Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to Doublecortin

Journal of Human Genetics

Volumn 43, Issue 3, 1998, Pages 169-177

  Omori, Yoshihiro ^a   Suzuki, Mikio ^a   Ozaki, Kouichi ^a   Harada, Yosuke ^a   Nakamura, Yusuke ^b   Takahashi, Ei Ichi ^a   Fujiwara, Tsutomu ^a  

^a OTSUKA PHARMACEUTICAL CO LTD   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

Author keywords

CaM kinase; Developmental nervous system; Double cortex; Doublecortin; KIAA0369; Lissencephaly; Neuropathy

Indexed keywords

MURINAE; VERTEBRATA;

DCAMKL1 PROTEIN, HUMAN; DCAMKL1 PROTEIN, MOUSE; DOUBLECORTIN PROTEIN; MICROTUBULE ASSOCIATED PROTEIN; NERVE PROTEIN; NEUROPEPTIDE; PROTEIN KINASE (CALCIUM,CALMODULIN); PROTEIN SERINE THREONINE KINASE;

ADULT; ALTERNATIVE RNA SPLICING; AMINO ACID SEQUENCE; ARTICLE; BRAIN CORTEX; CHROMOSOME 13; CHROMOSOME MAP; CONGENITAL MALFORMATION; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENETIC LINKAGE; GENETICS; HUMAN; MOLECULAR CLONING; MOLECULAR GENETICS; NERVOUS SYSTEM MALFORMATION; NUCLEAR LOCALIZATION SIGNAL; SEQUENCE HOMOLOGY; TISSUE DISTRIBUTION; X CHROMOSOME;

ADULT; ALTERNATIVE SPLICING; AMINO ACID SEQUENCE; CA(2+)-CALMODULIN DEPENDENT PROTEIN KINASE; CEREBRAL CORTEX; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 13; CLONING, MOLECULAR; FETUS; GENE EXPRESSION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LINKAGE (GENETICS); MICROTUBULE-ASSOCIATED PROTEINS; MOLECULAR SEQUENCE DATA; NERVE TISSUE PROTEINS; NERVOUS SYSTEM MALFORMATIONS; NEUROPEPTIDES; NUCLEAR LOCALIZATION SIGNALS; PROTEIN-SERINE-THREONINE KINASES; SEQUENCE HOMOLOGY, AMINO ACID; TISSUE DISTRIBUTION; X CHROMOSOME;

EID: 0031613727     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380050063     Document Type: Article

References (34)

