Gain-of-Function Mutation of KIT Ligand on Melanin Synthesis Causes Familial Progressive Hyperpigmentation
2009; Elsevier BV; Volume: 84; Issue: 5 Linguagem: Inglês
10.1016/j.ajhg.2009.03.019
ISSN1537-6605
AutoresZhiqiang Wang, Lizhen Si, Quan Tang, Debao Lin, Zhangjie Fu, Jing Zhang, Bin Cui, Yufei Zhu, Xianghua Kong, Min Deng, Yu Xia, Heng Xu, Weidong Le, Landian Hu, Xiangyin Kong,
Tópico(s)Mast cells and histamine
ResumoFamilial progressive hyperpigmentation (FPH) is an autosomal-dominantly inherited disorder characterized by hyperpigmented patches in the skin, present in early infancy and increasing in size and number with age. The genetic basis for FPH remains unknown. In this study, a six-generation Chinese family with FPH was subjected to a genome-wide scan for linkage analysis. Two-point linkage analysis mapped the locus for FPH at chromosome 12q21.31-q23.1, with a maximum two-point LOD score of 4.35 (Ø = 0.00) at D12S81. Haplotype analysis confined the locus within an interval of 9.09 cM, flanked by the markers D12S1667 and D12S2081. Mutation profiling of positional candidate genes detected a heterozygous transversion (c. 107A→G) in exon 2 of the KIT ligand (KITLG) gene, predicted to result in the substitution of a serine residue for an asparagine residue at codon 36 (p.N→S). This mutant "G" allele cosegregated perfectly with affected, but not with unaffected, members of the FPH family. Function analysis of the soluble form of sKITLG revealed that mutant sKITLGN36S increased the content of the melanin by 109% compared with the wild-type sKITLG in human A375 melanoma cells. Consistent with this result, the tyrosinase activity was significantly increased by mutant sKITLGN36S compared to wild-type control. To our knowledge, these data provided the first genetic evidence that the FPH disease is caused by the KITLGN36S mutation, which has a gain-of-function effect on the melanin synthesis and opens a new avenue for exploration of the genetic mechanism of FPH. Familial progressive hyperpigmentation (FPH) is an autosomal-dominantly inherited disorder characterized by hyperpigmented patches in the skin, present in early infancy and increasing in size and number with age. The genetic basis for FPH remains unknown. In this study, a six-generation Chinese family with FPH was subjected to a genome-wide scan for linkage analysis. Two-point linkage analysis mapped the locus for FPH at chromosome 12q21.31-q23.1, with a maximum two-point LOD score of 4.35 (Ø = 0.00) at D12S81. Haplotype analysis confined the locus within an interval of 9.09 cM, flanked by the markers D12S1667 and D12S2081. Mutation profiling of positional candidate genes detected a heterozygous transversion (c. 107A→G) in exon 2 of the KIT ligand (KITLG) gene, predicted to result in the substitution of a serine residue for an asparagine residue at codon 36 (p.N→S). This mutant "G" allele cosegregated perfectly with affected, but not with unaffected, members of the FPH family. Function analysis of the soluble form of sKITLG revealed that mutant sKITLGN36S increased the content of the melanin by 109% compared with the wild-type sKITLG in human A375 melanoma cells. Consistent with this result, the tyrosinase activity was significantly increased by mutant sKITLGN36S compared to wild-type control. To our knowledge, these data provided the first genetic evidence that the FPH disease is caused by the KITLGN36S mutation, which has a gain-of-function effect on the melanin synthesis and opens a new avenue for exploration of the genetic mechanism of FPH. Familial progressive hyperpigmentation (FPH [MIM %145250]), also called "melanosis universalis hereditaria," is a rare form of a congenital genetic disease causing hyperpigmentation. FPH was first reported by Chernosky in a two-generation family consisting of four individuals.1Chernosky M.E. Anderson D.E. Chang J.P. Shaw M.W. Romsdahl M.M. Familial progressive hyperpigmentation.Arch. Dermatol. 