- About this Journal
- Abstracting and Indexing
- Aims and Scope
- Article Processing Charges
- Articles in Press
- Author Guidelines
- Bibliographic Information
- Citations to this Journal
- Contact Information
- Editorial Board
- Editorial Workflow
- Free eTOC Alerts
- Publication Ethics
- Reviewers Acknowledgment
- Submit a Manuscript
- Subscription Information
- Table of Contents
Molecular Biology International
Volume 2011 (2011), Article ID 137459, 14 pages
Protein Methylation and Stress Granules: Posttranslational Remodeler or Innocent Bystander?
1Division of Hematology and Medical Oncology, Department of Medicine, Weill Medical College of Cornell University, New York, NY 1065, USA
2Biochemical Molecular Neurobiology Laboratory, Department of Molecular Biology, New York State Institute for Basic Research in Developmental Disabilities, 1050 Forest Hill Road, Staten Island, NY 10314, USA
Received 30 November 2010; Accepted 10 January 2011
Academic Editor: Jörg Kobarg
Copyright © 2011 Wen Xie and Robert B. Denman. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Stress granules contain a large number of post-translationally modified proteins, and studies have shown that these modifications serve as recruitment tags for specific proteins and even control the assembly and disassembly of the granules themselves. Work originating from our laboratory has focused on the role protein methylation plays in stress granule composition and function. We have demonstrated that both asymmetrically and symmetrically dimethylated proteins are core constituents of stress granules, and we have endeavored to understand when and how this occurs. Here we seek to integrate this data into a framework consisting of the currently known post-translational modifications affecting stress granules to produce a model of stress granule dynamics that, in turn, may serve as a benchmark for understanding and predicting how post-translational modifications regulate other granule types.
Stress granules are large, complex ribonucleoprotein particles that form in response to cellular insults such as heat shock, oxidative stress, energy deprivation, and glucose starvation [1–3]. They contain messenger RNA, small ribosomal subunits, eukaryotic initiation factors, and a host of RNA-Binding proteins. Stress granules are sites of RNA processing, and as such they are in dynamic equilibrium with other components of the cytosol and even the nucleus. For example, Kedersha et al. have shown that stress granules are reciprocally linked to polyribosome formation . Additionally, certain RNA-Binding proteins have been shown to shuttle between stress granules and processing bodies . Finally, fluorescence recovery after photobleaching studies (FRAP) have demonstrated that the components in stress granules can be replaced by their soluble counterparts in the cytosol to varying degrees and rates [5–7] leading one to the view that these entities can be modulated by a variety of forces that affect their composition (Figure 1).
Posttranslational modifications are known to affect protein-protein interactions between messenger ribonucleoprotein particles (mRNPs) [8, 9], so it is not surprising that they also play important roles in the assembly and remodeling of stress granules. In fact, the classic trigger for stress granule formation arising from heat shock or oxidative stress involves the phosphorylation of eukaryotic initiation factor 2α (eIF2α) [10–12]. In addition, other phosphorylation/dephosphorylation events also have been shown to affect stress granule composition, assembly, and disassembly [13–15].
Recent work has expanded the list of Posttranslational modifications that can affect stress granule composition and dynamics. These include the recruitment of calreticulin to stress granules by its arginylation , the dependence of histone deacetylase 6 (HDAC6) activity for stress granule formation , and the discovery that inhibiting the ubiquitin-proteasome system leads to stress granule disassembly even in the continued presence of eIF2α phosphorylation . Finally, studies originating from our laboratory have demonstrated that stress granules contain methylarginine-containing proteins [19, 20]. In this paper we will examine the results implicating a role for protein methylation in stress granule function. We will then endeavor to integrate protein methylation into a general scheme detailing how Posttranslational modifiers act on stress granules and possibly other granules as well.
2. RNA-Binding Proteins Containing RG Rich Regions Are Methylated on Specific Arginine Residues
RNA-Binding proteins are associated with virtually all aspects of cellular RNA metabolism. RNA Binding, however, is mediated by a relatively small number of protein domains whose type, repeat-number, and sequential order within a protein dictate the RNA-Binding properties of that protein. The structure and composition of many RNA-Binding domains such as the RRM (RNA recognition motif) are well defined. Others, however, are more heterogeneous. An RNA-Binding domain that has not been well defined is the RGG box . Nevertheless, it is clear that RNA-Binding proteins that harbor RGG boxes, or more precisely, RG-rich regions, play important roles in many aspects of RNA processing. They do so in two interrelated ways. First, glycine-flanked arginine residues within RGG repeat motifs serve as target sites for Type I protein arginine methyltransferases (PRMTs), and methylation of specific arginine residues can have varied effects on a protein’s RNA-Binding activity, its ability to interact with other proteins and its intracellular localization [22, 23]. Second, alternative splicing, in and around RG-rich domains has been shown to modulate both nucleic acid binding [24, 25] and protein methylation .
