2. DNA 6mA Methylation and Its Writers, Erasers, and Readers
DNA 6mA was first discovered in prokaryotes and it widely exists in many species, which involves in the regulation of DNA replication, repair, transcription, transposition, and cell defense. It is produced by the addition of the methyl group from S-adenosyl-
l-methionine (SAM) to N-6 of the adenine ring via specific methyltransferases
[3]. In recent years, it has been reported that 6mA exists in eukaryotes, such as green algae
[18],
C. elegans [19], and
Drosophila [20], but 6mA has been proved to exist at extremely low levels in most higher eukaryotes, especially in mammals.
DNA 6mA modification is a dynamic process including the addition and removal of methyl groups, coordinated via a complex system of methylases. These proteins are called writers and erasers. In eukaryotes, several methyltransferases have been reported (
Figure 1)
[21]. DNA N6 adenine methyltransferase 1 (DAMT-1) has been identified in
C. elegans to methylate 6mA via the knock down and overexpression of treatments. The DNA methyltransferases (DNMTs) family is known to act as 5mC methyltransferases in animals
[22]. The overexpression or depletion of DNMT1 lead to the increased or decreased levels of genomic 6mA
[23]. This suggested that DNMT1 may be a 6mA methyltransferase
[24]. Further analysis revealed that DNMT1 belongs to the MT-A70 domain-containing enzyme family which includes mRNA methyltransferases Ime4 and Kar4 in yeast, and the methyltransferase-like protein 3 (METTL3) and METL14 in humans
[25][26][27][25,26,27]. In mammals, METTL4 is a DNMT1 homologue and a paralogue of METTL3 and the methyltransferase-like protein14 (METTL14), which functions as a DNA 6mA methyltransferase. In the human genome, N-6 adenine-specific DNA methyltransferase 1 (N6AMT1) has reported as a methyltransferase, which contains the catalytic conserved motif NPPY
[28]. This conclusion has been demonstrated via structural analysis and silence/overexpression.
Figure 1. DNA 6mA modification is a dynamic process. Methyltransferases (writers), including N6AMT1, DAMT-1, DNMT1, and METTL4 add a methyl group to form 6mA. This process can be reversed via demethylases (erasers) such as DMAD, ALKBH1, NMAD-1, and FTO. In addition, binding proteins (readers) recognize and bind the 6mA site on DNA. Therefore, they also play an important role in the regulation of gene expression and cellular functions.
6mA modification is a reversible process, and there must be a demethylation process. 6mA demethylase (DMAD), as a ten-eleven translocation (TET) homologue in
Drosophila [20], tightly controls the demethylation of 6mA during embryonic development and tissue homeostasis. Loss of DMAD may result in severe developmental defects, while increasing the abundance of 6mA modifications. Interestingly, DMAD is expressed at higher levels in the
Drosophila brain than in the ovary. When DMAD was depleted, the levels of 6mA in the brain increased 100-fold
[29]. The ALKB protein family catalyzes the demethylation of various methylated DNA and RNA nucleotides. N6-methyladenine demethylase 1 (NMAD-1) is a member of the ALKB family. The deletion of
Nmad-1 in
C. elegans cells resulted in increased 6mA levels
[30]. Therefore, it can be stated that NMAD-1 is a 6mA demethylase. Another member of the ALKBHs (alkB homologs), ALKBH1, also showed to mediate the demethylation of 6mA in mouse and human cells
[31]. The 6mA levels were higher in glioblastoma cells compared with normal tissues, and the 6mA demethylase ALKBH1 has also been considered as a potential new target for cancer treatment
[32]. Further, it has been confirmed that the human fat mass and obesity-associated protein (FTO) not only is a demethylase of RNA m6A, but also demethylates DNA 6mA. In human cancer tissues, 6mA showed a downward trend, accompanied by the downregulation of N6AMT1 and the upregulation of ALKBH1. Therefore, the downregulation of genomic 6mA levels may promote tumorigenesis
[28].
It is important to note that the function of 6mA requires binding proteins in addition to methyltransferases and demethylases. These binding proteins, called readers, can recognize and bind 6mA sites on DNA and play a significant role in gene expression regulation and cell function
[33]. Protein readers, YTHDC5, YTHDF1, and YTHDF2, have been identified as bona fide 6mA regulators in type II testicular germ cell tumors (GCT) via reanalysis of the expression microarray data
[34]. Additionally, HNRNPC, which is highly expressed in GCT tissues and cell lines, was an “indirect reader” involved in the “6mA switch” that altered the local RNA structure, thereby triggering the RNA-binding motif and facilitating protein binding
[34]. In human mitochondria, the single-stranded DNA-binding protein 1 (SSBP1), containing the HNRNP and YTH domains, was thought to be a protein that recognized 6mA, and it preferentially bound to ssDNA along the heavy chain, consistent with the location of 6mA enrichment
[35][36][35,36]. The Jumu protein was an important transcription factor in
Drosophila, encoding 719 amino acids. It was the first FOX family protein with dual functions discovered, which could cause the large-scale modification of heterochromatin and has a specific recognition function. The Jumu protein has been reported to recognize and bind 6mA-modified DNA and act as a maternal factor to control the proper activation of the zygotic genome. Zelda, an essential precursor of the transcription factor for the maternal to zygotic transition (MZT), was one of the key target genes of Jumu. The study demonstrated that Jumu proteins regulated zygotic genome activation, at least in part by recognizing Zelda that controlled the 6mA mark, thereby regulating early embryogenesis
[37].
