Aβ peptide that accumulates in Alzheimer’s disease brain, derives from proteolytic processing of the amyloid precursor protein (APP) that exists in three main isoforms derived by alternative splicing. The isoform APP695, lacking exons 7 and 8, is predominately expressed in neurons and abnormal neuronal splicing of APP has been observed in the brain of patients with Alzheimer’s disease. Herein, we demonstrate that expression of the neuronal members of the ELAVL protein family (nELAVLs) correlate with APP695 levels in vitro and in vivo. Moreover, we provide evidence that nELAVLs regulate the production of APP695; by using a series of reporters we show that concurrent binding of nELAVLs to sequences located both upstream and downstream of exon 7 is required for its skipping, whereas nELAVL-binding to a highly conserved U-rich sequence upstream of exon 8, is sufficient for its exclusion. Finally, we report that nELAVLs block APP exon 7 or 8 definition by reducing the binding of the essential splicing factor U2AF65, an effect facilitated by the concurrent binding of AUF-1. Our study provides new insights into the regulation of APP pre-mRNA processing, supports the role for nELAVLs as neuron-specific splicing regulators and reveals a novel function of AUF1 in alternative splicing.
One of the hallmarks of Alzheimer’s disease (AD), the major cause of dementia in humans, is the abnormal deposition of aggregated amyloid-beta peptide (Αβ) in the brain1. Aβ is generated upon proteolytic cleavage of the parent amyloid precursor protein (APP), mutations of which have been associated with familial AD2. In mammals, APP is ubiquitously expressed, but most abundantly in the brain3,4. The gene contains 18 exons, four of which undergo alternative splicing (AS)3,5,6,7,8. In neurons, APP is present in three major isoforms: APP770 containing all exons, APP751 lacking exon 8 and APP695 lacking exons 7 and 8. APP770 and APP751 are ubiquitously expressed, whereas APP695 is predominately enriched in neurons3,6,7. It has been shown that APP695 is decreased, whereas APP770 is increased in the brain of AD patients9,10,11,12 and abnormal neuronal splicing of APP pre-mRNA has been associated with aberrant Aβ production13,14.
Along the same lines, AS is particularly prevalent in the nervous system15,16 and alterations in neural AS patterns have been linked to neurological disorders17. Tissue specific AS is regulated by a subset of RNA-binding proteins (RBPs), namely splicing regulators, that interact with RNA motifs on their target pre-mRNAs and affect their processing. In mammals, a highly abundant family of RBPs is the ELAVL-like (ELAVL) group of proteins that share significant homology with the Drosophila embryonic lethal and abnormal vision (ELAV) protein, shown to regulate AS in Drosophila neurons18,19. ELAVL protein family is comprised of four highly conserved members, the ubiquitously expressed ELAVL1 and the three predominantly neuronal RBPs ELAVL2, 3 and 4, collectively referred as neuronal ELAVL proteins (nELAVLs)20. At the molecular level, all members consist of three RNA-recognition motifs (RRM1-3) and a highly variable hinge region separating RRM2 and RRM3; RRM1 and RRM2 are mainly responsible for RNA-binding, whereas the hinge region is responsible for protein-protein interactions and contains signals for both nuclear localization and export21,22,23,24.
ELAVLs have been implicated in various biological processes and most of their functions were initially attributed to their ability to bind to specific AU-rich sequences (AU-rich elements, AREs) in the 3′untranslated region (UTR) of mammalian transcripts and increase the stability and/or translation of their targets25. More recent findings, suggest that at least nELAVLs bind with a higher affinity to U-rich sequences interspersed with guanosine (G) rather than adenosine residues (A), that are highly represented in intronic regions of target transcripts26. Consistently, in addition to the regulation of steady-state mRNA levels, nELAVLs have been also implicated in neuron-specific alternative RNA processing26 and nELAVL-mediated regulation of neuron-specific AS has been demonstrated for a small number of pre-mRNA targets27,28,29,30.
It has been previously shown that ELAVL4 binds to the 3′UTR of APP mRNA and increases its stability31. In the present study we provide evidence that nELAVLs are also critically involved in the regulation of neuron-specific AS of both human and mouse APP pre-mRNA. We report that APP695 expression correlates with nELAVLs in the human brain and cell lines and most importantly demonstrate that nELAVs but not the ubiquitous ELAVL1, promote the exclusion of both exons 7 and 8 from the pre-mRNA to generate APP695. Moreover, by using a series of artificial minigenes for human and mouse APP exons 7 and 8, we show that concurrent binding of nELAVLs to distal sequences located both upstream and downstream of exon 7 is required for its skipping, whereas nELAVL-binding to a highly conserved U-rich sequence just upstream of exon 8, is sufficient for its exclusion. Finally, we report that nELAVL proteins block exon definition by reducing the binding of the essential splicing factor U2AF65 to the 3′ splice site of both APP exons 7 and 8 and that this effect is facilitated by the concurrent binding of another ARE-binding protein AUF-1 to APP pre-mRNA. Taken together, our study provides new insights into a conserved neuronal mechanism for the regulation of APP695 expression and reveals a novel function of AUF-1 as an AS modulator.
Correlation between nELAVLs and APP695 expression
Both APP695 and nELAVLs are predominantly expressed in neurons3,20 indicating that a possible correlation between them may exist in vivo. To investigate this, we re-analyzed RNAseq data from 17 post-mortem human brain samples (9 AD patient and 8 control post-mortem brain samples; accession number GSE53699)32. More specifically, mRNA levels of isoforms APP770, APP751 and APP695 were normalized against total APP in each sample and associations between normalized APP isoform levels and mRNA levels of ELAVL1-4, as well as AUF-1 and TIA-1, two other RBPs sharing common targets with ELAVLs27,29,33,34, were investigated (Fig. 1A). Our analysis revealed a significant correlation of neuronal APP695 with nELAVLs (ELAVL2: Pearson r = 0.593, P < 0.05, ELAVL3: Pearson r = −0.510, P < 0.05, ELAVL4: Pearson r = 0.544, P < 0.05), but not with ELAV1, AUF-1 or TIA-1. Moreover, there was no correlation between the levels of nELAVLs and APP770 or APP751 isoforms (see Supplementary Table S1A,B) suggesting that in the human brain, nELAVL expression is specifically correlated with APP695 expression. It should be noted that unlike previous reports9,10,11,12 our differential expression analysis revealed no difference in the levels of APP isoforms between control and AD samples. No difference was either observed in nELAVL levels between the two groups.
