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Volumn 34, Issue 1, 2009, Pages 71-77

Evidence for both neuronal cell autonomous and nonautonomous effects of methyl-CpG-binding protein 2 in the cerebral cortex of female mice with Mecp2 mutation

Author keywords

Brain; MeCP2; Morphometry; Motor cortex; Mouse models; Rett syndrome; Spines

Indexed keywords

GREEN FLUORESCENT PROTEIN; METHYL CPG BINDING PROTEIN 2;

EID: 62149119249     PISSN: 09699961     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nbd.2008.12.016     Document Type: Article
Times cited : (64)

References (36)
  • 1
    • 0032830639 scopus 로고    scopus 로고
    • Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
    • Amir R.E., Van den Veyver I.B., Wan M., Tran C.Q., Francke U., and Zoghbi H.Y. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat. Genet. 23 (1999) 185-188
    • (1999) Nat. Genet. , vol.23 , pp. 185-188
    • Amir, R.E.1    Van den Veyver, I.B.2    Wan, M.3    Tran, C.Q.4    Francke, U.5    Zoghbi, H.Y.6
  • 2
    • 0026771999 scopus 로고
    • The neuropathology of the Rett syndrome
    • Armstrong D.D. The neuropathology of the Rett syndrome. Brain Dev. 14 Suppl (1992) S89-S98
    • (1992) Brain Dev. , vol.14 SUPPL
    • Armstrong, D.D.1
  • 3
    • 27144534968 scopus 로고    scopus 로고
    • Neuropathology of Rett syndrome
    • Armstrong D.D. Neuropathology of Rett syndrome. J. Child Neurol. 20 (2005) 747-753
    • (2005) J. Child Neurol. , vol.20 , pp. 747-753
    • Armstrong, D.D.1
  • 6
    • 0007679559 scopus 로고
    • Mapping of the Human Brain in normal and pathology: the single cell and fiber level, employing Lucifer Yellow microinjection, carbocyanine dyes tracing, immunofluorescence, and 3-D confocal laser scanning reconstruction
    • Belichenko P.V., and Dahlström A. Mapping of the Human Brain in normal and pathology: the single cell and fiber level, employing Lucifer Yellow microinjection, carbocyanine dyes tracing, immunofluorescence, and 3-D confocal laser scanning reconstruction. Neurosci. Protocol. 50 3 (1995) 1-30
    • (1995) Neurosci. Protocol. , vol.50 , Issue.3 , pp. 1-30
    • Belichenko, P.V.1    Dahlström, A.2
  • 7
    • 0027963287 scopus 로고
    • Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents
    • Belichenko P.V., Oldfors A., Hagberg B., and Dahlstrom A. Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents. NeuroReport 5 (1994) 1509-1513
    • (1994) NeuroReport , vol.5 , pp. 1509-1513
    • Belichenko, P.V.1    Oldfors, A.2    Hagberg, B.3    Dahlstrom, A.4
  • 8
    • 0030639079 scopus 로고    scopus 로고
    • Morphological study of neocortical areas in Rett syndrome
    • Belichenko P.V., Hagberg B., and Dahlstrom A. Morphological study of neocortical areas in Rett syndrome. Acta Neuropathol. 93 (1997) 50-61
    • (1997) Acta Neuropathol. , vol.93 , pp. 50-61
    • Belichenko, P.V.1    Hagberg, B.2    Dahlstrom, A.3
  • 10
    • 42149127627 scopus 로고    scopus 로고
    • Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome
    • Belichenko N.P., Belichenko P.V., Li H.H., Mobley W.C., and Francke U. Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome. J. Comp. Neurol. 508 (2008) 184-195
    • (2008) J. Comp. Neurol. , vol.508 , pp. 184-195
    • Belichenko, N.P.1    Belichenko, P.V.2    Li, H.H.3    Mobley, W.C.4    Francke, U.5
  • 11
    • 45849105557 scopus 로고    scopus 로고
    • MeCP2, a key contributor to neurological disease, activates and represses transcription
    • Chahrour M., Jung S.Y., Shaw C., Zhou X., Wong S.T., Qin J., and Zoghbi H.Y. MeCP2, a key contributor to neurological disease, activates and represses transcription. Science 320 (2008) 1224-1229
    • (2008) Science , vol.320 , pp. 1224-1229
    • Chahrour, M.1    Jung, S.Y.2    Shaw, C.3    Zhou, X.4    Wong, S.T.5    Qin, J.6    Zoghbi, H.Y.7
  • 12
    • 0035093830 scopus 로고    scopus 로고
    • Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
    • Chen R.Z., Akbarian S., Tudor M., and Jaenisch R. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nat. Genet. 27 (2001) 327-331
    • (2001) Nat. Genet. , vol.27 , pp. 327-331
    • Chen, R.Z.1    Akbarian, S.2    Tudor, M.3    Jaenisch, R.4
  • 13
    • 2942657302 scopus 로고    scopus 로고
    • Altered regulation of brain-derived neurotrophic factor protein in hippocampus following slice preparation
    • Danzer S.C., Pan E., Nef S., Parada L.F., and McNamara J.O. Altered regulation of brain-derived neurotrophic factor protein in hippocampus following slice preparation. Neuroscience 126 (2004) 859-869
    • (2004) Neuroscience , vol.126 , pp. 859-869
    • Danzer, S.C.1    Pan, E.2    Nef, S.3    Parada, L.F.4    McNamara, J.O.5
  • 15
    • 0036082812 scopus 로고    scopus 로고
    • Dendritic spine pathology: cause or consequence of neurological disorders?
    • Fiala J.C., Spacek J., and Harris K.M. Dendritic spine pathology: cause or consequence of neurological disorders?. Brain Res. Brain Res. Rev. 39 (2002) 29-54
    • (2002) Brain Res. Brain Res. Rev. , vol.39 , pp. 29-54
    • Fiala, J.C.1    Spacek, J.2    Harris, K.M.3
  • 16
    • 0035094767 scopus 로고    scopus 로고
    • A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
    • Guy J., Hendrich B., Holmes M., Martin J.E., and Bird A. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat. Genet. 27 (2001) 322-326
    • (2001) Nat. Genet. , vol.27 , pp. 322-326
    • Guy, J.1    Hendrich, B.2    Holmes, M.3    Martin, J.E.4    Bird, A.5
  • 17
    • 0024516981 scopus 로고
    • Rett syndrome: clinical peculiarities, diagnostic approach, and possible cause
    • Hagberg B.A. Rett syndrome: clinical peculiarities, diagnostic approach, and possible cause. Pediatr. Neurol. 5 (1989) 75-83
    • (1989) Pediatr. Neurol. , vol.5 , pp. 75-83
    • Hagberg, B.A.1
  • 18
    • 0029111944 scopus 로고
    • Rett syndrome: clinical peculiarities and biological mysteries
    • Hagberg B. Rett syndrome: clinical peculiarities and biological mysteries. Acta Paediatr. 84 (1995) 971-976
    • (1995) Acta Paediatr. , vol.84 , pp. 971-976
    • Hagberg, B.1
  • 19
    • 0020507697 scopus 로고
    • A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases
    • Hagberg B., Aicardi J., Dias K., and Ramos O. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases. Ann. Neurol. 14 (1983) 471-479
    • (1983) Ann. Neurol. , vol.14 , pp. 471-479
    • Hagberg, B.1    Aicardi, J.2    Dias, K.3    Ramos, O.4
  • 21
    • 34547118571 scopus 로고    scopus 로고
    • Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets
    • Jordan C., Li H.H., Kwan H.C., and Francke U. Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets. BMC Med .Genet. 8 (2007) 36
    • (2007) BMC Med .Genet. , vol.8 , pp. 36
    • Jordan, C.1    Li, H.H.2    Kwan, H.C.3    Francke, U.4
  • 23
    • 0033797735 scopus 로고    scopus 로고
    • Dendritic anomalies in disorders associated with mental retardation
    • Kaufmann W.E., and Moser H.W. Dendritic anomalies in disorders associated with mental retardation. Cereb. Cortex 10 (2000) 981-991
    • (2000) Cereb. Cortex , vol.10 , pp. 981-991
    • Kaufmann, W.E.1    Moser, H.W.2
  • 24
    • 0032932691 scopus 로고    scopus 로고
    • Morphological study of the entorhinal cortex, hippocampal formation, and basal ganglia in Rett syndrome patients
    • Leontovich T.A., Mukhina J.K., Fedorov A.A., and Belichenko P.V. Morphological study of the entorhinal cortex, hippocampal formation, and basal ganglia in Rett syndrome patients. Neurobiol. Dis. 6 (1999) 77-91
    • (1999) Neurobiol. Dis. , vol.6 , pp. 77-91
    • Leontovich, T.A.1    Mukhina, J.K.2    Fedorov, A.A.3    Belichenko, P.V.4
  • 25
    • 0028858681 scopus 로고
    • Neurotrophins regulate dendritic growth in developing visual cortex
