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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1999 Jul;65(1):104–110. doi: 10.1086/302467

Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster.

M Del Campo 1, M C Jones 1, A N Veraksa 1, C J Curry 1, K L Jones 1, J T Mascarello 1, Z Ali-Kahn-Catts 1, T Drumheller 1, W McGinnis 1
PMCID: PMC1378080  PMID: 10364522

Abstract

Vertebrates have four clusters of Hox genes (HoxA, HoxB, HoxC, and HoxD). A variety of expression and mutation studies indicate that posterior members of the HoxA and HoxD clusters play an important role in vertebrate limb development. In humans, mutations in HOXD13 have been associated with type II syndactyly or synpolydactyly, and, in HOXA13, with hand-foot-genital syndrome. We have investigated two unrelated children with a previously unreported pattern of severe developmental defects on the anterior-posterior (a-p) limb axis and in the genitalia, consisting of a single bone in the zeugopod, either monodactyly or oligodactyly in the autopod of all four limbs, and penoscrotal hypoplasia. Both children are heterozygous for a deletion that eliminates at least eight (HOXD3-HOXD13) of the nine genes in the HOXD cluster. We propose that the patients' phenotypes are due in part to haploinsufficiency for HOXD-cluster genes. This hypothesis is supported by the expression patterns of these genes in early vertebrate embryos. However, the involvement of additional genes in the region could explain the discordance, in severity, between these human phenotypes and the milder, non-polarized phenotypes present in mice hemizygous for HoxD cluster genes. These cases represent the first reported examples of deficiencies for an entire Hox cluster in vertebrates and suggest that the diploid dose of human HOXD genes is crucial for normal growth and patterning of the limbs along the anterior-posterior axis.

