Dyschromatosis symmetrica hereditaria (DSH) is a highly penetrant autosomal-dominant skin disease. It is characterized by a mixture of hyper- and hypo-pigmented macules on the dorsal aspects of the hands and feet (Figure 1). The disorder typically has its onset during infancy or early childhood, stops spreading before adolescence and lasts for life. It was clarified in 2003 that a heterozygous mutation in the adenosine deaminase acting on RNA1 gene (
The ADAR1 protein catalyzes the deamination of adenosine to inosine in double-stranded RNA [2, 3]. This modification is called RNA editing, more specifically A-I editing (Figure 2).
RNA editing is a post-transcriptional modification, and A-I editing is widely conserved in species ranging from roundworm to mammals. A-I editing had been considered a rare phenomenon in the coding region and this editing is known to create alterations of the codon or alternative splice sites that lead to different proteins in the target substrate. Representative substrate genes are the ionotropic AMPA glutamate receptor subunit 2  and the 5-HT2c serotonin receptor , which are both expressed in the brain and are associated with the some neurologic diseases .
However, the substrate gene for ADAR1 in the skin and the pathogenic mechanisms whereby mutation in
This chapter addresses DSH. First, we introduce the clinical and pathological features of DSH. Next, we introduce how
2. DSH, ADAR1 and RNA editing
2.1. Epidemiology and clinical features of DSH
Dyschromatosis symmetrica hereditaria (DSH; OMIM#127400; also called reticulate acropigmentation of Dohi) is an autosomal-dominant pigmentary genodermatosis with almost full penetrance. DSH was first described by Toyama [7, 8].
Clinically, the disorder is characterized by areas several millimeters in diameter of mixed hypopigmented and hyperpigmented macules distributed predominantly on the dorsal aspects of the hands and feet but sometimes extending to the dorsal aspects of the limbs (Figure 1). The lesions on the face are described as freckle-like macules with no hypopigmentation [9, 10]; some cases have been reported in which mixed areas of hypopigmented and hyperpigmented macules on the cheek were similar to those on the hands and feet . Patients who have strong skin manifestations on the limbs also tend to have lesions on face. The skin lesions do not show telangiectasia, atrophy or scaling. Skin manifestations are not observed on the palm, sole or mucosa.
DSH has been reported mainly from Japan and China; however, patients in South Korea , Taiwan , Thailand , India , Turkey  and Europe [16, 17] and patients of Hispanic ethnicity  have been reported.
The disorder typically develops during infancy or early childhood . Lesions first appear before the age of 6 years in 73% of cases, and the first appearance is usually on the limbs (83%) , particularly the hands and feet. This point can be useful in differentiating the disorder from dyschromatosis universalis symmetrica (DUH). The macules enlarge progressively , stop spreading before adolescence and last for life [19, 21]. The onset of lesions during adolescence has been reported in some patients .
The skin findings are more pronounced after sun exposure, although patients do not show photosensitivity [10, 20]. This differentiates the disorder from xeroderma pigmentosum (XP).
Interfamilial and intrafamilial variation has been reported. The clinical features are not always similar among patients in a pedigree . We have encountered a family in which the patient has only faint hypopigmented macules on the backs of the fingers and the patient’s children have mixtures of hyper- and hypopigmented macules in all the limbs.
The characteristic clinical features of typical DSH can be clearly differentially diagnosed from similar hereditary pigmentary disorders as follows . Acropigmentatio reticularis (Kitamura) (ARK) is characterized by atrophic pigmented macules on the dorsum of the hands and feet, and palmoplantar pits and pigmentation. It is autosomal dominant, as is DSH.
DUH shows hypo- and hyper-pigmented macules that are similar to those of DSH on the trunk as well as the extremities. It has been reported to be autosomal dominant and autosomal recessive.
It had been though that those two diseases were related to DSH. However, when mutation of the
Mild cases or the early stages of child DSH are sometimes difficult to differentiate from xeroderma pigmentosum (XP) . In such cases, the diagnosis of XP can usually be obtained by following up on skin lesions such as xerosis, atrophy, telangiectasia and skin tumors of sun-exposed areas as they grow up, photosensitivity test, and ultimately gene analysis [24, 25].
2.2. Histopathology of DSH
Histological studies have showed increased melanin pigmentation in the basal layer of hyperpigmented lesions, along with pigmentary incontinence and largely absent melanin in the hypopigmented macule [13, 23].