To examine if this correlation also applies in vitro, levels of ELAVLs and APP isoforms were assayed in different cell lines and mouse primary cortical neurons, the later serving as a cell model for APP695-specific AS. As shown in Fig. 1B and C, similar to cortical neurons, significant levels of APP695 mRNA and protein were detected only in cells, where nELAVL expression was also observed. In contrast, there was no obvious association between APP695 and ELAVL1 expression (Fig. 1B and C) or between nELAVLs and APP isoforms generated by AS of exon 15 (see Supplementary Fig. S1A–C). To gain further support, nELAVL and APP695 levels were also examined in SH-SY5Y and CAD neuroblastoma cells upon differentiation into a neuron-like phenotype. Compared to their controls, differentiated SH-SY5Y and CAD cells, as evident by the upregulation of neuronal markers βΙΙΙ tubulin and SAP97, displayed an increase of both nELAVLs and APP695 levels, whereas changes in ELAVL1 expression did not correspond to those of APP695 (Fig. 1D). It thus appears that a strong correlation between nELAVLs and APP695 generation exists both in vitro and in vivo.
nELAVLs promote the exclusion of exons 7 and 8 from the endogenous APP pre-mRNA
The correlation between nELAVLs and APP695 expression suggests a role for these RBPs in the regulation of APP695-specific AS. To test this hypothesis, SK-N-SH cells, that express no nELAVLs, were transfected with an expression vector bearing either one Elavl or no insert (empty) as a control and the effect of ELAVLs on the AS pattern of APP exons 7 and 8 was assayed by RT-PCR with primers that allow the simultaneous detection of all four different splicing events (Fig. 2A). As shown in Fig. 2B, overexpression of ELAVL3 or ELAVL4 led to a significant decrease in the percentage of full-length APP mRNA (APP770: ANOVA, F(4,14) = 5.429, P < 0.05 and Bonferroni post-hoc) along with a significant increase in the percentage of APP mRNA lacking both exons 7 and 8 (APP695: ANOVA, F(4,14) = 12.075, P < 0.01 and Bonferroni post-hoc); in contrast, no difference was observed on the percentage of APP transcripts lacking either only exon 7 (APP714, undetectable) or only exon 8 (APP751). Notably, ELAVL overexpression had no effect on the AS pattern of APP exon 15 (see Supplementary Fig. S1A–C). Total RNA from the above transfected cells was also used in a series of RT-qPCR experiments with primers specific for APP770, APP751 and APP695. Our analysis revealed that in contrast to the ubiquitous ELAVL1, overexpression of ELAVL2, ELAVL3 or ELAVL4 resulted in a significant reduction of APP770 relative expression by 35%, 53% or 49% (Fig. 2C; ANOVA, F(4,14) = 22.573, P < 0.001 and Bonferroni post-hoc), along with a significant 3.8-fold, 4.5-fold or 5-fold upregulation of APP695, respectively (Fig. 2D; ANOVA, F(4,14) = 31.707, P < 0.001 and Bonferroni post-hoc). No difference was observed on APP751 relative expression (Fig. 2E). Induction of APP695-specific AS by nELAVLs was also evident at the protein level (Fig. 2F) and similar results were also obtained from a comparable set of experiments performed in Neuro-2a cells (see Supplementary Fig. S2A–C).
To gain further insight, Neuro-2a cells expressing nELAVLs and APP695, were transfected with an expression vector carrying a shRNA specific for each nElavl or GFP mRNA, as a control. Reduction of nELAVL-expression was verified at the mRNA and protein level (see Supplementary Fig. S3) and its effect on the AS pattern of App exons 7 and/or 8 was assayed by RT-qPCR. As depicted in Fig. 2G, reduction of ELAVL2, ELAVL3 or ELAVL4 levels resulted in increased inclusion of App exons 7 and 8 by 33%, 66% and 56%, respectively (App770/App: ANOVA, F(3,15) = 8.118, P = 0.003 and Bonferroni post-hoc). Consistently, a significant decrease in the relative expression of App751 by ~30% (Fig. 3C, ANOVA, F(3,15) = 32.182, P < 0.001 and Bonferroni post-hoc) and of App695 by ~20% (Fig. 3D, ANOVA, F(3,15) = 14.386, P < 0.001 and Bonferroni post-hoc) was also observed. Collectively, the experiments described above demonstrate that nELAVLs play a critical role in the exclusion of exons 7 and 8 from both the human and the mouse APP mRNA.
nELAVLs interact with the APP pre-mRNA
We next examined whether nELAVLs interact with the APP pre-mRNA by performing RIP using a mouse anti-ELAVL antibody, followed by RT-PCR with primers amplifying sequences flanking exon/intron boundaries of exons 7 and 8 (Fig. 3A). To discriminate between ELAVL1- and nELAVL-binding, ELAVL complexes were immunoprecipitated from nuclear extracts of SK-N-SH cells expressing only ELAVL1 (Fig. 3B) and SH-SY5Y cells expressing all ELAVLs (Fig. 3C). As shown in Fig. 3, APP pre-mRNA was detected only in the immunoprecipitate of SH-SY5Y cells, whereas in both immunoprecipitates no GAPDH pre-mRNA was present (data not shown). To verify this selective association, APP pre-mRNA levels were also assayed in the ELAVL-immunoprecipitates’ supernatant by RT-qPCR; consistently, compared to IgGs controls, APP pre-mRNA appeared depleted in the supernatant only when nuclear extracts from SH-SY5Y cells were used (Fig. 3C; Student’s t-test, *P < 0.05, **P < 0.01). Finally, significant levels of App pre-mRNA were also detected in ELAVL-complexes immunoprecipitated from nuclear extracts of Neuro-2a cells (Fig. 3D, Student’s t-test, *P < 0.05, **P < 0.01). Our results combined point to a preferential association of nELAVLs to the human and mouse APP pre-mRNA, supporting their role in neuron-specific processing of these pre-mRNAs.
nELAVLs suppress the inclusion of either both exons 7 and 8, or only exon 8 in transcripts from artificial minigenes
It has been predicted that nELAVLs regulate AS of exons flanked by U-rich sequences interspersed with purine residues, usually within 250 nucleotides (nts) of intron/exon boundaries26. Our initial analysis of human and mouse genomic regions surrounding APP exons 7 and 8 revealed several sequences encoding for such U-rich blocks close to splice sites, as well as deep in the intervening intron 7 (see Supplementary Tables S2 and S3). To confirm that these are nELAVL-binding sites, we re-analyzed 17 human brain HITS-CLIP datasets for nELAVL-RNP complexes (accession number GSE53699)32 and show a large number of CLIP tags in these predicted U-rich blocks (Fig. 4A). To validate that these blocks are the cis-acting elements responsible for nELAVL-induced exon 7 and 8 skipping, we initially constructed two artificial minigenes containing either the human (APPE78) or the mouse (AppE78) genomic sequence, extending from ~500 nts upstream of exon 7 to ~500 nts downstream of exon 8 (Fig. 4B). Each minigene was then co-transfected along with an ELAVL2-, ELAVL3- or ELAVL4- expression vector in SK-N-SH cells and the effect of nELAVLs on the inclusion of exons 7 and 8 was assayed by RT-PCR using primers specific for the flanking artificial exons (Fig. 4B). As shown in Fig. 4C, all nELAVLs -but most efficiently ELAVL4, which for that reason was used in all our subsequent experiments- promoted the generation of transcripts lacking exons 7 and 8. In general, nELAVLs displayed a more dramatic effect on the AS of mouse transcript compared to the human, probably due to other differences in the cis-acting elements among the two species. Interestingly, all nELAVLs appeared very potent in inducing exon 8 –but not exon 7- skipping separately, a finding that was not observed in our initial transfection experiments. It thus seems that despite differences in the regulation of exon 8 AS between endogenous and APPE78/AppE78 minigenes, the latter constructs appear sufficient for evaluating the regulation of APP695-specific AS by nELAVLs.