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Selected References

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  1. Boles R. G., Pober B. R., Gibson L. H., Willis C. R., McGrath J., Roberts D. J., Yang-Feng T. L. Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review. Am J Med Genet. 1995 Jan 16;55(2):155–160. doi: 10.1002/ajmg.1320550204. [DOI] [PubMed] [Google Scholar]
  2. Chiang C., Litingtung Y., Lee E., Young K. E., Corden J. L., Westphal H., Beachy P. A. Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function. Nature. 1996 Oct 3;383(6599):407–413. doi: 10.1038/383407a0. [DOI] [PubMed] [Google Scholar]
  3. Davis A. P., Capecchi M. R. Axial homeosis and appendicular skeleton defects in mice with a targeted disruption of hoxd-11. Development. 1994 Aug;120(8):2187–2198. doi: 10.1242/dev.120.8.2187. [DOI] [PubMed] [Google Scholar]
  4. Davisson M. T., Cattanach B. M. The mouse mutation ulnaless on chromosome 2. J Hered. 1990 Mar-Apr;81(2):151–153. [PubMed] [Google Scholar]
  5. Dollé P., Izpisúa-Belmonte J. C., Brown J. M., Tickle C., Duboule D. HOX-4 genes and the morphogenesis of mammalian genitalia. Genes Dev. 1991 Oct;5(10):1767–1767. doi: 10.1101/gad.5.10.1767. [DOI] [PubMed] [Google Scholar]
  6. Dollé P., Izpisúa-Belmonte J. C., Falkenstein H., Renucci A., Duboule D. Coordinate expression of the murine Hox-5 complex homoeobox-containing genes during limb pattern formation. Nature. 1989 Dec 14;342(6251):767–772. doi: 10.1038/342767a0. [DOI] [PubMed] [Google Scholar]
  7. Duboule D. The vertebrate limb: a model system to study the Hox/HOM gene network during development and evolution. Bioessays. 1992 Jun;14(6):375–384. doi: 10.1002/bies.950140606. [DOI] [PubMed] [Google Scholar]
  8. Favier B., Le Meur M., Chambon P., Dollé P. Axial skeleton homeosis and forelimb malformations in Hoxd-11 mutant mice. Proc Natl Acad Sci U S A. 1995 Jan 3;92(1):310–314. doi: 10.1073/pnas.92.1.310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Fromental-Ramain C., Warot X., Messadecq N., LeMeur M., Dollé P., Chambon P. Hoxa-13 and Hoxd-13 play a crucial role in the patterning of the limb autopod. Development. 1996 Oct;122(10):2997–3011. doi: 10.1242/dev.122.10.2997. [DOI] [PubMed] [Google Scholar]
  10. Fujimoto M., Kantaputra P. N., Ikegawa S., Fukushima Y., Sonta S., Matsuo M., Ishida T., Matsumoto T., Kondo S., Tomita H. The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32. J Hum Genet. 1998;43(1):32–36. doi: 10.1007/s100380050033. [DOI] [PubMed] [Google Scholar]
  11. Hérault Y., Fraudeau N., Zákány J., Duboule D. Ulnaless (Ul), a regulatory mutation inducing both loss-of-function and gain-of-function of posterior Hoxd genes. Development. 1997 Sep;124(18):3493–3500. doi: 10.1242/dev.124.18.3493. [DOI] [PubMed] [Google Scholar]
  12. Hérault Y., Hraba-Renevey S., van der Hoeven F., Duboule D. Function of the Evx-2 gene in the morphogenesis of vertebrate limbs. EMBO J. 1996 Dec 2;15(23):6727–6738. [PMC free article] [PubMed] [Google Scholar]
  13. Izpisúa-Belmonte J. C., Tickle C., Dollé P., Wolpert L., Duboule D. Expression of the homeobox Hox-4 genes and the specification of position in chick wing development. Nature. 1991 Apr 18;350(6319):585–589. doi: 10.1038/350585a0. [DOI] [PubMed] [Google Scholar]
  14. Kaufman T. C., Lewis R., Wakimoto B. Cytogenetic Analysis of Chromosome 3 in DROSOPHILA MELANOGASTER: The Homoeotic Gene Complex in Polytene Chromosome Interval 84a-B. Genetics. 1980 Jan;94(1):115–133. doi: 10.1093/genetics/94.1.115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Knezevic V., De Santo R., Schughart K., Huffstadt U., Chiang C., Mahon K. A., Mackem S. Hoxd-12 differentially affects preaxial and postaxial chondrogenic branches in the limb and regulates Sonic hedgehog in a positive feedback loop. Development. 1997 Nov;124(22):4523–4536. doi: 10.1242/dev.124.22.4523. [DOI] [PubMed] [Google Scholar]
  16. Kondo T., Zákány J., Innis J. W., Duboule D. Of fingers, toes and penises. Nature. 1997 Nov 6;390(6655):29–29. doi: 10.1038/36234. [DOI] [PubMed] [Google Scholar]
  17. Lewis E. B. A gene complex controlling segmentation in Drosophila. Nature. 1978 Dec 7;276(5688):565–570. doi: 10.1038/276565a0. [DOI] [PubMed] [Google Scholar]