1971; 103: 581-598Crossref PubMed Scopus (43) Google Scholar The onset of the pigmentation was either at birth or in early infancy, and irregular patches increased with age in size, number, and confluence.2Rebora A. Parodi A. Universal inherited melanodyschromatosis: A case of melanosis universalis hereditaria?.Arch. Dermatol. 1989; 125: 1442-1443Crossref PubMed Scopus (14) Google Scholar This process was rapid during childhood and slower during adolescence, and it resulted in extensive hyperpigmentation of the conjunctive face, neck, trunk, limbs, lips, oral mucosa, palms, and soles.3Ling D.B. Lo T. Familial progressive hyperpigmentation: A family study in China.Br. J. Dermatol. 1991; 125: 607Crossref PubMed Scopus (9) Google Scholar FPH was determined to be an autosomal-dominant inheritable disease, after Rebora's report on an Italian family in 1989 and Lin's report on a Han family from China in 1991.2Rebora A. Parodi A. Universal inherited melanodyschromatosis: A case of melanosis universalis hereditaria?.Arch. Dermatol. 1989; 125: 1442-1443Crossref PubMed Scopus (14) Google Scholar, 3Ling D.B. Lo T. Familial progressive hyperpigmentation: A family study in China.Br. J. Dermatol. 1991; 125: 607Crossref PubMed Scopus (9) Google Scholar The first locus for FPH was reported at chromosome 19p13.1-pter, spanning 45.58 cM between D19S593 and 19pter in 2006.4Zhang C. Deng Y. Chen X. Wu X. Jin W. Li H. Yu C. Xiong Y. Zhou L. Chen Y. Linkage of a locus determining familial progressive hyperpigmentation (FPH) to chromosome 19p13.1-pter in a Chinese family.Eur. J. Dermatol. 2006; 16: 246-250PubMed Google Scholar However, no candidate gene has been identified in this region, and the genetic basis and pathologic mechanisms of FPH remain unknown. In an effort to localize the gene for FPH, we undertook an entire genome scan in the six-generation Chinese family with FPH reported by Lin.3Ling D.B. Lo T. Familial progressive hyperpigmentation: A family study in China.Br. J. Dermatol. 1991; 125: 607Crossref PubMed Scopus (9) Google Scholar We found significant evidence for linkage of the FPH-responsible gene to chromosome 12q21.31-q23.1. Subsequently, a missense mutation in the KITLG gene (OMIM ∗184785) was identified as being associated with human FPH. We investigated a six-generation family, from a rural area of Shandong Province of China, with typical features of FPH. A complete family history was obtained, and 18 affected individuals (nine males and nine females) were identified. Careful physical examination revealed that all of the affected individuals in this family manifested pigmentation disorders without the association of any other system disease (Figure 1). For example, patient IV-1 (Figure 1A) is an affected 53-year-old male with hyperpigmentation on his hands, palms, limbs, conjunctive face, neck, trunk, and soles. None of the affected members in this family was found to have skin cancer. The pedigrees with FPH showed an autosomal-dominant inheritance pattern (Figure 1C). This research has been approved by the ethical review committees of the appropriate institutions. In total, 25 family members participated in this study, but only 17 are informative for linkage analysis. Samples of peripheral blood were obtained from all available family members after informed consent was obtained, and genomic DNA was extracted with the QIAmp DNA Blood kit (QIAGEN, Germany). A genome-wide screening was performed in this family for determination of the chromosomal regions linked to FPH, with the use of 382 fluorescent microsatellite markers covering 22 autosomes at a resolution of approximately 10 cM (Linkage Mapping Set Version 2, Perkin Elmer). PCR amplification was performed in a total volume of 10 μl, with the use of a PTC-225 DNA Engine Tetrad (MJ Research, USA) and standard conditions. PCR products were electrophoresed on a 5% standard denaturing polyacrylamide gel with an Applied Biosystems 377XL DNA Sequencer. The size of the allele was determined on the basis of an internal size standard (GeneScan 400HD ROX, Perkin Elmer) in each lane, and results were analyzed with GeneScan 3.0 and Genotyper 2.1 software (Perkin Elmer). A two-point linkage analysis was conducted with the use of the LINKAGE V5.10 software package,5Lathrop G.M. Lalouel J.M. Easy calculations of lod scores and genetic risks on small computers.Am. J. Hum. Genet. 