glutamine to alanine in YTHDF2aa 230−383 (Fig. S1E), and the mutated protein essentially failed to form as many and large LLPS under the same assay condition (Fig. S1F and S1G). Similarly, another phase separation protein MED1 contains conserved serine (S) rich region, and this serine bias is necessary for MED1 phase separation (Sabari et al., 2018). To test whether YTHDF2 forms LLPS in cell, we overexpressed EGFP-YTHDF2 in mouse embryonic stem (mES) cells and human U2OS cells. FRAP assays showed YTHDF2 forms LLPS in both cell lines (Fig. 1C and 1D).
Previous studies suggested that RNA plays a crucial role in protein phase separation. For instance, RNA has been shown to facilitate HP1 alpha phase separation on heterochromatin (Strom et al., 2017). Given that YTHDF2 preferentially binds m6A RNA (Wang et al., 2014), we hypothesized that m6A RNA might promote YTHDF2-mediated phase separation. To test this idea, we constructed a portion of the YTHDF2 protein containing aa 230 to its C terminus (aa 579), which includes both the LC and the YTH domains (Fig. 1A). We identified a condition (13 μmol/L YTHDF2, 37 mmol/L NaCl, 0.74 μmol/L RNA, 10% PEG8000) under which the recombinant YTHDF2aa 230−579 protein barely formed LLPS with RNA oligos containing no m6A in vitro (Fig. S1H, right and S1I). Importantly, however, under the same assay condition, RNA oligos containing one m6A modification induced liquid like droplet formation (Fig. S1H, left and S1I). In addition, we found this phase separation enhancement appears to be dependent on the number of m6A in the RNA. As shown in Fig. 1E, phase separation mediated by YTHDF2 increases in a manner that is dependent on the number of m6A sites in the RNA oligos (50 bp RNAs containing either 0, 1, 5, or 10 m6A). These results are consistent with the recent reports that RNA oligos containing multiple m6A methylation sites robustly induce droplet formation by YTHDF2 (Gao et al., 2019; Ries et al., 2019). Consistently, induction of phase separation of YTHDF2 by m6A RNAs seems to be dependent on the YTH domain, as even the RNA containing 10 m6A failed to enhance phase separation in vitro when the m6A-binding capability of the YTH domain is compromised (YTHDF2aa 230−579 carrying W432A, W486A) (Li et al., 2014) (Fig. 1F). To corroborate this finding, we investigated whether binding of YTHDF2 to m6A is necessary for phase separation in vivo by expressing wildtype and the m6A-binding defective YTHDF2 (YTH mutated (W432A, W486A)) in mouse ES cells. While wildtype YTHDF2 formed droplets in cell, YTH mutated YTHDF2 did not (Fig. 1G), indicating that the ability of YTHDF2 to bind m6A RNA is necessary for YTHDF2 LLPS in vivo. To further confirm this finding, we asked whether YTHDF2 forms LLPS in cells lacking the mRNA m6A enzymatic complex, METTL3 or METTL14 (Fig. S1J). We detected no YTHDF2 droplets in these cells (Fig. 1G), further supporting the notion that m6A promotes YTHDF2 LLPS in cells.
In summary, we provide both in vitro and in vivo data demonstrating that m6A enhances phase separation of YTHDF2. Although recombinant YTHDF2 itself can phase separate in vitro, m6A modification significantly enhances this ability, and in vivo, YTHDF2 LLPS may in fact be dependent on binding m6A mRNAs.
While this manuscript was in preparation, several groups reported that YTHDF family proteins display phase separation potential (Fu and Zhuang, 2019; Gao et al., 2019; Ries et al., 2019) stimulated by m6A RNA (Gao et al., 2019; Ries et al., 2019), consistent with our finding that m6A promotes the phase separation potential of YTHDF2.
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FOOTNOTES
H.S. was sponsored by Shanghai Rising-Star Program (19QA1401300) and the National Natural Science Foundation of China (Grant Nos. 81874157 and 31601060). Research was also supported by funds from Fudan University. Y.S. is an American Cancer Society Research Professor.
J.W. and L.W. carried out all the experiments described in this manuscript. H.M. and Y.S. directed all the experiments with input from J.D. H.S. and Y.S. conceived the project and co-wrote the manuscript.
Y.S. is a co-founder of Constellation Pharmaceuticals, Inc. and Athelas Therapeutics Inc.
J.W., L.W., J.D., Y.G.S., H.M., and H.S. declare that they have no conflict of interest.
This article does not contain any studies with human or animal subjects performed by the any of the authors.
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Wang, J., Wang, L., Diao, J. et al. Binding to m6A RNA promotes YTHDF2-mediated phase separation. Protein Cell 11, 304–307 (2020). https://doi.org/10.1007/s13238-019-00660-2
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DOI: https://doi.org/10.1007/s13238-019-00660-2