A fly view on the roles and mechanisms of the m⁶A mRNA modification and its players

ABSTRACT

RNA modifications are an emerging layer of posttranscriptional gene regulation in eukaryotes. N⁶-methyladenosine (m⁶A) is among the most abundant modifications in mRNAs (mRNAs) that was shown to influence many physiological processes from yeast to mammals. Like DNA methylation, m⁶A in mRNA is dynamically regulated. A conserved methyltransferase complex catalyzes the deposition of the methyl group on adenosine, which can be removed by specific classes of demethylases. Furthermore, YTH-domain containing proteins can recognize this modification to mediate m⁶A-dependent activities. Here we review the functions and mechanisms of the main m⁶A players with a particular focus on Drosophila melanogaster.

KEYWORDS:

• Drosophila
• m⁶A
• neurogenesis
• RNA modifications
• Sex lethal
• splicing

Introduction

Epigenetic modifications regulate gene expression in response to changes in environmental cues. While the effect of DNA and chromatin modifications has been well studied, the role of RNA modifications on gene expression during organismal development and human disease is only starting to be unveiled. More than 100 modifications have so far been discovered; most of them were found on highly abundant RNAs such as transfer and rRNAs.^1,2 One of the most prevalent modifications on mRNA is N⁶-methyladenosine (m⁶A). Two independent groups developed a few years ago a method called MeRIP-seq (methylated RNA immunoprecipitation sequencing) enabling for the first time a global mapping of m⁶A to the transcriptome.^3,4 These studies revealed the presence of m⁶A in more than 10,000 transcripts of mRNAs and long noncoding RNAs with enrichments around stop codons, in the 3′ untranslated regions (UTRs) and within long internal exons as well as in alternatively spliced ones.^3,4 A consensus sequence for m⁶A was derived from these and subsequent genome-wide studies, which consists of RRACH where R represents purine and H a non-guanine base.^3-5

m⁶A formation is catalyzed by a methyltransferase complex, composed of METTL3, METTL14 and WTAP^6-10 (Fig. 1). METTL3 catalyzes S-adenosyl methionine (SAM)-mediated transfer of methyl group to N⁶-position of adenosine base, while METTL14 is thought to be catalytically inactive with a structural role for facilitating METTL3 activity.^11-13 WTAP, instead, appears essential to stabilize the interaction between the two METTL proteins.⁷ The three components of the core complex localize in nuclear speckles and recognize the previously derived consensus sequence RRACH.^6,14 However, since only a subset of sites is methylated in vivo, additional subunits of the complex, such as KIAA1429 and RBM15, have been proposed to function in guiding the methylation to targeted sites.¹⁵

Figure 1. m⁶A mRNA pathway in vertebrates and Drosophila melanogaster. The m⁶A methyltransferase complex is composed of five factors. In Drosophila, the methyltransferase complex controls neural development and sex determination via its nuclear reader YT521-B. The precise functions or roles of Virilizer and its vertebrate homolog KIAA1429 remain to be identified. No demethlyase has been found so far in Drosophila.

The m⁶A modification was shown to modulate several physiological processes by regulating many aspects of mRNA processing, including splicing, mRNA decay and translation (for a recent review see^16,17). Most of these functions are mediated by members of the YTH-domain family of proteins, which specifically recognize modified adenosines and serve as m⁶A readers.^3,18,19 Vertebrates have five and Arabidopsis have thirteen members of YTH domain proteins, while only two members of the YTH domain family proteins exist in Drosophila; the nuclear YT521-B and the yet uncharacterized cytoplasmic protein CG6422.^20-22 Both Drosophila proteins share high homology to their human counterparts in the YTH region, but low degree of similarities are observed outside the YTH domain.

m⁶A is dynamically regulated in mammals as it can be reverted by oxidative demethylation via the activity of two demethylases, FTO and ALKBH5. Their differential specificity toward m⁶A may rely on distinct temporal and spatial expression^23,24 as well as on the sequence context surrounding the methylated adenosine.²⁵ Accordingly, FTO has recently been shown to act primarily on N⁶-methylated adenosine that is introduced at the first position after the cap.²⁶

Our recent work uncovers the in vivo roles of m⁶A in Drosophila melanogaster and identifies several major regulators. Some of these regulators bear distinct functions, suggesting that they also have m⁶A-independent roles. Here we summarize our current knowledge about the m⁶A players in Drosophila, and compare their functions with homologs in other species.