1984; 36: 460-465PubMed Google Scholar under an autosomal-dominant genetic model, with a disease-allele frequency of 0.0001, evenly shared allele frequency, full penetrance, and no sex difference. Pedigree drawing and haplotype construction were carried out with the use of the Cyrillic v2.0 software (Cyrillic Software, UK). An initial genome-wide scan identified a locus for FPH at chromosome 12q. The maximum two-point LOD score obtained was 4.35 with marker D12S81, at a recombination frequency of Ø = 0.00 (Table 1). The analysis of additional markers (D12S83, D12S326, D12S1708, D12S1667, D12S351, D12S101, D12S2081, D12S346, D12S78; Table 1) further confirmed the initial result. Conversely, no significant linkage with markers on other chromosomal regions was found in this FPH family (Table S1, available online).Table 1Two-Point LOD Score Result between the Disease Gene and Ten Markers of Chromosome 12q21.31-q23.1Two-Point LOD Score at ØMarker0.000.010.050.10.20.30.4D12S83–∞–4.69–2.05–1.04–0.260.020.07D12S326–3.95–0.270.270.370.290.150.06D12S17082.942.882.652.341.731.120.54D12S1667–0.632.763.102.932.291.510.72D12S814.354.263.923.482.561.620.73D12S3512.942.882.622.301.641.00.44D12S1014.134.053.733.312.441.550.70D12S2081–∞–0.520.070.240.280.210.11D12S346–∞0.551.091.171.030.740.38D12S78–∞–0.240.420.630.680.540.30 Open table in a new tab Pedigree and haplotype analyses were carried out, and three recombinations were identified (Figure 1C). First, an affected male individual (IV-1) had a recombination between D12S1667 and D12S81. Second, an affected female (V-12) had a recombination between D12S1708 and D12S1667. For the affected individual (V-3), recombination took place between D12S101 and D12S2081. All of the combined information indicates that FPH maps to the region of chromosome 12q21.31-q23.1 spanning approximately 9.09 cM and flanked by markers D12S1667 and D12S2081. The above physical interval contained about 81 defined genes, and KITLG (GeneID: 4254) could be a plausible candidate gene on the basis of chromosome position and previous function analysis.6Kunisada T. Yoshida H. Yamazaki H. Miyamoto A. Hemmi H. Nishimura E. Shultz L.D. Nishikawa S. Hayashi S. Transgene expression of steel factor in the basal layer of epidermis promotes survival, proliferation, differentiation and migration of melanocyte precursors.Development. 1998; 125: 2915-2923PubMed Google Scholar, 7Grichnik J.M. Burch J.A. Burchette J. Shea C.R. The SCF/KIT pathway plays a critical role in the control of normal human melanocyte homeostasis.J. Invest. Dermatol. 1998; 111: 233-238Crossref PubMed Scopus (169) Google Scholar Sequencing of the KITLG gene was initially performed on genomic DNA derived from patient V-5. Upon complete analysis of the coding and the adjacent intron regions of KITLG, a heterozygous c.107A →G transversion in exon 2 of KITLG was identified in this patient but was not present in unaffected members (Figures 2A and 2B). The transversion caused an asparagine→serine exchange at amino acid 36 of the KITLG protein sequence. This mutant "G" allele cosegregated perfectly with family members affected with FPH, but not with unaffected members. We confirmed that c.107A →G was not listed in the NCBI SNP database (dbSNP). Furthermore, we used sequencing to exclude it as a SNP in a panel of 296 normal, unrelated, healthy Chinese individuals. These results indicated that KITLG N36S was a mutation. KITLG, also known as steel factor, stem cell factor, and mast cell growth factor, binds to and activates KIT and plays a crucial role in the development and maintenance of the melanocyte lineage in adult skin.7Grichnik J.M. Burch J.A. Burchette J. Shea C.R. The SCF/KIT pathway plays a critical role in the control of normal human melanocyte homeostasis.J. Invest. Dermatol. 