Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR

Molecular and Cellular Probes

Volumn 13, Issue 3, 1999, Pages 199-202

  Corrado, L ^a   Colapietro, P ^a   Larizza, L ^a   Riva, P ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

Human WHN gene; Retinal 4 gene; Sodium dicarboxylate cotransporter gene; STR; YAC contig

Indexed keywords

CARRIER PROTEIN; CONTIG; CRYSTALLIN; DICARBOXYLIC ACID; RETINAL; TRANSCRIPTION FACTOR;

ARTICLE; CHROMOSOME 17Q; GENE CONSTRUCT; GENE MAPPING; GENETIC POLYMORPHISM; HUMAN; MARKER GENE; NEUROFIBROMATOSIS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SODIUM TRANSPORT; YEAST ARTIFICIAL CHROMOSOME;

EID: 0033153278     PISSN: 08908508     EISSN: None     Source Type: Journal    
DOI: 10.1006/mcpr.1999.0237     Document Type: Article

References (12)

1. Schorpp, M., Hofmann, M., Neil Dear, T. & Boehm, T. (1997). Characterization of mouse and human nude genes. Immunogenetics 46, 509-15.
2. Segré, J., Nemhauser, J. L., Taylor, B. A., Nadeau, J. & Lander, E. S. (1995). Positional cloning of the nude locus: Genetic, physical and transcription maps of the region and mutations in the mouse and rat. Genomics 28, 549-59.
3. Schuddekopf, K., Schorpp, M. & Boehm, T. (1996). The whn transcription factor encoded by the nude locus contains an evolutionary conserved and functionally indispensable activation domain. Genetics 96, 9661-4.
4. Nehls, M., Kyewsky, B., Messerle, M., Waldschutz, R., Schuddekopf, K., Smith, A. J. H. & Boehm, T. (1996). Two genetically separable steps in the differentiation of thymicepithelium. Science 272, 886-9.
5. Nehls, M., Pfeifer, D., Schorpp, M., Hedrich, H. & Boehm, T. (1994). New member of the winged-helix protein family disrupted in mouse and rat nude mutations. Nature 372, 103-7.
6. Chumakov, I. M., Ringault, P., Le Gall, I. et al. (1995). A YAC contig map of the human genome. Nature 377, 175-297.
7. Nelson, D., Ledbetter, S. A., Corbo, L. et al. (1989). Alu polymerase chain reaction: A method for rapid isolation of human specific sequences from complex DNA sources. Proceedings of the National Academy of Science USA 86, 6686-90.
8. Munroe, D. J., Haas, M., Bric, E., Whitton, T., Aburatani, H., Hunter, K., Waard, D. & Hosman, D.E. (1994). Ire-bubble PCR: A rapid method for efficient and representative amplification of human genomic DNA sequences from complex sources. Genomics 19, 506-14.
9. Nelson, D. L., Ballabio, A., Victoria, M. A. et al. (1991). Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: Identification of clones associated with a disease locus. Proceedings of the National Academy of Science USA 88, 6157-61.
10. Riva, P., Castorina, P., Manoukian, S., Dalprà, L., Doneda, L. & Larizza, L. (1996). Characterization of a cytogenetic 17q11.2 deletion in a NF1 patient with a contiguous gene syndrome. Human Genetics 98, 646-50.
11. Fain, P. R., Goldgar, D. E., Wright, E. C. et al. (1989). Markers tightly linked to NF1 locus on chromosome 17. Cytogenetic Cell Genetics 51, 996.
12. Schlake, T., Schorpp, M., Nehls, M. & Boehm, T. (1997). The nude gene encodes a sequence-specific DNA binding protein with homologs in organisms that lack an anticipatory immune system. Proceedings of the National Academy of Science USA 94, 3842-7.