Identification of minimal sequences required for nELAVL-mediated exclusion of APP exon 8
Since nELAVLs appeared very potent in inducing APP exon 8 skipping from the generated minigenes, we initially examined the cis-elements that affect this process. For this reason, we generated a series of minigenes consisting of the human (APPE8) or mouse (AppE8) exon 8 and progressively shorter regions of their flanking introns fostering a progressively reduced number of U-rich blocks (Fig. 5A). Each minigene was co-transfected into SK-N-SH cells along with an ELAVL4-expressing vector (or the empty vector as a control) and the effect of ELAVL4 on exon 8 inclusion was assayed by RT-PCR. Overall, co-transfection of each minigene with Elavl4 resulted in the generation of two transcripts and in all cases 50–60% of generated transcripts did not contain exon 8; no such effect was evident in control co-transfections with the empty expressing vector (Fig. 5B). Notably, APPE8.4 and AppE8.5 primary transcripts contained only one U-rich block spanning the last 47 nts of intron 7 that are highly conserved in human, mouse and rat (Fig. 5A and data not shown). To test the importance of this U-rich region in ELAVL4-mediated exon 8 exclusion, point mutations were inserted into APPE8.4 and AppE8.5 (Fig. 5A) and wild-type and mutant minigenes were co-transfected in SK-N-SH cells along with Elavl4 (Fig. 5B). Our analysis showed that compared to wild-type transcripts that were processed to exclude exon 8 at 54% (APPE8.4) and 52% (AppE8.5), mutant APPE8.4 and AppE8.5 transcripts showed significantly reduced exon 8 exclusion at 23% (Student’s t-test, ***P < 0.001) and 26% (Student’s t-test, ***P < 0.001), respectively. To verify that these sequences are nELAVL-targets, biotinylated riboprobes generated by wild-type and mutant APPE8.4/AppE8.5 minigenes were incubated with Neuro-2a whole cell lysates and the association of nELAVLs was assayed by immunoblotting after pull-down with streptavidin-coated beads. As shown in Fig. 5C, nELAVLs strongly associated with wild-type transcripts, but this association was reduced in the case of mutants. Notably, ELAVL1-binding was also evident, but with a much weaker affinity. Taken together, our results indicate that nELAVLs induce exon 8 skipping from both the human and mouse APP pre-mRNA through binding to a conserved U-rich sequence immediately upstream of this alternative exon; all other U-rich sequences flanking this exon play a minor, if any role, in this process.
Concurrent binding of ELAVL4 to sequences located upstream and downstream of APP exon 7 is required for its skipping
Based on our above observations, to identify the cis-elements on APP pre-mRNA that participate in nELAVL-mediated exclusion of exon 7, we initially generated a human (APPE7.1) and a mouse (AppE7.1) minigene encoding for transcripts containing U-rich elements close to the upstream splice site of exon 7 (Fig. 6A). Interestingly, similar to control minigenes lacking T-rich intronic regions, co-transfection of APP7.1 or App7.1 with Elavl4 resulted in the generation of only full-length transcripts (Fig. 6B), indicating that binding of ELAVL4 upstream of exon 7 is not sufficient for its skipping. Since our HITS-CLIP analysis revealed strong nELAVL-binding to U-rich blocks located deep in intron 7 (Fig. 4A), we next examined whether these sequences participate in nELAVL-mediated APP exon 7 skipping. Therefore, we generated a series of human (APPE7.2-4) and mouse (AppE7.2-7.5) minigenes consisting of the same upstream intronic region, exon 7 and varying lengths of the downstream intron encoding for progressively more U-rich blocks (Fig. 6A). Co-transfection of Elavl4 with each of the latter minigenes promoted the generation of transcripts lacking exons 7; notably, transcripts generated from minigenes with progressively more nELAVL-binding sites downstream of exon 7, were processed to exclude exon 7 at progressively higher levels (Fig. 6B). Nevertheless, these downstream sequences were not sufficient for ELAVL4-mediated exclusion of exon 7, in the absence of U-rich blocks in the upstream intron 6 (APPE7.5-7 and AppE7.6-8; Fig. 6B). Binding of nELAVLs to sequences both upstream and downstream of exon 7 was verified by RNA pull-down assays using biotinylated riboprobes from human and mouse minigenes containing T-rich regions either only upstream (APP7.1 or AppE7.1), or only downstream (APP7.7 and AppE7.8) of exon 7 (Fig. 6C). Taken together, our results indicate that concurrent binding of nELAVLs both upstream and deeply downstream of exon 7 is required for its exclusion from the human and mouse APP mRNA.
ELAVL4 interfere with the recognition of 3′ splice site of APP exon 7 and exon 8 by reducing U2AF65 binding
Given that ELAVL4-binding upstream of APP exons 7 or 8 is necessary for their skipping, we next examine whether ELAVL4 hinders the interaction of the essential splicing factor U2AF65 (U2 small nuclear ribonucleoprotein (snRNP) auxiliary factor 65 kDa) with the upstream 3′ splice site of these exons. For this reason, SK-N-SH cells were co-transfected with progressively increased amounts of an ELAVL4-expression plasmid and whole cell lysates of transfected cells were used in a series of RNA pull down assays using the biotinylated riboprobes APPE7.4 and APPE8.4, to which nELAVLs bind and efficiently induce skipping of exons 7 and 8, respectively; APPE7control bearing no nELAVL-binding sites, was also used as control. As shown in Fig. 7, ELAVL4 reduced U2AF65 binding to APPE7.4 and APPE8.4 transcripts in a dose-dependent way (APPE7.4: ANOVA, F(2,8) = 31.337, P = 0.001 and Bonferroni post-hoc; APPE8.4: ANOVA, F(2,8) = 119.805, P < 0.001 and Bonferroni post-hoc) and this effect was not observed when control transcripts were used. Notably, ELAVL4 appeared to be more potent in displacing U2AF65 from APPE8.4 transcript, as a ~40% reduction was also observed in the presence of half the amount of ELAVL4. It thus appears that nELAVLs may interfere with the binding of U2AF65 to the 3′ splice site of APP exons 7 and 8.
