메뉴 건너뛰기




Volumn 52, Issue 8, 2011, Pages 5933-5940

Altered Expression of the Transcription Factor Mef2c during Retinal Degeneration in Rpe65 -/- Mice

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; MYOCYTE ENHANCER FACTOR 2; MYOCYTE ENHANCER FACTOR 2C; OPSIN; RHODOPSIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR NR2E3; TRANSCRIPTION FACTOR NRL; TRANSDUCIN; UNCLASSIFIED DRUG; BASIC LEUCINE ZIPPER TRANSCRIPTION FACTOR; CARRIER PROTEIN; EYE PROTEIN; MEF2C PROTEIN, MOUSE; MYOGENIC FACTOR; NR2E3 PROTEIN, MOUSE; NRL PROTEIN, MOUSE; ORPHAN NUCLEAR RECEPTOR; RPE65 PROTEIN, MOUSE;

EID: 80053328408     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.10-6978     Document Type: Article
Times cited : (8)

References (51)
  • 1
    • 33747664256 scopus 로고    scopus 로고
    • Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene
    • El Matri L, Ambresin A, Schorderet DF, et al. Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene. Graefes Arch Clin Exp Ophthalmol. 2006;244:1104-1112.
    • (2006) Graefes Arch Clin Exp Ophthalmol. , vol.244 , pp. 1104-1112
    • El Matri, L.1    Ambresin, A.2    Schorderet, D.F.3
  • 2
    • 20944447776 scopus 로고    scopus 로고
    • Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success
    • Jacobson SG, Aleman TS, Cideciyan AV, et al. Identifying photoreceptors in blind eyes caused by RPE65 mutations: prerequisite for human gene therapy success. Proc Natl Acad Sci U S A. 2005;102: 6177-6182.
    • (2005) Proc Natl Acad Sci U S A. , vol.102 , pp. 6177-6182
    • Jacobson, S.G.1    Aleman, T.S.2    Cideciyan, A.V.3
  • 3
    • 23744447355 scopus 로고    scopus 로고
    • Rpe65 is the retinoid isomerase in bovine retinal pigment epithelium
    • Jin M, Li S, Moghrabi WN, Sun H, Travis GH. Rpe65 is the retinoid isomerase in bovine retinal pigment epithelium. Cell. 2005;122: 449-459.
    • (2005) Cell. , vol.122 , pp. 449-459
    • Jin, M.1    Li, S.2    Moghrabi, W.N.3    Sun, H.4    Travis, G.H.5
  • 5
    • 33646353950 scopus 로고    scopus 로고
    • RPE65 is an iron(II)-dependent isomerohydrolase in the retinoid visual cycle
    • Moiseyev G, Takahashi Y, Chen Y, et al. RPE65 is an iron(II)-dependent isomerohydrolase in the retinoid visual cycle. J Biol Chem. 2006;281:2835-2840.
    • (2006) J Biol Chem. , vol.281 , pp. 2835-2840
    • Moiseyev, G.1    Takahashi, Y.2    Chen, Y.3
  • 6
    • 17344366357 scopus 로고    scopus 로고
    • Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle
    • Redmond TM, Yu S, Lee E, et al. Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle. Nat Genet. 1998;20: 344-351.
    • (1998) Nat Genet. , vol.20 , pp. 344-351
    • Redmond, T.M.1    Yu, S.2    Lee, E.3
  • 7
    • 13444271841 scopus 로고    scopus 로고
    • Clinical phenotypes in carriers of Leber congenital amaurosis mutations
    • Galvin J, Fishman G, Stone E, Koenekoop R. Clinical phenotypes in carriers of Leber congenital amaurosis mutations. Ophthalmology. 2005;112:349-356.
    • (2005) Ophthalmology. , vol.112 , pp. 349-356
    • Galvin, J.1    Fishman, G.2    Stone, E.3    Koenekoop, R.4
  • 8
    • 17944379443 scopus 로고    scopus 로고
    • New views on RPE65 deficiency: The rod system is the source of vision in a mouse model of Leber congenital amaurosis
    • Seeliger M, Grimm C, Stahlberg F, et al. New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis. Nat Genet. 2001;29:70-74.
