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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 2006 Oct 17;79(6):1105–1109. doi: 10.1086/509789

Mutations in the Gene Encoding the Wnt-Signaling Component R-Spondin 4 (RSPO4) Cause Autosomal Recessive Anonychia

C  Bergmann 1,*, J  Senderek 1,*, D  Anhuf 1, C T  Thiel 1, A B  Ekici 1, P  Poblete-Gutiérrez 1, M  van Steensel 1, D  Seelow 1, G  Nürnberg 1, H H  Schild 1, P  Nürnberg 1, A  Reis 1, J  Frank 1, K  Zerres 1
PMCID: PMC1698700  PMID: 17186469

Abstract

Anonychia is an autosomal recessive disorder characterized by the congenital absence of finger- and toenails. In a large German nonconsanguineous family with four affected and five unaffected siblings with isolated total congenital anonychia, we performed genomewide mapping and showed linkage to 20p13. Analysis of the RSPO4 gene within this interval revealed a frameshift and a nonconservative missense mutation in exon 2 affecting the highly conserved first furin-like cysteine-rich domain. Both mutations were not present among controls and were shown to segregate with the disease phenotype. RSPO4 is a member of the recently described R-spondin family of secreted proteins that play a major role in activating the Wnt/β-catenin signaling pathway. Wnt signaling is evolutionarily conserved and plays a pivotal role in embryonic development, growth regulation of multiple tissues, and cancer development. Our findings add to the increasing body of evidence indicating that mesenchymal-epithelial interactions are crucial in nail development and put anonychia on the growing list of congenital malformation syndromes caused by Wnt-signaling–pathway defects. To the best of our knowledge, this is the first gene known to be responsible for an isolated, nonsyndromic nail disorder.


Anonychia (MIM 206800) is defined as the absence of finger- and toenails.1 Usually, anonychia and its milder phenotypic variant hyponychia occur as a feature of genetic syndromes and may be associated with significant limb anomalies. Well-known examples are Coffin-Siris syndrome (MIM 135900), different ectodermal dysplasias (MIM 129490, MIM 300291, MIM 224900), nail-patella syndrome (MIM 161200), and brachydactyly type B (MIM 113000). Most of these syndromes are transmitted in an autosomal dominant mode. In contrast, isolated, nonsyndromic anonychia without additional features is a rare entity that may present either as a so-called partial autosomal dominant form that affects only the thumbs2 or—in its most severe, autosomal recessively inherited variant—with involvement of all digits and toes.3 So far, no gene or locus has been reported for nonsyndromic anonychia.

We describe a large, nonconsanguineous German family with four children afflicted with isolated total congenital anonychia (fig. 1). Both parents and five siblings were unaffected. Further family history was unremarkable. Affected individuals were of normal height and proportionate stature and were not different in any aspect, besides anonychia, from their healthy siblings. In any affected individual, anonychia had been present since birth. X-rays of the right upper limb and foot of individual II-8 showed normal results (fig. 2). No additional malformations were found on clinical examination of affected siblings, neither of ectodermal structures nor of sensory organs. There was no report of inner abnormalities in any affected individual, and an additional abdominal ultrasound performed in individual II-8 showed normal results. All siblings were of normal intelligence. The youngest affected sibling is 36 years old, the eldest currently 47 years old. All affected individuals have healthy children with normal nails.

Figure  1. .

Figure  1. 

Top left, Pedigree of the German nonconsanguineous family with isolated total congenital anonychia, with four affected and five unaffected siblings. Top right and middle right, Hands and feet of affected individual II-8, showing isolated total congenital anonychia. Middle left, Maternally transmitted guanine nucleotide insertion leading to a frameshift and premature truncation of the corresponding protein (c.92_93insG, p.Leu31fs). Bottom left, paternal nonconservative RSPO4 missense mutation c.218G→A leading to an amino acid exchange from cysteine to tyrosine at position 73 (p.Cys73Tyr). Bottom right, Multiple protein sequence alignment, generated with the program ClustalW with use of translation from genome assemblies and expressed sequences. Sequence comparison shows that the identified RSPO4 missense mutation c.218G→A (p.Cys73Tyr) affects an amino acid (displayed on a grayish background) that is highly conserved in evolution.

Figure  2. .

Figure  2. 

X-ray of the right hand of affected individual II-8, showing no skeletal alteration or any degenerative or inflammable joint process.

We obtained blood samples after receiving informed consent from all individuals of this family (who were all adults) and extracted genomic DNA using standard procedures. To identify the causative disease locus in this family, we undertook a genomewide linkage scan using a panel of microsatellite markers with an average distance of 10 cM (Weber panel Version 10 [Research Genetics]), an ABI3100 sequence analyzer, and Genotyper software v3.7 (Applied Biosystems) (table 1). We achieved marker saturation by use of existing and newly generated microsatellite markers. We performed two-point LOD score calculations by use of the LINKAGE program package, with help from the computer programs LINKRUN and MKS, with an autosomal recessive, fully penetrant model. We identified two regions with multipoint LOD scores >2, on chromosome 10 and chromosome 20 (fig. 3). The candidate interval on chromosome 10 comprised 27.7 Mb between the flanking markers D10S1214 and D10S1221. The candidate region on chromosome 20p could be further refined by typing additional microsatellite markers from the draft human genome sequence to a 7.8-Mb region on chromosome 20p13 flanked by D20S1155 and the newly established STR marker AL021879. At about the same time, consanguineous pedigrees with autosomal recessively inherited anonychia were reported to be linked to the same region on chromosome 20.4

Table 1. .