AUF-1 cooperates with nELAVLs in the regulation of APP695-specific AS
nELAVLs have been shown to regulate AS through binding to intronic sequences in competition with other splicing factors27,29. Given that AUF-1 and TIA-1 have been shown to share common targets with ELAVLs27,28,33,34, we initially examined whether regions of APP pre-mRNA essential for nELAVL-induced exon 7 and 8 skipping are also targets of these RBPs. Our analysis revealed a strong association of AUF-1 (especially isoforms p45 and p42)- but not TIA-1- with riboprobes from human or mouse APP pre-mRNA shown to be also bound by nELAVLs (Fig. 8A,B and data not shown). To test the functional importance of this association SK-N-SH cells were transfected with either AUF-1 (encoding for p42 isoform) or an shRNA targeting all AUF-1 transcripts. Intriguingly, changes in AUF-1 level (see Supplementary Fig. S4A) had no effect on the AS pattern of APP exons 7 and 8, as assessed by RT-qPCR (Fig. 8C). To examine whether nELAVLs compete with AUF-1 to regulate APP695-specific AS, a series of co-transfection experiments was performed using the human or mouse APPE78 minigene and a combination of ELAVL4- and p42 AUF1- expression plasmids in various ratios (Fig. 8D,E). Consistent with the role of ELAVL4 as a splicing factor, in our control experiments, levels of alternative transcripts were gradually reduced following the decrease in the amount of ELAVL4-expression plasmid. Interestingly, when AUF-1 was co-expressed with ELAVL4, levels of transcripts lacking both exons 7 and 8, but not those lacking only exon 8, were significantly increased by 2-3 folds compared to their controls, suggesting that AUF-1 enhances ELAVL4-induced APP695 specific AS. To verify the latter synergistic function, Auf-1 expression was silenced in Neuro2a cells that express significant levels of nELAVLs and APP695 (see Supplementary Fig. S4B). As predicted, reduction of AUF-1 levels in these cells resulted in a significant 45% increase of App770 along with a significant 35% decrease of App695 relative expression (Student’s t-test, P = 0.002 and P = 0.004, respectively); in contrast no difference was observed on App751 abundance. Finally, to test whether AUF-1 facilitates U2AF65 displacement by nELAVLs, SK-N-SH were co-transfected with equal amounts of ELAVL4- and AUF-1- expression plasmids and whole cell lysates of the transfected cells were used in RNA pull down assays using APPE7.4 biotinylated riboprobes. As shown in Fig. 8G, compared to controls, in the presence of suboptimal levels of ELAVL4, no significant reduction of U2AF65 binding to APP7.4 transcript was observed. Interestingly, upon AUF-1 overexpression U2AF65-binding was increased by ~90%; nevertheless when ELAVL4 was co-expressed along with AUF-1 a significant decrease of U2AF65-binding was observed compared to all other conditions (ANOVA, F3,11 = 25,391, P < 0.001 and Bonferroni post-hoc). Taken together, our observations suggest that ELAVL4 uses AUF-1 as a cofactor to promote exclusion of exons 7 and 8 from the APP pre-mRNA.
In the present study, we report that nELAVLs, as opposed to ubiquitous ELAVL1, are critically involved in neuronal-specific AS of human and mouse APP pre-mRNA, by promoting the exclusion of exons 7 and 8. Moreover, we demonstrate the mechanism by which nELAVLs regulate this process and provide evidence supporting that AUF-1 facilitates nELAVL-induced APP695-specific AS.
By using a series of minigenes, we identified cis-elements on the APP pre-mRNA important for nELAVL-mediated exon 7 or 8 skipping and report that an evolutionary conserved U-rich sequence immediately upstream of exon 8 acts as a splicing repressor and is important for nELAVL-mediated skipping of this exon. Our observations are consistent with the position-dependent model for AS regulation by RBPs, according to which preferential binding of RBPs in close proximity to the 3′ splice site of the target exon is usually associated with exon skipping, while binding within approximately 300 nts downstream of the exon is associated with exon inclusion35,36,37. However, this simple position-based rule did not apply to nELAVL-mediated APP exon 7 skipping, that appeared to be dependent on the concurrent binding of nELAVLs to U-rich sequences both upstream and downstream of this target exon. Our latter result is in agreement with the nELAVL-RNA map recently reported26; consistently nELAVLs have been shown to promote exon 23a exclusion from neurofibromin 1 (NF1) pre-mRNA by binding on either flanking intron of this exon29. All previous studies examining the role of nELAVLs in AS have reported nELAVL-binding in close proximity to splice sites27,29,30. Herein, we provide evidence that nELAVLs are also able to control AS by binding to distal intronic sequences, as ELAVL4-induced exon 7 exclusion was dependent on the interaction of ELAVL4 with U-rich sequences located deeply in the downstream intron 7.
Notably, although nELAVLs were able to promote exclusion of either exon 7 or exon 8 from their respective artificial transcripts, when their effect on the endogenous APP pre-mRNA was examined, a significant change was observed only in the level of transcripts lacking both these two exons. It thus appears that in the case of nELAVL-mediated regulation of APP AS, adjacent exons 7 and 8 behave as a “joint cassette exon”. An interesting question arises how nELAVLs promote the concurrent exclusion of these two exons from the endogenous mRNA. Given the existence of nELAVL-binding sites upstream of exon 7, as well as throughout its downstream intron 7, a possible mechanism in which nELAVLs regulate splicing is by binding and multimerizing along the pre-mRNA. Along the same lines, herein we show that ELAVL4-mediated exon 7 skipping was progressively more efficient on transcripts with progressively more distal U-rich blocks. Consistently, nELAVLs, as well as the Drosophila homologue ELAV exists as multimers and multimerized ELAV has been shown to be functionally important on Drosophila ewg RNA AS24,38,39. Multimerization of nELAVLs may provide a mechanism to bring into close proximity the distant RNA-processing signals of APP exons 6 and 9 by looping out the intronic sequence containing exons 7 and 8 and thus increasing the frequency of their skipping. Alternatively, it might interfere with the interaction of spliceosomal components and thus affect proper exon recognition. Both the above mechanisms have been proposed for the splicing regulator hnRNPA140,41 and nELAVLs have been shown to promote NF1 exon 23a skipping by preventing binding of core splicing factors29. Herein, we show that nELAVLs interfere with binding of U2AF65 to the 3′ splice site of both exons 7 and 8. Interestingly, although in the case of exon 8 it appears to involve competition for binding to the same target, this is unlikely to account for the reduced binding of U2AF64 upstream of exon 7, given that nELAVLs bind to sequences located more than 300 nts away from intron/exon boundaries of exon 7.
In all experiments described herein, although nELAVLs promoted exclusion of APP exons 7 and 8, abundant expression of transcripts containing these two exons was still observed. We speculated that this might be attributed to either the presence of endogenous factors that may function competitively, or to the deficiency of an unknown splicing regulator in the transfected cells. It has been previously reported that nELAVLs regulate neuron-specific AS of the calcitonin/GCRP and NF1 pre-mRNAs, by binding to intronic U-rich sequences in competition with the ubiquitously expressed TIA-1/TIAR, which will otherwise promote exon inclusion27,29. A similar mechanism is unlikely to apply in the case of nELAVL-regulated APP AS, since TIA-1 did not interact with the APP pre-mRNA regions participating in this process. Recently, AUF-1 has been shown to share many common target RNAs with ELAVL1 and compete or cooperate with ELAVL1 in the translational activation of these targets33. Moreover, AUF-1 binding has been observed at intronic sites and silencing of AUF-1 has been associated with alterations in the levels of selected groups of alternative transcripts34. In the present study, we provide evidence that AUF-1 acts as a cofactor of nELAVLs in the regulation of APP695-spesific AS; AUF-1, more specifically isoforms p45 and/or p42, binds to APP pre-mRNA regions shown to be nELAVL-targets and despite its minor effect on the AS pattern of exons 7 and 8 in the absence of nELAVLs, AUF-1 silencing in cells expressing nELAVLs results in increased inclusion of exon 7 and 8 in APP transcripts. To our knowledge, this study provides the first evidence that AUF-1 directly modulates AS events. Although the mechanism, by which AUF-1 facilitates nELAVL-induced APP695-specific awaits further investigation, an interesting possibility is that local changes in RNA structure may account for this synergistic effect. Previous studies have demonstrated that binding of AUF-1 is able to alter the local conformation of its RNA targets42,43. Although the functional significance of local RNA structural remodeling by AUF-1 remains unclear, a logical functional consequence of this effect is to control accessibility for additional RNA-binding factors and thus influence RNA fate depending on the presence of RBPs within the cell. In that respect, it’s noteworthy that in the absence of nELAVLs binding of p42 AUF-1 to APPE7 transcripts increased U2AF65-binding, whereas in the presence of ELAVL4 enhanced nELAVL-mediated U2AF65 displacement, probably through facilitating ELAVL4-binding to this target sequence.