According to precise histochemical studies, Masson-Fontana stain reveals a remarkable decrease or total absence of melanin in the hypochromic-achromic epidermis [13, 23]. Split-dopa preparations were reported to show an obvious decrease in melanocyte number in the hypomelanotic area (45-167 cells/mm2) and the surrounding pigmented skin (119-204 cells/mm2), as compared with the 16 normal control persons (1,217+/-282 cells/mm2 on the dorsal hands and 821-1,154 cells/mm2 on the dorsal feet) . There was an increase in melanocyte size but not number in the hyperchromic area, and the dendrites were very elongated and numerous, suggesting that melanosome transfer from melanocytes to keratinocytes was active . Another study also indicated a lower density of dopa-positive melanocytes in the hypo-pigmented macules of DSH patients than in normal skin at same site from normal pigmented controls . Electron microscopy showed melanocytic abnormalities in the hypomelanotic skin, i.e., a numerical decrease, fatty degeneration, swollen mitochondria, vacuolization of the cytoplasm, large cytoplasmic vacuole formation and condensed irregularly shaped nuclei [13, 23]. The keratinocytes located in the vicinity of the melanocytes contained few melanosomes. In some keratinocytes, the melanosome complex containing more than 15 melanosomes were recognized . The hyperpigmented area showed a lot of slight larger melanosomes in the melanocytes, and the adjacent keratinocytes showed many singly dispersed melanosomes . The aggregated melanosome were also found in the keratinocyte in hyperpigmented macules . In the hyperpigmented macules, the number of melanosomes in the melanocytes was somewhat smaller than in adjacent keratinocytes, which suggests that the melanosome transfer from melanocytes to keratinocytes is more active than melanosome production in the melanocyte .
2.3. Identifying the causative gene of DSH
In 2003, Miyamura et al. determined that a heterozygous mutation of the adenosine deaminase acting on RNA1 gene (
In identifying the causative gene of DSH , whole-genome-wide scan (linkage analysis) using 343 microsatellite markers in three pedigrees of DSH (88 people, including 41 patients) was done at first. The results of linkage analysis indicated that the DSH locus was on the long arm of chromosome 1. Next, to narrow the interval of the region containing the DSH locus, haplotype analysis was carried out, and the results suggested that the DSH gene lay between two microsatellite markers, D1S2715 and D1S2777. Haplotype analysis using novel single-nucleotide polymorphisms showed a final DSH genetic interval of approximately 500 kbp. There were 9 genes in this interval, including the
The ADAR1 protein catalyzes the deamination of adenosine to inosine in double-stranded RNA [2, 3]. ADAR1 is in the ADAR protein family, which includes ADAR1 , ADAR2  and ADAR3 . As RNA editing enzymes, all ADAR family members contain several double-stranded RNA-binding domains (dsRBDs) and a conserved catalytic deaminase domain in the C-terminal region . Differences in the number and spacing of the dsRBDs, nuclear localization signals and the presence of additional domains create the variants (Figure 2A).
ADAR1 has two isoforms of different sizes: interferon-inducible ADAR1-p150 (150kDa) and constitutively expressed ADAR1-p110 (110kDa) (Figure 2B) . Both contain three dsRBDs, but they differ in that the p150 variant contains two Z-DNA binding domains and a nuclear export signal, whereas the p110 variant contains only a single Z-DNA binding domain and no export signal. Consequently, ADAR1-p110 localizes mainly to the nucleus, whereas ADAR1-p150 is found in both the cytoplasm and the nucleus. Resulting from alternative promoters, the two variants may play different cellular roles. Although the ADAR1-p110 promoter is constitutively active, the ADAR1-p150 promoter is interferon-inducible, suggesting a role in response to cellular stresses such as viral infection .
ADAR1 catalyzes the deamination of adenosine to inosine in double-stranded RNA substrates in the step of post-transcription processing  (Figure 3). Inosine acts as guanine during translation, which results in codon alterations or alternative splicing sites  and thus leads to functional changes in proteins. It is expressed ubiquitously, including in the skin , but only a few known target genes for ADAR1 are expressed in specific tissues, including ionotropic glutamate receptor   and the serotonin receptor 2C subtype in the brain , and hepatitis δ virus antigen in the liver . Fifteen sites of amino acid substitution by A-I editing have been identified to date . The substrate gene edited by ADAR1 in the skin is still unknown, and it remains to clarify how ADAR1 causes DSH. The structure and function of ADAR1 are detailed later.