    • (2001) Nat Genet. , vol.29 , pp. 70-74
    • Seeliger, M.1    Grimm, C.2    Stahlberg, F.3
  • 9
    • 0141707934 scopus 로고    scopus 로고
    • Spontaneous activity of opsin apoprotein is a cause of Leber congenital amaurosis
    • Woodruff ML, Wang Z, Chung HY, Redmond TM, Fain GL, Lem J. Spontaneous activity of opsin apoprotein is a cause of Leber congenital amaurosis. Nat Genet. 2003;35:158-164.
    • (2003) Nat Genet. , vol.35 , pp. 158-164
    • Woodruff, M.L.1    Wang, Z.2    Chung, H.Y.3    Redmond, T.M.4    Fain, G.L.5    Lem, J.6
  • 10
    • 68949164901 scopus 로고    scopus 로고
    • Bax-induced apoptosis in Leber's congenital amaurosis: A dual role in rod and cone degeneration
    • Hamann S, Schorderet DF, Cottet S. Bax-induced apoptosis in Leber's congenital amaurosis: a dual role in rod and cone degeneration. PLoS ONE. 2009;4:e6616.
    • (2009) PLoS ONE. , vol.4
    • Hamann, S.1    Schorderet, D.F.2    Cottet, S.3
  • 11
    • 0032437107 scopus 로고    scopus 로고
    • Transcriptional control of muscle development by myocyte enhancer factor-2 (MEF2) proteins
    • Black BL, Olson EN. Transcriptional control of muscle development by myocyte enhancer factor-2 (MEF2) proteins. Annu Rev Cell Dev Biol. 1998;14:167-196.
    • (1998) Annu Rev Cell Dev Biol. , vol.14 , pp. 167-196
    • Black, B.L.1    Olson, E.N.2
  • 12
    • 38049147787 scopus 로고    scopus 로고
    • MEF2: A central regulator of diverse developmental programs
    • Potthoff MJ, Olson EN. MEF2: a central regulator of diverse developmental programs. Development. 2007;134:4131-4140.
    • (2007) Development. , vol.134 , pp. 4131-4140
    • Potthoff, M.J.1    Olson, E.N.2
  • 13
    • 0029994419 scopus 로고    scopus 로고
    • Mutational analysis of the DNA binding, dimerization, and transcriptional activation domains of MEF2C
    • Molkentin JD, Black BL, Martin JF, Olson EN. Mutational analysis of the DNA binding, dimerization, and transcriptional activation domains of MEF2C. Mol Cell Biol. 1996;16:2627-2636.
    • (1996) Mol Cell Biol. , vol.16 , pp. 2627-2636
    • Molkentin, J.D.1    Black, B.L.2    Martin, J.F.3    Olson, E.N.4
  • 14
    • 0030911475 scopus 로고    scopus 로고
    • Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C
    • Lin Q, Schwarz J, Bucana C, Olson EN. Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C. Science. 1997;276:1404-1407.
    • (1997) Science. , vol.276 , pp. 1404-1407
    • Lin, Q.1    Schwarz, J.2    Bucana, C.3    Olson, E.N.4
  • 15
    • 0141449169 scopus 로고    scopus 로고
    • mef2c is activated directly by myogenic basic helix-loop-helix proteins during skeletal muscle development in vivo
    • Dodou E, Xu S-M, Black BL. mef2c is activated directly by myogenic basic helix-loop-helix proteins during skeletal muscle development in vivo. Mech Dev. 2003;120:1021-1032.
    • (2003) Mech Dev. , vol.120 , pp. 1021-1032
    • Dodou, E.1    Xu, S.-M.2    Black, B.L.3
  • 16
    • 20044377250 scopus 로고    scopus 로고
    • Transgenic mice that express Cre recombinase under control of a skeletal muscle-specific promoter from mef2c
    • Heidt AB, Black BL. Transgenic mice that express Cre recombinase under control of a skeletal muscle-specific promoter from mef2c. Genesis. 2005;42:28-32.