3. Asymmetrically Dimethylated RNA-Binding Proteins Are Found in SGs
The fragile X mental retardation protein (FMRP) contains an RG-rich region, which is encoded by alternatively spliced exon 15 . Our discovery that this region could be methylated in vitro  led us to wonder if the methylation had any functional consequences on FMRP biology. Specifically, we were interested in testing whether methylation may be a trigger for the incorporation or release of FMRP from neuronal granules. Since biochemical studies pointed to the fact that methylation was required for FMRP to interact with its paralog, FXR1P , we wished to investigate whether the FMRP/FXR1P content was altered in granules when cells were hypomethylated. Initial immunostaining studies showed that endogenous FMRP forms small cytoplasmic granules  that were present in a wide variety of cultured cells . These granules were unique because they did not colocalize with other known granule markers, nor did they contain mRNA or methylated proteins. In addition, when HeLa cells were treated with adenosine 2′,3′ dialdehyde (AdOx), a general methylation inhibitor, the number of cells harboring such granules increased .
As a control for these studies we examined the cellular methylation state and its effect upon FMRP in stress granules. Here we clearly demonstrated that upon cellular hypomethylation a portion of the FMRP is lost from stress granules as its colocalization with stress granule markers such as TIA1 and PABP decreases. This change correlated with a decrease of FXR1P in FMRP-containing stress granules (Figure 2), a loss of FMRP in FXR1P immunoprecipitates, and with an increased association of FMRP with smaller cytoplasmic granules .
To confirm that AdOx treatment truly resulted in decreased cellular methylation we conducted Western blotting [19, 27] and immunostaining studies  using two antibodies that detect subsets of asymmetrically dimethylated (aDMA) proteins (Figure 3). Both assays showed a dose-dependent decrease in asymmetrically dimethylated proteins. However, the decreases for individual proteins were not uniform as they are most likely linked to the rate of protein turnover . In keeping with this observation, stress granules from AdOx-treated cells stain positive for asymmetrically dimethylated proteins, although much more weakly so than nontreated cells .
Because the antibodies used to detect asymmetrically dimethylated proteins are incompletely characterized and validated [33, 34] the identities of most of the methylated proteins that they detect in stress granules are not wellknown. Nevertheless, over the years a list of experimentally methylated RNA-Binding proteins that are recruited to stress granules upon a variety of cellular insults has grown (Table 1). These 14 proteins demonstrate that changes in cellular methylation have the potential for significantly modulating the composition and the function of stress granules. For example, the cold inducible response protein, CIRP, is methylated on arginines 94, 105, and 116 of its C-terminal RG-rich region. AdOx treatment completely blocks CIRP’s nuclear export and its subsequent recruitment into stress granules . On the other hand, as mentioned above, AdOx treatment reduces, but does not completely block, the recruitment of FMRP into stress granules.
4. The limitations of AdOx Studies
Is methylation obligate for stress granule formation? This turns out to be a much more difficult question to answer than one might think. The reason seems to be a function of the stability of the products of N-methylation reactions and the general dearth of cellular demethylases. As mentioned above, inhibiting cellular methylation with AdOx results in an increase in hypomethylated proteins, which are readily observed by comparing the patterns of AdOx-treated versus nontreated protein extracts by Western blotting with anti-methylarginine antibodies [1, 19] or by in vitro methylation . Nevertheless, Chen et al. have shown that the changes in methylation upon AdOx treatment are specifically associated with new protein synthesis. Most cellular methylation does not change. That is, once a protein is methylated it generally remains so until it is turned over . Because of the background of methylated and partially methylated proteins in cells treated with AdOx one would need a means of monitoring both stress granule formation and the methylation status of each methylated protein that associates with stress granules to determine whether methylation plays a role in stress granule assembly. Currently, the lack of antibodies that specifically recognize only the methylated or non-methylated forms of particular RNA-Binding proteins precludes attacking the problem in this manner.
To try to circumvent this requirement we sought a paradigm in which we could monitor the recruitment of a newly synthesized methylatable protein into stress granules in the presence of AdOx. We chose FMRP because it has been demonstrated that its overexpression is sufficient for forming stress granules in the absence of cellular stressors and that this effect is mediated by its methylatable RG-rich domain . Thus, we treated HeLa cells with AdOx and subsequently transfected them with a plasmid that produces EGFP-FMRP in its continuous presence. We determined that AdOx treatment had no effect on the expression efficiency of EGFP-FMRP or its ability to make cytoplasmic granules that sometimes contained other stress granule markers . However, two caveats prevent us from definitively concluding that protein methylation is not absolutely required for stress granule formation. First we noted that unlike endogenous FMRP, EGFP-FMRP granules contained asymmetrically that dimethylated proteins even in the presence of AdOx , and our experimental protocol does not allow us to distinguish whether EGFP-FMRP recruits endogenous methylated protein to form stress granules or vice versa. Second, we have not demonstrated whether or not EGFP-FMRP is methylated in the presence of AdOx. Thus, the question of whether methylation is required for stress granule formation will necessitate further study.
5. Are the Proteins Found in Stress Granules Methylated before or after Stress Granule Formation?
Other important questions that have yet to be addressed are where and when are the methylated proteins found in stress granules methylated? More specifically, is there any evidence that protein arginine methyltransferases are associated with stress granules? The importance of this question cannot be underestimated. If proteins cannot be methylated, dimethylated, or hyper-/hypomethylated while, they are in stress granules, it is extremely unlikely that protein methylation would play a direct role in stress granule remodeling.