The m⁶A methyltransferase complex

Ime4

The corresponding homolog of METTL3 (or MTA in plants) in Drosophila is Ime4 (Inducer of meiosis 4 in yeast) (Fig. 2), which was the first subunit of the methyltransferase complex shown to bind S-Adenosyl methionine (SAM) and to transfer the methyl group from the SAM donor to N⁶-position of adenosine.²⁷ A phylogenetic analysis of METTL3 revealed that many species ranging from yeast to human contain a conserved protein,²⁸ which plays essential roles in development, but apparently is absent in fission yeast S. pombe and C. elegans.²⁰ Sporulation is affected in budding yeast S. cerevisae that lack Ime4²⁹ and abnormal growth and seed development is observed in A. thaliana upon loss of MTA^30,31 (Table 1). Knock out of METTL3 prevents naïve embryonic stem cells to differentiate and leads to early embryonic lethality in mice.³² In zebrafish, METTL3 is enriched in brain regions and its depletion leads to increased apoptosis in embryos.⁸ In contrast, Drosophila Ime4 knock out flies survive to adulthood, but are flightless.^21,22 In addition, they display severe locomotion defects in orientation, walking speed and activity due to impaired neuronal functions. Also, defects in oogenesis due to altered Notch signaling have been reported.²⁸ Intriguingly, female Ime4 mutant flies show altered splicing of Sxl, the master regulator of sex determination and dosage compensation in flies. In the soma, Sxl determines female physiognomy through regulation of alternative splicing of transformer (tra) and prevents dosage compensation in females by inhibition of male-specific lethal 2 (msl-2).³³ In addition, Sxl is also required to initiate germ cell differentiation, but this pathway is independent of the sex determination pathway mediated by Tra. Consistently, genetic interaction between Ime4 and Sxl mutants show increased female lethality during development due to compromised dosage compensation and sexual transformations in the absence of msl-2. Furthermore, female germ cell differentiation defects were observed revealing a fine-tuning function of the m⁶A modification in the sex determination pathway. Initial links to the sex determination pathway have further been indicated by the interaction of Arabidopsis MTA with Fip37, the homolog of Fl(2)d in flies, previously identified to play a role in Drosophila sex determination³⁰ (see below).

Figure 2. Domain-structure comparison of m⁶A writers and readers between Drosophila and Human. Comparison of the different proteins was based on uniprot (www.uniprot.org). Homology between similar domains was analyzed via protein BLAST from NCBI. Individual domains of Spenito were compared with RBM15; YT521-B with YTHDC1 and CG6422 with YTHDF2 (Hs - homo sapiens, Dm - Drosophila melanogaster).

Table 1. Components of the m⁶A methyltransferase complex and their biologic roles.