1. 2+/calmodulin-dependent protein kinase isoforms in rat brain. J Neurosci 15: 6797-6808
2. D'Arcangelo G, Miao GG, Chen SC, Soares HD, Morgan JI, Curran T (1995) A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature 374: 719-723
3. des Portes V, Pinard JM, Billuart P, Vinet MC, Koulakoff A, Carrie A, Gelot A, Dupuis E, Motte J, Berwald-Netter Y, Catala M, Kahn A, Beldjord C, Chelly J (1998) A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. Cell 92: 51-61
4. Enslen H, Tokumitsu H, Soderling TR (1995) Phosphorylation of CREB by CaM-kinase IV activated by CaM-kinase IV kinase. Biochem Biophys Res Commun 207: 1038-1043
5. Frohman MA, Dush MK, Martin GR (1988) Rapid production of full-length cDNAs from rare transcripts: Amplification using a single gene-specific oligonucleotide primer. Proc Natl Acad Sci USA 85: 8998-9002
6. Gallagher PJ, Herring BP (1991) The carboxyl terminus of the smooth muscle myosin light chain kinase is expressed as an independent protein, telokin. J Biol Chem 266: 23945-23952
7. Gleeson JG, Allen KM, Fox JW, Lamperti ED, Berkovic S, Scheffer I, Cooper EC, Dobyns WB, Minnerath SR, Ross ME, Walsh CA (1998) Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein Cell 92: 63-72
8. 2+/calmodulin-dependent protein kinases. Annu Rev Biochem 61: 559-601
9. Hicks GR, Raikhel NV (1995) Protein import into the nucleus: An integrated view. Ann Rev Cell Dev Biol 11: 155-188
10. 2+/calmodulin-dependent protein kinase type Gr in rat cerebellar cortex. Proc Natl Acad Sci USA 88: 2850-2853
11. Johnson JE, Birren SJ, Anderson DJ (1990) Two rat homologues of Drosophila achaetescute specifically expressed in neuronal precursors. Nature 346: 858-861
12. Jouet M, Rosenthal A, Armstrong G, MacFarlane J, Stevenson R, Paterson J, Metzenberg A, Ionasescu V, Temple K, Kenwrick S (1994) X-linked spastic paraplegia (SPG1). MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene. Nat Genet 7: 402-407
13. Kamm KE, Stull JT (1989) Regulation of smooth muscle contractile elements by second messengers. Annu Rev Physiol 51: 299-313
14. Lee JE, Hollenberg SM, Snider L, Turner DL, Lipnick N, Weintraub H (1995) Conversion of Xenopus ectoderm into neurons by NeuroD, a basic hehx-loop-helix protein. Science 268: 836-844
15. Lichter P, Ledbetter DH, Ward DC (1990) Fluorescence in situ hybridization with Alu and L1 polymerase chain reaction probes for rapid characterization of human chromosomes in hybrid cell lines. Proc Natl Acad Sci USA 87: 6634-6638
16. Lisman J (1994) The CaM kinase II hypothesis for the storage of synaptic memory. Trends Neurosci 17: 406-412
17. Mumm S, Zucchi I, Pilia G (1997) SOX3 gene maps near DXS984 in Xq27.1, within candidate regions for several X-linked disorders. Am J Med Genet 72: 376-378
18. Nagase T, Ishikawa K, Nakajima D, Ohira M, Seki N, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (1997) Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro. DNA Res 4: 141-150
19. Nairn AC, Picciotto MR (1994) Calcium/calmodulin-dependent protein kinases. Semin Cancer Biol 5: 295-303
20. Radhakrishna U, Blouin J-L, Mehenni H, Mehta TY, Sheth FJ, Sheth JJ, Solanki JV, Antonarakis SE (1997) The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region. Am J Med Genet 71: 80-86
21. Rugh R (1990) The mouse: Its reproduction and development. Oxford University Press, New York
22. 2+/ calmodulin-dependent protein kinase II. Differential expression in rat brain and aorta. J Biol Chem 268: 14443-14449
23. Silver DL, Vorotnikov AV, Watterson DM, Shirinsky VP, Sellers JR (1997) Sites of interaction between kinase-related protein and smooth muscle myosin. J Biol Chem 272: 25353-25359
24. Slee JJ, Smart RD, Viljoen DL (1991) Deletion of chromosome 13 in Moebius syndrome. J Med Genet 28: 413-414
25. Soderling TR (1993) Calcium/calmodulin-dependent protein kinase II: Role in learning and memory. Mol Cell Biochem 128: 93-101
26. Stabile M, Cavaliere ML, Scarano G, Fels A, Valiani R, Ventruto V (1984) Abnormal BAEP in a family with Moebius syndrome: Evidence for supranuclear lesion Clin Genet 25: 459-463
27. Takahashi E, Hori T, O'Connell P, Leppert M, White R (1990) R-banding and nonisotopic in situ hybridization: Precise localization of the human type II collagen gene (COL2A1). Hum Genet 86: 14-16
28. Takahashi E, Yamauchi M, Tsuji H, Hitomi A, Meuth M, Hori T (1991) Chromosome mapping of the human cytidine-5′-triphosphate synthetase (CTPS) gene to band 1p34.1-p34.3 by fluorescence in situ hybridization. Hum Genet 88: 119-121
29. Uwanogho D, Rex M, Cartwright EJ, Pearl G, Healy C, Scotting PJ, Sharpe PT (1995) Embryonic expression of the chicken Sox2, Sox3 and Sox11 genes suggests an interactive role in neuronal development. Mech Dev 49: 23-36
30. Walter M, Spillet D, Thomas P, Weissenbach J, Goodfellow P (1994) A method for constructing radiation hybrid maps of whole genomes. Nat Genet 7: 22-28
31. Watanahe TK, Fujiwara T, Kawai A, Shimizu F, Takami S, Hirano H, Okuno S, Ozaki K, Takeda S, Shimada Y, Nagata M, Takaichi A, Takahashi E, Nakamura Y, Shin S (1996a) Cloning, expression, and mapping of UBE2I, a novel gene encoding a human homologue of yeast ubiquitin-conjugatmg enzymes which are critical for regulating the cell cycle. Cytogenet Cell Genet 72: 86-89
32. Watanabe TK, Fujiwara T, Shimizu F, Okuno S, Suzuki M, Takahashi E, Nakamura Y, Hirai Y (1996b) Cloning, expression, and mapping of TCTEL1, a putative human homologue of murine Tctel, to 6q. Cytogenet Cell Genet 73: 153-156
33. Wolff DJ, Gustashaw KM, Zurcher V, Ko L, White W, Weiss L, Van Dyke DL, Schwartz S, Willard HF (1997) Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern. Hum Genet 100: 256-261
34. Wright E, Hargrave MR, Christiansen J, Cooper L, Kun J, Evans T, Gangadharan U, Greenfield A, Koopman P (1995) The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos. Nat Genet 9: 15-20