Because of its known association with ribosomes , we were particularly attracted by the possibility that PRMT3 might be found in stress granules. Therefore, we measured the subcellular distribution of PRMT3 in the presence and absence of arsenite treatment by confocal immunofluorescence microscopy using endogenous FXR1P as a stress granule marker (Figure 4). We found that in the presence of arsenite PRMT3 was found in perinuclear cytoplasmic granules that colocalized with FXR1P-containing stress granules. Interestingly, pretreatment of the cells with AdOx resulted in the relocation of most of PRMT3 to the nucleus, effectively eliminating the colocalization (not shown). The basis of this effect is currently unknown. In contrast, we found that neither class II PRMT (PRMT5 nor PRMT7) colocalized with TIA1-containing stress granules. These data support the hypothesis that asymmetric dimethylation, but not symmetric dimethylation, may be modulated directly on stress granules. However, additional experiments, for example, Förster resonance energy transfer (FRET) studies, will be required to confirm the colocalization of PRMT3 in stress granules.
6. A Link between Stress Granules, Symmetric Dimethylation, and Splicing?
Although we found no evidence for the association of stress granules with class II protein arginine methyltransferases we still endeavored to ascertain whether stress granules contained symmetrically dimethylated (sDMA) proteins. To this end we treated HeLa cells with arsenite and then immunostained them with antibodies that recognize TIA1 and a subset of all symmetrically dimethylated proteins. We observed significant colocalization, indicating that stress granules unequivocally harbor symmetrically dimethylated proteins (Figure 5) .
The antibody (SYM10) that was used to detect symmetrically dimethylated arginine residues was raised to the peptide RsDMAGRsDMAGRsDMAGRsDMAG . In fact, Boisvert et al. detected more than 29 potential symmetrically dimethylated proteins in immunoprecipitation reactions using this antibody  (Figure 3). Most of the identified proteins were associated directly or indirectly with pre-mRNA splicing. Of particular interest here were the core spliceosomal proteins (SmB/B′, SmD1/D3, and U6 small nuclear RNA-associated Sm-like proteins Lsm4 and Lsm8), which have been shown to contain symmetric dimethylarginine  and are known epitopes for the SYM10 antibody .
Previous studies have shown that a large number of stress granule constituents also play a role in splicing (Table 2). However, since many of these proteins also have alternative functions, for example, as translational regulators, an operational link between stress granule function and splicing has not been clearly established. For example, the exon-junction complex (EJC) protein, MLN51, is recruited to stress granules upon oxidative stress, but other minimal constituents of the EJC (MAGOH, Y14 and EIF4AIII) are not. Thus, it is unlikely that EJC function would be relevant for stress granule biology. Nevertheless, our data showing symmetrically that dimethylated proteins were associated with stress granules suggested a potential functional link might occur between stress granules and the spliceosome. To address this question we immunostained arsenite-treated HeLa cells with core components of the spliceosome and its precursor, the SMN-PRMT5 complex. We found that neither the major spliceosomal proteins anti-SYM10 recognizes, that is, SmD3 and SmB/B′, nor SMN-PRMT5 complex components, PRMT5 and SMN, were associated with stress granules (Figures 4 and 6). Thus, the identities of the symmetrically dimethylated proteins that are present in stress granules must still be determined. More importantly, however, the data rule out the possibility that stress granules function in spliceosomal chaperoning or spliceosomal triage.
7. Modeling the Effects of Posttranslational Modifications on Stress Granule Dynamics
While our understanding of the mechanisms by which Posttranslational modifications regulate and remodel stress granules is incomplete, it is nevertheless clear that they do so in an intricate and often hierarchical way (Figure 7).
Of all the Posttranslational modifications affecting stress granules, phosphorylation, by far, exhibits the most varied effects and has the largest repertoire of affected target proteins. Phosphorylation can directly trigger stress granule assembly via the eIF2α pathway , or this can occur by the dephosphorylation of Ras-GTPase-activating protein SH3 domain binding protein 1 (G3BP1) . In addition, phosphorylation can have a direct bearing on the composition of stress granules through recruitment or remodeling. For example, cytosolic phosphorylation of mRNA-bound hnRNPA1 by MAP kinase interacting serine/threonine kinase (Mnk1/2) results in its recruitment into pre-existing stress granules . Similarly, phosphorylation of the Ras homolog gene A (RhoA) by Rho-associated coil-coil containing protein kinase (ROCK1) leads to its recruitment into pre-existing stress granules; however, in this case active ROCK1 is also recruited into stress granules, and this action prevents cellular apoptosis . Likewise, the scaffold protein WDR62 can recruit active c-jun N-terminal kinase (JNK) into stress granules and P-bodies , although the target(s) of the kinase within these mRNPs or its function have yet to be elucidated. Finally, phosphorylation also can affect stress granule disassembly. Recruitment of active focal adhesion kinase (FAK) to stress granules results in the phosphorylation of growth receptor bound protein 7 (Grb7) causing it is dissociation from the RNA-Binding protein HuR and consequently its release from stress granules . This remodeling event is crucial for the disassembly of nascent stress granules following stress.
