Assignment of the genes encoding the human chloride channels, CLCNKA and CLCNKB, to 1p36 and of CLCN3 to 4q32-q33 by in situ hybridization

Genomics

Volumn 36, Issue 2, 1996, Pages 372-374

  Saito Ohara, Fumiko ^a   Uchida, Shinichi ^a   Takeuchi, Yasuo ^a   Sasaki, Sei ^a   Hayashi, Aiko ^a   Marumo, Fumiaki ^a   Ikeuchi, Tatsuro ^a  

^a TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE; CHLORIDE CHANNEL; COMPLEMENTARY DNA;

ARTICLE; CHROMOSOME 1P; CHROMOSOME 4Q; FLUORESCENCE IN SITU HYBRIDIZATION; GENE ASSIGNMENT; GENOME; HUMAN; PRIORITY JOURNAL;

EID: 0030249306     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0479     Document Type: Article

References (18)

1. 1. Adachi, S., Uchida, S., Ito, H., Hata, M., Hiroe, M., Marumo, F., and Sasaki, S. (1994). Two isoforms of a chloride channel predominantly expressed in thick ascending limb of Henle'sloop and collecting ducts of rat kidney. J. Biol. Chem. 269: 17677-17683.
2. 2. Borsani, G., Rugarli, E. I., Taglialatela, M., Wong, C., and Ballabio, A. (1995). Characterization of a human and murine gene (CLCN3) sharing similarities to voltage-gated chloride channels and to a yeast integral membrane protein. Genomics 27: 131-141.
3. 3. Fidlerova, H., Senger, G., Kost, M., Sanseau, P., and Sheer, D. (1994). Two simple procedures for releasing chromatin from routinely fixed cells for fluorescence in situ hybridization. Cytogenet. Cell Genet. 65: 203-205.
4. 4. Fisher, S. E., Black, G. C. M., Lloyd, S. E., Hatchwell, E., Wrong, O., Thakker, R. V., and Craig, I. W. (1994). Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis). Hum. Mol. Genet. 3: 2053-2059.
5. 5. Gill, J. R., and Bartter, F. C. (1978). Evidence for a prostaglandin-independent defect in chloride reabsorption in the loop of Henle as a proximal cause by Bartter's syndrome. Am. J. Med. 65: 766-772.
6. 6. Jentsch, T. J., Steinmeyer, K., and Schwarz, G. (1990). Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes. Nature 348: 510-514.
7. 7. Kawasaki, M., Uchida, S., Monkawa, T., Myawaki, A., Mikoshiba, K., Marumo, F., and Sasaki, S. (1994). Cloning and expression of a protein kinase C-regulated chloride channel abundantly expressed in rat brain neuronal cells. Neuron 12: 597-604.
8. 8. Kimberling, W. J., Kumar, S., Gabow, P. A., Kenyon, J. B., Connolly, C. J., and Somlo, S. (1993). Autosomal dominant polycystic kidney disease; Localization of the second gene to chromosome 4q13-q23. Genomics 18: 467-472.
9. 9. Meyer-Kleine, C., Steinmeyer, K., Ricker, K., Jentsch, T. J., and Koch, M. C. (1995). Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCNUI) leading to myotonia. Am. J. Hum. Genet. 57: 1325-1334.
10. 10. Peters, D. J. M., Spruit, L., Saris, J. J., Ravine, D., Sandkuijl, L. A., Fossdal, R., Boersma, J., van Eijk, R., Norby, S., Constantinou-Deltas, C. D., Pierides, A., Brissenden, J. E., Frants R. R., van Ommen, G.-J. B., and Breuning, M. H. (1993). Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease. Nature Genet. 5: 359-362.
11. 11. Saito, F., Yamamoto, T., Horikoshi, M., and Ikeuchi, T. (1994). Direct mapping of the human TATA box-binding protein (TBP) gene to 6q27 by fluorescence in situ hybridization. Jpn. J. Hum. Genet. 39: 421-425.
12. 12. Saito, F., Sasaki, S., Chepelinsky, A. B., Fushimi., K., Marumo, F., and Ikeuchi, T. (1995). Human AQP2 and MIP genes, two members of the MIP family, map within chromosome band 12q13 on the basis of two-color FISH. Cytogenet. Cell Genet. 68: 45-48.
13. 13. Saito, F., Yamaguchi, T., Komuro, A., Tobe, T., Ikeuchi, T., Tomita, M., and Nakajima, H. (1995). Mapping of the newly identified biliverdin-IXb reductase gene (BLVRB) to human chromosome 19q13.13 → q13.2 by fluorescence in situ hybridization. Cytogenet. Cell Genet. 71: 179-181.
14. 14. Simon, D. B., Nelson-Williams, C., Bia, M. J., Ellison, D., Karet, F. E., Molina, A. M., Vaara, I., Iwata, F., Cushner, H. M., Koolen, M., Gainza, F. J., Gitelman, H. J., and Lifton, R. P. (1996). Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. Nature Genet. 12: 24-30.
15. 15. Steinmeyer, K., Ortland, C., and Jentsch, T. J. (1991). Primary structure and functional expression of a developmentally regulated skeletal muscle chloride channel. Nature 354: 301-304.
16. 16. Take, C., Ikeda, K., Kurosawa, T., and Kurokawa, K. (1991). Increased chloride reabsorption as an inherited renal tubular defect in familial type II pseudohypo-aldosteronism. N. Engl. J. Med. 324: 472-476.
17. 17. Uchida, S., Sasaki, S., Furukawa, T., Hiraoka, M., Imai, T., Hirata, Y., and Marumo, F. (1993). Molecular cloning of a chloride channel that is regulated by dehydration and expressed predominantly in kidney medulla. J. Biol. Chem. 268: 3821-3824.
18. 18. Uchida, S., Sasaki, S., Nitta, K., Uchida, K., Horita, S., Nihei, H., and Marumo, F. (1995). Localization and functional characterization of rat kidney-specific chloride channel, CIC-K1. J. Clin. Invest. 95: 104-113.