1998; 111: 233-238Crossref PubMed Scopus (169) Google Scholar, 8Anderson D.M. Lyman S.D. Baird A. Wignall J.M. Eisenman J. Rauch C. March C.J. Boswell H.S. Gimpel S.D. Cosman D. et al.Molecular cloning of mast cell growth factor, a hematopoietin that is active in both membrane bound and soluble forms.Cell. 1990; 63: 235-243Abstract Full Text PDF PubMed Scopus (712) Google Scholar, 9Copeland N.G. Gilbert D.J. Cho B.C. Donovan P.J. Jenkins N.A. Cosman D. Anderson D. Lyman S.D. Williams D.E. Mast cell growth factor maps near the steel locus on mouse chromosome 10 and is deleted in a number of steel alleles.Cell. 1990; 63: 175-183Abstract Full Text PDF PubMed Scopus (477) Google Scholar, 10Russell E.S. Hereditary anemias of the mouse: A review for geneticists.Adv. Genet. 1979; 20: 357-459Crossref PubMed Scopus (822) Google Scholar, 11Manova K. Bachvarova R.F. Huang E.J. Sanchez S. Pronovost S.M. Velazquez E. McGuire B. Besmer P. c-kit receptor and ligand expression in postnatal development of the mouse cerebellum suggests a function for c-kit in inhibitory interneurons.J. Neurosci. 1992; 12: 4663-4676Crossref PubMed Google ScholarKITLG exists in two alternatively spliced transcripts, differing in exon 6. The smaller splice variant of KITLG, lacking exon 6, encodes a primarily membrane-bound form of KITLG (mKITLG).12Huang E.J. Nocka K.H. Buck J. Besmer P. Differential expression and processing of two cell associated forms of the kit-ligand: KL-1 and KL-2.Mol. Biol. Cell. 1992; 3: 349-362Crossref PubMed Scopus (272) Google Scholar In contrast, the larger precursor contains exon 6, which codes for a membrane-proximal extracellularly located protease-cleavage site. This site is readily cleaved by cell-surface proteases for production of a soluble KITLG molecule (sKITLG).13Flanagan J.G. Chan D.C. Leder P. Transmembrane form of the kit ligand growth factor is determined by alternative splicing and is missing in the Sld mutant.Cell. 1991; 64: 1025-1035Abstract Full Text PDF PubMed Scopus (607) Google Scholar The primary translation product of both KITLG mRNAs contains a 25 aa signal sequence at the N terminus, not found in the mature form of the proteins.8Anderson D.M. Lyman S.D. Baird A. Wignall J.M. Eisenman J. Rauch C. March C.J. Boswell H.S. Gimpel S.D. Cosman D. et al.Molecular cloning of mast cell growth factor, a hematopoietin that is active in both membrane bound and soluble forms.Cell. 1990; 63: 235-243Abstract Full Text PDF PubMed Scopus (712) Google Scholar Many studies have shown that the KIT and KITLG genes play a critical role in the development of the melanocyte and melanin synthesis in fish, salamanders, avians, and mammals, although the expression pattern of KIT and KITLG among different species is variable. In addition, the dependence of melanocytes on KIT/KITLG signaling for survival or proliferation shows species-specific differences.12Huang E.J. Nocka K.H. Buck J. Besmer P. Differential expression and processing of two cell associated forms of the kit-ligand: KL-1 and KL-2.Mol. Biol. Cell. 1992; 3: 349-362Crossref PubMed Scopus (272) Google Scholar, 14Hultman K.A. Bahary N. Zon L.I. Johnson S.L. 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Crawford J. Jimenez F. Kurtzberg J. Buchanan M. Blackwell S. Clark R.E. Hitchcock M.G. Human recombinant stem-cell factor induces melanocytic hyperplasia in susceptible patients.J. Am. Acad. Dermatol. 1995; 33: 577-583Abstract Full Text PDF PubMed Scopus (54) Google Scholar, 28Bellet J.S. Obadiah J.M. Frothingham B.M. Kurtzberg J. Grichnik J.M. A patient with extensive stem cell factor-induced hyperpigmentation.Cutis. 2003; 71: 149-152PubMed Google Scholar Biopsies taken from the hyperpigmented areas of FPH patients displayed strong hyperpigmentation of the epidermia and increased melanin in the basal layer, but no increase in the number of melanocytes within the epidermis.2Rebora A. Parodi A. Universal inherited melanodyschromatosis: A case of melanosis universalis hereditaria?.Arch. Dermatol. 