LOD Score Data for Chromosomes 10 and 20

Chromosome and Position LOD Score NPL Score P Informativity
Chromosome 10:
 .00 −13.822492 −.573142 .859375 .811315
 2.86 −1.938632 −.172976 .421875 .582592
 5.72 −.900282 .237033 .234375 .491290
 8.58 −.301249 .662147 .234375 .471094
 11.44 .110500 1.108011 .234375 .515610
 14.30 .414527 1.580727 .140625 .657019
 16.08 .483845 1.594740 .140625 .660038
 17.86 .535067 1.611783 .140625 .673747
 19.64 .567594 1.631802 .140625 .697169
 21.42 .578384 1.654749 .140625 .730847
 23.20 .560123 1.680586 .140625 .776981
 24.36 .521674 1.686149 .140625 .802739
 25.52 .453916 1.692859 .140625 .835366
 26.68 .333943 1.700672 .140625 .875583
 27.84 .088157 1.709544 .140625 .926083
 29.00 −6.822926 1.719426 .140625 1.000000
 30.64 .856069 1.762825 .015625 .866986
 32.28 1.104381 1.797109 .015625 .788036
 33.92 1.225349 1.822675 .015625 .734387
 35.56 1.291396 1.839829 .015625 .700467
 37.20 1.323717 1.848786 .015625 .684918
 38.12 1.328376 1.843667 .015625 .676700
 39.04 1.325265 1.836000 .015625 .674017
 39.96 1.314218 1.825780 .015625 .676576
 40.88 1.294516 1.812996 .015625 .684457
 41.80 1.264734 1.797627 .015625 .698176
 41.82 1.263945 1.797211 .015625 .698481
 41.84 1.263150 1.796794 .015625 .698790
 41.86 1.262349 1.796376 .015625 .699102
 41.88 1.261543 1.795956 .015625 .699420
 41.90 1.260730 1.795535 .015625 .699745
 43.04 1.199961 1.756346 .015625 .711695
 44.18 1.109516 1.713088 .140625 .734171
 45.32 .966671 1.665637 .140625 .767390
 46.46 .697958 1.613845 .140625 .814102
 47.60 1.557547 .140625 .888636 −6.590196
 48.74 −1.250954 1.577088 .140625 .893416
 49.88 −1.049511 1.598450 .140625 .902286
 51.02 −1.024437 1.621661 .140625 .915123
 52.16 −1.175601 1.646752 .140625 .932487
 53.30 −6.825668 1.673757 .140625 .956747
 53.86 1.443266 2.052412 .015625 .901350
 54.42 1.752742 2.442580 .015625 .886910
 54.98 1.937380 2.844488 .015625 .894812
 55.54 2.070971 3.258374 .015625 .925517
 56.10 2.176644 3.684484 .015625 1.000000
 56.34 2.176196 3.682546 .015625 .998753
 56.58 2.175797 3.680789 .015625 .997883
 56.82 2.175448 3.679213 .015625 .997258
 57.06 2.175149 3.677818 .015625 .996857
 57.30 2.174899 3.676604 .015625 .996713
 57.66 2.174102 3.673363 .015625 .994597
 58.02 2.173417 3.670530 .015625 .993060
 58.38 2.172843 3.668103 .015625 .991942
 58.74 2.172381 3.666082 .015625 .991207
 59.10 2.172031 3.664466 .015625 .990842
 59.32 2.171873 3.663678 .015625 .990803
 59.54 2.171756 3.663042 .015625 .990908
 59.76 2.171680 3.662556 .015625 .991166
 59.98 2.171647 3.662221 .015625 .991597
 60.20 2.171655 3.662038 .015625 .992268
 60.22 2.171643 3.661987 .015625 .992283
 60.24 2.171631 3.661939 .015625 .992302
 60.26 2.171619 3.661891 .015625 .992325
 60.28 2.171608 3.661845 .015625 .992352
 60.30 2.171597 3.661800 .015625 .992389
 60.40 2.171302 3.660483 .015625 .991431
 60.50 2.171016 3.659199 .015625 .990617
 60.60 2.170739 3.657946 .015625 .989875
 60.70 2.170470 3.656724 .015625 .989192
 60.80 2.170209 3.655533 .015625 .988562
 62.26 2.164898 3.635009 .015625 .976102
 63.72 2.161423 3.621133 .015625 .969648
 65.18 2.159784 3.613847 .015625 .967907
 66.64 2.159982 3.613123 .015625 .970853
 68.10 2.162017 3.618957 .015625 .980000
 68.42 2.142698 3.616549 .015625 .957001
 68.74 2.122628 3.614457 .015625 .941817
 69.06 2.101729 3.612682 .015625 .929869
 69.38 2.079907 3.611224 .015625 .920197
 69.70 2.057058 3.610081 .015625 .912387
 70.88 1.960658 3.603075 .015625 .889199
 72.06 1.838878 3.600351 .015625 .882554
 73.24 1.670560 3.601902 .015625 .890900
 74.42 1.391393 3.607733 .015625 .916483
 75.60 .338006 3.617858 .015625 .976002
 76.58 .359932 3.539859 .015625 .948603
 77.56 .365445 3.464913 .015625 .931756
 78.54 .357042 3.392885 .015625 .920075
 79.52 .335658 3.323645 .015625 .912531
 80.50 .301009 3.257065 .015625 .909286
 82.16 .221510 2.938901 .015625 .857513
 83.82 .089546 2.627674 .015625 .835104
 85.48 −.119658 2.321753 .015625 .832311
 87.14 −.488215 2.019535 .015625 .850962
 88.80 −5.131500 1.719426 .140625 .910479
 89.86 −1.124280 1.675626 .140625 .809393
 90.92 −.727556 1.630636 .140625 .740541
 91.98 −.497598 1.584447 .140625 .684926
 93.04 −.343611 1.537039 .140625 .638436
 94.10 −.234429 1.488386 .140625 .599112
 98.52 −.029553 1.271161 .234375 .492907
 102.94 −.046463 1.027462 .234375 .459669
 107.36 −.233979 .751054 .234375 .490440
 111.78 −.673779 .433452 .234375 .589229
 116.20 −5.362968 .063683 .234375 .794357
 117.32 −3.693738 .026691 .234375 .758733
 118.44 −3.694394 −.011703 .234375 .768489
 119.56 −3.932102 −.051613 .234375 .805640
 120.68 −4.491026 −.093157 .234375 .872634
 121.80 −13.822492 −.136462 .421875 1.000000
 123.26 −3.914463 −.038117 .234375 .902700
 124.72 −3.407335 .042009 .234375 .844640
 126.18 −3.235219 .104377 .234375 .804612
 127.64 −3.317401 .149345 .234375 .778452
 129.10 −6.262274 .177174 .234375 .765241
 131.26 −2.878196 .189584 .234375 .741330
 133.42 −2.733289 .164976 .234375 .742660
 135.58 −2.868831 .103029 .234375 .768551
 137.74 −3.365977 .002966 .234375 .823832
 139.90 −13.822492 −.136462 .421875 .937188
 140.40 −5.166596 −.122758 .234375 .892549
 140.90 −4.476299 −.109837 .234375 .860217
 141.40 −4.164445 −.097686 .234375 .832992
 141.90 −4.116894 −.086293 .234375 .809376
 142.40 −6.204296 −.075647 .234375 .788813
 146.46 −.750165 −.044719 .234375 .499708
 150.52 −.323259 −.074176 .234375 .391086
 154.58 −.244677 −.164515 .421875 .403903
 158.64 −.518801 −.319478 .484375 .541759
 162.70 −13.822492 −.546295 .484375 .899303
 164.40 −3.311111 −.495144 .484375 .752945
 166.10 −2.819883 −.443336 .484375 .679131
 167.80 −2.616737 −.391340 .484375 .642130
 169.50 −2.642169 −.339606 .484375 .636089
 171.20 −4.786508 −.288589 .484375 .662478
 172.54 −1.453826 −.247775 .484375 .625899
 173.88 −1.172033 −.209244 .421875 .622275
 175.22 −1.074798 −.173134 .421875 .644024