Deacetylation can also have wide-ranging effects on stress granule assembly and recruitment; however, unlike phosphorylation, in which a number of different kinases affect specific targets and effect specific functions, the effects of deacetylation flow through a single multifunctional enzyme, histone deacetylase 6 (HDAC6) . Thus, HDAC6’s deacetylase domains promote stress granule formation via their ability to bind dephosphorylated G3BP1; however, deacetylase activity is not required to mediate this effect. Nevertheless, HDAC6 activity is required for stress granule formation since mouse embryonic fibroblasts (MEFs) lacking wild-type HDAC6 are unable to do so. Furthermore, HDAC6’s zinc finger ubiquitin binding domain is necessary for the recruitment of ubiquitinated proteins into stress granules, ultimately connecting stress granule dynamics to the ubiquitin-proteasome system and the ubiquitin conjugating system. Finally, HDAC6’s ability to interact with microtubules links a functional microtubule network to stress granule formation.
O-linked N-acetylglucosamine modification (O-GlcNAc) has also been associated with stress assembly . This modification, which occurs to a number of stress granule incorporated proteins most notably ribosomal proteins (rpsl), likely assists in the aggregation phase of stress granule formation as studies have shown that eIF2α phosphorylation is simultaneously required.
Other less well-studied Posttranslational modifications can also cause the modified proteins to be recruited into stress granules. Arginylation of calreticulin by the cytosolic enzyme arginine tRNA protein transferase (ATE1) following its stress-induced exit from the endoplasmic reticulum leads efficient incorporation into pre-existing stress granules . Likewise, ubiquitinated proteins can also be incorporated into stress granules, following transient proteasome inhibition with MG132 as can the ubiquitin ligase, Roquin . However, the role these proteins play in stress granule function is unknown.
Finally, the level of expression of various RNA-Binding proteins (RBPs) may influence their Posttranslational modification(s) and indirectly affect stress granule dynamics. Although most work has focused on the artificial overexpression of RBPs (TIA1/TIAR, FMRP, and G3BP) comparable nonequilibrium conditions could occur during development or in particular disease states such that the expression of a particular RBP exceeds the capacity of its Posttranslational modification enzymes or vice versa. For example, it has been reported that G3BP levels are decreased in fragile X syndrome . This suggests that there may be a relative increase in the ratio of phosphorylated/dephosphorylated G3BP, which potentially could affect the assembly, composition or function of stress granules in fragile X patients.
8. Locating the Role of Protein Methylation in the Model
How does Posttranslational protein methylation fit within the overall landscape of stress granule Posttranslational modifiers? While our knowledge of this process is still in its infancy certain tentative conclusions can be drawn. First, it is apparent from the rather large number of methylated proteins that are associated with stress granules that the potential for modulating stress granule composition is great. In this regard, protein methylation resembles phosphorylation more than arginylation. On the other hand, it appears more likely that protein methylation plays its role in stress granule recruitment and remodeling, rather than in its assembly or disassembly. This is particularly true of sDMA-modified proteins whose modification occurs in the cytosol rather than in the granules and CIRP whose methylation is required for exiting the nucleus. Nevertheless, the fact that PRMT3 may associate with stress granules holds out the possibility that direct aDMA methylation or hypermethylation may occur on certain stress granules. Interestingly, PRMT3 is unique among the family of protein arginine methyltransferases in that it contains a zinc finger binding domain , which may via protein-protein interactions also link it to other Posttranslational modifiers like HDAC6. It is certain to say that the role protein methylation plays in stress granule function is rife for future investigations.
9. Concluding Remarks: Looking to the Future
Lastly, can we make any inferences between the Posttranslational processes that regulate stress granules and those affecting other granule types? First, we should distinguish between what exactly is meant by granules types. Clearly, there are two classes of large mRNP-complexes, those that are common to all cells (polyribosomes, stress granules, and P-bodies) and those that are unique to different cells (germ granules, oocyte foci, neuronal transport granules). Regardless of the class, it has been shown that they all contain common core constituents [7, 67]. Thus, there should be some underlying similarities by which they are Posttranslationally regulated. We have been particularly intrigued by the common features of stress granules and neuronal transport granules (Table 3) which may suggest that common assembly and disassembly mechanisms apply to each. Nevertheless, their distinguishing characteristics allow the possibility of unique means of Posttranslational regulation, for example, the receptor-mediated remodeling of neuronal transport granules.
Because the various granule types that have been distinguished to date share common proteins, one might expect that those proteins which are modified prior to granule formation would have two possible fates: either they would sort identically to different granules or the modification might be used to differentially sort them to specific granule types, for example, stress granules versus P-bodies. While this has been a largely uncharted area of investigation it is interesting to note that Qi et al. have demonstrated that prolyl 4-hydroxylation of Ago2 is required for its recruitment into P-bodies but not stress granules .