Taken together our results suggest a neuronal mechanism, conserved in human and mouse, for the regulation of APP695 production by nELAVLs. To date a few factors have been proposed to regulate APP exon 7 and/or exon 8 skipping. RNA-binding proteins Fox -1 and -2 (RBFOX1 and 2), have been shown to induce exon 7, but not exon 8, exclusion44, whereas the Elav-like family 1 (CELF1), a CUG-binding protein, has been shown to induce APP exon 8 skipping45. Intriguingly, APP714 lacking only exon 7 has a relative high expression in skeletal muscles6 where RBFox1 and 2 are abundantly expressed46, whereas APP751 lacking only exon 8 and CELF1 are ubiquitously expressed3,6,47. Interestingly, SC35 and hnRNPA1 have been also involved in the exclusion of both APP exons 7 and 813. However, neither SC35, nor hnRNPA1 are neuronal-specific48,49. APP695, lacking both exons 7 and 8, is predominantly expressed in neurons3,6, where nELAVLs are also predominantly expressed20,26. Herein, we provide evidence that a similar association exists also in cell lines in vitro and manipulation of nELAVL levels in neuroblastoma cells leads to changes of endogenous APP695 relative expression. Although keeping in mind that neuroblastoma cells have been shown to express alterations in AS patterns compared to neuronal cells50, our bioinformatics’ analysis showing a strong correlation between APP695 and nELAVLs levels in the human brain, suggests that nELAVLs may play an orchestrating role in the regulation of APP695-specific RNA processing in vivo.
APP695 is principally neuronal and in neurons is present at relatively high levels compared to the other two major isoforms APP770 and APP7513,6. Until recently no conclusive functional differences have been ascribed to these different isoforms apart from the protease inhibitor role of the Kunitz-type protease inhibitor (KPI) domain encoded by exon 7; nevertheless, efficiency of Aβ production appears to be affected by the APP isoform13,14,51 and alterations in neuronal splicing of APP have been observed in the brain of AD patients, with numerous studies reporting a decrease in neuronal APP695 along with an increase in full-length APP7709,10,11,12. Of note, unlike latter reports, herein we failed to detect differences in APP isoform levels (as well as nELAVL levels) between control and AD samples, most possibly due to the small sample size and the observed high intra-group heterogeneity (see also original article 32). However, taking into account our results suggesting a strong correlation of APP695 and nELAVL levels in the human brain, we speculate that a deficiency of nELAVLs could contribute to the reduced APP695 relative levels reported elsewhere9,10,11,12. Although this speculation awaits future investigation, it’s noteworthy that previous studies have reported alterations in nELAVL protein levels31,52 or binding profile32 in the brain of AD patients.
Taken together, our results suggest that nELAVLs play an orchestrating role in the regulation of neuronal APP695-specific RNA processing, facilitated by AUF-1. Since nELAVLs have been also involved in the regulation of APP steady-state levels31, it appears that they play a key role in the post-transcriptional regulation of APP expression, alterations of which have been linked to AD.
To generate cDNA sequences of Elavl1, Elavl2, Elavl3, and Elavl4, reverse transcription (RT) and polymerase chain reaction (PCR) were carried out using RNA isolated from CD1 mouse cells brain and specific primers for each cDNA (see Supplementary Table S5). PCR products were inserted into the pcDNA3.1/V5-His-TOPO vector (Invitrogen), and the cDNAs were further subcloned into the EcoRV and XhoI sites of pCAGGS-IRES-GFP vector. In order to generate shRNA specific for human AUF-1 and LacZ mRNA, Block-iT U6 RNAi Entry vector Kit (Invitrogen) as well as AUF-1 shRNA oligos (see Supplementary Table S5) and LacZ shRNA oligos (provided by Invitrogen) were used. The AUF-1 expression plasmids53 were a kind gift of Dr. P. Naveilhan (University of Nantes, France), the five shRNA expression plasmids, each containing a shRNA targeting Elavl2, Elavl3 and Elavl4 or eGFP transcript30 were kindly provided by Dr. H. Lou (Case Western Reserve University, Cleveland, USA) and the two pSilencer plasmids containing no insert or a shRNA targeting all Auf-1 transcripts33, were provided by Dr. M. Gorospe (National Institutes of Health, Baltimore MD, USA).
The minigene vector constructed consists of sequences from the pcDNA6.2-GW/EmGFP plasmid (backbone vector; Invitrogen), the splice donor sequence of EF1 exon1 [SD, a gift of Dr. A. Klinakis, Biomedical Research Foundation Academy of Athens (BRFAA), Greece] and an adenoviral splice acceptor (SA, provided by Dr. L. Zagoraiou, BRFAA, Greece). SD and SA sequences were PCR-amplified using SD and SA primers, respectively (see Supplementary Table S5). SD product was cloned into the pcDNA3.1/V5-His-TOPO vector, digested with BamHI and XhoI, blunted and inserted into the DraI site of pcDNA6.2-GW/EmGFP vector replacing the EmGFP coding sequence. SA product was digested with BamHI and XhoI and inserted into the same sites of the pcDNA6.2 vector.
The APPE78 sequences used in this study consist of a part of the human or mouse APP genomic sequence extending from ~500 nucleotides (nts) upstream of exon 7 up to ~500 nts downstream of exon 8. To generate APPE78 and AppE78 minigenes, human and mouse sequences were PCR-amplified from HEK293 cell and mouse CD1 genomic DNA, using APP7_514 F and APP8_505 R or App7_512 F and App8_487 R primers, respectively. PCR products were digested with NotI and SalI and cloned into the same sites of the above minigene vector. To obtain the series of APPE7 (containing exon 7 and parts of its flanking introns) and APPE8 (containing exon 8 and parts of its flanking introns) minigenes, desired sequences were PCR-amplified using as templates APPE78 or AppE78 sequences and the appropriate combination of primers (primer sequences are summarized in Supplementary Table S5). PCR products were digested with NotI and SalI and were inserted either into the same sites of the minigene vector or into the NotI and XhoI sites of the DNA3.1 vector that was further linearized and used as a template for in vitro transcription.
