Molecular cloning and characterization of a novel developmentally regulated gene, Bdm1, showing predominant expression in postnatal rat brain

被引:27
作者
Yamauchi, Y
Hongo, S
Ohashi, T
Shioda, S
Zhou, CJ
Nakai, Y
Nishinaka, N
Takahashi, R
Takeda, F
Takeda, M
机构
[1] Showa Univ, Sch Med, Dept Biochem, Shinagawa Ku, Tokyo 1428555, Japan
[2] Showa Univ, Sch Med, Dept Anat, Shinagawa Ku, Tokyo 1428555, Japan
来源
MOLECULAR BRAIN RESEARCH | 1999年 / 68卷 / 1-2期
关键词
Bdm1; brain development; cDNA cloning; mRNA expression; in situ hybridization;
D O I
10.1016/S0169-328X(99)00084-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Postnatal development, such as synapse refinement, is necessary for the establishment of a mature and functional central nervous system (CNS). Using differential display analysis, we identified a novel gene, termed Bdm1, that is more abundantly expressed in the adult brain than in the embryonic brain. The full-length Bdm1 cDNA is 2718 base pairs long and contains an open reading frame of 1059 base pairs encoding a 38-kDa protein. Northern blot analysis revealed that expression of Bdm1 mRNA in the brain was weak on embryonic days and increased in the early postnatal period. Bdm1 mRNA was significantly expressed in the brain and heart, but there was no or little expression in other tissues. During the differentiation of mouse carcinoma cells P19 to neuron-like cells by retinoic acid, Bdm1 mRNA was up-regulated almost parallel to neurofilament mRNA. Expression of Bdm1 mRNA was observed appreciably in PC12 cells after neuronal differentiation but not in the nonneural cell,lines examined. In situ hybridization demonstrated that Bdm1 was expressed widely in the olfactory bulb, cerebral cortex, hippocampus, cerebellum, thalamus, and medulla oblongata. Taken together, these data suggest that Bdm1 gene plays a role in the early postnatal development and function of neuronal cells. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:149 / 158
页数:10
相关论文
共 27 条
[1]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[2]   REGRESSIVE EVENTS IN NEUROGENESIS [J].
COWAN, WM ;
FAWCETT, JW ;
OLEARY, DDM ;
STANFIELD, BB .
SCIENCE, 1984, 225 (4668) :1258-1265
[3]   Molecular cloning and functional expression of mouse connexin-30, a gap junction gene highly expressed in adult brain and skin [J].
Dahl, E ;
Manthey, D ;
Chen, Y ;
Schwarz, HJ ;
Chang, YS ;
Lalley, PA ;
Nicholson, BJ ;
Willecke, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (30) :17903-17910
[4]  
DURRANT I, 1995, GENE PROBES, V1, P189
[5]   FLUORESCENT DIFFERENTIAL DISPLAY - ARBITRARILY PRIMED RT-PCR FINGERPRINTING ON AN AUTOMATED DNA SEQUENCER [J].
ITO, T ;
KITO, K ;
ADATI, N ;
MITSUI, Y ;
HAGIWARA, H ;
SAKAKI, Y .
FEBS LETTERS, 1994, 351 (02) :231-236
[6]  
JACOBSON M, 1991, DEV NEUROBIOL, P41
[7]  
Jacobson M., 1991, DEV NEUROBIOL, P223, DOI DOI 10.1007/978-1-4757-4954-0_6
[8]   MOLECULAR MECHANISMS OF DEVELOPMENTAL NEURONAL DEATH [J].
JOHNSON, EM ;
DECKWERTH, TL .
ANNUAL REVIEW OF NEUROSCIENCE, 1993, 16 :31-46
[9]   CLONING AND DEVELOPMENTAL EXPRESSION OF THE MURINE NEUROFILAMENT GENE FAMILY [J].
JULIEN, JP ;
MEYER, D ;
FLAVELL, D ;
HURST, J ;
GROSVELD, F .
MOLECULAR BRAIN RESEARCH, 1986, 1 (03) :243-250
[10]   Homocysteine-respondent genes in vascular endothelial cells identified by differential display analysis - GRP78/BiP and novel genes [J].
Kokame, K ;
Kato, H ;
Miyata, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (47) :29659-29665