METTL3
Human	METTL3	•METTL3 KD leads to circadian clock period elongation.^81
		•METTL3 promotes translation independently of its catalytic activity.^34
		•METTL3 KD prevents differentiation of hESC.^74
Mouse	Mettl3	•Mettl3 KO in naïve mESC leads to hyper naïve ground state, while in primed mESC boost cell differentiation.^32
		•Mettl3 KO leads to embryonic lethality.^32
Zebrafish	METTL3	•Morpholino depletion leads to developmental defects during embryogenesis.^8
A. thaliana	MTA	•MTA disruption results in embryonic lethality.^30
		•MTA reduction leads to various developmental and organ definition defects.^31
S. cerevisiae	Ime4	•Ime4 is required for sporulation and meiosis.^64,82
D. melanogaster	Ime4	•Ime4 inactivation leads to defects during oogenesis.^83
		•Ime4 KO affects fly locomotion due to impaired neuronal function.^21,22
		•Ime4 regulates splicing of Sxl and fine tunes sex determination.^21,22
METTL14
Human	METTL14	•Structural component of the methyltransferase complex.^7,8,11-13
S. cerevisiae	Kar4	•Transcriptional activator required for karyogamy.^35,84
D. melanogaster	Mettl14	•Mettl14 KO affects fly locomotion due to impaired neuronal functions.^22
		•Mettl14 regulates splicing of Sxl and fine tunes sex determination.^21, 22
WTAP
Human	WTAP	•Structural component of the mehyltransferase complex required for METTL3-METTL14 stabilization.^7,8
Mouse	WTAP	•WTAP KO results in early embryonic lethality.^39
Zebrafish	WTAP	•WTAP morpholinos display defects in head and brain development.^8
S. cerevisiae	Mum2	•Mum2 is required for meiotic mRNA methylation as part of the MIS complex (Mum2, Ime4, Slz1).^82
D. melanogaster	Fl(2)d	•Fl(2)d is required for splicing of Sxl and its KO leads to embryonic lethality.^41
		•Fl(2)d controls retinal development.^44
		•Structural component of the methyltransferase complex, required for Ime4-Mettl14 stabilization.^22
RBM15, RBM15B
Human	RBM15,RBM15B	•RBM15 fusion with MKL1 is associated with acute megakaryoblastic leukemia.^50
		•RBM15 and RBM15B are components of the methyltransferase complex, responsible for complex recruitment to targeted sites.^15
Mouse	RBM15, RBM15B	•Loss of RBM15 leads to embryonic lethality.^47
		•RBM15 controls hematopoiesis, B-cell and megakaryocyte differentiation.^47–49
D. melanogaster	Nito	•Nito regulates wingless signaling and photoreceptor development.^51,52
		•Nito is required for splicing of Sxl.^53
		•Component of the methyltransferase complex.^22

Ime4 is a 68 kilodalton (kDa) protein with a nuclear localization signal. Ime4 co-localizes extensively with RNA Pol II on Drosophila polytene chromosomes suggesting global co-transcriptional deposition of m⁶A.²¹ However, m⁶A levels in Drosophila mRNAs measured by dot blot and LC-MS/MS analyses are low, indicating that more methyl groups might initially be incorporated but are then removed by intron removal or demethylation. Alternatively, the methyltransferase complex, despite being widely present on chromosomes, might be active only under certain conditions. MeRIP-seq analysis with mRNA from Drosophila S2 embryonic cells also points toward lower m⁶A levels compared to vertebrates as around one thousand putative m⁶A sites were identified in Drosophila, while at least 10,000 sites were identified in various vertebrate cells.^3,4,22 Whether m⁶A modification is more abundant and plays more prominent roles in Drosophila neuronal cells remains to be investigated. Nevertheless the consensus RRACH was present in most of the m⁶A peaks, and enrichment near start and stop codons was also observed, suggesting conserved functions and regulatory mechanisms.

Intriguingly, a novel function for mammalian METTL3, independent of its m⁶A catalytic activity, was recently found. A fraction of METTL3 localizes in the cytoplasm and was shown to promote translation of a subset of RNAs containing m⁶A peaks in 3′UTRs by interaction with the eIF3b subunit of the translation initiation complex.³⁴ Whether Drosophila Ime4 has a similar role in the cytoplasm remains to be investigated.