Cell culture and transfections
Human HEK293, HeLa, SK-N-SH, SH-SY5Y and mouse Neuro-2a cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum (FBS) (Invitrogen). Mouse CAD cells were maintained in DMEM containing 8% FBS and mouse primary cortical neurons were prepared as before54. All cells were maintained at 5% CO2 and 37 °C. To induce neuronal differentiation, SH-SY5Y cells were treated with 10 μΜ retinoic acid for 7 days and CAD cells were deprived of FBS for the same time period. Transfection of SK-N-SH and Neuro-2a cells was carried out using Lipofectamine 2000 (Invitrogen) following manufacturer’s recommendations. Co-transfections using APP minigene constructs and RBP expression plasmids were generally performed in a 1:10 ratio, unless otherwise stated. Transfected cells were harvested 48 hours after transfection.
Whole cell lysate and nuclear extract preparation
Whole-cell lysates used for immunoblotting were prepared in a lysis buffer containing 20 mM Tris pH 7.5, 150 mM NaCl, 1 mM EDTA, 1%Triton X-100 and a protease inhibitor cocktail (Complete®, Roche). For RNA pull-down assays (see below), Neuro-2a cells were lysed in NT2 buffer (50 mM Tris pH 7.4, 150 mM NaCl, 1mMMgCl2, 0.05% NP40, protease inhibitor cocktail) supplemented with RNAse inhibitors (RNaseOUT, Invitrogen). In both cases, cellular debris was pelleted by centrifugation at 13,000 rpm for 10 min. In order to obtain nuclear extracts, cells were initially lysed in HLB buffer (10 mM Tris pH 7.4, 10 mMNaCl, 3 mM MgCl2, 1 mM EGTA, 0.1% NP40 and inhibitors for proteases and RNAses). Nuclei were pelleted by centrifugation at 2,500 rpm for 15 min, resuspended in RIP buffer (25 mM Tris pH 7.4, 150 mM KCl, 5 mM EDTA, 0.5% NP40 and protease and RNase inhibitors) and mechanically sheared using a dounce homogenizer. Nuclear membrane and debris were pelleted by centrifugation at 13,000 rpm for 10 min. Protein content in both whole cell lysates and nuclear extracts was determined by the Broadford assay (BioRad).
Immunoblotting was carried out as previously described54. Briefly, equal amounts of whole cell extracts (30 μg) or equal volumes of pull-down materials were analyzed by 10% SDS-PAGE under reducing conditions. The molecular weight of proteins was confirmed using prestained protein ladder (PageRuler, Fermentas). The R1(57) anti-APP C-terminal rabbit antibody55, a kind gift of Dr. S. Efthimiopoulos (University of Athens, Greece) and the rabbit anti-AUF-1 antibody (07-260, Millipore) were used in a dilution 1:2000, the mouse anti-ELAVL and the rabbit anti-U2AF65 antibodies (3A2 and H300, respectively; all from Santa Cruz Biotechnology) in a dilution 1:1000 and the mouse anti-SAP97 (K64/15 UC Davis/NIH NeuroMab Facility and Antibodies Inc.) in a 1:50 dilution. Finally, the mouse anti-β-tubulin, the mouse anti-βΙΙΙ-tubulin (T5201 and T8660, respectively from Sigma) and the mouse anti-GAPDH-HRP conjugated (HRP-60004 from Proteintech) antibodies were used in a dilution 1:5000. All secondary HRP-conjugated antibodies (Santa Cruz Biotechnology) were used in a 1:5000 dilution. Each sample was tested in duplicate and samples obtained from three independent experiments were used for analysis. Densitometric analysis of immunoblotting images was performed using the image analysis software Image J (NIH, USA).
RNA isolation and RT-PCR
Total RNA was extracted from cells using the RNAzol Reagent (Molecular Research Center, Inc) according to the manufacturer’s protocol, or from RIP material (see below) by acidic phenol/chlorophorm extraction. One microgram of RNA isolated from cells or total RNA isolated from RIP immunoprecipitates, was reverse transcribed by the M-MLV reverse transcriptase (Invitrogen) using random hexamer primers. Semi-quantitative PCRs were performed using Kappa Taq polymerase (Kappa Biosystems) and specific primers (see Supplementary Table S6). Amplification bands were quantified by densitometric analysis using the image analysis software Image J (NIH, USA). The effect of RBPs on APP RNA processing was calculated as a percentage exon(s) exclusion [(exon(s) exclusion/exon(s) exclusion + exons(s) inclusion)] averaged by three independent experiments. Quantitative real-time PCR (qPCR) was carried out in the Light Cycler 96 instrument (Roche) using Platinum Taq polymerase (Invitrogen), SYBR Green Reagent (Roche) and primers specific for either each APP isoform cDNA or APP genomic sequences; total APP cDNA and intronic GAPDH were used for normalization (see Supplementary Table S6). Specificity of amplification products was confirmed by their dissociation curves. Each sample was tested in triplicates and samples obtained from three to four independent experiments were used for analysis of relative expression by the comparative CT method.
Ribonucleoprotein immunoprecipitation (RIP)
RIP analysis was performed as previously described31. Briefly, nuclear extracts were incubated for 4–6 hours at 4 °C with protein A/G Sepharose beads (Santa Cruz Biotechnology) coated with the mouse anti-ELAVL antibody or control mouse IgGs (Santa Cruz Biotechnology). RNA was isolated from both immunoprecipitates and their supernatants by acidic phenol/chlorophorm extraction and was further studied by semi-quantitative RT-PCR and RT-qPCR analysis, respectively. Binding of APP or App primary transcripts was verified by RT-PCR with primers specific for intronic regions of the pre-mRNA of each species, whereas binding specificity was ensured by the absence of GAPDH pre-mRNA, a known non target of nELAVs27, in immunoprecipitates (for primers see Supplementary Table S6).
RNA pull-down assay
One microgram of linearized plasmid carrying the desired sequence was used as template for in vitro transcription with T7 RNA polymerase (Takara). Labeling of riboprobes was achieved with addition of biotin-11-CTP (Roche) in the nucleotide mix. Biotinylated probes were purified with acidic phenol/chlorophorm and used for RNA pull-down assays as previously described56. Briefly, 1 μg of biotinylated RNA was incubated with 100 μg of Neuro-2a whole extracts and RNA-proteins complexes were precipitated using streptavidin coated beads. For the detection of competitive binding, 0.4 μg of biotinylated RNA was incubated with 100 μg of whole cell lysate from transfected SK-N-SH cells and RNA-proteins complexes were precipitated as described above. To detect nELAVL-, AUF-1- or U2AF65- binding to the biotinylated transcripts, equal of volume of precipitates and their supernatants were analyzed by immunoblotting.
Mean values were derived from at least three experiments. Depending on the number of groups examined, comparisons were carried out using either Student’s t-test (two groups) or one-Way ANOVA and Bonferroni post-hoc analysis (more than two groups). Significance was defined as P < 0.05. Statistical analysis was performed using the SPSS software (Release 10.0.1, SPSS, Chicago, IL, USA).