    • (2005) Genesis. , vol.42 , pp. 28-32
    • Heidt, A.B.1    Black, B.L.2
  • 17
    • 0027243922 scopus 로고
    • Myocyte enhancer factor (MEF) 2C: A tissue-restricted member of the MEF-2 family of transcription factors
    • Martin JF, Schwarz JJ, Olson EN. Myocyte enhancer factor (MEF) 2C: a tissue-restricted member of the MEF-2 family of transcription factors. Proc Natl Acad Sci U S A. 1993;90:5282-5286.
    • (1993) Proc Natl Acad Sci U S A. , vol.90 , pp. 5282-5286
    • Martin, J.F.1    Schwarz, J.J.2    Olson, E.N.3
  • 18
    • 0028279115 scopus 로고
    • Mef2 gene expression marks the cardiac and skeletal muscle lineages during mouse embryogenesis
    • Edmondson DG, Lyons GE, Martin JF, Olson EN. Mef2 gene expression marks the cardiac and skeletal muscle lineages during mouse embryogenesis. Development. 1994;120:1251-1263.
    • (1994) Development. , vol.120 , pp. 1251-1263
    • Edmondson, D.G.1    Lyons, G.E.2    Martin, J.F.3    Olson, E.N.4
  • 19
    • 0029085629 scopus 로고
    • Expression of mef2 genes in the mouse central nervous system suggests a role in neuronal maturation
    • Lyons GE, Micales BK, Schwarz J, Martin JF, Olson EN. Expression of mef2 genes in the mouse central nervous system suggests a role in neuronal maturation. J Neurosci. 1995;15:5727-5738.
    • (1995) J Neurosci. , vol.15 , pp. 5727-5738
    • Lyons, G.E.1    Micales, B.K.2    Schwarz, J.3    Martin, J.F.4    Olson, E.N.5
  • 20
    • 3142705929 scopus 로고    scopus 로고
    • Myocyte enhancer factor-2 transcription factors in neuronal differentiation and survival
    • Heidenreich KA, Linseman DA. Myocyte enhancer factor-2 transcription factors in neuronal differentiation and survival. Mol Neurobiol. 2004;29:155-166.
    • (2004) Mol Neurobiol. , vol.29 , pp. 155-166
    • Heidenreich, K.A.1    Linseman, D.A.2
  • 21
    • 0027409049 scopus 로고
    • MEF2C, a MADS/MEF2-family transcription factor expressed in a laminar distribution in cerebral cortex
    • Leifer D, Krainc D, Yu YT, et al. MEF2C, a MADS/MEF2-family transcription factor expressed in a laminar distribution in cerebral cortex. Proc Natl Acad Sci U S A. 1993;90:1546-1550.
    • (1993) Proc Natl Acad Sci U S A. , vol.90 , pp. 1546-1550
    • Leifer, D.1    Krainc, D.2    Yu, Y.T.3
  • 22
    • 48249090873 scopus 로고    scopus 로고
    • Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo
    • Li H, Radford JC, Ragusa MJ, et al. Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo. Proc Natl Acad Sci U S A. 2008;105:9397-9402.
    • (2008) Proc Natl Acad Sci U S A. , vol.105 , pp. 9397-9402
    • Li, H.1    Radford, J.C.2    Ragusa, M.J.3
  • 23
    • 0033595764 scopus 로고    scopus 로고
    • Neuronal activity-dependent cell survival mediated by transcription factor MEF2
    • Mao Z, Bonni A, Xia F, Nadal-Vicens M, Greenberg ME. Neuronal activity-dependent cell survival mediated by transcription factor MEF2. Science. 1999;286:785-790.
    • (1999) Science. , vol.286 , pp. 785-790
    • Mao, Z.1    Bonni, A.2    Xia, F.3    Nadal-Vicens, M.4    Greenberg, M.E.5
  • 24
    • 70450257883 scopus 로고    scopus 로고
    • A novel microdeletion syndrome involving 5q14.3-q15: Clinical and molecular cytogenetic characterization of three patients
    • Engels H, Wohlleber E, Zink A, et al. A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients. Eur J Hum Genet. 2009;17: 1592-1599.
