Isolation and characterization of a novel gene close to the human phosphoinositide-specific phospholipase C β3 gene on chromosomal region 11q13

Genomics

Volumn 31, Issue 3, 1996, Pages 380-384

  Lagercrantz, Jacob ^a   Carson, Emma ^a   Larsson, Catharina ^a   Nordenskjöld, Magnus ^a   Weber, Günther ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; PHOSPHATIDYLINOSITIDE; PHOSPHOLIPASE C;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CHROMOSOME 11Q; CHROMOSOME 2; CHROMOSOME 22; CHROMOSOME 4; CHROMOSOME 7; CHROMOSOME MAP; COSMID; GENE EXPRESSION; HOUSEKEEPING GENE; HUMAN; HUMAN CELL; HYBRID CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROMOTER REGION;

ANIMALIA;

EID: 0030026141     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0063     Document Type: Article

References (22)

1. Carrier, L., Hengstenberg, C., Beckmann, J. S., Guicheney, P., Dufour, C., Bercovici, J., Dausse, E., Berebbi-Bertrand, I., Wisnewsky, C., Pulvenis, D., Fetler, L., Vignal, A., Weissenbach, J., Hillaire, D., Feingold, J., Bouhour, J. B., Hagege, A., Desnos, M., Isnard, R., Dubourg, O., Komajda, M., and Schwartz, K. (1993). Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11. Nature Genet. 4: 311-313.
2. Chou, P. Y., and Fasman, G. D. (1978). Empirical predictions of protein conformation. Annu. Rev. Biochem. 47: 251-276.
3. Faisst, S., and Meyer, S. (1992). Compilation of vertebrate-encoded transcription factors. Nucleic Acids Res. 20: 3-26.
4. Fujimori, M., Wells, S. A., and Nakamura, Y. (1992). Fine-scale mapping of the gene responsible for multiple endocrine neoplasia type I (MENI). Am. J. Hum. Genet. 50: 399-403.
5. Grimmond, S., Weber, G., Larsson, C., Walters, M., Teh, B., Shepherd, J., Nordenskjöld, M., and Hayward, N. (1995). Exclusion of the 13-kDa rapamycin binding protein gene (FKBP2) as a candidate gene for multiple endocrine neoplasia type 1. Hum. Genet. 95: 455-458.
6. Hofmann, W., Royer, H. D., Drechsler, M., Schneider, S., and Royer-Pokora, B. (1993). Characterization of the transcriptional regulatory region of the human WT1 gene. Oncogene 8: 3123-3132.
7. Kadonaga, J. T., Jones, K. A., and Tjian, R. (1986). Promoter-specific activation of RNA polymerase II transcription by Sp1. Trends Biochem. Sci. 11: 20-23.
8. Lagercrantz, J., Carson, E., Phelan, C., Grimmond, S., Rosén, A., Daré, E., Nordenskjöld, M., Hayward, N. K., Larsson, C., and Weber, G. (1995). Genomic organization and complete cDNA sequence of the human phosphoinositide-specific phospholipase C β3 gene (PLCB3). Genomics 26: 467-472.
9. Larsson, C., Lardelli, M., White, I., and Lendahl, U. (1994). The human NOTCH1, 2, and 3 genes are located at chromosome positions 9q34, 1p13-p11, and 19p13.2-p13.1 in regions of neoplasia-associated translocation. Genomics 24: 253-258.
10. Larsson, C., Skogseid, B., Öberg, K., Nakamura, Y., and Norden skjöld, M. (1988). Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature 332: 85-87.
11. Larsson, C., Weber, G., Kvanta, E., Lewis, K., Janson, M., Jones, C., Glaser, T., Evans, G., and Nordenskjöld, M. (1992). Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus. Hum. Genet. 89: 187-193.
12. Leppert, M., Baird, L., Anderson, K. L., Otterud, B., Lupski, J. R., and Lewis, R. A. (1994). Bardet - Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous. Nature Genet. 7: 108-112.
13. Li, B., Adams, C. C., and Workman, J. L. (1994). Nucleosome binding by the constitutive transcription factor Sp1. J. Biol. Chem. 269: 7756-7763.
14. Lu, Q., Wallrath, L. L., and Elgin, S. C. (1994). Nucleosome positioning and gene regulation. J. Cell. Biochem. 55: 83-92.
15. Mount, S. M. (1982). A catalogue of splice junction sequences. Nucleic Acids Res. 10: 459-472.
16. Sanger, F., Nicklen, S., and Coulson, A. R. (1977). DNA sequencing with chain-terminating inhibitors. Proc. Natl. Acad. Sci. USA 74: 5463-5467.
17. Sinke, R. J., Weghuis, D. O., Suijkerbuijk, R. F., Tanigami, A., Nakamura, Y., Larsson, C., Weber, G., de Jong, B., Oosterhuis, J. W., Molenaar, W. M., and Geurts van Kessel, A. (1994). Molecular characterization of a recurring complex chromosomal translocation in two human extragonadal germcell tumors. Cancer Genet. Cytogenet. 73: 11-16.
18. Teh, B. T., Cardinal, J., Shepherd, J., Hayward, N. K., Weber, G., Cameron, D., and Larsson, C. (1995). Genetic mapping of the multiple endocrine neoplasia type 1 locus at 11q13. J. Int. Med. 238: 249-253.
19. Uberbacher, E. C., and Mural, R. J. (1991). Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach. Proc. Natl. Acad. Sci. USA 88: 11261-11265.
20. Viskochil, D., Buchberg, A. M., Xu, G., Cawthon, R. M., Stevens, J., Wolff, R. K., Culver, M., Carey, J. C., Copeland, N. G., Jenkins, N. A., White, R., and O'Connell, P. (1990). Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus. Cell 62: 187-192.
21. Weber, G., Friedman, E., Grimmond, S., Hayward, N. K., Phelan, C., Skogseid, B., Gobi, A., Zedenius, J., Sandelin, K., Teh, B. T., Carson, E., White, I., Öberg, K., Shepherd, J., Nordenskjöld, M., and Larsson, C. (1994). The phospholipase C β3 gene located in the MEN1 region shows loss of expression in endocrine tumors. Hum. Mol. Genet. 3: 1775-1781.
22. Zabarovsky, E. R., and Allikmets, R. L. (1986). An improved technique for the efficient construction of gene libraries by partial filling-in of cohesive ends. Gene 1551: 119-123.