 176.56 −1.161200 −.139617 .421875 .694806
 177.90 −5.307711 −.108906 .234375 .803001
Chromosome 20:
 .00 2.423638 3.684484 .015625 .989978
 .02 2.423562 3.684342 .015625 .989732
 .04 2.423487 3.684202 .015625 .989523
 .06 2.423412 3.684063 .015625 .989329
 .08 2.423338 3.683925 .015625 .989145
 .10 2.423264 3.683789 .015625 .988969
 .76 2.420946 3.679112 .015625 .984275
 1.42 2.419228 3.675805 .015625 .981689
 2.08 2.418111 3.673865 .015625 .980580
 2.74 2.417594 3.673291 .015625 .980781
 3.40 2.417678 3.674083 .015625 .982297
 3.66 2.417769 3.674290 .015625 .982796
 3.92 2.417954 3.674710 .015625 .983507
 4.18 2.418232 3.675342 .015625 .984419
 4.44 2.418603 3.676186 .015625 .985536
 4.70 2.419067 3.677242 .015625 .986871
 4.74 2.419142 3.677402 .015625 .987073
 4.78 2.419219 3.677568 .015625 .987282
 4.82 2.419299 3.677739 .015625 .987497
 4.86 2.419380 3.677915 .015625 .987718
 4.90 2.419464 3.678096 .015625 .987947
 5.12 2.419941 3.679069 .015625 .989176
 5.34 2.420484 3.680195 .015625 .990589
 5.56 2.421094 3.681472 .015625 .992200
 5.78 2.421770 3.682901 .015625 .994055
 6.00 2.422514 3.684484 .015625 .996354
 6.44 2.422303 3.683266 .015625 .995707
 6.88 2.422311 3.682658 .015625 .995790
 7.32 2.422536 3.682658 .015625 .996478
 7.76 2.422978 3.683266 .015625 .997798
 8.20 2.423638 3.684484 .015625 1.000000
 9.60 2.418638 3.672194 .015625 .988142
 11.00 2.415669 3.666061 .015625 .982493
 12.40 2.414729 3.666061 .015625 .981277
 13.80 2.415819 3.672194 .015625 .984408
 15.20 2.418936 3.684484 .015625 .993229
 15.30 2.418638 3.683721 .015625 .992349
 15.40 2.418350 3.682989 .015625 .991618
 15.50 2.418072 3.682290 .015625 .990960
 15.60 2.417805 3.681621 .015625 .990358
 15.70 2.417548 3.680985 .015625 .989807
 15.72 2.417497 3.680856 .015625 .989697
 15.74 2.417446 3.680729 .015625 .989588
 15.76 2.417396 3.680603 .015625 .989481
 15.78 2.417346 3.680479 .015625 .989377
 15.80 2.417296 3.680356 .015625 .989274
 16.26 2.402473 3.616546 .015625 .974271
 16.72 2.387427 3.553516 .015625 .963903
 17.18 2.372130 3.491238 .015625 .955663
 17.64 2.356549 3.429690 .015625 .949028
 18.10 2.340650 3.368844 .015625 .943839
 18.12 2.339947 3.366197 .015625 .943628
 18.14 2.339243 3.363551 .015625 .943421
 18.16 2.338538 3.360906 .015625 .943218
 18.18 2.337833 3.358262 .015625 .943020
 18.20 2.337127 3.355620 .015625 .942831
 18.22 2.335567 3.349189 .015625 .941284
 18.24 2.334005 3.342758 .015625 .939984
 18.26 2.332441 3.336330 .015625 .938778
 18.28 2.330875 3.329902 .015625 .937636
 18.30 2.329306 3.323476 .015625 .936541
 18.32 2.327731 3.317035 .015625 .935462
 18.34 2.326153 3.310596 .015625 .934418
 18.36 2.324573 3.304158 .015625 .933402
 18.38 2.322991 3.297721 .015625 .932411
 18.40 2.321406 3.291286 .015625 .931444
 19.22 2.253007 3.024822 .015625 .898429
 20.04 2.179818 2.760751 .015625 .876006
 20.86 2.100844 2.498736 .015625 .860225
 21.68 2.014782 2.238444 .015625 .849862
 22.50 1.919883 1.979541 .015625 .844453
 22.52 1.917427 1.973204 .015625 .844324
 22.54 1.914964 1.966868 .015625 .844201
 22.56 1.912494 1.960533 .015625 .844081
 22.58 1.910017 1.954199 .015625 .843966
 22.60 1.907534 1.947865 .015625 .843854
 23.80 1.743738 1.568009 .140625 .840750
 25.00 1.541528 1.190153 .234375 .847434
 26.20 1.273452 .813264 .234375 .864284
 27.40 .862436 .436311 .234375 .893256
 28.60 −.434900 .058259 .234375 .942226
 28.62 −.535670 .051943 .234375 .943462
 28.64 −.664504 .045627 .234375 .944747
 28.66 −.844528 .039309 .234375 .946098
 28.68 −1.149529 .032991 .234375 .947549
 28.70 −7.200503 .026673 .234375 .949261
 29.12 −2.682250 −.027535 .234375 .955363
 29.54 −2.629849 −.081878 .234375 .962748
 29.96 −2.804522 −.136375 .234375 .971595
 30.38 −3.280056 −.191044 .421875 .982427
 30.80 −17.575493 −.245905 .484375 .997650
 30.84 −9.638976 −.311361 .484375 .952840
 30.88 −9.307118 −.376818 .484375 .937601
 30.92 −9.305147 −.442277 .484375 .937940
 30.96 −9.573983 −.507735 .484375 .953860
 31.00 −12.269465 −.573195 .859375 .999362
 31.02 −12.325924 −.573184 .859375 .999475
 31.04 −12.414116 −.573173 .859375 .999593
 31.06 −12.556562 −.573162 .859375 .999717
 31.08 −12.826556 −.573152 .859375 .999849
 31.10 −17.575493 −.573142 .859375 1.000000
 31.12 −13.468746 −.660477 .859375 .954875
 31.14 −13.417577 −.747813 .859375 .939310
 31.16 −13.593653 −.835149 .859375 .939310
 31.18 −14.070704 −.922485 .906250 .954875
 31.20 −17.575493 −1.009821 1.000000 1.000000
 32.48 −5.872531 −.969173 .906250 .873024
 33.76 −4.779617 −.930131 .906250 .787859
 35.04 −4.190805 −.892766 .859375 .720256
 36.32 −3.811727 −.857141 .859375 .665016
 37.60 −3.550800 −.823315 .859375 .619701
 41.16 −3.177208 −.739150 .859375 .536085
 44.72 −3.137892 −.670490 .859375 .506255
 48.28 −3.410878 −.618666 .859375 .528065
 51.84 −4.235787 −.585414 .859375 .609142
 55.40 −17.575493 −.573142 .859375 .803361
 56.98 −5.453980 −.415987 .484375 .684035
 58.56 −4.527463 −.253724 .484375 .617131
 60.14 −4.149167 −.084994 .234375 .575625
 61.72 −4.102505 .091561 .234375 .554466
 63.30 −4.168811 .277311 .234375 .552599
 64.72 −1.879491 .589531 .234375 .466750
 66.14 −1.398610 .847528 .234375 .455461
 67.56 −1.281234 1.049933 .234375 .492007
 68.98 −1.523008 1.195434 .234375 .581027
 70.40 −3.266411 1.282746 .234375 .774705
 72.48 −1.138050 1.083509 .234375 .647943
 74.56 −.651584 .894249 .234375 .568205
 76.64 −.418451 .713340 .234375 .509180
 78.72 −.294835 .539243 .234375 .465398
 80.80 −.238499 .370491 .234375 .434528
 82.76 −.234274 .215095 .234375 .416334
 84.72 −.278492 .062033 .234375 .408540
 86.68 −.388827 −.089835 .234375 .411679
 88.64 −.635660 −.241642 .421875 .427553
 90.60 −6.386105 −.394530 .484375 .465457
 92.74 −.508718 −.381091 .484375 .442746
 94.88 −.136055 −.370811 .484375 .443192
 97.02 .110283 −.363559 .484375 .462379
 99.16 .305072 −.359244 .484375 .504284
 101.30 .472183 −.357812 .484375 .592887