In contrast, modifications that occur directly on granules would likely be unique to those granules. Furthermore, it is clear that specific proteins differentiate the various granule types and this would provide unique possibilities for Posttranslational regulation. For example, it has recently been shown that the phosphorylation of Dcp2 at S137 and the phosphorylation of Ago2 at S387 are required for their accumulation in P-bodies . Additionally, the repertoire of Posttranslational modifications need not be restricted to those that modify stress granules. Future studies will undoubtedly uncover a wealth of new Posttranslationally modified granule proteins, and these data will have to be integrated into comprehensive models of how these granules are formed and how they function. Until that time we have the general outline provided by Posttranslationally modified stress granules.
Protein methylation impinges upon stress granule dynamics in a number of ways that are beginning to be, but are not yet fully, defined. Time will tell if protein methylation is a true driver of stress granule stress granule assembly, disassembly, or remodeling, or whether it simply tags along, an innocent bystander on various RNA-Binding proteins that are recruited to these granules through different mechanisms.
All of the antibodies mentioned in this paper have been described in the authors’ published works [19, 20, 26, 33] with the exception of anti-SmB/B′ (Santa Cruz, sc25372), anti-SmD3 (Sigma HPA001170), and anti-SMN (2B1), a kind gift from Dr. Gideon Dreyfuss, University of Pennsylvania.
This work was funded in part by the New York State Research Foundation for Mental Hygiene. W. Xie was supported by a FRAXA Research Foundation grant to R. B. Denman.
- F. de Leeuw, T. Zhang, C. Wauquier, G. Huez, V. Kruys, and C. Gueydan, “The cold-inducible RNA-binding protein migrates from the nucleus to cytoplasmic stress granules by a methylation-dependent mechanism and acts as a translational repressor,” Experimental Cell Research, vol. 313, no. 20, pp. 4130–4144, 2007.
- T. Grouši, P. Ivanov, I. Frýdlová et al., “Robust heat shock induces eIF2α-phosphorylationin-dependent assembly of stress granules containing eIF3 and 40S ribosomal subunits in budding yeast, Saccharomyces cerevisiae,” Journal of Cell Science, vol. 122, no. 12, pp. 2078–2088, 2009.
- K. Fujimura, J. Katahira, F. Kano, Y. Yoneda, and M. Murata, “Microscopic dissection of the process of stress granule assembly,” Biochimica et Biophysica Acta, vol. 1793, no. 11, pp. 1728–1737, 2009.
- N. Kedersha, M. R. Cho, W. Li et al., “Dynamic shuttling of TIA-1 accompanies the recruitment of mRNA to mammalian stress granules,” Journal of Cell Biology, vol. 151, no. 6, pp. 1257–1268, 2000.
- N. Kedersha, G. Stoecklin, M. Ayodele et al., “Stress granules and processing bodies are dynamically linked sites of mRNP remodeling,” Journal of Cell Biology, vol. 169, no. 6, pp. 871–884, 2005.
- A. Baguet, S. Degot, N. Cougot et al., “The exon-junction-complex-component metastatic lymph node 51 functions in stress-granule assembly,” Journal of Cell Science, vol. 120, no. 16, pp. 2774–2784, 2007.
- J. R. Buchan and R. Parker, “Eukaryotic stress granules: the ins and outs of translation,” Molecular Cell, vol. 36, no. 6, pp. 932–941, 2009.
- S. Ceman, W. T. O'Donnell, M. Reed, S. Patton, J. Pohl, and S. T. Warren, “Phosphorylation influences the translation state of FMRP-associated polyribosomes,” Human Molecular Genetics, vol. 12, no. 24, pp. 3295–3305, 2003.
- I. Barlat, F. Maurier, M. Duchesne, E. Guitard, B. Tocque, and F. Schweighoffer, “A role for Sam68 in cell cycle progression antagonized by a spliced variant within the KH domain,” Journal of Biological Chemistry, vol. 272, no. 6, pp. 3129–3132, 1997.
- P. Anderson and N. Kedersha, “Stressful initiations,” Journal of Cell Science, vol. 115, no. 16, pp. 3227–3234, 2002.
- S. Mokas, J. R. Mills, C. Garreau et al., “Uncoupling stress granule assembly and translation initiation inhibition,” Molecular Biology of the Cell, vol. 20, no. 11, pp. 2673–2683, 2009.
- N. Kedersha, S. Chen, N. Gilks et al., “Evidence that ternary complex (eIF2-GTP-tRNA)-Deficient preinitiation complexes are core constituents of mammalian stress granules,” Molecular Biology of the Cell, vol. 13, no. 1, pp. 195–210, 2002.
- N. P. Tsai, P. C. Ho, and L. N. Wei, “Regulation of stress granule dynamics by Grb7 and FAK signalling pathway,” The EMBO Journal, vol. 27, no. 5, pp. 715–726, 2008.
- S. Guil, J. C. Long, and J. F. Cáceres, “hnRNP A1 relocalization to the stress granules reflects a role in the stress response,” Molecular and Cellular Biology, vol. 26, no. 15, pp. 5744–5758, 2006.
- N. P. Tsai and L. N. Wei, “RhoA/ROCK1 signaling regulates stress granule formation and apoptosis,” Cellular Signalling, vol. 22, no. 4, pp. 668–675, 2010.
