Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein

Mammalian Genome

Volumn 8, Issue 5, 1997, Pages 371-375

  Taylor, Catherine ^a   Wadey, Roy ^a   O'Donnell, Hilary ^a   Roberts, Catherine ^a   Mattei, Marie Geneviève ^b   Kimber, Wendy L ^c   Wynshaw Boris, Anthony ^c   Scambler, Peter J ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b INSERM   (France)

^c NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADHESION RECEPTOR; CELL ADHESION MOLECULE; COMPLEMENTARY DNA; MEMBRANE PROTEIN;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; CHROMOSOME MAP; COMPARATIVE STUDY; DIGEORGE SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENETICS; HUMAN; MOLECULAR CLONING; MOLECULAR GENETICS; MOUSE; NUCLEOTIDE SEQUENCE; SEQUENCE HOMOLOGY; SPECIES DIFFERENCE;

AMINO ACID SEQUENCE; ANIMALS; CELL ADHESION MOLECULES; CHROMOSOME MAPPING; CLONING, MOLECULAR; DIGEORGE SYNDROME; DNA, COMPLEMENTARY; GENE EXPRESSION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MEMBRANE PROTEINS; MICE; MOLECULAR SEQUENCE DATA; SEQUENCE HOMOLOGY, AMINO ACID; SPECIES SPECIFICITY;

ANIMALIA; MURINAE;

EID: 0031136322     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900445     Document Type: Article

References (18)

1. Augusseau S, Jouk S, Jalbert P, Priur M (1986) DiGeorge syndrome and 22q11 rearrangements. Hum Genet 74, 206
2. Bucan M, Gatalica B, Nolan P, Chung A, Leroux A, Grossman MH, Nadeau J, Emanuel BS, Budarf M (1993) Comparative map of 9 chromosome 22q loci in the laboratory mouse. Hum Mol Genet 2, 1245-1252
3. Budarf ML, Collins J, Gong W, Roe B, Wang Z, Bailey LC, Sellinger B, Michaud D, Driscoll DA, Emanuel BS (1995) Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene. Nature Genet 10, 269-278
4. Cattanach B, Evans H (1994) Molecular Mechanisms in Radiation Mutagenesis and Carcinogenesis. Commission of the European Communities Report EUR 15294
5. Demczuk S, Aledo R, Zucman J, Delattre O, Desmaze C, Dauphinot L, Jalbert P, Rouleau GA, Thomas G, Aurias A (1995) Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity. Hum Mol Genet 4, 551-558
6. Halford S, Wilson DI, Daw SCM, Roberts C, Wadey R, Kamath S, Wickremasinghe A, Burn J, Goodship J, Mattei M-G, Moorman AFM, Scambier PJ (1993) Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome. Hum Mol Genet 2, 1577-1582
7. Heisterkamp N, Mulder MP, Langeveld A, ten Hoeve J, Wang Z, Roe B, Groffen J (1995) Localization of the human mitochondrial citrate transporter protein gene to chromosome 22q11 in the DiGeorge syndrome critical region. Genomics 29, 451-456
8. Kajiwara K, Nagasawa H, Shimizu-Nishikawa K, Ookura T, Kimura M, Sugaya E (1996) Cloning of SEZ-12 encoding seizure-related and membrane bound adhesion protein. Biochem Biophys Res Commun 222, 144-148
9. Kirby ML, Gale TF, Stewart DE (1983) Neural crest cells contribute to normal aorticopulmonary septation. Science 220, 1059-1061
10. Levy A, Demczuk S, Aurias A, Depetris D, Mattel MG, Philip N (1995) Interstitial 22q11 deletion excluding the ADU breakpoint in a patient with DCS. Hum Mol Genet 4, 2417-2418
11. Lindsay EA, Halford S, Wadey R, Scambler PJ, Baldini A (1993) Molecular cytogenetic characterisation of the DiGeorge syndrome region using fluorescence in situ hybridisation. Genomics 17, 403-407
12. Mattei MG, Halford S, Scambler PJ (1994) Mapping of the Tuplel gene to mouse chromosome 16A-B1. Genomics 23, 717-718
13. Ramirez-Solis R, Liu P, Bradley A (1995) Chromosome engineering in mice. Nature 378, 720-724
14. Rizzu P, Lindsay EA, Taylor C, O'Donnell H, Scambler PJ, Baldini A (1996) Cloning and comparative mapping of a gene deleted in DiGeorge and velocardiofacial syndromes conserved in the C. elegans genome. Mamm Genome 7, 639-643
15. Sutherland HF, Wadey R, McKie JM, Taylor C, Atif U, Johnstone KA, Halford S, Kamath S, Kim U-J, Goodship JA, Baldini A, Scambler PJ (1996) Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome. Am J Hum Genet 59, 23-31
16. Wadey R, Daw S, Taylor C, Atif U, Kamath S, Halford S, O'Donnell H, Wilson D, Goodship JA, Burn J, Scambler PJ (1995) Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with the DiGeorge syndrome. Hum Mol Genet 4, 1027-1034
17. Wilkinson D (1992) Whole mount in situ hybridisation of vertebrate embryos. In In situ Hybridisation: A Practical Approach, D. Wilkinson, ed. (Oxford:IRL Press), pp 75-84
18. Wilson DI, Burn J, Scambler P, and Goodship J (1993) Syndrome of the month: DiGeorge syndrome. Part of CATCH-22. J Med Genet 30, 852-856