1989; 125: 1442-1443Crossref PubMed Scopus (14) Google Scholar, 3Ling D.B. Lo T. Familial progressive hyperpigmentation: A family study in China.Br. J. Dermatol. 1991; 125: 607Crossref PubMed Scopus (9) Google Scholar, 4Zhang C. Deng Y. Chen X. Wu X. Jin W. Li H. Yu C. Xiong Y. Zhou L. Chen Y. Linkage of a locus determining familial progressive hyperpigmentation (FPH) to chromosome 19p13.1-pter in a Chinese family.Eur. J. Dermatol. 2006; 16: 246-250PubMed Google Scholar, 29Zanardo L. Stolz W. Schmitz G. Kaminski W. Vikkula M. Landthaler M. Vogt T. Progressive hyperpigmentation and generalized lentiginosis without associated systemic symptoms: A rare hereditary pigmentation disorder in south-east Germany.Acta Derm. Venereol. 2004; 84: 57-60Crossref PubMed Scopus (19) Google Scholar To determine the effects of the p.N36S substitution in KITLG on the melanin synthesis, we expressed the soluble form of wild-type (WT) sKITLG and mutant sKITLGN36S in Escherica coli and purified the expression products for further analysis (Figure S1). Coomassie brilliant blue staining revealed a single band for each construct (WT and mutant) after SDS-PAGE, and western blot analysis showed that both bands could be recognized by human KITLG antibody (Figure S1). The A375 human pigmented melanoma cells were treated with WT and mutant sKITLGN36S, then melanin content was measured. Our results indicate that the two types of sKITLG can increase the melanin content of each cell in treated A375 cells; melanin content increased from 16.2 pg per cell (WT sKITLG) to 33.9 pg per cell (mutant sKITLGN36S). Compared with the WT sKITLG, the mutant sKITLGN36S significantly increased the melanin content, up to 209%. This indicated that the mutant sKITLGN36S had a greater melanin-synthesis function than its WT form (Figure 2C). Many reports have shown that tyrosinase is essential in melanin synthase.30Luo D. Chen H. Searles G. Jimbow K. 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Sci. 2008; 49: 115-123Abstract Full Text Full Text PDF PubMed Scopus (28) Google Scholar Consistent with the improved ability of the mutant sKITLGN36S to induce melanin synthesis, the tyrosinase activity increased significantly in A375 cells after treatment with mutant sKITLGN36S, compared to treatment with the WT sKITLG (Figure 2D). Together, all of these results indicate that the mutant sKITLGN36S protein had the ability to increase melanin synthesis. These results are consistent with the biopsies of FPH patients who displayed increased melanin in the basal layer (Figure 1B).3Ling D.B. Lo T. Familial progressive hyperpigmentation: A family study in China.Br. J. Dermatol. 1991; 125: 607Crossref PubMed Scopus (9) Google Scholar However, there was no proliferation difference found for treated A375 cells between the WT and mutant sKITLG (data not shown). Although our experimental data show that the soluble form of p.N36S mutant KITLG can increase the melanin synthesis in A375 cells, we cannot exclude the role of the membrane-bound form of mutant KITLG for hyperpigmentation in FPH families. Indeed, reports have indicated that mouse melanocytes require the membrane-bound form of KITLG for survival.6Kunisada T. Yoshida H. Yamazaki H. Miyamoto A. Hemmi H. Nishimura E. Shultz L.D. Nishikawa S. Hayashi S. Transgene expression of steel factor in the basal layer of epidermis promotes survival, proliferation, differentiation and migration of melanocyte precursors.Development. 1998; 125: 2915-2923PubMed Google Scholar Additional work will be required for determination of whether the membrane-bound form of mutant KITLG plays a role in melanin synthesis. Several human genetic diseases, such as dyschromatosis universalis hereditaria (DUH [MIM %127500]), dyschromatosis symmetrica hereditaria (DSH [MIM #127400]), and xeroderma pigmentation (XP [MIM #278700]), show some overlap with FPH. DUH and DSH are pigmentary dermatoses most commonly seen in Japanese and Korean individuals. DUH is characterized by hyperpigmented and hypopigmented flecks and spots over much of the body.35Stuhrmann M. Hennies H.C. Bukhari I.A. Brakensiek K. Nurnberg G. Becker C. Huebener J. Miranda M.C. Frye-Boukhriss H. Knothe S. et al.Dyschromatosis universalis hereditaria: Evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23.Clin. Genet. 