- M. A. Carpio, C. Lopez Sambrooks, E. S. Durand, and M. E. Hallak, “The arginylation-dependent association of calreticulin with stress granules is regulated by calcium,” Biochemical Journal, vol. 429, no. 1, pp. 63–72, 2010.
- S. Kwon, Y. Zhang, and P. Matthias, “The deacetylase HDAC6 is a novel critical component of stress granules involved in the stress response,” Genes & Development, vol. 21, no. 24, pp. 3381–3394, 2007.
- R. Mazroui, S. Di Marco, R. J. Kaufman, and I. E. Gallouzi, “Inhibition of the ubiquitin-proteasome system induces stress granule formation,” Molecular Biology of the Cell, vol. 18, no. 7, pp. 2603–2618, 2007.
- N. Dolzhanskaya, G. Merz, J. M. Aletta, and R. B. Denman, “Methylation regulates the intracellular protein-protein and protein-RNA interactions of FMRP,” Journal of Cell Science, vol. 119, no. 9, pp. 1933–1946, 2006.
- N. Dolzhanskaya, W. Xie, G. Merz, and R. B. Denman, “EGFP-FMRP granules are proto-stress granules and a poor surrogate for endogenous FMRP,” Journal of Biophysics and Structural Biology. In press, http://precedings.nature.com/documents/5442/version/1.
- L. Redish, J. Shen, J. R. Currie, and R. B. Denman, “The RGG box: a domain in search of a consensus,” Current Topics in Biochemical Research, pp. 93–109, 2004.
- J. M. Aletta and J. C. Hu, “Protein arginine methylation in health and disease,” Biotechnology Annual Review, vol. 14, pp. 203–224, 2008.
- N. Dolzhanskaya, C. Dobkin, A. El Idrissi, R. P. Bauchwitz, and R. B. Denman, “Protein arginine methylation in fragile X mouse models: a cause of phenotypic diversity in fragile X syndrome?” in The Molecular Basis of Fragile X Syndrome, Y. J. Sung and R. B. Denman, Eds., pp. 245–265, Research Signposts, Trivandrum, India, 2005.
- L. A. Dempsey, L. A. Hanakahi, and N. Maizels, “A specific isoform of hnRNP D interacts with DNA in the LR1 heterodimer: canonical RNA binding motifs in a sequence-specific duplex DNA binding protein,” Journal of Biological Chemistry, vol. 273, no. 44, pp. 29224–29229, 1998.
- L. A. Dempsey, M. J. Li, A. Depace, P. Bray-Ward, and N. Maizels, “The human HNRPD locus maps to 4q21 and encodes a highly conserved protein,” Genomics, vol. 49, no. 3, pp. 378–384, 1998.
- N. Dolzhanskaya, G. Merz, and R. B. Denman, “Alternative splicing modulates protein arginine methyltransferase-dependent methylation of fragile X syndrome mental retardation protein,” Biochemistry, vol. 45, no. 34, pp. 10385–10393, 2006.
- R. B. Denman, “EGFP-FMRP granules are proto-granules that can be shunted to stress granules during a stress response,” Nature Precedings. submitted.
- F. Kayali, H. L. Montie, J. A. Rafols, and D. J. DeGracia, “Prolonged translation arrest in reperfused hippocampal cornu ammonis 1 is mediated by stress granules,” Neuroscience, vol. 134, no. 4, pp. 1223–1245, 2005.
- E. E. Eichler, S. Richards, R. A. Gibbs, and D. L. Nelson, “Fine structure of the human FMR1 gene,” Human Molecular Genetics, vol. 2, no. 8, pp. 1147–1153, 1993.
- R. B. Denman, N. Dolzhanskaya, and Y. J. Sung, “Regulating a translational regulator: mechanisms cells use to control the activity of the fragile X mental retardation protein,” Cellular and Molecular Life Sciences, vol. 61, no. 14, pp. 1714–1728, 2004.
- Y.-J. Sung, N. Dolzhanskaya, and R. B. Denman, “Searching for common ground: the fragile X mental retardation protein as a core element of RNA granules,” in New Research in Fragile X Syndrome, J. J. Uppner, Ed., pp. 117–134, Nova Scientific, 2007.
- D. H. Chen, K. T. Wu, C. J. Hung, M. Hsieh, and C. Li, “Effects of adenosine dialdehyde treatment on in vitro and in vivo stable protein methylation in heLa cells,” Journal of Biochemistry, vol. 136, no. 3, pp. 371–376, 2004.
- P. Duan, YE. Xu, B. Birkaya et al., “Generation of polyclonal antiserum for the detection of methylarginine proteins,” Journal of Immunological Methods, vol. 320, no. 1-2, pp. 132–142, 2007.
- F. M. Boisvert, J. Côté, M. C. Boulanger, and S. Richard, “A proteomic analysis of arginine-methylated protein complexes,” Molecular & Cellular Proteomics, vol. 2, no. 12, pp. 1319–1330, 2003.
- A. Frankel and S. Clarke, “RNase treatment of yeast and mammalian cell extracts affects in vitro substrate methylation by type I protein arginine N-methyltransferases,” Biochemical and Biophysical Research Communications, vol. 259, no. 2, pp. 391–400, 1999.