    • McAllister A.K., Lo D.C., and Katz L.C. Neurotrophins regulate dendritic growth in developing visual cortex. Neuron 15 (1995) 791-803
    • (1995) Neuron , vol.15 , pp. 791-803
    • McAllister, A.K.1    Lo, D.C.2    Katz, L.C.3
  • 26
    • 33646164398 scopus 로고    scopus 로고
    • Temporal shift in methyl-CpG binding protein 2 expression in a mouse model of Rett syndrome
    • Metcalf B.M., Mullaney B.C., Johnston M.V., and Blue M.E. Temporal shift in methyl-CpG binding protein 2 expression in a mouse model of Rett syndrome. Neuroscience 139 (2006) 1449-1460
    • (2006) Neuroscience , vol.139 , pp. 1449-1460
    • Metcalf, B.M.1    Mullaney, B.C.2    Johnston, M.V.3    Blue, M.E.4
  • 27
    • 33745890228 scopus 로고    scopus 로고
    • TrkB binds and tyrosine-phosphorylates Tiam1, leading to activation of Rac1 and induction of changes in cellular morphology
    • Miyamoto Y., Yamauchi J., Tanoue A., Wu C., and Mobley W.C. TrkB binds and tyrosine-phosphorylates Tiam1, leading to activation of Rac1 and induction of changes in cellular morphology. Proc. Natl. Acad. Sci. U. S. A. 103 (2006) 10444-10449
    • (2006) Proc. Natl. Acad. Sci. U. S. A. , vol.103 , pp. 10444-10449
    • Miyamoto, Y.1    Yamauchi, J.2    Tanoue, A.3    Wu, C.4    Mobley, W.C.5
  • 28
    • 27144431761 scopus 로고    scopus 로고
    • Natural history of Rett syndrome
    • Nomura Y., and Segawa M. Natural history of Rett syndrome. J Child Neurol. 20 (2005) 764-768
    • (2005) J Child Neurol. , vol.20 , pp. 764-768
    • Nomura, Y.1    Segawa, M.2
  • 29
    • 58549109636 scopus 로고    scopus 로고
    • X chromosome dosage compensation: how mammals keep the balance
    • Payer B., and Lee J.T. X chromosome dosage compensation: how mammals keep the balance. Annu. Rev. Genet. 42 (2008) 733-772
    • (2008) Annu. Rev. Genet. , vol.42 , pp. 733-772
    • Payer, B.1    Lee, J.T.2
  • 30
    • 0036829488 scopus 로고    scopus 로고
    • Rett syndrome. Current status and new vistas
    • Percy A.K. Rett syndrome. Current status and new vistas. Neurol. Clin. 20 (2002) 1125-1141
    • (2002) Neurol. Clin. , vol.20 , pp. 1125-1141
    • Percy, A.K.1
  • 31
    • 42449108258 scopus 로고    scopus 로고
    • Rett syndrome: recent research progress
    • Percy A.K. Rett syndrome: recent research progress. J. Child Neurol. 23 (2008) 543-549
    • (2008) J. Child Neurol. , vol.23 , pp. 543-549
    • Percy, A.K.1
  • 32
    • 0035234670 scopus 로고    scopus 로고
    • Neurotrophins as synaptic modulators
    • Poo M.M. Neurotrophins as synaptic modulators. Nat. Rev., Neurosci. 2 (2001) 24-32
    • (2001) Nat. Rev., Neurosci. , vol.2 , pp. 24-32
    • Poo, M.M.1
  • 33
    • 0014011176 scopus 로고
    • [On a unusual brain atrophy syndrome in hyperammonemia in childhood]
    • Rett A. [On a unusual brain atrophy syndrome in hyperammonemia in childhood]. Wien. Med. Wochenschr. 116 (1966) 723-726
    • (1966) Wien. Med. Wochenschr. , vol.116 , pp. 723-726
    • Rett, A.1
  • 35
    • 33750941251 scopus 로고    scopus 로고
    • Dysregulation of brain-derived neurotrophic factor expression and neurosecretory function in Mecp2 null mice
    • Wang H., Chan S.A., Ogier M., Hellard D., Wang Q., Smith C., and Katz D.M. Dysregulation of brain-derived neurotrophic factor expression and neurosecretory function in Mecp2 null mice. J. Neurosci. 26 (2006) 10911-10915
    • (2006) J. Neurosci. , vol.26 , pp. 10911-10915
    • Wang, H.1    Chan, S.A.2    Ogier, M.3    Hellard, D.4    Wang, Q.5    Smith, C.6    Katz, D.M.7
  • 36
    • 1542344372 scopus 로고    scopus 로고
    • X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of Rett syndrome
    • Young J.I., and Zoghbi H.Y. X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of Rett syndrome. Am. J. Hum. Genet. 74 (2004) 511-520
    • (2004) Am. J. Hum. Genet. , vol.74 , pp. 511-520
    • Young, J.I.1    Zoghbi, H.Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.