  18. McGinnis W., Krumlauf R. Homeobox genes and axial patterning. Cell. 1992 Jan 24;68(2):283–302. doi: 10.1016/0092-8674(92)90471-n. [DOI] [PubMed] [Google Scholar]
  19. Mortlock D. P., Innis J. W. Mutation of HOXA13 in hand-foot-genital syndrome. Nat Genet. 1997 Feb;15(2):179–180. doi: 10.1038/ng0297-179. [DOI] [PubMed] [Google Scholar]
  20. Mortlock D. P., Post L. C., Innis J. W. The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation. Nat Genet. 1996 Jul;13(3):284–289. doi: 10.1038/ng0796-284. [DOI] [PubMed] [Google Scholar]
  21. Muragaki Y., Mundlos S., Upton J., Olsen B. R. Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13. Science. 1996 Apr 26;272(5261):548–551. doi: 10.1126/science.272.5261.548. [DOI] [PubMed] [Google Scholar]
  22. Nelson C. E., Morgan B. A., Burke A. C., Laufer E., DiMambro E., Murtaugh L. C., Gonzales E., Tessarollo L., Parada L. F., Tabin C. Analysis of Hox gene expression in the chick limb bud. Development. 1996 May;122(5):1449–1466. doi: 10.1242/dev.122.5.1449. [DOI] [PubMed] [Google Scholar]
  23. Nixon J., Oldridge M., Wilkie A. O., Smith K. Interstitial deletion of 2q associated with craniosynostosis, ocular coloboma, and limb abnormalities: cytogenetic and molecular investigation. Am J Med Genet. 1997 Jun 13;70(3):324–327. [PubMed] [Google Scholar]
  24. Peichel C. L., Prabhakaran B., Vogt T. F. The mouse Ulnaless mutation deregulates posterior HoxD gene expression and alters appendicular patterning. Development. 1997 Sep;124(18):3481–3492. doi: 10.1242/dev.124.18.3481. [DOI] [PubMed] [Google Scholar]
  25. Qiu M., Bulfone A., Ghattas I., Meneses J. J., Christensen L., Sharpe P. T., Presley R., Pedersen R. A., Rubenstein J. L. Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches. Dev Biol. 1997 May 15;185(2):165–184. doi: 10.1006/dbio.1997.8556. [DOI] [PubMed] [Google Scholar]
  26. Ramer J. C., Ladda R. L., Frankel C. A., Beckford A. A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2. Am J Med Genet. 1989 Mar;32(3):359–363. doi: 10.1002/ajmg.1320320318. [DOI] [PubMed] [Google Scholar]
  27. Ramer J. C., Mowrey P. N., Robins D. B., Ligato S., Towfighi J., Ladda R. L. Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformations. Am J Med Genet. 1990 Nov;37(3):392–400. doi: 10.1002/ajmg.1320370320. [DOI] [PubMed] [Google Scholar]
  28. Riddle R. D., Johnson R. L., Laufer E., Tabin C. Sonic hedgehog mediates the polarizing activity of the ZPA. Cell. 1993 Dec 31;75(7):1401–1416. doi: 10.1016/0092-8674(93)90626-2. [DOI] [PubMed] [Google Scholar]
  29. Shabtai F., Klar D., Halbrecht I. Partial monosomy of chromosome 2. Delineable syndrome of deletion 2 (q23-q31). Ann Genet. 1982;25(3):156–158. [PubMed] [Google Scholar]
  30. Stuart J. J., Brown S. J., Beeman R. W., Denell R. E. A deficiency of the homeotic complex of the beetle Tribolium. Nature. 1991 Mar 7;350(6313):72–74. doi: 10.1038/350072a0. [DOI] [PubMed] [Google Scholar]
  31. Tickle C. Vertebrate limb development. Curr Opin Genet Dev. 1995 Aug;5(4):478–484. doi: 10.1016/0959-437x(95)90052-i. [DOI] [PubMed] [Google Scholar]
  32. Yokouchi Y., Sasaki H., Kuroiwa A. Homeobox gene expression correlated with the bifurcation process of limb cartilage development. Nature. 1991 Oct 3;353(6343):443–445. doi: 10.1038/353443a0. [DOI] [PubMed] [Google Scholar]
  33. Zeltser L., Desplan C., Heintz N. Hoxb-13: a new Hox gene in a distant region of the HOXB cluster maintains colinearity. Development. 1996 Aug;122(8):2475–2484. doi: 10.1242/dev.122.8.2475. [DOI] [PubMed] [Google Scholar]
  34. Zákány J., Duboule D. Synpolydactyly in mice with a targeted deficiency in the HoxD complex. Nature. 1996 Nov 7;384(6604):69–71. doi: 10.1038/384069a0. [DOI] [PubMed] [Google Scholar]
  35. Zákány J., Fromental-Ramain C., Warot X., Duboule D. Regulation of number and size of digits by posterior Hox genes: a dose-dependent mechanism with potential evolutionary implications. Proc Natl Acad Sci U S A. 1997 Dec 9;94(25):13695–13700. doi: 10.1073/pnas.94.25.13695. [DOI] [PMC free article] [PubMed] [Google Scholar]

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