3.ミエリン欠損モデルマウスの病因病態解析

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Published in日本疾患モデル学会記録 Vol. 22; pp. 47 - 53
Main Authors 李, 正花, 山村, 研一, 尾池, 雄一
Format Journal Article
LanguageJapanese
Published 公益社団法人 日本実験動物学会 05.07.2006
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ISSN0918-8991
1884-4197
DOI10.1538/expanim1992.22.47

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Author 尾池, 雄一
李, 正花
山村, 研一
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  organization: 熊本大学発生医学研究センター臓器形成分野
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  fullname: 尾池, 雄一
  organization: 熊本大学発生医学研究センター臓器形成分野
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References 25) Lo, P.C.H. and Frasch, M. A novel KH-domain protein mediates cell adhesion processes in Drosophila. Dev. Biol. 190, 241-256, 1997.
15) Bannister, A.J. and Kouzarides, T. CBP-induced stimulation of c-Fos activity is abrogated by Ela. EMBO J., 14, 4758-4762, 1995.
22) Wang, C., Kuo, F., Fujiwara, Y., Gilliland, D.G., Golub, T.R. and Orkin, S.H. Yolk sac angiogenic defect and intra-embryonic apoptosis in mice lacking the Ets-related factor TEL. EMBO J. 16, 4374-4383, 1997.
6) Ebersole, T.A., Chen, Q., Justice, M.J. and Artzt, K. The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteins. Nat. Genet. 12, 260-265, 1996.
11) Larocque, D., Pilotte, J., Chen, T., Cloutier, F., Massie, B., Pedraza, L., Couture, R., Lasko, P., Almazan, G. and Richard, S. Nuclear retention of MBP mRNAs in the quaking viable mice. Neuron 36, 815-829, 2002.
4) Bode, C.V. Ethylnitrosourea mutagenesis and the isolation of mutant alleles for specific genes located in the T region of mouse chromosome 17. Genetics 108, 457-470, 1984.
13) Petrij, F., Giles, R.H., Dauwerse, H.G., Saris, J. J., Hennekam, R.C.M., Masuno, M., Tommerup, N., van Ommen, G.B., Goodman, R.H., Peters, D.J.M. and Breuning, M.H. Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP. Nature, 376, 348-351, 1995.
24) Larocque, D., Pilotte, J., Chen, T., Cloutier, F., Massie, B., Pedraza, L., Couture, R., Lasko, P., Almazan, G. and Richard, S. Nuclear retention of MBP mRNAs in the quaking viable mice. Neuron 36, 815-829, 2002.
26) Takakura, N., Huang, X.-L., Naruse, T., Hamaguchi, I., Dumont, D.J., Yancopoulos, G.D. and Suda, T. Critical role of the TIE2 endothelial receptor in the development of definitive hematopoiesis. Immunity 9, 677-686, 1998.
16) Arias, J., Alberts, A.S., Brindle, P., Claret, F.X., Smeal, T., Karin, M., Feramisco, J. and Montominy, M. Activation of cAMP and mitogen responsive genes relies on a common nuclear factor. Nature, 370, 226-229, 1994.
19) Chakravarti, D., Lamorte, V.J., Nelson, M.C., Nakajima, T., Schulman, I.G., Juguilon, H., Montominy, M. and Evans, R.M. Role of CBP/P300 in nuclear receptor signalling. Nature, 383, 99-103, 1996.
10) Liu, Z.H., Luyten, I., Bottomley, M.J., Messias, A.C., Sophie, H.M., Spranger, R., Zanier, K., Krämer, A. and Sattler, M. Structural basis for recognition of the intron branch site RNA by splicing factor 1. Science 294, 1098-1101, 2001.
18) Kamei, Y., Xu, L., Heinzel, T., Torchia, J., Kurokawa, R., Gloss, B., Lin, S., Heyman, R.A., Rose, D.W., Glass, C.K. and Rosenfeld, M.G. A CBP integrator complex mediates transcriptional activation and AP-1 inhibition by nuclear receptors. Cell, 85, 403-414, 1996.
5) Justice, M.J. and Bode, V.C. Three ENU-induced alleles of the murine quaking locus are recessive embryonic lethal mutations. Genet. Res. 51, 95-102, 1988.
12) Chrivia, J.C., Kwok, R.P.S., Lamb, N., Hagiwara, M., Montominy, M.R. and Goodman, R.H. Phosphorylated CREB binds specifically to the nuclear protein CBP. Nature, 365, 855-859, 1993.
7) Kondo, T., Furuta, T., Mitsunaga, K., Ebersole, T.A., Shichiri, M., Wu, J., Artzt, K., Yamamura, K. and Abe, K. Genomic organization and expression analysis of the mouse qkI locus. Mamm. Genome 10, 662-669, 1999.