2.4. Gene analysis of the
ADAR1 in DSH patients
Since identification of the
The two mutations p.Q102fs and p.H216fs [9, 39] that were found in the
2.5. Homodimerization of ADAR1
Homodimerization was demonstrated to be essential for the enzyme activity of ADAR1 . Having one monomer defective for the deaminase domain (E396A) halves the dimer function. Taken together, these data indicate that a deaminase mutant chimeric dimer (E396A/WT) is able to bind dsRNA but that only one functional active site is formed and the result is, therefore, only partial activity . This result may indicate that ADAR1 mutation in the deaminase domain generates haploinsufficiency. However, site-selective RNA editing activity of 5HT2cR RNA by heterodimer was found to be decreased to 30% . These results may indicate a complex effect at each site by this enzyme.
In contrast, the A-I editing activity of the dsRNA binding mutant chimeric dimer (Mut/WT) is completely lost . This is because of the defective dsRBDs of one monomer, and it suggests that cooperative interactions of functional dsRBDs in both ADAR dimer subunits are required for dsRNA binding. When one monomer in the dimer complex is unable to bind the dsRNA, then the dimer complex is excluded from binding the substrate. It shows activity. As previously indicated, in DSH patients, a disproportionately high number of mutations are identified in the deaminase domain relative to the dsRBDs of ADAR1. It may be that mutations identified in the deaminase domain are less severe, because the chimeric dimers that are expected to form still retain some editing activity .
The likely ratio of monomer subunits in a dimer is 1:2:1 for (WT/WT), (Mut/WT) and (Mut/Mut), suggesting that a heterozygous deaminase mutation would not have as strong an effect due to the dimer’s ability to maintain partial activity. In contrast, mutations are rarely found in the dsRBDs, because these alterations would have a more dominant effect when paired with a wild-type partner, thus greatly reducing ADAR function. Under this assumption, the reduced activity for ADAR could be as low as one-quarter with only (WT/WT) dimers having editing activity, and this may be below a threshold for survival and may possibly be selected out naturally during development. ADAR dimerization can be a potential source of modulation for RNA editing activity, and these ADAR (EAA) mutants may prove interesting for future studies
2.6. Neurological complications
In 1994, Patrizi
On the basis of the known crystal structure , it was predicted that ADAR1 G1007R would introduce an additional positively charged arginine residue on the RNA-binding face of the deaminase domain very close to the active site . In fact, the ADAR1 G1007R mutant has efficient RNA-binding ability, similar in level to that of wild-type ADAR1, but it does not edit dsRNA; however, other mutant ADAR1 partially edit. So, the dominant negative effect gives these additional neurological symptoms of DSH [44, 45].
The ionotropic glutamate receptor [33, 34] is a known target gene for ADAR1. Glutamate receptors are expressed at high levels in the brain, including in the basal ganglia , and glutamatergic overactivity has been suggested to contribute to the occurrence of dystonia [47, 48]. ADAR1 catalyzes RNA editing at the Q/R sites of the glutamate receptor subunits GluR5 and GluR6, and reduces the Ca2+ permeability of glutamate receptors . Therefore, mutation in
Furthermore, increased Ca2+ influx through glutamate receptors is known to be toxic to neurons, and that toxicity may induce various neurological abnormalities . Increases in intracellular Ca2+ levels have also been reported to be the underlying mechanism of tissue calcification . Therefore, mutations in
The patient’s mother had the same mutation in p.G1007R as her son, but she showed no neurological problems, which suggests that some unknown mechanism is involved in the development of dystonia, mental deterioration and brain calcification . It will be necessary to observe whether she develops neurological symptoms later. This mechanism, as well as the unknown molecular pathogenesis of the skin lesion, should be clarified.
2.7. More ADAR functions than A-I editing of the coding region of mRNA
Only a few sites of A-I editing by ADAR1 had been found in the coding region. Recently it was reported that 85% of all the transcripts are edited by A-I editing , and A-I editing regulated gene expression much more than had been thought.
New A-I editing sites have been found by next-generation sequencing . Also, ADAR1 is now known to frequently target 5’ and 3’ untranslated regions (UTRs) and intronic retrotransposon elements, such as Alu and long interspersed elements (LINE/SINEs). Further, several primary microRNA (miRNA) intermediates undergo A-I editing [55-58]. 99% of the identified A-I editing sites are in non-coding RNA . It was reported that ADARs regulate the expression of microRNA and redirect silencing targets by A-I editing of miRNA [55, 57, 58]. There is extensive interaction between the RNA editing and RNA interference (RNAi) pathways . However, the overview of physiologic significance of non-coding RNA editing still remains to be clarified, including whether those non-coding RNA editing is involved in the pathogenesis of DSH.