Figure  3. .

Figure  3. 

Genomewide linkage data generated using a panel of microsatellite markers with an average distance of 10 cM (Weber panel Version 10 [Research Genetics]), an ABI3100 sequence analyzer, and Genotyper software v3.7 (Applied Biosystems).

Given the multitude of genes in the chromosome 20p13 region, we aimed to further narrow the candidate interval. Under the hypothesis of distant parental consanguinity, we additionally performed a genomewide screening for homozygous regions in an affected individual of the family (individual II-7 in fig. 1) by use of the 100K Affymetrix SNP set of arrays (table 2). With a Perl script (available from the authors on request), genotypes from the SNP array and STR analysis were merged and sorted according to their physical positions. Homozygous stretches of ⩾10 adjacent SNPs in the candidate region were detected, and all genes or ESTs contained in these homozygous segments were analyzed by direct sequencing. However, no change was identified that cosegregated with the disease phenotype.

Table 2. .

Screen for Homozygous Regions in Affected Individual II-7 for the Critical Region on Chromosome 20, Performed Using the 100K Affymetrix SNP Set of Arrays

SNP dbSNP ID Position Genotype in Individual II-7
SNP_A-1658549 rs6077288 86460 ab
SNP_A-1658659 rs1858594 86555 ab
SNP_A-1643135 rs1858597 95685 aa
SNP_A-1748257 rs722829 117701 aa
SNP_A-1734968 rs1342841 161423 bb
SNP_A-1667902 rs1342842 161523 aa
SNP_A-1669428 rs2077713 166783 bb
SNP_A-1669546 rs1418259 167011 bb
SNP_A-1669686 rs10485818 168303 aa
SNP_A-1670947 rs8124344 168757 bb
SNP_A-1671055 rs10485819 169018 aa
SNP_A-1697158 rs513522 200165 aa
SNP_A-1697340 rs8117711 200721 aa
SNP_A-1730843 rs10485820 546278 bb
SNP_A-1655167 rs1114734 642894 ab
SNP_A-1675086 rs750160 649631 ab
SNP_A-1702909 rs2317024 691220 aa
SNP_A-1647500 rs910858 691827 aa
SNP_A-1734892 rs2282051 774513 ab
SNP_A-1714865 rs473958 867023 bb
SNP_A-1659077 rs6140882 915957 bb
SNP_A-1660215 rs3787573 1048669 aa
SNP_A-1664614 rs1923876 1176093 bb
SNP_A-1654694 rs651329 1181837 bb
SNP_A-1654816 rs387035 1182243 aa
SNP_A-1654922 rs10485821 1182390 ab
SNP_A-1727214 rs10485822 1194412 bb
SNP_A-1744743 rs912108 1220405 ab
SNP_A-1725538 rs1294689 1317198 ab
SNP_A-1715626 rs1294690 1319697 bb
SNP_A-1717662 rs6042018 1332298 aa
SNP_A-1646540 rs6042209 1354212 ab
SNP_A-1679564 rs1884389 1358582 aa
SNP_A-1675439 rs1884390 1358818 ab
SNP_A-1646717 rs10485823 1367846 bb
SNP_A-1744699 rs6042588 1421397 ab
SNP_A-1712119 rs6135095 1422405 aa
SNP_A-1696958 rs10485824 1466100 ab
SNP_A-1678257 rs2246154 1476038 aa
SNP_A-1744065 rs2253429 1490954 bb
SNP_A-1726910 rs3848788 1491066 bb
SNP_A-1660338 rs1438106 1607461 ab
SNP_A-1661933 rs1550266 1608689 ab
SNP_A-1754312 rs202548 1610999 aa
SNP_A-1731217 rs202546 1611539 nocall
SNP_A-1679304 rs1438101 1629609 bb
SNP_A-1756893 rs1438098 1629929 aa
SNP_A-1719826 rs1347741 1646963 aa
SNP_A-1746432 rs202518 1653474 ab
SNP_A-1726869 rs621884 1674963 ab
SNP_A-1661214 rs200891 1739920 bb
SNP_A-1664383 rs2318132 1752466 aa
SNP_A-1706300 rs156331 1774988 aa
SNP_A-1646447 rs2206698 1885475 aa
SNP_A-1650069 rs10485703 1908313 bb
SNP_A-1698440 rs7269557 1973036 aa
SNP_A-1703676 rs4814966 2022922 ab
SNP_A-1706137 rs6047163 2094285 aa
SNP_A-1667302 rs6132407 2119630 ab
SNP_A-1649128 rs6113161 2119649 bb
SNP_A-1702639 rs10485598 2119679 aa
SNP_A-1651382 rs6082345 2119927 ab
SNP_A-1647343 rs1610302 2144559 aa
SNP_A-1699664 rs3895160 2232440 bb
SNP_A-1699812 rs10485599 2232776 bb
SNP_A-1706526 rs84825 2248608 aa
SNP_A-1706694 rs84823 2249308 aa
SNP_A-1724346 rs214827 2266723 bb
SNP_A-1710836 rs4053458 2338880 bb
SNP_A-1664109 rs10485600 2348503 bb
SNP_A-1751935 rs2143863 2388652 bb
SNP_A-1744973 rs1109009 2405788 bb
SNP_A-1511055 rs1109010 2405887 bb
SNP_A-1678926 rs4815266 2406160 bb
SNP_A-1645368 rs6076199 2419755 ab
SNP_A-1673331 rs6083460 2424631 ab
SNP_A-1711205 rs6083461 2424778 ab
SNP_A-1724097 rs10485601 2542190 ab
SNP_A-1724211 rs6115181 2542254 ab
SNP_A-1724333 rs10485602 2542502 ab
SNP_A-1724441 rs10485603 2543515 ab
SNP_A-1708716 rs6051366 2692438 ab
SNP_A-1682092 rs6115686 2746326 bb
SNP_A-1745528 rs6138900 2747040 aa
