Regional localization and molecular characterization of a DNA sequence on the long arm of chromosome 22
Short Communications
Received:
Revised:
- 23 Downloads
- 3 Citations
Summary
A human genomic DNA fragment, p22hom13 (D22S16), was isolated from a chromosome 22-specific library. After elimination of repetitive sequences, a single copy BamHI-EcoRI fragment was subcloned into pTZ18. By using mouse/human somatic cell hybrids and in situ hybridization, the new DNA probe was mapped to chromosome 22q13-qter. Its application in the analysis of the distal part of chromosome 22 and its diagnostic use in translocations are discussed.
Keywords
Internal Medicine Metabolic Disease Somatic Cell Regional Localization Molecular Characterization
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
Preview
Unable to display preview. Download preview PDF.
References
- Arwert F, Porck HJ, Fràter-Schröder M, Brahl C, Geurts van Kessel A, Westerveld A, Meera Khan P, Zang K, Frants RR, Kortbeek HT, Eriksson AW (1986) Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells. Hum Genet 74:378–381CrossRefPubMedGoogle Scholar
- Camargo N, Cervenka J (1982) Patterns of DNA replication of human chromosomes. Am J Hum Genet 34:757–780PubMedGoogle Scholar
- Chapelle A de la, Herva R, Koivisto M, Aula P (1981) A deletion in chromosome 22 can cause DiGeorge syndrome. Hum Genet 57:253–256CrossRefPubMedGoogle Scholar
- deKlein A, Kessel AG van, Grosveld G, Bartram CR, Hagemeijer A, Bootsma D, Spurr NK, Heisterkamp N, Groffen J, Stephenson JR (1982) A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia. Nature 300:765–767Google Scholar
- Dumanski JP, Carlbom E, Collins VP, Nordenskjöld M (1987) Deletion mapping of a loss on human chromosome 22 involved in the oncogenesis of meningioma. Proc Natl Acad Sci USA 84:9275–9279PubMedGoogle Scholar
- Fitzgerald PH (1976) Evidence that chromosome band 22q12 is concerned with cell proliferation in chronic myeloid leukaemia. Hum Genet 33:269–274CrossRefPubMedGoogle Scholar
- Fraccaro M, Lindsten J, Ford CE, Iselius L (1980) The 11q;22q translocation: a European collaborative analysis of 43 cases. Hum Genet 56:21–51PubMedGoogle Scholar
- Hsu LYF, Hirschhorn K (1979) The trisomy 22 syndrome and the cat eye syndrome. In: Yunis JJ (ed) New chromosomal syndromes. Academic Press, New York London, pp 73–85Google Scholar
- Kaplan JC, Carritt B (1987) Report of the committee on the genetic constitution of chromosomes 20, 21, and 22. (9th International Workshop on Human Gene Mapping) Cytogenet Cell Genet 46: 257–276PubMedGoogle Scholar
- Kessel E, Pfeifer RA (1977) Remarks on the problem of trisomy 22. Hum Genet 37:111–116CrossRefPubMedGoogle Scholar
- Krumlauf R, Jeanpierre M, Young BD (1982) Construction and characterization of genomic libraries from specific human chromosomes. Proc Natl Acad Sci USA 79:2971–2975PubMedGoogle Scholar
- Limon J, Rao U, DalCin P, Gibas Z, Sandberg A (1986) Translocation (13;22) in a hemangiopericytoma. Cancer Genet Cytogenet 21:309–318CrossRefPubMedGoogle Scholar
- Maniatis T, Fritsch EF, Sambrook J (eds) (1982) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NYGoogle Scholar
- Mattei MG, Philip N, Passage E, Moisan JP, Mandel JL, Mattei JF (1985) DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome. Hum Genet 69:268–271PubMedGoogle Scholar
- Meese E, Blin N (1987) Simultaneous isolation of high molecular weight DNA and RNA from limited amounts of tissues and cells. Gene Anal Techn 4:45–49CrossRefGoogle Scholar
- Meese E, Blin N, Zang KD (1987) Loss of heterozygosity and the origin of meningioma. Hum Genet 77:349–351CrossRefPubMedGoogle Scholar
- Metzdorf R, Göttert E, Blin N (1988) A novel repetitive DNA from human chromosome 22. Chromosoma 97:154–158CrossRefPubMedGoogle Scholar
- Nakai H, Yamamoto Y, Kuroki U (1979) Partial trisomy of 11 and 22 due to familial translocation t(11;22)(q231;q111), inherited in three generations. Hum Genet 51:349–355CrossRefPubMedGoogle Scholar
- Seizinger BR, Martuza RL, Gusella JF (1986) Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma. Nature 322:644–647CrossRefPubMedGoogle Scholar
- Seizinger BR, Monte S de la, Atkins L, Gusella JF, Martuza RL (1987) Molecular genetic approach to human meningioma: loss of genes on chromosome 22. Proc Natl Acad Sci USA 84:5419–5423PubMedGoogle Scholar
- Thomas PS (1980) Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc Natl Acad Sci USA 77:5201–5205PubMedGoogle Scholar
Copyright information
© Springer-Verlag 1989