Mettl14

The corresponding homolog of METTL14 in Drosophila is Mettl14 (Fig. 2). Mettl14 is an essential component of the methyltransferase complex and contains, like Ime4, a catalytic domain.^7-10 However, recent structural studies revealed that steric constraints from side groups near the putative SAM binding pocket prevent METTL14 to accommodate SAM and is therefore catalytically inactive.^11-13 Rather, METTL14 was shown to stabilize the interaction between the methyltransferase complex and RNA by forming a charged grove at the interface of METTL3 and METTL14 for RNA accommodation.^11-13 These studies therefore indicate that METTL3 requires METTL14 for its activity. Drosophila Mettl14 shares a 62% identity with human ortholog and sequence comparison shows that side chains, which prevent accommodation of SAM in METTL14 are conserved. Both proteins lack aromatic residues that interact with acceptor adenine as well as residues that enable formation of hydrogen bonds with SAM in METTL3 protein. Loss of function of Mettl14 in Drosophila is reminiscent to the loss of function of Ime4, suggesting that they act together^21,22 (Table 1). Furthermore, quantitative mass spectrometry analysis revealed an interaction at a one to one ratio and show that the stability of both proteins depends on each other.²² Interestingly, the ortholog of METTL14 in yeast, Kar4, can bind DNA and possesses transcriptional activity.³⁵ Whether this function is related to m⁶A methylation and whether similar functions linked to transcription exist for METTL14 in other species is currently unknown.

Fl(2)d

Female-Lethal(2)D is the ortholog of mammalian WTAP (Wilms' tumor 1 associated protein), a nuclear protein that was found to interact with splicing factors and other proteins involved in RNA processing³⁶ (Fig. 2). Its localization to nuclear speckles depends on the presence of BCLAF1 and THRAP3. WTAP was initially found in a yeast two-hybrid screen to identify interactors of Wilms' tumor 1 protein (WT1).¹⁴ WT1 encodes several protein isoforms that can either interact with DNA and act in transcription, or bind RNA and colocalize with splicing factors.³⁷ Intriguingly, isoforms binding to RNA are required for sex determination in mice, since male mutants lacking these isoforms undergo sex reversal due to reduced levels of sex-determining region Y (SRY) protein.³⁸ Whether m⁶A and WTAP are involved in this function remains to be addressed. WTAP knock out mice show embryonic lethality and defects in cell cycle progression^36,39 (Table 1). Drosophila Fl(2)d also colocalizes with several splicing factors in the nucleus and regulates m⁶A levels.^22,40 Accordingly, its expression pattern strictly correlates with the level of m⁶A during development, supporting the notion that, in Drosophila, m⁶A metabolism is primarily dependent on the presence of a functional methyltransferase complex, and less so from potential demethylases (see below). Its depletion strongly compromises the interaction between Ime4 and Mettl14.²²

Fl(2)d was among the first proteins identified to be required for sex-specific alternative splicing of Sxl and tra.^41,42 In contrast to Ime4 and Mettl14, fl(2)d is essential during development and analysis of sexual mosaics showed male somatic transformations in females, which is also observed in transheterozygous Ime4, sxl female mutants made viable by the lack of msl-2.¹⁷ Lethality of fl(2)d mutant females thus suggests other roles, independent of its activity within the methyltransferase complex. In line with these observations, depletion of WTAP in zebrafish also causes more severe developmental defects compared with the loss of METTL3.⁸ Furthermore, gel filtration experiments indicate that human WTAP co-fractions with METTL3 and METTL14 at a size of 300 kDa, but is also present at a higher molecular weight, supporting its association in distinct complexes.⁷

fl(2)d encodes for two isoforms generated via alternative 5′ splice site selection in the 5′UTR. A long isoform contains an N-terminal histidine and glutamine rich region, found in many transcription factors.⁴³ This isoform interacts with Sine Oculis (So) to control retinal development.⁴⁴ Interestingly, fl(2)d splicing is regulated via m⁶A located near the proximal splice site. Depletion of methyltransferase complex components leads to increased usage of the distal splice site and formation of the long protein isoform, but whether this impacts on m⁶A methylosome activity awaits further investigation.²²

Virilizer

Virlizer (Vir) is the ortholog of KIAA1429, which was found in a mass spectrometry-based approach as an interacting protein of the core components of the methyltransferase complex (Fig. 2). Its depletion severely reduces m⁶A levels on mRNA.^9,22 Vir is a large nuclear protein of 1854 amino acids, and like Fl(2)d has essential functions as null mutants are lethal. Like Fl(2)d, Vir is also required for female specific alternative splicing of Sxl^45,46 (Table 1). In vir2F female mutants, ectopic expression of Sxl is sufficient to rescue female lethality. The precise role of Vir and its human homolog in the context of m⁶A biogenesis awaits further investigation.