- R. Mazroui, M. E. Hout, S. Tremblay, C. Fillion, Y. Labelle, and E. W. Khandjian, “Trapping of messenger RNA by fragile X mental retardation protein into cytoplasmic granules induces translation repression,” Human Molecular Genetics, vol. 11, no. 24, pp. 3007–3017, 2002.
- R. Swiercz, D. Cheng, D. Kim, and M. T. Bedford, “Ribosomal protein rpS2 is hypomethylated in PRMT3-deficient mice,” Journal of Biological Chemistry, vol. 282, no. 23, pp. 16917–16923, 2007.
- F. M. Boisvert, J. Côté, M. C. Boulanger et al., “Symmetrical dimethylarginine methylation is required for the localization of SMN in Cajal bodies and pre-mRNA splicing,” Journal of Cell Biology, vol. 159, no. 6, pp. 957–969, 2002.
- H. Brahms, L. Meheus, V. de Brabandere, U. Fischer, and R. Lührmann, “Symmetrical dimethylation of arginine residues in spliceosomal Sm protein and the Sm-like protein LSm4, and their interaction with the SMN protein,” RNA, vol. 7, no. 11, pp. 1531–1542, 2001.
- S. Sen, I. Talukdar, and N. J. G. Webster, “SRp20 and CUG-BP1 modulate insulin receptor exon 11 alternative splicing,” Molecular and Cellular Biology, vol. 29, no. 3, pp. 871–880, 2009.
- M. C. Didiot, Z. Tian, C. Schaeffer, M. Subramanian, J. L. Mandel, and H. Moine, “The G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancer,” Nucleic Acids Research, vol. 36, no. 15, pp. 4902–4912, 2008.
- T. Kashima, N. Rao, C. J. David, and J. I. Manley, “hnRNP A1 functions with specificity in repression of SMN2 exon 7 splicing,” Human Molecular Genetics, vol. 16, no. 24, pp. 3149–3159, 2007.
- T. Revil, J. Pelletier, J. Toutant, A. Cloutier, and B. Chabot, “Heterogeneous nuclear ribonucleoprotein K represses the production of pro-apoptotic Bcl-xS splice isoform,” Journal of Biological Chemistry, vol. 284, no. 32, pp. 21458–21467, 2009.
- J. L. Kabat, S. Barberan-Soler, and A. M. Zahler, “HRP-2, the Caenorhabditis elegans homolog of mammalian heterogeneous nuclear ribonucleoproteins Q and R, is an alternative splicing factor that binds to UCUAUC splicing regulatory elements,” Journal of Biological Chemistry, vol. 284, no. 42, pp. 28490–28497, 2009.
- J. M. Izquierdo, “Hu antigen R (HuR) functions as an alternative pre-mRNA splicing regulator of Fas apoptosis-promoting receptor on exon definition,” Journal of Biological Chemistry, vol. 283, no. 27, pp. 19077–19084, 2008.
- S. Sen, I. Talukdar, Y. Liu, J. Tam, S. Reddy, and N. J.G. Webster, “Muscleblind-like 1 (Mbnl1) promotes insulin receptor exon 11 inclusion via binding to a downstream evolutionarily conserved intronic enhancer,” Journal of Biological Chemistry, vol. 285, no. 33, pp. 25426–25437, 2010.
- S. Pedrotti, P. Bielli, M. P. Paronetto et al., “The splicing regulator Sam68 binds to a novel exonic splicing silencer and functions in SMN2 alternative splicing in spinal muscular atrophy,” The EMBO Journal, vol. 29, no. 7, pp. 1235–1247, 2010.
- H. H. Chen, J. G. Chang, R. M. Lu, T. Y. Peng, and W. Y. Tarn, “The RNA binding protein hnRNP Q modulates the utilization of exon 7 in the survival motor neuron 2 (SMN2) gene,” Molecular and Cellular Biology, vol. 28, no. 22, pp. 6929–6938, 2008.
- J. K. Bose, I. F. Wang, L. Hung, W. Y. Tarn, and C. K. J. Shen, “TDP-43 overexpression enhances exon 7 inclusion during the survival of motor neuron pre-mRNA splicing,” Journal of Biological Chemistry, vol. 283, no. 43, pp. 28852–28859, 2008.
- H. N. Yeowell, L. C. Walker, D. M. Mauger, P. Seth, and M. A. Garcia-Blanco, “TIA nuclear proteins regulate the alternate splicing of lysyl hydroxylase 2,” Journal of Investigative Dermatology, vol. 129, no. 6, pp. 1402–1411, 2009.
- H. Zhu, M. N. Hinman, R. A. Hasman, P. Mehta, and H. Lou, “Regulation of neuron-specific alternative splicing of neurofibromatosis type 1 pre-mRNA,” Molecular and Cellular Biology, vol. 28, no. 4, pp. 1240–1251, 2008.
- N. Skoko, M. Baralle, E. Buratti, and F. E. Baralle, “The pathological splicing mutation c.6792C > G in NF1 exon 37 causes a change of tenancy between antagonistic splicing factors,” FEBS Letters, vol. 582, no. 15, pp. 2231–2236, 2008.