    • (2009) Eur J Hum Genet. , vol.17 , pp. 1592-1599
    • Engels, H.1    Wohlleber, E.2    Zink, A.3
  • 25
    • 74549139226 scopus 로고    scopus 로고
    • MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations
    • Le Meur N, Holder-Espinasse M, Jaillard S, et al. MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations. J Med Genet. 2010;47:22-29.
    • (2010) J Med Genet. , vol.47 , pp. 22-29
    • le Meur, N.1    Holder-Espinasse, M.2    Jaillard, S.3
  • 26
    • 77957555139 scopus 로고    scopus 로고
    • Refining the phenotype associated with MEF2C haploinsufficiency
    • Novara F, Beri S, Giorda R, et al. Refining the phenotype associated with MEF2C haploinsufficiency. Clin Genet. 2010;78:471-477.
    • (2010) Clin Genet. , vol.78 , pp. 471-477
    • Novara, F.1    Beri, S.2    Giorda, R.3
  • 27
    • 77952715676 scopus 로고    scopus 로고
    • Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression
    • Zweier M, Gregor A, Zweier C, et al. Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression. Hum Mutat. 2010;31:722-733.
    • (2010) Hum Mutat. , vol.31 , pp. 722-733
    • Zweier, M.1    Gregor, A.2    Zweier, C.3
  • 29
    • 0036501462 scopus 로고    scopus 로고
    • Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice
    • Kennan A, Aherne A, Palfi A, et al. Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice. Hum Mol Genet. 2002;11:547-557.
    • (2002) Hum Mol Genet. , vol.11 , pp. 547-557
    • Kennan, A.1    Aherne, A.2    Palfi, A.3
  • 31
    • 3543082672 scopus 로고    scopus 로고
    • -/- mouse retina: Identification of retinal disease candidates and transcriptional regulatory targets of Nrl
    • -/- mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl. Hum Mol Genet. 2004;13:1487-1503.
    • (2004) Hum Mol Genet. , vol.13 , pp. 1487-1503
    • Yoshida, S.1    Mears, A.J.2    Friedman, J.S.3
  • 32
    • 0031788318 scopus 로고    scopus 로고
    • Differential expression of peroxisome proliferator-activated receptor-alpha,-beta, and-gamma during rat embryonic development
    • Braissant O, Wahli W. Differential expression of peroxisome proliferator-activated receptor-alpha,-beta, and-gamma during rat embryonic development. Endocrinology. 1998;139:2748-2754.
    • (1998) Endocrinology. , vol.139 , pp. 2748-2754
    • Braissant, O.1    Wahli, W.2
  • 33
    • 15544371180 scopus 로고    scopus 로고
    • The photoreceptorspecific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes
    • Peng G-H, Ahmad O, Ahmad F, Liu J, Chen S. The photoreceptorspecific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes. Hum Mol Genet. 2005;14:747-764.
    • (2005) Hum Mol Genet. , vol.14 , pp. 747-764
    • Peng, G.-H.1    Ahmad, O.2    Ahmad, F.3    Liu, J.4    Chen, S.5
  • 34
    • 33646942503 scopus 로고    scopus 로고
    • Myocyte enhancer factors 2A and 2C induce dilated cardiomyopathy in transgenic mice
    • Xu J, Gong NL, Bodi I, Aronow BJ, Backx PH, Molkentin JD. Myocyte enhancer factors 2A and 2C induce dilated cardiomyopathy in transgenic mice. J Biol Chem. 2006;281:9152-9162.
    • (2006) J Biol Chem. , vol.281 , pp. 9152-9162
    • Xu, J.1    Gong, N.L.2    Bodi, I.3    Aronow, B.J.4    Backx, P.H.5    Molkentin, J.D.6
  • 35
    • 61649107865 scopus 로고    scopus 로고
    • Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family
    • Escher P, Gouras P, Roduit R, et al. Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family. Hum Mutat. 2009;30:342-351.