2008; 73: 566-572Crossref PubMed Scopus (34) Google Scholar DSH shows a characteristic mixture of hyperpigmented and hypopigmented macules of various sizes, limited largely to the dorsal aspects of the hands and feet.36Suenaga M. Genetical studies on skin diseases. VII. Dyschromatosis universalis hereditaria in 5 generations.Tohoku J. Exp. Med. 1952; 55: 373-376Crossref PubMed Scopus (26) Google Scholar FPH can be differentiated from DSH and DUH on the basis of the absence of hypopigmented lesions in patients. In addition, the genes for DSH and DUH have previously been mapped to chromosomes 1q21.3, 6q24.2-q25.2, and 12q21-q23.35Stuhrmann M. Hennies H.C. Bukhari I.A. Brakensiek K. Nurnberg G. Becker C. Huebener J. Miranda M.C. Frye-Boukhriss H. Knothe S. et al.Dyschromatosis universalis hereditaria: Evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23.Clin. Genet. 2008; 73: 566-572Crossref PubMed Scopus (34) Google Scholar, 37Xing Q.H. Wang M.T. Chen X.D. Feng G.Y. Ji H.Y. Yang J.D. Gao J.J. Qin W. Qian X.Q. Wu S.N. et al.A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2.Am. J. Hum. 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The genetics of the hereditary xeroderma pigmentosum syndrome.Biochimie. 2002; 84: 49-60Crossref PubMed Scopus (70) Google Scholar Although XP also resembles FPH hyperpigmentation, FPH does not show the atrophy, xerosis, or skin tumors usually observed in XP. FPH is also likely to be a heterogenous disease, given that C. Zhang et al. mapped the gene responsible for FPH to chromosome 19p13.1-pter, spanning 45.58 cM between D19S593 and 19pter, using genome screening on a three-generation Chinese family. However, there was no gene reported to be responsible for FPH in this family.4Zhang C. Deng Y. Chen X. Wu X. Jin W. Li H. Yu C. Xiong Y. Zhou L. Chen Y. Linkage of a locus determining familial progressive hyperpigmentation (FPH) to chromosome 19p13.1-pter in a Chinese family.Eur. J. Dermatol. 2006; 16: 246-250PubMed Google Scholar In the current work, we have mapped the dominant FPH gene to the region at chromosome 12q21.31-q23.1. Candidate-gene analysis revealed that mutant KITLGN36S was the critical gene for FPH in this family. Protein-function analysis confirmed that the soluble form of mutant sKITLGN36S can increase the melanin content significantly in A375 human pigmented melanoma cells, compared with the WT. In conclusion, this report identified the p.N36S transversion of KITLG responsible for inherited FPH. The data show that the soluble mutant form, sKITLG, produces a gain-of-function defect in melanin synthesis, possibly triggering hyperpigmentation of skin in patients. These results will provide important clues for understanding of the molecular mechanism of pigmentation in FPH and increase our ability to develop effective intervention strategies. We thank all members of the TPT-PS family for participation in this study, and we thank Donghua Chen, Minhua Jin, and Jianqun Wang for their support. This work is supported by the National High Technology Research and Development Program of China (2006AA02Z330, 2006AA02A301), the National Basic Research Program of China (2007CB512202, 2007CB512100, 2004CB518603), the National Natural Science Foundation of China, Key Program (30530450), the Knowledge Innovation Program of the Chinese Academy of Sciences (KSCX1-YW-R-74), and the E-Institutes of Shanghai Municipal Education Commission. Download .pdf (.1 MB) Help with pdf files Document S1. One Table and One Figure The URLs for data presented herein are as follows:NCBI dbSNP Database, http://www.ncbi.nlm.nih.gov/projects/SNP/Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim/
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