SNP_A-1695854 rs10485604 2884204 aa
SNP_A-1679212 rs10485605 2942534 bb
SNP_A-1680244 rs1178015 2944423 bb
SNP_A-1646349 rs1127354 3141842 aa
SNP_A-1698232 rs6051727 3235121 bb
SNP_A-1698374 rs2422865 3235142 bb
SNP_A-1698494 rs6037541 3235704 bb
SNP_A-1714687 rs750702 3303228 ab
SNP_A-1754371 rs979332 3381158 ab
SNP_A-1713301 rs238688 3473701 aa
SNP_A-1653542 rs235590 3482340 bb
SNP_A-1731032 rs235577 3489633 bb
SNP_A-1732467 rs237640 3492216 aa
SNP_A-1734365 rs170977 3496089 aa
SNP_A-1716148 rs6115970 3562336 aa
SNP_A-1720425 rs910652 3675970 aa
SNP_A-1667738 rs674110 3676026 bb
SNP_A-1653410 rs2253977 3887140 ab
SNP_A-1686052 rs910952 4141694 bb
SNP_A-1725623 rs835882 4157772 bb
SNP_A-1659863 rs8123338 4237066 aa
SNP_A-1662001 rs6076657 4249757 aa
SNP_A-1702641 rs2422925 4251877 ab
SNP_A-1744893 rs3904872 4260153 ab
SNP_A-1672182 rs159782 4295347 aa
SNP_A-1719620 rs6116326 4300738 aa
SNP_A-1650469 rs531043 4335440 aa
SNP_A-1705213 rs10485512 4354221 bb
SNP_A-1706989 rs297733 4357955 ab
SNP_A-1686202 rs6139437 4416930 ab
SNP_A-1743877 rs6139438 4417090 ab
SNP_A-1739387 rs6133127 4417883 ab
SNP_A-1690629 rs297765 4435111 ab
SNP_A-1651549 rs4141626 4492193 bb
SNP_A-1691367 rs2326536 4510141 ab
SNP_A-1696219 rs1884917 4524069 ab
SNP_A-1701904 rs1981105 4562486 bb
SNP_A-1664548 rs4813709 4567157 aa
SNP_A-1744980 rs16989992 4602135 aa
SNP_A-1745100 rs10485513 4603602 aa
SNP_A-1742759 rs2326510 4649211 ab
SNP_A-1757716 rs7264576 4665456 ab
SNP_A-1685511 rs968432 4690282 bb
SNP_A-1749994 rs6116566 4810642 bb
SNP_A-1750126 rs8126036 4811943 bb
SNP_A-1737405 rs1715366 4847842 ab
SNP_A-1655282 rs1715372 4858589 ab
SNP_A-1647474 rs1519860 4871286 ab
SNP_A-1641862 rs3730453 5042524 bb
SNP_A-1642160 rs3730448 5043137 aa
SNP_A-1643745 rs3626 5043771 aa
SNP_A-1644005 rs3730441 5044470 aa
SNP_A-1652937 rs10485482 5086590 bb
SNP_A-1729580 rs6085020 5096597 ab
SNP_A-1757437 rs10485483 5106354 aa
SNP_A-1701497 rs2295509 5111263 aa
SNP_A-1739875 rs6053189 5127579 ab
SNP_A-1703622 rs6107598 5148227 ab
SNP_A-1755577 rs10485484 5226869 bb
SNP_A-1755731 rs927102 5227315 bb
SNP_A-1755841 rs927103 5227335 aa
SNP_A-1749407 rs4815785 5229253 aa
SNP_A-1757736 rs4815787 5229807 bb
SNP_A-1643246 rs3746682 5231256 aa
SNP_A-1643558 rs7263438 5232251 aa
SNP_A-1645113 rs10485485 5232380 bb
SNP_A-1660103 rs6053291 5239760 aa
SNP_A-1679440 rs6516015 5240086 bb
SNP_A-1694262 5278801 aa
SNP_A-1695756 rs6116754 5280049 aa
SNP_A-1722190 rs4813744 5289009 bb
SNP_A-1702884 rs10485486 5326152 ab
SNP_A-1703062 rs10485487 5326864 aa
SNP_A-1703226 rs6085143 5327486 aa
SNP_A-1703334 rs10485488 5327548 bb
SNP_A-1650582 rs6053374 5335789 aa
SNP_A-1753888 rs10485489 5376300 aa
SNP_A-1754018 rs10485490 5376494 aa
SNP_A-1755509 rs10485492 5376989 bb
SNP_A-1680810 rs2273372 5490092 ab
SNP_A-1745047 rs6107653 5490471 ab
SNP_A-1709751 rs6053520 5516662 ab
SNP_A-1663062 rs805764 5624783 bb
SNP_A-1686030 rs6053733 5763074 ab
SNP_A-1645129 rs237091 5769185 aa
SNP_A-1652077 rs6053753 5789624 aa
SNP_A-1652237 rs1632590 5790094 aa
SNP_A-1707009 rs1699236 5790468 bb
SNP_A-1711764 rs6053754 5790518 ab
SNP_A-1679502 rs1343178 5791440 aa
SNP_A-1642781 rs6085297 5791479 ab
SNP_A-1655468 rs1699230 5793855 bb
SNP_A-1655606 rs1777356 5794123 aa
SNP_A-1702570 rs1287059 5830562 ab
SNP_A-1749610 rs10485493 5853250 aa
SNP_A-1749730 rs2821 5853779 aa
SNP_A-1756982 rs10485494 5867378 aa
SNP_A-1710047 rs6117011 5870830 aa
SNP_A-1644337 rs1005517 5873219 aa
SNP_A-1648143 rs236114 5883385 ab
SNP_A-1705441 5889999 aa
SNP_A-1693306 rs10485495 5920728 aa
SNP_A-1693430 rs6139886 5921189 bb
SNP_A-1745043 rs10485496 6056749 aa
SNP_A-1669205 rs947465 6076201 bb
SNP_A-1668959 rs1774886 6076223 ab
SNP_A-1687245 rs3897510 6077268 aa
SNP_A-1738041 rs6038393 6178133 bb
SNP_A-1696274 rs10485704 6179883 nocall
SNP_A-1657057 rs6038397 6186141 bb
SNP_A-1748358 rs6085500 6269349 aa
SNP_A-1672329 rs3920632 6284597 ab
SNP_A-1679527 rs2182710 6311207 ab
SNP_A-1679637 rs2148815 6311480 aa
SNP_A-1683169 rs355530 6322170 ab
SNP_A-1664464 rs2876032 6347494 ab
SNP_A-1719375 rs6139980 6355642 ab
SNP_A-1649288 rs6038495 6370001 bb
SNP_A-1744725 rs6139993 6370570 aa
SNP_A-1704821 rs6117260 6370697 aa
SNP_A-1751481 rs6117261 6373158 bb