Spenito

Spenito (Nito) has two orthologs in mammals: RBM15 and RBM15B (Fig. 2). Mice lacking RBM15 die at embryonic day 9.5 and display defects in heart, spleen, vasculature as well as in hematopoiesis, B-cell and megakaryocyte differentiation^47-49 (Table 1). A well-characterized chromosomal aberration involving RBM15 and Megakaryoblastic leukemia 1 (MKL1) is associated with acute megakaryoblastic leukemia,⁵⁰ demonstrating also the pivotal role of RBM15 in cancer. In Drosophila, Nito promotes Wingless signaling⁵¹ and its overexpression in the eye leads to defects in photoreceptor development,⁵² while its depletion in ovaries results in stem cell tumor appearance.⁵³ The loss of Nito affects Sxl splicing and gives rise to male somatic transformations, which is in agreement with the role of other m⁶A components in sex determination.⁵³ Furthermore, Nito interacts with subunits of the methyltransferase complex and its depletion drastically decreases m⁶A levels.²² Interestingly, RBM15 was also recently found to regulate m⁶A levels in human cells and to control X-chromosome inactivation for dosage compensation in female cells via m⁶A-methylation of XIST, which in turn promotes transcriptional repression of the inactive X chromosome.¹⁵ RBM15 binds near m⁶A sites on XIST mRNA and on other transcripts and is predicted to recruit the methyltransferase complex to its target transcripts. RBM15 interacts with RNA directly via its RRM domains and was also shown to interact with the Setd1b protein, an H3K4me3 histone methlyltransferase, via its SPOC domain.⁸⁵ The importance of the individual motif for RBM15/Nito function in regards to m⁶A activity awaits further investigation.

Demethylases

In vertebrates, methylation of adenosine is reversible due to the activity of two demethylases, namely FTO and ALKBH5.^24,54 FTO demethylates m⁶A through N⁶-hydroxymethyladenosine (hm⁶A) and N⁶-formyladenosine (f⁶A) intermediates.^55,56 A recent study showed that FTO preferentially acts on N⁶,2′-O-dimethyladenosine (m⁶A_m) modification adjacent to mRNA cap, which in turn negatively affects mRNA stability.²⁶ FTO loss of function leads to postnatal growth retardation, altered locomotor activity, defects of signaling in dopaminergic neurons and reduced fat mass.^23,57-62 Likewise, overexpression of FTO results in obesity.⁶³ Another m⁶A demethylase, ALKBH5, was later found to play a role in male fertility.²⁴ In contrast to vertebrates, the specificity of m⁶A occupancy in yeast seems to be determined by the restricted expression of the methyltransferase complex.⁶⁴ Similarly, alignment of FTO and ALKBH5 nucleotide sequences to the Drosophila genome failed to identify homologs in flies. FTO appearance is concomitant to the vertebrate clade, with the exception of homologs present in diverse marine eukaryotic algae.⁶⁵ Despite the fact that ALKBH5 is also absent, additional members of the ALKBH family that localize into the cytoplasm are present. However, depletion of these candidates, either individually or in combination, has no consequence on the m⁶A/A ratio (Lence et al, unpublished), indicating that these factors are not functional in flies in regards to their ability to demethylate m⁶A on mRNA. Additional studies will be necessary to address whether other unknown demethylases are required to fine-tune m⁶A levels in this organism.