    • (2009) Hum Mutat. , vol.30 , pp. 342-351
    • Escher, P.1    Gouras, P.2    Roduit, R.3
  • 36
    • 70350716547 scopus 로고    scopus 로고
    • Mutations in the DNA-binding domain of NR2E3 affect in vivo dimerization and interaction with CRX
    • Roduit R, Escher P, Schorderet DF. Mutations in the DNA-binding domain of NR2E3 affect in vivo dimerization and interaction with CRX. PloS ONE. 2009;4:e7379.
    • (2009) PloS ONE. , vol.4
    • Roduit, R.1    Escher, P.2    Schorderet, D.F.3
  • 37
    • 0030064117 scopus 로고    scopus 로고
    • The basic motif-leucine zipper transcription factor Nrl can positively regulate rhodopsin gene expression
    • Rehemtulla A, Warwar R, Kumar R, Ji X, Zack DJ, Swaroop A. The basic motif-leucine zipper transcription factor Nrl can positively regulate rhodopsin gene expression. Proc Natl Acad Sci U S A. 1996;93:191-195.
    • (1996) Proc Natl Acad Sci U S A. , vol.93 , pp. 191-195
    • Rehemtulla, A.1    Warwar, R.2    Kumar, R.3    Ji, X.4    Zack, D.J.5    Swaroop, A.6
  • 38
    • 0035860776 scopus 로고    scopus 로고
    • Nrl and Sp nuclear proteins mediate transcription of rod-specific cGMP-phosphodiesterase beta-subunit gene: Involvement of multiple response elements
    • Lerner LE, Gribanova YE, Ji M, Knox BE, Farber DB. Nrl and Sp nuclear proteins mediate transcription of rod-specific cGMP-phosphodiesterase beta-subunit gene: involvement of multiple response elements. J Biol Chem. 2001;276:34999-35007.
    • (2001) J Biol Chem. , vol.276 , pp. 34999-35007
    • Lerner, L.E.1    Gribanova, Y.E.2    Ji, M.3    Knox, B.E.4    Farber, D.B.5
  • 39
    • 2442425295 scopus 로고    scopus 로고
    • Functional analysis of the rod photoreceptor cGMP phosphodiesterase alpha-subunit gene promoter: Nrl and Crx are required for full transcriptional activity
    • Pittler SJ, Zhang Y, Chen S, et al. Functional analysis of the rod photoreceptor cGMP phosphodiesterase alpha-subunit gene promoter: Nrl and Crx are required for full transcriptional activity. J Biol Chem. 2004;279:19800-19807.
    • (2004) J Biol Chem. , vol.279 , pp. 19800-19807
    • Pittler, S.J.1    Zhang, Y.2    Chen, S.3
  • 40
    • 48649108204 scopus 로고    scopus 로고
    • Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors
    • Oh EC, Cheng H, Hao H, Jia L, Khan NW, Swaroop A. Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors. Brain Res. 2008;1236:16-29.
    • (2008) Brain Res. , vol.1236 , pp. 16-29
    • Oh, E.C.1    Cheng, H.2    Hao, H.3    Jia, L.4    Khan, N.W.5    Swaroop, A.6
  • 41
    • 78649986068 scopus 로고    scopus 로고
    • Neural retina leucine-zipper regulates the expression of Ppp2r5c, the regulatory subunit of protein phosphatase 2A, in photoreceptor development
    • Kim JW, Jang SM, Kim CH, An JH, Kang EJ, Choi KH. Neural retina leucine-zipper regulates the expression of Ppp2r5c, the regulatory subunit of protein phosphatase 2A, in photoreceptor development. FEBS Lett J. 2010;277:5151-5160.
    • (2010) FEBS Lett J. , vol.277 , pp. 5151-5160
    • Kim, J.W.1    Jang, S.M.2    Kim, C.H.3    An, J.H.4    Kang, E.J.5    Choi, K.H.6
  • 42
    • 0030725687 scopus 로고    scopus 로고
    • Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation
    • Furukawa T, Morrow EM, Cepko CL. Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation. Cell. 1997;91:531-541.
    • (1997) Cell. , vol.91 , pp. 531-541
    • Furukawa, T.1    Morrow, E.M.2    Cepko, C.L.3
  • 44
    • 0035977135 scopus 로고    scopus 로고
    • Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes
    • Blackshaw S, Fraioli RE, Furukawa T, Cepko CL. Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes. Cell. 2001;107:579-589.