SNP_A-1730018 rs6117277 6396678 bb
SNP_A-1642052 rs6085569 6401105 aa
SNP_A-1642184 rs6054292 6402661 bb
SNP_A-1682410 rs6054303 6411512 aa
SNP_A-1680452 rs6038520 6411617 bb
SNP_A-1647841 rs10485705 6416261 aa
SNP_A-1647975 rs1970008 6416371 aa
SNP_A-1651587 rs4815908 6426585 bb
SNP_A-1727122 rs1411296 6437010 aa
SNP_A-1694686 rs6054326 6444783 bb
SNP_A-1668478 rs2423161 6457880 aa
SNP_A-1726100 rs1576448 6476208 bb
SNP_A-1749729 rs2180686 6477470 bb
SNP_A-1748998 rs958435 6524785 aa
SNP_A-1749126 rs1321450 6524904 aa
SNP_A-1706835 rs6107847 6532196 aa
SNP_A-1641928 rs1407027 6564872 bb
SNP_A-1657009 rs967417 6568893 ab
SNP_A-1683451 rs6038571 6582566 ab
SNP_A-1685441 rs6054434 6591207 bb
SNP_A-1655813 rs4456770 6600150 aa
SNP_A-1690772 rs1040568 6610817 bb
SNP_A-1692657 rs2223753 6615135 aa
SNP_A-1694010 rs2206920 6616179 ab
SNP_A-1738408 rs1015151 6638502 bb
SNP_A-1739584 rs6085660 6639069 aa
SNP_A-1724222 rs235713 6659863 bb
SNP_A-1688071 rs235746 6729631 bb
SNP_A-1690513 rs2224191 6755276 aa
SNP_A-1701319 rs723511 6786358 bb
SNP_A-1739150 rs1500537 6787124 aa
SNP_A-1742024 rs7352437 6791835 aa
SNP_A-1742414 rs10485706 6797366 bb
SNP_A-1742504 rs1500540 6797414 bb
SNP_A-1658220 rs6085728 6850150 aa
SNP_A-1647506 rs6085729 6850171 bb
SNP_A-1753527 rs10485707 6861788 bb
SNP_A-1673578 rs6140124 6862617 aa
SNP_A-1687998 rs717087 6862914 bb
SNP_A-1682257 rs10485708 6874675 aa
SNP_A-1682569 rs6038661 6875369 bb
SNP_A-1720315 rs6054633 6893366 ab
SNP_A-1689406 rs4815957 6911796 ab
SNP_A-1700682 rs6085806 6912082 ab
SNP_A-1667810 rs3885922 6915730 aa
SNP_A-1733455 rs2209988 6916506 aa
SNP_A-1756164 rs952793 6918831 bb
SNP_A-1736600 rs6107905 6927153 bb
SNP_A-1695399 rs6077130 6940288 aa
SNP_A-1643518 rs2209981 6940657 bb
SNP_A-1725236 rs6038683 6941629 aa
SNP_A-1669941 rs995636 6956824 aa
SNP_A-1664181 rs10485709 6958593 aa
SNP_A-1755918 rs2149642 6962445 bb
SNP_A-1676255 rs1157366 7011136 aa
SNP_A-1676547 rs10485710 7011749 bb
SNP_A-1676659 rs10485711 7012147 aa
SNP_A-1689121 rs232648 7016436 aa
SNP_A-1695748 rs232659 7042138 bb
SNP_A-1695912 rs232658 7042370 aa
SNP_A-1696019 rs232657 7042534 aa
SNP_A-1684826 rs10485712 7044163 bb
SNP_A-1699692 rs1473708 7057325 aa
SNP_A-1705166 rs6038726 7084322 aa
SNP_A-1742894 rs10485713 7084468 aa
SNP_A-1743022 rs10485714 7085322 aa
SNP_A-1740265 rs6117692 7135711 aa
SNP_A-1643083 rs6038742 7143389 aa
SNP_A-1743073 rs926915 7143749 bb
SNP_A-1731047 rs1013214 7144831 aa
SNP_A-1734178 rs724940 7147413 aa
SNP_A-1681541 rs4140470 7155479 ab
SNP_A-1747581 rs6085938 7168930 ab
SNP_A-1738210 rs720010 7174248 ab
SNP_A-1644144 rs6140226 7174483 ab
SNP_A-1695184 rs2326909 7207469 bb
SNP_A-1695326 rs4239769 7207687 aa
SNP_A-1695448 rs4239770 7207836 bb
SNP_A-1695566 rs4239771 7207881 aa
SNP_A-1695684 rs10485715 7207925 bb
SNP_A-1714398 rs724084 7223683 bb
SNP_A-1741192 rs2423191 7241535 bb
SNP_A-1742648 rs6054906 7242903 bb
SNP_A-1729676 rs2224053 7254965 aa
SNP_A-1726852 rs6054926 7263982 bb
SNP_A-1682695 rs2423243 7324672 aa
SNP_A-1704945 rs2326931 7395191 ab
SNP_A-1676683 rs6108011 7500504 bb
SNP_A-1680133 rs6108015 7515858 aa
SNP_A-1757816 rs6086141 7570826 bb
SNP_A-1727604 rs6140362 7573506 aa
SNP_A-1727694 rs2050081 7575224 bb
SNP_A-1727786 rs6108030 7575294 aa
SNP_A-1644520 rs6086149 7586703 aa
SNP_A-1726944 rs2143197 7604210 bb
SNP_A-1743225 rs4816018 7604614 aa
SNP_A-1685392 rs6140387 7627577 aa
SNP_A-1693699 rs6133460 7628047 aa
SNP_A-1670630 rs6133466 7628673 aa
SNP_A-1689084 rs6140394 7638957 aa
SNP_A-1701533 rs6140410 7685540 aa
SNP_A-1716078 rs2092380 7704027 bb
SNP_A-1717970 rs730270 7721702 bb
SNP_A-1688228 rs10485717 7758099 aa
SNP_A-1688346 rs6086234 7758380 aa
SNP_A-1746174 rs2423290 7766261 bb
SNP_A-1665124 rs2423291 7767221 bb
SNP_A-1729033 rs2423292 7767432 bb
SNP_A-1726969 7769472 bb
SNP_A-1728540 rs2423302 7771854 bb
SNP_A-1755882 rs2423311 7782237 aa
SNP_A-1684174 rs2205824 7797927 bb
SNP_A-1689769 rs4816025 7798038 aa
SNP_A-1650176 rs2205823 7798116 aa
SNP_A-1736495 rs6086260 7799039 bb
SNP_A-1749454 rs6038971 7809041 bb
SNP_A-1753921 rs2223276 7830106 bb
SNP_A-1715157 rs941426 7853050 ab
SNP_A-1669273 rs941425 7853283 ab
SNP_A-1758225 rs2423334 7853947 ab
SNP_A-1694324 rs6133519 7908865 aa