m⁶A binding YTH proteins

YT521-B

YT521-B is the closest ortholog of YTHDC1 (Fig. 2). The YTH domain was initially found as an RNA binding domain recognizing the hexanucleotide GCAUAC sequence, based on in vitro SELEX experiments.¹⁸ More recently, proteins of the YTH-domain family were recognized as specific binders of m⁶A RNA modification.³ A number of crystal structures revealed the mechanism of this binding by the hydrophobic pocket and aromatic residues.^19,66-68 A 50-fold increase in binding to methylated in comparison to non methylated residues was observed.¹⁹ YTHDC1 is localized in the nucleus and is involved in splicing regulation via m⁶A-in long exons. This mechanism involves the YTHDC1-mediated recruitment of the splicing regulator SRSF3 and the exclusion of SRSF10.⁶⁹ YTHDC1 was also recently shown to induce X chromosome inactivation in human via binding to m⁶A on Xist RNA.¹⁵ The precise mechanism of YTHDC1 in this process is currently unclear. Interactome studies indicate its association with members of Polycomb group complexes, suggesting that YTHDC1, via its ability to recognize m⁶A, may facilitate the binding of gene-silencing proteins to Xist RNA. The sub-nuclear distribution of YTHDC1 is controlled via its association with the KH-domain containing Sam68 protein and this interaction is abolished upon YTHDC1 phosphorylation by p59^fyn kinase.^70,71 In Drosophila, YT521-B is enriched in the embryonic neuroectoderm and in heads of adult flies.²² It localizes to the nucleus and specifically binds m⁶A-modified transcripts.^21,22 In particular, YT521-B assists Sxl in repressing inclusion of the male-specific alternative exon by binding to nearby intronic m⁶A sites.²¹ Consistent with the observation in mammals, Drosophila YT521-B regulates most of m⁶A-dependent splicing events (about 60 to 70% overlap with Ime4). Intron retention and alternative splicing in 5′UTRs are overrepresented. This regulation influences the number of upstream AUGs in 5′UTRs, suggesting that m⁶A-regulated alternative splicing affects translation. Furthermore, YT521-B appears to be the main mediator of m⁶A-dependent processes in vivo, as flies lacking a functional YT521-B resemble the phenotypes observed in mutants for methyltransferase complex components.^21,22 Using SILAC-based proteomic analysis of YT521-B, several potential interactors were found, which includes many predicted mRNA binding proteins, such as the KH-domain containing Quaking related-family proteins, Hrb27C, Syp, Imp and others. The relevance of these interactions, however, awaits further validations.

CG6422

The closest vertebrate ortholog of CG6422 is YTHDF2 (Fig. 2). YTHDF2 is a cytoplasmic protein that belongs to the YTH-domain containing family of proteins. It was identified as an m⁶A binding protein in a pull-down experiment with a methylated probe.³ Its role in mRNA decay was the first study providing a functional mechanism of m⁶A modification in the mRNA life cycle.⁷² YTHDF2 binds m⁶A predominantly in the 3′UTR of mRNAs via its C-terminally located YTH domain. Its N-terminal Glutamine/Proline-rich region interacts directly with CNOT1, a component of the CCR4-NOT deadenylase complex, guiding methylated mRNAs to processing bodies.⁷³ This function appears important in human embryonic cells to degrade mRNA encoding pluripotency factors, eventually allowing for differentiation.^32,74 Likewise, in zebrafish, YTHDF2 is required for maternal mRNA clearance during the maternal to zygotic transition.⁷⁵ Interestingly, YTHDF2 was shown to re-localize to the nucleus under stress conditions and to specifically bind m⁶A in the 5′UTRs of the newly transcribed mRNAs. This binding protects m⁶A sites from FTO-mediated demethylation, which in turn enhances cap-independent translation of heat shock responsive transcripts.⁵⁶ Further m⁶A can also serve on its own to direct cap-independent translation. eIF3 was shown to directly bind m⁶A in the 5′UTR of mRNA upon UV-irradiation or heat-shock conditions, allowing the recruitment of the 43S pre-initiation complex independently of the m⁷G cap modification.⁷⁶ Hence, translation of stress-induced transcripts is enabled by this mechanism when translation of other cellular transcripts is shut down. YTHDF1 is another cytoplasmic YTH-domain containing protein in vertebrates that binds m⁶A around stop codon and in the 3′UTR. YTHDF1 was shown to enhance protein production by direct interaction with eIF3.⁷⁶ Recently, a third protein, YTHDF3, was shown to act cooperatively with YTHDF1 and YTHDF2, to promote translation and mRNA decay, respectively.^77,78 In Drosophila, CG6422 localizes in the cytoplasm but does not re-localize to the nucleus upon heat shock or under UV-irradiation (Lence et al, unpublished). Consistent also with a possible role in the maternal to zygotic transition its expression is high in the first two hours of embryogenesis and decreases during development.²² Its function in the context of m⁶A and potential roles in translation and/or mRNA decay await further investigation.