17 samples from 9 AD patient and 8 control post-mortem brain samples, subjected to NGS expression analyses and nELAVL HITS-CLIP, were retrieved from GEO repository (accession number GSE53699)32. Raw Seq data were initially quality checked with FastQC57 and further processed for adapter removal with a combined use of Minion58 and Trimgalore59. Following pre-processing, quantification of expression at gene and at transcript level was performed using Kallisto60. GRCh38 and Ensembl 81 were utilized as reference genomes and transcriptomes, respectively. All downstream analyses were implemented using R/Bioconductor61. The data had an average of 60 million PE reads. Initial standard differential expression analysis revealed that samples exhibited high heterogeneity, even within the same group. We found that this high level of intra-group variance diminished the number of differentially expressed transcripts between control and AD samples, an observation that was also noted by the authors of the original manuscript32. Subsequently, APP isoform levels were normalized against APP gene expression in each sample. Associations between normalized APP isoform expression and Hu, TIA-1, and AUF-1 mRNA expression were investigated. Pearson Correlation Coefficient was calculated for all pairs to produce a correlation map. HITS-CLIP libraries had a mean value of ~10 M aligned reads. The adopted pipeline identified clusters of nELAVL binding corresponding to enriched regions with a 10 reads minimum coverage. The final set of nELAVL binding regions comprises peaks present in at least 2 samples.
Panels in figures were prepared from uncropped images deposited in Supplementary Material (Supplementary Figs S5–S12). For clarity reasons gel images were inverted and brightness and contrast adjustments were applied.
How to cite this article: Fragkouli, A. et al. Neuronal ELAVL proteins utilize AUF-1 as a co-partner to induce neuron-specific alternative splicing of APP. Sci. Rep. 7, 44507; doi: 10.1038/srep44507 (2017).
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Selkoe, D. J. Alzheimer’s disease: genes, proteins and therapy. Physiol Rev. 81, 741–766 (2001).
Brouwers, N., Sleegers, K. & Van Broeckhoven, C. Molecular genetics of Alzheimer’s disease: an update. Ann Med. 40, 562–583 (2008).
Tanzi, R. E. et al. Amyloid beta protein gene: cDNA, mRNA distribution and genetic linkage near the Alzheimer locus. Science, 235, 880–884 (1987).
Schmechel, D. E. et al. Cellular localization of messenger RNA encoding amyloid-beta-protein in normal tissue and in Alzheimer disease. Alzheimer Dis. Assoc. Disord. 2, 96–111 (1988).
König, G. et al. Identification and differential expression of a novel alternative splice isoform of the beta A4 amyloid precursor protein (APP) mRNA in leukocytes and brain microglial cells. J. Biol. Chem. 267, 10804–10809 (1992).
Sandbrink, R., Masters, C. L. & Beyreuther, K. Beta A4-amyloid protein precursor mRNA isoforms without exon 15 are ubiquitously expressed in rat tissues including brain, but not in neurons. J. Biol. Chem. 269, 1510–1517 (1994).
Tsukahara, T., Kunika, N., Momoi, T. & Arahata, K. Regulation of alternative splicing in the amyloid precursor protein (APP) mRNA during neuronal and glial differentiation of P19 embryonal carcinoma cells. Brain Res. 679, 178–183 (1995).
Tang, K. et al. Identification of a novel alternative splicing isoform of human amyloid precursor protein gene, APP639. Eur. J. Neurosci. 18, 102–108 (2003).
Johnson, S. A. et al. Selective reduction of mRNA for the β-amyloid precursor protein that lacks a Kunitz-type protease inhibitor motif in cortex from Alzheimer brains. Exp. Neurol. 102, 264–268 (1988).
Tanaka, S. et al. Tissue-specific expression of three types of β-protein precursor mRNA: enhancement of protease inhibitor-harboring types in Alzheimer’s disease brain. Biochem. Biophys. Res Commun. 165, 1406–1414 (1989).
Moir, R. D. et al. Relative increase in Alzheimer’s disease of soluble forms of cerebral Abeta amyloid protein precursor containing the Kunitz protease inhibitory domain. J. Biol. Chem. 273, 5013–2019 (1998).
Matsui, T. et al. Expression of APP pathway mRNAs and proteins in Alzheimer’s disease. Brain Res. 1161, 116–123 (2007).
Donev, R., Newall, A., Thome, J. & Sheer, D. A role of SC35 and hnRNPA1 in the determination of amyloid precursor protein isoforms. Mol. Psychiatry 12, 681–690 (2007).
Belyaev, N. D. et al. The transcriptionally active amyloid precursor protein (APP) intracellular domain is preferentially produced from the 695 isoform of APP in a β-secretase-dependent pathway. J. Biol. Chem. 285, 41443–41454 (2010).
De La Grange, P., Gratadou, L., Delord, M., Dutertre, M. & Auboeuf, D. Splicing factor and exon profiling across human tissues. Nucleic Acids Res. 38, 2825–2838 (2010).
Merkin, J., Russell, C., Chen, P. & Burge, C. B. Evolutionary dynamics of gene and isoform regulation in mammalian tissues. Science, 338, 1593–1599 (2012).
Licatalosi, D. D. & Darnell, R. B. Splicing regulation in neurologic disease. Neuron. 52, 93–101 (2006).
Lisbin, M. J., Qiu, J. & White, K. The neuron-specific RNA-binding protein ELAV regulates neuroglian alternative splicing in neurons and binds directly to its pre-mRNA. Genes Dev. 15, 2546–2461 (2001).
Soller, M. & White, K. ELAV inhibits 3′-end processing to promote neural splicing of ewg pre-mRNA. Genes Dev. 17, 2526–2538 (2003).
Okano, H. J. & Darnell, R. B. A hierarchy of Hu RNA binding proteins in developing and adult neurons. J. Neurosci. 17, 3024–3037 (1997).
Sakai, K., Kitagawa, Y. & Hirose, G. Analysis of the RNA recognition motifs of human neuronal ELAV-like proteins in binding to a cytokine mRNA. Biochem. Biophys. Res. Commun. 256, 263–268 (1999).
Fan, X. C. & Steitz, J. A. HNS, a nuclear-cytoplasmic shuttling sequence in HuR. Proc. Natl. Acad. Sci. USA 95, 15293–15298 (1998).
Kasashima, K., Terashima, K., Yamamoto, K., Sakashita, E. & Sakamoto, H. Cytoplasmic localization is required for the mammalian ELAV‐like protein HuD to induce neuronal differentiation. Genes Cells 4, 667–683 (1999).
Hinman, M. N., Zhou, H. L., Sharma, A. & Lou, H. All three RNA recognition motifs and the hinge region of HuC play distinct roles in the regulation of alternative splicing. Nucleic Acids Res. 41, 5049–5061 (2013).
Colombrita, C., Silani, V. & Ratti, A. ELAV proteins along evolution: Back to the nucleus? Mol. Cell Neurosci. 56, 447–455 (2013).
Ince-Dunn, G. et al. Neuronal Elav-like (Hu) proteins regulate RNA splicing and abundance to control glutamate levels and neuronal excitability. Neuron 75, 1067–1080 (2012).
Zhu, H., Hasman, R. A., Barron, V. A., Luo, G. & Lou, H. A nuclear function of Hu proteins as neuron-specific alternative RNA processing regulators. Mol. Biol. Cell. 17, 5105–5114 (2006).
Belavia, D. et al. Notch3 and the Notch3-upregulated RNA-binding protein HuD regulate Ikaros alternative splicing. EMBO J. 26, 1670–1680 (2007).
Zhu, H., Hinman, M. N., Hasman, R. A., Mehta, P. & Lou, H. Regulation of neuron-specific alternative splicing of neurofibromatosis type 1 pre-mRNA. Mol. Cell Biol. 28, 1240–1251 (2008).