Thus, we next prioritized genes within the mapped critical interval on 20p13 for mutational screening, on the basis of putative function and expression data, using the University of California–Santa Cruz (UCSC) human genome database. Initially, we designed primers (see Primer3 Web site) for the entire coding and adjacent intronic regions of the SOX12 (MIM 601947), TCF15 (MIM 601010), SCRT2 (GenBank accession number NM_033129), RSPO4 (GenBank accession number NM_001029871), SNPH (GenBank accession number NM_014723), TGM3 (MIM 600238), TGM6 (GenBank accession number NM_198994), ADRA1D (MIM 104219), and BMP2 (MIM 112261) genes and performed direct sequencing using genomic DNA of an affected individual (individual II-7 in fig. 1) on an ABI PRISM 310 genetic analyzer (Applied Biosystems). Primer sequences are available on request.

No convincing change was identified in any of the other candidates; however, we detected two mutations in exon 2 of the RSPO4 gene and confirmed segregation of the changes with the phenotype in this family. Neither mutation has been described previously in public domain databases. As shown in figure 1, the maternally transmitted mutation was a guanine nucleotide insertion leading to a frameshift and premature truncation of the corresponding protein (c.92_93insG, p.Leu31fs) (GenBank accession number NP_001025042). Sixty healthy German controls tested by BglI restriction enzyme analysis were negative for this change, further corroborating its pathogenicity. On the paternal allele, the nonconservative missense mutation c.218G→A, which leads to an amino acid exchange from cysteine to tyrosine at position 73 (p.Cys73Tyr), was identified. The affected residue is highly conserved in evolution, was not found among 300 German white control chromosomes tested by HpyCH4III restriction enzyme analysis and, thus, is thought to be pathogenic too.