17) Dai, P., Akimura, H., Tanaka, Y., Hou, D., Yasukawa, T., Kanei-Ishii, C., Takahashi, T. and Ishii, S. CBP as a transcriptional coactivator of c-Myb. Genes Dev., 10, 528-540, 1996.
2) Samorajski, T., Friede, R.L. and Reimer, P.R. Hypomyelination in the quaking mouse. A model for the analysis of disturbed myelin formation. J. Neuropathol. Exp. Neurol. 29, 507-523, 1970.
3) Watanabe, I. and Bingle, G.J. Dysmyelination in “quaking” mouse. Electron microscope study. J. Neuropathol. Exp. Neurol. 31, 352-369, 1972.
21) Visvader, J.E., Fujiwara, Y. and Orkin, S.H. Unsuspected role for the T-cell leukemia protein SCL/tal-1 in vascular development. Genes Dev. 12, 473-479, 1998.
9) Hardy, R.J. Molecular defects in the dysmyelinating mutant quaking. J. Neurosci. Res. 51, 417-422, 1998.
20) Tanaka, Y., Naruse, I., Maekawa, T., Masuya, H., Shiroishi, T. and Ishii, S. Abnormal skeletal patterning in embryos lacking a single Cbp allele: a partial similarity with Rubinstein-Taybi syndrome. Proc. Natl. Acad. Sci. USA, 94, 10215-10220, 1997.
23) Xue, Y., Gao, X., Lidsell, C.E., Norton, C.R., Chang, B., Hicks, C., Gendron-Maguire, M., Rand, E.B., Weinmaster, G. and Gridley, T. Embryonic lethality and vascular defects in mice lacking the Notch ligand Jaggedl. Human Mol. Genet. 8, 723-730, 1999.
8) Vernet, C. and Artzt, K. STAR, a gene family involved in signal transduction and activation of RNA. Trends Genet. 13, 479-484, 1997.
1) Sidman, R.L., Dickie, M.M. and Apple, S.H. Mutant mice (quaking and jimpy) with deficient myelination in the central nervous system. Science 144, 309-312, 1964.
14) Kwok, R.P.S., Lundblad, J.R., Chrivia, J.C., Richards, J.P., Bachinger, H.P., Brennan, R.G., Roberts, S.G.E., Green, M.R. and Goodman, R.H. Nuclear protein CBP is a coactivator for the transcription factor CREB. Nature, 370, 223-226, 1994.
References_xml – reference: 2) Samorajski, T., Friede, R.L. and Reimer, P.R. Hypomyelination in the quaking mouse. A model for the analysis of disturbed myelin formation. J. Neuropathol. Exp. Neurol. 29, 507-523, 1970.
– reference: 11) Larocque, D., Pilotte, J., Chen, T., Cloutier, F., Massie, B., Pedraza, L., Couture, R., Lasko, P., Almazan, G. and Richard, S. Nuclear retention of MBP mRNAs in the quaking viable mice. Neuron 36, 815-829, 2002.
– reference: 13) Petrij, F., Giles, R.H., Dauwerse, H.G., Saris, J. J., Hennekam, R.C.M., Masuno, M., Tommerup, N., van Ommen, G.B., Goodman, R.H., Peters, D.J.M. and Breuning, M.H. Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP. Nature, 376, 348-351, 1995.
– reference: 22) Wang, C., Kuo, F., Fujiwara, Y., Gilliland, D.G., Golub, T.R. and Orkin, S.H. Yolk sac angiogenic defect and intra-embryonic apoptosis in mice lacking the Ets-related factor TEL. EMBO J. 16, 4374-4383, 1997.
– reference: 23) Xue, Y., Gao, X., Lidsell, C.E., Norton, C.R., Chang, B., Hicks, C., Gendron-Maguire, M., Rand, E.B., Weinmaster, G. and Gridley, T. Embryonic lethality and vascular defects in mice lacking the Notch ligand Jaggedl. Human Mol. Genet. 8, 723-730, 1999.
– reference: 24) Larocque, D., Pilotte, J., Chen, T., Cloutier, F., Massie, B., Pedraza, L., Couture, R., Lasko, P., Almazan, G. and Richard, S. Nuclear retention of MBP mRNAs in the quaking viable mice. Neuron 36, 815-829, 2002.
– reference: 25) Lo, P.C.H. and Frasch, M. A novel KH-domain protein mediates cell adhesion processes in Drosophila. Dev. Biol. 190, 241-256, 1997.
– reference: 16) Arias, J., Alberts, A.S., Brindle, P., Claret, F.X., Smeal, T., Karin, M., Feramisco, J. and Montominy, M. Activation of cAMP and mitogen responsive genes relies on a common nuclear factor. Nature, 370, 226-229, 1994.