Wang, H., Molfenter, J., Zhu, H. & Lou, H. Promotion of exon 6 inclusion in HuD pre-mRNA by Hu protein family members. Nucleic Acids Res. 38, 3760–3770 (2010).
Kang, M. J. et al. HuD regulates coding and noncoding RNA to induce APP → Aβ processing. Cell Rep. 7, 1401–1409 (2014).
Scheckel, C. et al. Regulatory consequences of neuronal ELAV-like protein binding to coding and non-coding RNAs in human brain. Elife 5, e10421 (2016).
Lal, A. et al. Concurrent versus individual binding of HuR and AUF1 to common labile target mRNAs. EMBO J. 23, 3092–3102 (2004).
Yoon, J. H. et al. PAR-CLIP analysis uncovers AUF-1 impact on target RNA fate and genome integrity. Nat. Commun. 5, 5248 (2014).
Ule, J. et al. An RNA map predicting Nova-dependent splicing regulation. Nature 444, 580–586 (2006).
Llorian, M. et al. Position-dependent alternative splicing activity revealed by global profiling of alternative splicing events regulated by PTB. Nat. Struct. Mol. Biol. 17, 1114–1123 (2010).
Barash, Y. et al. Deciphering the splicing code. Nature 465, 53–59 (2010).
Kasashima, K., Sakashita, E., Saito, K. & Sakamoto, H. Complex formation of the neuron‐specific ELAV‐like Hu RNA‐binding proteins. Nucleic Acids Res. 30, 4519–4526 (2002).
Soller, M. & White, K. ELAV multimerizes on conserved AU4-6 motifs important for ewg splicing regulation. Mol. Cel. Biol. 25, 7580–7591 (2005).
Blanchette, M. & Chabot, B. Modulation of exon skipping by high‐affinity hnRNP A1‐binding sites and by intron elements that repress splice site utilization. EMBO J. 18, 1939–1952 (1999).
Damgaard, C. K., Tange, T. O. & Kjems, J. hnRNP A1 controls HIV-1 mRNA splicing through cooperative binding to intron and exon splicing silencers in the context of a conserved secondary structure. RNA 8, 1401–1415 (2002).
Wilson, G. M., Sutphen, K., Moutafis, M., Sinha, S. & Brewer, G. Structural remodeling of an A+U-rich RNA element by cation or AUF1 binding. J. Biol. Chem. 276, 38400–38409 (2001).
Zucconi, B. E. et al. Alternatively expressed domains of AU-rich element RNA-binding protein 1 (AUF1) regulate RNA-binding affinity, RNA-induced protein oligomerization, and the local conformation of bound RNA ligands. J. Biol. Chem. 285, 39127–39139 (2010).
Alam, S., Suzuki, H. & Tsukahara, T. Alternative splicing regulation of APP exon 7 by RBFox proteins. Neurochem. Int. 78, 7–17 (2014).
Poleev, A., Hartmann, A. & Stamm, S. A trans-acting factor, isolated by the three-hybrid system that influences alternative splicing of the amyloid precursor protein minigene. Eur. J. Biochem. 267, 4002–4010 (2000).
Zhang, C. et al. Defining the regulatory network of the tissue-specific splicing factors Fox-1 and Fox-2. Genes Dev. 22, 2550–2563 (2008).
Good, P. J., Chen, Q., Warner, S. J. & Herring, D. C. A Family of Human RNA-binding Proteins Related to the Drosophila Bruno Translational Regulator. J. Biol. Chem. 275, 28583–28592 (2000).
Zhang, W. J. & Wu, J. Y. Functional properties of p54, a novel SR protein active in constitutive and alternative splicing. Mol. Cell Biol. 16, 5400–5408 (1996).
Hanamura, A., Cáceres, J. F., Mayeda, A., Franza, B. R. Jr. & Krainer, A. R. Regulated tissue-specific expression of antagonistic pre-mRNA splicing factors. RNA 4, 430–444 (1998).
Huo, Q. et al. Splicing changes in SMA mouse motoneurons and SMN-depleted neuroblastoma cells: evidence for involvement of splicing regulatory proteins. RNA Biol. 11, 1430–1446 (2014).
Ben Khalifa, N. et al. Structural features of the KPI domain control APP dimerization, trafficking, and processing. FASEB 26, 855–867 (2012).
Amadio, M. et al. nELAV proteins alteration in Alzheimer’s disease brain: a novel putative target for amyloid-beta reverberating on AbetaPP processing. J. Alzheimer’s Dis. 16, 409–419 (2008).
Hambardzumyan, D. et al. AUF-1 and Hu proteins in the developing rat brain: implication in the proliferation and differentiation of neural progenitors. J. Neurosci. Res. 87, 1296–1209 (2009).
Fragkouli, A. & Doxakis, E. miR-7 and miR-153 protect neurons against MPP+-induced cell death via upregulation of mTOR pathway. Front. Cell Neurosci. 8, 182 (2014).
Fotinopoulou, A. et al. BRI2 Interacts with Amyloid Precursor Protein (APP) and Regulates Amyloid β (Aβ) Production. J. Biol. Chem. 280, 30768–30772 (2005).
Tsai, M. C. et al. Long noncoding RNA as modular scaffold of histone modification complexes. Science 329, 689–693 (2010).
Andrews, S. FastQC: A quality control tool for high throughput sequence data (2015).
Davis, M. P., van Dongen, S., Abreu-Goodger, C., Bartonicek, N. & Enright, A. J. Kraken: a set of tools for quality control and analysis of high-throughput sequence data. Methods 63, 41–49 (2013).
Krueger, F. Trim Galore!: A wrapper tool around Cutadapt and FastQC to consistently apply quality and adapter trimming to FastQ files (2015).
Bray, N. L., Pimentel, H., Melsted, P. & Pachter, L. Near-optimal probabilistic RNA-seq quantification. Nature biotechnology 34, 525–527 (2016).
Gentleman, R. C. et al. Bioconductor: open software development for computational biology and bioinformatics. Genome Biol. 5, R80 (2004).
We would like to acknowledge the following individuals for providing antibodies and plasmids: Dr. S. Efthimiopoulos at the University of Athens (Greece), Dr. H. Lou at Case Western Reserve University (Cleveland, USA), Dr. P. Naveilhan at the University of Nantes (France), and Drs. A. Klinakis and L. Zagoraiou at the BRFAA (Greece). We thank members of Doxakis laboratory Maria Paschou, Chrysanthi Charalampous and Margarita Zacharogianni for critical reading of the manuscript. This work was supported by the Greek Secretariat for Research and Development (GSRT, 12RUS-11-65 to E.D.) and by the John S. Latsis Public Benefit Foundation (Program “Scientific projects” 2015 to A.F.). The sole responsibility for its content lies with the authors.
The authors declare no competing financial interests.
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Fragkouli, A., Koukouraki, P., Vlachos, I. et al. Neuronal ELAVL proteins utilize AUF-1 as a co-partner to induce neuron-specific alternative splicing of APP. Sci Rep 7, 44507 (2017). https://doi.org/10.1038/srep44507
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