3. The Potential Functions of DNA 6mA Methylation
The 6mA modification has been well described in prokaryotes to play roles in foreign DNA cleavage, virus defense, and DNA damage repair
[38][39][40][41][38,39,40,41]. The potential function of 6mA modification in mammals remains an active area of ongoing research. In addition to providing binding sites for effector proteins, one potential effect of the 6mA modification was to directly alter the overall structure of DNA. Early crystal structures suggested that 6mA may also alter DNA secondary structure
[42]. Meanwhile, 6mA affected DNA double helix formation by altering the base pair stability and base stacking
[40][42][40,42]. Similar to the main function of 5mC, 6mA modification has been found to play a role in regulating gene expression in different species
[43]. The 6mA modification reduced the thermal stability of the DNA chain, which in turn changed the curvature of the DNA chain; thus, 6mA at a specific position affected the interaction of transcription factor-related elements
[44]. 6mA modification acted as an epigenetic mark that affected the chromatin structure and gene expression patterns in a heritable manner. Recent studies showed that the coordination of 6mA and histone modification H3K4me2 contributed to the transgenerational epigenetic control
[19], and 6mA was mainly present at ApT dinucleotides around the transcription start site (TSS) with a bimodal distribution and appeared to mark the active genes in Chlamydomonas. Furthermore, a genome-wide map of 6mA and its genomic distribution suggested a potential epigenetic role for 6mA in regulating gene expression
[18]. Together, these findings suggested 6mA functions as an epigenetic mark in eukaryotes.
In mouse embryonic stem cells, 6mA was associated with the repression and silencing of genes, particularly those on the X chromosome, and was known to play an important role in cell fate decisions. During the first 120 h of zebrafish embryonic development, the 6mA levels rose steadily from a pluripotent cell to a nearly fully formed individual, and the same pattern was observed in mouse embryonic days 7–21
[45]. With the continuous improvement of detection technology, 6mA modification has been detected in humans and is confirmed to be related to various diseases. It has been reported that 6mA was involved in the pathogenesis of essential hypertension
[46]. The 6mA levels in leukocytes of all hypertension models were significantly reduced and could return to normal levels after successful hypertension treatment. The decreased 6mA levels in leukocytes and vascular smooth muscle cells (VSMCs) of the hypertensive models in vivo and in vitro were due to the increased ALKBH1 content. The 6mA was a sensitive marker for the development, diagnosis, and treatment of hypertension
[46]. Moreover, 6mA was involved in the regulation of fatty liver degeneration. In patients with fatty liver degeneration, significantly increased the 6mA levels and downregulated ALKBH1 have been found
[47]. Integrative analysis of transcriptome and chromatin immunoprecipitation-sequencing revealed that ALKBH1 directly bound and specifically demethylated the 6mA of genes involved in fatty acid uptake and lipogenesis, thereby reducing hepatic lipid accumulation
[47]. Importantly, ALKBH1 overexpression was sufficient to suppress lipid uptake and synthesis and attenuate diet-induced hepatic steatosis and insulin resistance. ALKBH1-induced 6mA played an integral role in hepatic fatty acid metabolism as an epigenetic repressor and provided a potential therapeutic target for treatment.
Aberrant DNA methylation has been shown to be associated with tumorigenesis. Recent reports indicated that 6mA participated in the progression and tumorigenesis of several cancers, such as breast cancer
[48], gastric cancer
[49], liver cancer
[28], lung cancer,
[50] and glioma
[32]. Reduction in N6AMT1 in clinical breast cancer tissues correlated with 6mA intensity and predicted poorer survival of patients
[48]. Functionally, the knockdown of N6AMT1 significantly decreased the 6mA levels in DNA and promoted colony formation and the migration of breast cancer cells, whereas the overexpression of N6AMT1 had the opposite effect. Mechanistically, N6AMT1 acted as a methyltransferase for 6mA formation and repressed the gene expression of key cell cycle inhibitors such as RB1 and TP53, which was also the first study on the regulation and function of 6mA modification in breast cancer progression and prognosis.
The 6mA levels were apparently tissue specific, with the highest 6mA levels observed in the brain. It is well known that environmental exposure may induce epigenetic changes. What need to be pointed out here is that environmental factors in vivo and in vitro are inseparable from the expression level of 6mA. Yao et al. demonstrated that 6mA in the mouse brain was a dynamic change in response to environmental stress, and the change in 6mA was related to the expression of neuronal genes and LINE transposon. Stress-induced 6mA changes significantly related to genes which are associated with neuropsychiatric disorders. These results implicated that 6mA may play a key epigenetic role in mammalian brain development and pathogenesis
[51]. Substantial evidence showed that physiological and psychological stress can alter DNA methylation of key stress-related genes in the mouse brain
[52][53][52,53]. The prefrontal cortex (PFC), responsible for the highest-order cognitive abilities, is particularly vulnerable to chronic stress and plays an important role in depression. It has also been reported that after characterizing the dynamics of 6mA under starvation in the single-cell model organism, Tetrahymena thermophila, single-molecule real-time sequencing (SMRT-sequencing) showed that the 6mA levels in starved cells were significantly lower compared with the DNA 6mA levels in vegetatively growing cells
[54]. In summary, environmental factors are extremely important for the influence of 6mA in different model organisms.
6mA is emerging as a crucial DNA epigenetic mark to regulate gene expression in eukaryotes. Current researchers explored the role of 6mA dysregulation and 6mA modulators in human diseases, especially in cancers
[55]. However, the study of 6mA in mammals is still in its infancy, so further studies are needed to confirm the characterization of 6mA in mammals and expand
theour knowledge of the biological functions of 6mA in human diseases, especially the physiological significance of its high abundance in the mammalian brain.