– reference: 8) Vernet, C. and Artzt, K. STAR, a gene family involved in signal transduction and activation of RNA. Trends Genet. 13, 479-484, 1997.
– reference: 18) Kamei, Y., Xu, L., Heinzel, T., Torchia, J., Kurokawa, R., Gloss, B., Lin, S., Heyman, R.A., Rose, D.W., Glass, C.K. and Rosenfeld, M.G. A CBP integrator complex mediates transcriptional activation and AP-1 inhibition by nuclear receptors. Cell, 85, 403-414, 1996.
– reference: 3) Watanabe, I. and Bingle, G.J. Dysmyelination in “quaking” mouse. Electron microscope study. J. Neuropathol. Exp. Neurol. 31, 352-369, 1972.
– reference: 10) Liu, Z.H., Luyten, I., Bottomley, M.J., Messias, A.C., Sophie, H.M., Spranger, R., Zanier, K., Krämer, A. and Sattler, M. Structural basis for recognition of the intron branch site RNA by splicing factor 1. Science 294, 1098-1101, 2001.
– reference: 1) Sidman, R.L., Dickie, M.M. and Apple, S.H. Mutant mice (quaking and jimpy) with deficient myelination in the central nervous system. Science 144, 309-312, 1964.
– reference: 26) Takakura, N., Huang, X.-L., Naruse, T., Hamaguchi, I., Dumont, D.J., Yancopoulos, G.D. and Suda, T. Critical role of the TIE2 endothelial receptor in the development of definitive hematopoiesis. Immunity 9, 677-686, 1998.
– reference: 7) Kondo, T., Furuta, T., Mitsunaga, K., Ebersole, T.A., Shichiri, M., Wu, J., Artzt, K., Yamamura, K. and Abe, K. Genomic organization and expression analysis of the mouse qkI locus. Mamm. Genome 10, 662-669, 1999.
– reference: 12) Chrivia, J.C., Kwok, R.P.S., Lamb, N., Hagiwara, M., Montominy, M.R. and Goodman, R.H. Phosphorylated CREB binds specifically to the nuclear protein CBP. Nature, 365, 855-859, 1993.
– reference: 20) Tanaka, Y., Naruse, I., Maekawa, T., Masuya, H., Shiroishi, T. and Ishii, S. Abnormal skeletal patterning in embryos lacking a single Cbp allele: a partial similarity with Rubinstein-Taybi syndrome. Proc. Natl. Acad. Sci. USA, 94, 10215-10220, 1997.
– reference: 17) Dai, P., Akimura, H., Tanaka, Y., Hou, D., Yasukawa, T., Kanei-Ishii, C., Takahashi, T. and Ishii, S. CBP as a transcriptional coactivator of c-Myb. Genes Dev., 10, 528-540, 1996.
– reference: 21) Visvader, J.E., Fujiwara, Y. and Orkin, S.H. Unsuspected role for the T-cell leukemia protein SCL/tal-1 in vascular development. Genes Dev. 12, 473-479, 1998.
– reference: 14) Kwok, R.P.S., Lundblad, J.R., Chrivia, J.C., Richards, J.P., Bachinger, H.P., Brennan, R.G., Roberts, S.G.E., Green, M.R. and Goodman, R.H. Nuclear protein CBP is a coactivator for the transcription factor CREB. Nature, 370, 223-226, 1994.
– reference: 19) Chakravarti, D., Lamorte, V.J., Nelson, M.C., Nakajima, T., Schulman, I.G., Juguilon, H., Montominy, M. and Evans, R.M. Role of CBP/P300 in nuclear receptor signalling. Nature, 383, 99-103, 1996.
– reference: 9) Hardy, R.J. Molecular defects in the dysmyelinating mutant quaking. J. Neurosci. Res. 51, 417-422, 1998.
– reference: 5) Justice, M.J. and Bode, V.C. Three ENU-induced alleles of the murine quaking locus are recessive embryonic lethal mutations. Genet. Res. 51, 95-102, 1988.
– reference: 6) Ebersole, T.A., Chen, Q., Justice, M.J. and Artzt, K. The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteins. Nat. Genet. 12, 260-265, 1996.
– reference: 15) Bannister, A.J. and Kouzarides, T. CBP-induced stimulation of c-Fos activity is abrogated by Ela. EMBO J., 14, 4758-4762, 1995.
– reference: 4) Bode, C.V. Ethylnitrosourea mutagenesis and the isolation of mutant alleles for specific genes located in the T region of mouse chromosome 17. Genetics 108, 457-470, 1984.
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Title 3.ミエリン欠損モデルマウスの病因病態解析
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