- Q. Liu and G. Dreyfuss, “A novel nuclear structure containing the survival of motor neurons protein,” The EMBO Journal, vol. 15, no. 14, pp. 3555–3565, 1996.
- H. Tourrière, K. Chebli, L. Zekri et al., “The RasGAP-associated endoribonuclease G3BP assembles stress granules,” Journal of Cell Biology, vol. 160, no. 6, pp. 823–831, 2003.
- T. Wasserman, K. Katsenelson, S. Daniliuc, T. Hasin, M. Choder, and A. Aronheim, “A novel c-Jun N-terminal kinase (JNK)-binding protein WDR62 is recruited to stress granules and mediates a nonclassical JNK activation,” Molecular Biology of the Cell, vol. 21, no. 1, pp. 117–130, 2010.
- T. Ohn, N. Kedersha, T. Hickman, S. Tisdale, and P. Anderson, “A functional RNAi screen links O-GlcNAc modification of ribosomal proteins to stress granule and processing body assembly,” Nature Cell Biology, vol. 10, no. 10, pp. 1224–1231, 2008.
- C. G. Vinuesa, M. C. Cook, C. Angelucci et al., “A RING-type ubiquitin ligase family member required to repress follicular helper T cells and autoimmunity,” Nature, vol. 435, no. 7041, pp. 452–458, 2005.
- N. Zhong, W. Ju, D. Nelson, C. Dobkin, and W. T. Brown, “Reduced mRNA for G3BP in fragile X cells: evidence of FMR1 gene regulation,” American Journal of Medical Genetics, vol. 84, no. 3, pp. 268–271, 1999.
- A. Frankel and S. Clarke, “PRMT3 is a distinct member of the protein arginine N-methyltransferase family: conferral of substrate specificity by a zinc-finger domain,” Journal of Biological Chemistry, vol. 275, no. 42, pp. 32974–32982, 2000.
- K. G. Chernov, A. Barbet, L. Hamon, L. P. Ovchinnikov, P. A. Curmi, and D. Pastré, “Role of microtubules in stress granule assembly: microtubule dynamical instability favors the formation of micrometric stress granules in cells,” Journal of Biological Chemistry, vol. 284, no. 52, pp. 36569–36580, 2009.
- Y. Kanai, N. Dohmae, and N. Hirokawa, “Kinesin transports RNA: isolation and characterization of an RNA-transporting granule,” Neuron, vol. 43, no. 4, pp. 513–525, 2004.
- G. Elvira, S. Wasiak, V. Blandford et al., “Characterization of an RNA granule from developing brain,” Molecular and Cellular Proteomics, vol. 5, no. 4, pp. 635–651, 2006.
- N. Dolzhanskaya, G. Merz, and R. B. Denman, “Oxidative stress reveals heterogeneity of FMRP granules in PC12 cell neurites,” Brain Research, vol. 1112, no. 1, pp. 56–64, 2006.
- P. W. Vanderklish and G. M. Edelman, “Differential translation and fragile X syndrome,” Genes, Brain and Behavior, vol. 4, no. 6, pp. 360–384, 2005.
- L. N. Antar, R. Afroz, J. B. Dictenberg, R. C. Carroll, and G. J. Bassell, “Metabotropic glutamate receptor activation regulates fragile X mental retardation protein and Fmr1 mRNA localization differentially in dendrites and at synapses,” Journal of Neuroscience, vol. 24, no. 11, pp. 2648–2655, 2004.
- L. N. Antar, J. B. Dictenberg, M. Plociniak, R. Afroz, and G. J. Bassell, “Localization of FMRP-associated mRNA granules and requirement of microtubules for activity-dependent trafficking in hippocampal neurons,” Genes, Brain and Behavior, vol. 4, no. 6, pp. 350–359, 2005.
- P. Anderson and N. Kedersha, “RNA granules,” Journal of Cell Biology, vol. 172, no. 6, pp. 803–808, 2006.
- S. H. Kim, W. K. Dong, I. J. Weiler, and W. T. Greenough, “Fragile X mental retardation protein shifts between polyribosomes and stress granules after neuronal injury by arsenite stress or in vivo hippocampal electrode insertion,” Journal of Neuroscience, vol. 26, no. 9, pp. 2413–2418, 2006.
- Y. De Diego Otero, L. A. Severijnen, G. van Cappellen, M. Schrier, B. Oostra, and R. Willemsen, “Transport of fragile X mental retardation protein via granules in neurites of PC12 cells,” Molecular and Cellular Biology, vol. 22, no. 23, pp. 8332–8341, 2002.
- H. H. Qi, P. P. Ongusaha, J. Myllyharju et al., “Prolyl 4-hydroxylation regulates Argonaute 2 stability,” Nature, vol. 455, no. 7211, pp. 421–424, 2008.
- J. H. Yoon, E. J. Choi, and R. Parker, “Dcp2 phosphorylation by Ste20 modulates stress granule assembly and mRNA decay in Saccharomyces cerevisiae,” Journal of Cell Biology, vol. 189, no. 5, pp. 813–827, 2010.