    • (2001) Cell. , vol.107 , pp. 579-589
    • Blackshaw, S.1    Fraioli, R.E.2    Furukawa, T.3    Cepko, C.L.4
  • 45
    • 0035734382 scopus 로고    scopus 로고
    • Nrl is required for rod photoreceptor development
    • Mears AJ, Kondo M, Swain PK, et al. Nrl is required for rod photoreceptor development. Nat Genet. 2001;29:447-452.
    • (2001) Nat Genet. , vol.29 , pp. 447-452
    • Mears, A.J.1    Kondo, M.2    Swain, P.K.3
  • 46
    • 79952385781 scopus 로고    scopus 로고
    • Nuclear receptor Rev-erb alpha (Nr1d1) functions in concert with Nr2e3 to regulate transcriptional networks in the retina
    • Mollema NJ, Yuan Y, Jelcick AS, et al. Nuclear receptor Rev-erb alpha (Nr1d1) functions in concert with Nr2e3 to regulate transcriptional networks in the retina. PLoS ONE. 2011;6: e17494.
    • (2011) PLoS ONE. , vol.6
    • Mollema, N.J.1    Yuan, Y.2    Jelcick, A.S.3
  • 47
    • 0035203948 scopus 로고    scopus 로고
    • The Mef2c gene is a direct transcriptional target of myogenic bHLH and MEF2 proteins during skeletal muscle development
    • Wang DZ, Valdez MR, McAnally J, Richardson J, Olson EN. The Mef2c gene is a direct transcriptional target of myogenic bHLH and MEF2 proteins during skeletal muscle development. Development. 2001;128:4623-4633.
    • (2001) Development. , vol.128 , pp. 4623-4633
    • Wang, D.Z.1    Valdez, M.R.2    McAnally, J.3    Richardson, J.4    Olson, E.N.5
  • 48
    • 0034671652 scopus 로고    scopus 로고
    • Myocyte enhancer factors-2B and-2C are required for adhesion related kinase repression of neuronal gonadotropin releasing hormone gene expression
    • Allen MP, Xu M, Zeng C, Tobet SA, Wierman ME. Myocyte enhancer factors-2B and-2C are required for adhesion related kinase repression of neuronal gonadotropin releasing hormone gene expression. J Biol Chem. 2000;275:39662-39670.
    • (2000) J Biol Chem. , vol.275 , pp. 39662-39670
    • Allen, M.P.1    Xu, M.2    Zeng, C.3    Tobet, S.A.4    Wierman, M.E.5
  • 49
    • 44849094592 scopus 로고    scopus 로고
    • Myocyte enhancer factor 2A is transcriptionally autoregulated
    • Ramachandran B, Yu G, Li S, Zhu B, Gulick T. Myocyte enhancer factor 2A is transcriptionally autoregulated. J Biol Chem. 2008;283:10318-10329.
    • (2008) J Biol Chem. , vol.283 , pp. 10318-10329
    • Ramachandran, B.1    Yu, G.2    Li, S.3    Zhu, B.4    Gulick, T.5
  • 50
    • 33144473786 scopus 로고    scopus 로고
    • A calcium-regulated MEF2 sumoylation switch controls postsynaptic differentiation
    • Shalizi A, Gaudilliere B, Yuan Z, et al. A calcium-regulated MEF2 sumoylation switch controls postsynaptic differentiation. Science. 2006;311:1012-1017.
    • (2006) Science. , vol.311 , pp. 1012-1017
    • Shalizi, A.1    Gaudilliere, B.2    Yuan, Z.3
  • 51
    • 33644641674 scopus 로고    scopus 로고
    • Phosphorylation-facilitated sumoylation of MEF2C negatively regulates its transcriptional activity
    • Kang J, Gocke CB, Yu H. Phosphorylation-facilitated sumoylation of MEF2C negatively regulates its transcriptional activity. BMC Biochem. 2006;7:5.
    • (2006) BMC Biochem. , vol.7 , pp. 5
    • Kang, J.1    Gocke, C.B.2    Yu, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.