RSPO4 spans ∼44 kb of genomic DNA and comprises five exons that encode a secreted protein of 234 aa.5 The R-spondin protein family was only recently described and comprises four independent gene products in mammals that are widely expressed and are predicted to share a common organization with substantial structural homologies.6 It is noteworthy that each of the five exons constitutes a predicted structural domain. Although the N-terminal signal peptide sequences (exon 1) share only relatively weak conservation, the two adjacent cysteine-rich furin-like domains encoded by exons 2 and 3 and the single thrombospondin (TSP-1) motif that is encoded by exon 4 display significant similarity among protein family members. Finally, the C-terminal basic region encoded by exon 5 is of varying length and scores as a nuclear localization signal.

The R-spondin proteins were recently shown to play a major role in activating the Wnt/β-catenin signaling pathway.5,7 Wnt signaling is known to be evolutionarily conserved and pivotal for embryonic development by regulation of cell morphology, proliferation, and motility.5,8,9 Its inappropriate activation has been reported in several human cancers.10 All four human R-spondin family members, as well as a splice variant of RSPO4 (GenBank accession number NM_001040007), were recently shown to be able to induce proliferation of intestinal epithelium.5 The functions of R-spondins essentially overlap with those of the canonical Wnt ligands by binding to the Frizzled (Fzd) family receptors (MIM 606143) and the low-density lipoprotein–related receptor (LRP) 5 (MIM 603506) or LRP6 coreceptor (MIM 603507), ultimately leading to gene activation by β-catenin (MIM 116806) and the T-cell factor (TCF)-lymphoid enhancer factor (LEF) family transcription factor complex (MIM 153245). A minimum of 10 different Fzd-related receptors are known in the human genome, and it might be hypothesized that a greater degree of selectivity is achieved through specific responses of cells to Wnt or R-spondin ligands that may be dictated by the available, possibly cell-line– or tissue-specific Fzd receptor(s) on the cell surface.11 Moreover, it has recently been shown that mouse R-spondin proteins increase the activity of Wnt ligands, possibly through a direct interaction.7 There is also evidence of independent receptor-signaling pathways of R-spondin proteins that may intersect those of Wnt only at the β-catenin level.5 This adds to the growing body of evidence that a wide range of soluble ligands is capable of activating the β-catenin transduction complex, expanding well beyond the canonical Wnt-Fzd system. On the other hand, as noted above, R-spondins contain furin-like domains. Furin is a subtilisin family serine protease that is involved in the processing of many different proteins (MIM 136950).12 Notably, the Dickkopf (DKK) proteins (MIM 605189), regulators of Wnt activity, possess furin cleavage sites13; thus, it is conceivable that the R-spondin family may indirectly regulate Wnt-pathway activity through regulation of DKK activation.

It is noteworthy that both RSPO4 mutations detected in our family affect the highly conserved first furin-like cysteine-rich domain. Experimental data suggest that a shortened RSPO4 protein comprising just the two furin-like regions is sufficient for β-catenin stabilization, further supporting the harmful character of the identified mutations. Evidence of the pathogenicity of the missense change c.218G→A (p.Cys73Tyr) is striking, particularly given that the cysteine residues within the furin-like domains are strictly conserved among R-spondins and in evolution (fig. 1).5 RSPO4 mutation analysis in further families may answer the intriguing question of whether mutations in domains other than the highly conserved furin-like regions result in a similar clinical phenotype or allow for a residual protein function, conceivably giving rise to a milder expression pattern with hyponychia. Likewise, it may also be hypothesized that RSPO4 mutations in other functionally important regions might lead to a more severe phenotype, with skeletal involvement and reduction defects of distal limbs.

This hypothesis fits the long-standing argument of bone-dependent nail formation and, in particular, the observation that nail development depends on correct dorso-ventral polarization.14 Embryonic development of the human fingernails begins at the 8th or 9th wk of gestation and ends by the 20th wk, with completion of the toenails lagging ∼4 wk behind.15 Recent molecular data have indicated a crucial role for epithelial-mesenchymal interaction at different developmental stages in terms of proper nail development. These critical first steps require expression of Wnt7a (MIM 601570), Noggin (MIM 602991), Bmp4 (bone morphogenetic protein 4 [MIM 112262]), and Lmx1b (MIM 602575), among others.16,17 Mutations in LMX1B cause nail-patella syndrome (MIM 161200), and it has been suggested that the LIM-domain homeobox protein Lmx1b is required for dorsal specification and hence for nail development.18 Indeed, it turns out that Wnt-7a induces the expression of Lmx1b in the dorsal limb mesenchyme. In the ventral limb bud, Engrailed-1 (MIM 131290) represses Wnt-7a expression.19 Thus, it is conceivable that, in the absence of RSPO4, Wnt-7a activity in the developing limb is reduced. In that scenario, the establishment of dorsal-ventral polarity in the developing limb would be disturbed, and the nail would finally fail to be specified. Pertinent confirmation of this idea could be obtained, for instance, by conditional knockout experiments in mice.

Acknowledgments

The authors thank the family in this study for their cooperation. This work was supported by the START program of the medical faculty of Aachen University (START JF/KZ, Research Protocol No. 44/2001).

Web Resources

The URLs for data presented herein are as follows:

  1. ClustalW, http://www.ebi.ac.uk/clustalw/
  2. GenBank, http://www.ncbi.nlm.nih.gov/Genbank/
  3. Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim/
  4. Primer3 Web site, http://frodo.wi.mit.edu/cgi-bin/primer3/primer3_www.cgi
  5. UCSC Genome Browser, http://genome.ucsc.edu/

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