The human BARX2 gene: Genomic structure, chromosomal localization, and single nucleotide polymorphisms

Genomics

Volumn 62, Issue 3, 1999, Pages 456-459

  Hjalt, Tord Å ^a   Murray, Jeffrey C ^a  

^a UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOMAL LOCALIZATION; CHROMOSOME 11Q; CRANIOFACIAL DEVELOPMENT; GENE EXPRESSION; GENETIC POLYMORPHISM; GENOME; HOMEOBOX; HUMAN; MULTIPLE MALFORMATION SYNDROME; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RIEGER SYNDROME;

MAMMALIA; UMBILICUS;

EID: 0033572214     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1999.6037     Document Type: Article

References (20)

1. Dausset, J., Cann, H., Cohen, D., Lathrop, M., Lalouel, J. M., and White, R. (1990). Centre d'etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genome. Genomics 6: 575-577.
2. Higashijima, S., Kojima, T., Michiue, T., Ishimaru, S., Emori, Y., and Saigo, K. (1992a). Dual Bar homeo box genes of Drosophila required in two photoreceptor cells, R1 and R6, and primary pigment cells for normal eye development. Genes Dev. 6: 50-60.
3. Higashijima, S., Michiue, T., Emori, Y., and Saigo, K. (1992b). Subtype determination of Drosophila embryonic external sensory organs by redundant homeo box genes BarH1 and BarH2. Genes Dev. 6: 1005-1018.
4. Jones, F. S., Kioussi, C., Copertino, D. W., Kallunki, P., Holst, B. D., and Edelman, G. M. (1997). HBarx2, a new homeobox gene of the Bar class, is expressed in neural and craniofacial structures during development. Proc. Natl. Acad. Sci. USA 94: 2632-2637.
5. Kojima, T., Sone, K., Michiue, T., and Saigo, K. (1993). Mechanism of induction of Bar-like eye malformation by transient overexpression of Bar homeobox genes in Drosophila melanogaster. Genetica 88: 85-91.
6. Krasner, A., Wallace, L., Thiagalingam, A., Jones, C., Lengauer, C., Minahan, L., Kalikin, L., Feinberg, A. F., Jabs, E. W., Baylin, S. B., Ball, D. W., and Nelkin, B. D. (1997). GenBank Accession No. AF031924.
7. Mucchielli, M-L., Mitsadis, T. A., Raffo, S., Brunet, J-F., Proust, J-P., and Goridis, C. (1997). Mouse Otlx2/RIEG expression in the odontogenic epithelium precedes tooth initiation and requires mesenchyme-derived signals for its maintenance. Dev. Biol. 189: 275-284.
8. Mucchielli, M.-L., Martinez, S., Pattyn, A., Goridis, C., and Brunet, J.-F. (1996). Otlx2, an Otx related homeobox gene expressed in the pituitary gland and in a restricted pattern in the forebrain. Mol. Cell. Neurosci. 8: 258-271.
9. Murray, J. C., Bennett, S. R., Kwitek, A. E., Small, K. W., Schinzel, A., Alward, W. L., Weber, J. L., Bell, G. I., and Buetow, K. H. (1992). Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4. Nat. Genet. 2: 46-49.
10. Phillips, J. C., del Bono, E. A., Haines, J. L., Pralea, A. M., Cohen, J. S., Greff, L. J., and Wiggs, J. L. (1996). A second locus for Rieger syndrome maps to chromosome 13q14. Am. J. Hum. Genet. 59: 613-619.
11. Pivnick, E. K., Velagaleti, G. V. N., Wilroy, R. S., Smith, M. E., Rose, S. R., Tipton, R. E., and Tharapel, A. T. (1996). Jacobsen syndrome: Report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11(q23q25) and review of 52 cases. J. Med. Genet. 33; 772-778.
12. Sato, M., Kojima, T., Michiue, T., and Saigo, K. (1999). Bar homeobox genes are latitudinal prepattern genes in the developing Drosophila notum whose expression is regulated by the concerted functions of decapentaplegic and wingless. Development 126: 1457-1466.
13. Schinzel, A., Auf der Maur, P., and Moser, H. (1977). Partial deletion of long arm of chromosome 11(del(11) (q23)): Jacobsen syndrome. J. Med. Genet. 14: 438-444.
14. Semenza, G. L. (1998). "Transcription Factors and Human Disease," Oxford Univ. Press, London.
15. Semina E. V., Datson, N. A., Leysens, N. J., Zabel, B. U., Carey, J. C., Bell, G. I., Bitoun, P., Lindgren, C. Stevenson, T., Frants, R. R., van Ommen, G., and Murray J. C. (1996a). Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. Am. J. Hum. Genet. 59: 1288-1296.
16. Semina, E. V., Ferrell, R. E., Mintz-Hittner, H. A., Bitoun, P., Alward, W. L. M., Reiter, R. S., Funkhauser, C., Daack-Hirsch, S., and Murray, J. C. (1998). A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Nat. Genet. 19: 167-170.
17. Semina, E. V., Funkhauser, C., Bitoun, P., Alward, W. L. M., Daack-Hirsh, S., Amendt, B., Ludwig, B., and Murray, J. C. (1999). Spectrum and frequency of PITX2/RIEG mutations in patients with Rieger syndrome and related ocular anomalies. The American Society of Human Genetics 1999 Annual Meeting, Am. J. Hum. Genet. 65(Suppl.): A490.
18. Semina E. V., Reiter R., Leysens N. J., Alward, W. L. M., Small, K. W., Datson, N. A., Siegel-Bartelt, J., Bierke-Nelson, D., Bitoun, P., Zabel, B. U., Carey, J. C., and Murray, J. C. (1996b). Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nat. Genet. 14: 392-399.
19. Shapiro, M. B., and Senepathy, P. (1987). RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression. Nucleic Acids Res. 15: 7155-7174.
20. Smith, D. M., and Tabin, C. J. (1999). Chick Barx2b, a marker for myogenic cells also expressed in branchial arches and neural structures. Mech. Dev. 80: 203-206.