Conclusion and future directions

With the advance of novel techniques, m⁶A was found on thousands of mRNA sites in several species. Several recent studies demonstrated its role in nearly all aspects of mRNA processing, via a group of YTH-domain family proteins, but also by altering the binding of some RNA interacting proteins to their recognition sites via m⁶A-mediated changes in RNA secondary structure or “RNA switches”.^10,79 The players that catalyze, remove and recognize the modification are conserved across evolution, although with exceptions.

While the precise molecular function of the core methyltransferase complex, including METTL3, METTL14 and WTAP is almost solved; the role of the other co-factors remains less understood. KIAA1429 and its fly homolog Vir, interact with other components of the methlyltransferase complex and regulate m⁶A levels, but their molecular functions are currently unknown. RBM15 binds near methylated sites and its absence prevents recruitment of the methlytransferase complex to its targeted sites. While this model provides an elegant explanation on why only a subset of m⁶A sites is methylated, it remains to be explored whether RBM15 is sufficient to recruit the complex and to induce m⁶A or whether other players are also involved? Intriguingly, RBM15 was shown to interact with chromatin binding proteins via its SPOC domain and has the ability to influence histone marks. Whether RBM15 provides a link between methylated RNA and the chromatin state is therefore an attractive possibility. In fact, it is likely that m⁶A deposition happens co-transcriptionally, as m⁶A regulates splicing and several sites were found in introns.^3,21 Thus, future research will reveal the dynamics of m⁶A deposition and its distribution in relation with transcription and chromatin features.

Loss of components of the Drosophila methyltransferase leads to neuronal and sex determination defects, but how m⁶A precisely regulates these processes remains to be determined. It will be interesting to examine whether other m⁶A functions could be revealed upon stress conditions or in a sensitive context when the dosage of important players involved in specific physiological processes is reduced? Intriguingly, the loss of Ime4 and Mettl14 gives rise to milder phenotypes compared with the depletion of the other complex components such as Nito, Fl(2)d and Vir. This suggests m⁶A-independent functions for these subunits, or else, they may work with distinct m⁶A methyltransferases.

Once the RNA is methylated it can be recognized by a different set of reader proteins and/or the methylation can be removed by the activity of demethylases. Several questions on how selectivity is achieved remain open. Likely, competition exists at individual m⁶A sites for various proteins to bind and protect the m⁶A or to remove it. In addition, binding of other RNA binding proteins such as hnRNPC or ELAV/Hu family proteins might be regulated by m⁶A RNA switches and/or concomitant binding of YTH proteins.^3,79,80 Therefore, sequence context for m⁶A sites is a key to which proteins will bind and which regulatory program will be initiated; as for example, distinct members of the YTHDF proteins can initiate translation or mRNA decay. Overall, the fate of each m⁶A-modified mRNA should take into consideration the “place and time” including the m⁶A position within mRNA, the sequence context, the expression levels of m⁶A regulators as well as the cell type and its developmental stage. Therefore, we foresee that the study of single gene reporters will bring additional mechanistic insights into these questions.

Disclosure of potential conflict of interest

No potential conflicts of interest were disclosed.

Funding

T. Lence and J-Y Roignant are supported by the Marie Curie CIG (334288), the Deutsche Forschungsgemeinschaft (DFG) SPP1935 Grant (RO 4681/4–1) and the European COST action (CA16120). M. Soller is supported by the Biotechnology and Biological Science Research Council (BBSRC).