Additionally, in these miRNA/siRNA pathways, an editing-independent effect of inhibition of RNAi by ADARs was reported .
2.8. DSH murine models
Wang et al. generated an Adar1 knockout (KO) murine model  that lacks exons 12–15, corresponding to the catalytic RNA-editing domain. Hartner et al.  created a KO mouse that has the homozygous deletion of exons 7-9 or exons 2-13.
In the Adar-/- mouse with homozygous deletion exons 7-9 or exons 2-13, the liver sizes in fatal mice were the same as in wild-type mice until E11.0 - 11.25, and they did not increase further, whereas wild-type and Adar+/- embryo livers enlarged by up to 50% between E11.5 and 12.5 . Reduced cell density and blood accumulation were observed by microscopy in Adar-/- fatal livers, perhaps resulting from massive cell death. Embryonic hematopoietic tissues were significantly reduced in the yolk sac, fetal liver and peripheral blood compared with wild-type and Adar+/- embryos. There were no morphological abnormalities in other tissues .
In KO mice with the homozygous deletions of exons 12-15, widespread apoptosis was detected in many tissues of the Adar-/- mouse embryos collected live from E10.5 to E11.5, particularly in the heart, liver and vertebra, despite their normal gross appearance . Fibroblasts derived from Adar-/- embryos were also prone to apoptosis induced by serum deprivation. Those results demonstrated that ADAR1 is essential to embryogenesis and suggested that it functions to promote the survival of numerous tissues by editing one or more double-stranded RNAs required for protection against stress-induced apoptosis ].
KO mice with different mutant alleles showed the same result of fatal lethality at E11.5–12.5 [60, 61].
Interestingly nonsense mutations that encode proteins similar to those in the knockout mice have been reported in DSH patients, such as R328X  or Y989X . Notably, DSH patients are heterozygous for the
The previously described KO mice had disruptions of both the p110 and p150 isoforms [60, 61]. To circumvent the embryonic lethality associated with simultaneous disruption of p110 and p150, a selective p150-isoform-disrupted mouse was generated in which the promoter and exon 1A region of the p150 isoform of Adar1 were specifically targeted, while the expression of p110 was left intact . Selective disruption of p150 alone resulted in embryonic lethality from E11-E12, similar to the time point of embryonic lethality seen previously with disruption of p110 and p150 [60, 61]. These results indicate that the p150 isoform of ADAR1 plays a critically important role in embryogenesis. Furthermore, they raise the possibility that the embryonic lethality seen in the previously described
To investigate in more depth the role of ADAR1 in skin, an epidermis-specific Adar1 knockout murine model was established . In this model, Adar1 gene deletion was induced by tamoxifen exposure. First we administrated tamoxifen orally to ten K14-Adar1 mice (FVB background) at the age of 6 weeks old for 5 consecutive days. Eight of these treated mice died within three weeks after treatment, developing a phenotype that included dramatically decreased aggressiveness, thin body shape, fur loss, poor skin resiliency, skin rash and bleeding . In the FVB mice, H–E stained sections revealed massive necrosis in the epidermis and few remaining hair follicles in the dermis. Thickening of the interfollicular epidermis (IFE) and the stratum corneum were observed, while skin ulcers were observed in some other areas . In the B6 mice, epidermal necrosis was not observed but increased keratinocytes and thickened stratum corneum were evident. p150-specific Adar1-deleted newborn B6 mouse showed death in a subset of the hair follicles. These results support an essential role for ADAR1 in the epidermis during the first hair follicle developmental cycle .
The RNA editing mechanism has been gaining much attention. A-I editing has been shown to affect a wide variety of RNA transcripts, both protein coding and noncoding sequences. Its relationship with some neurological diseases, e.g., amyotrophic lateral sclerosis [50, 65-67], epilepsy , depression  and schizophrenia , has been clarified. In the skin, although the expression of ADAR1 is recognized, its function remains unknown. Various functions of ADAR have been successively clarified. In DSH patients, if a new function of ADAR1 or a new target gene of ADAR1 were to be identified, it would not only help to elucidate the pathogenesis of DSH, but also be one step toward clarifiying RNA editing in the skin. For dermatologists, it is also very interesting how this characteristic skin manifestation, a mixture of pigmented and depigmented macules with a unique distribution of eruptions in the extremities, develops.
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