FMRP and myelin protein expression in oligodendrocytes

Molecular and Cellular Neuroscience

Volumn 56, Issue , 2013, Pages 333-341

  Giampetruzzi, Anthony ^a   Carson, John H ^a   Barbarese, Elisa ^a  

^a UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

Author keywords

Fragile X mental retardation protein; Fragile X syndrome; Myelin; Oligodendrocyte; Translation

Indexed keywords

FRAGILE X MENTAL RETARDATION PROTEIN; MESSENGER RNA; MYELIN BASIC PROTEIN; MYELIN PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; FRAGILE X SYNDROME; IN VITRO STUDY; MOUSE; MYELINATION; NONHUMAN; OLIGODENDROGLIA; PREMATURITY; PRIORITY JOURNAL; PROTEIN EXPRESSION; STEM CELL; WILD TYPE;

FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; MYELIN; OLIGODENDROCYTE; TRANSLATION;

ANIMALS; FRAGILE X MENTAL RETARDATION PROTEIN; HUMANS; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MYELIN BASIC PROTEIN; OLIGODENDROGLIA; RATS; RATS, SPRAGUE-DAWLEY; RNA, MESSENGER;

EID: 84882790019     PISSN: 10447431     EISSN: 10959327     Source Type: Journal    
DOI: 10.1016/j.mcn.2013.07.009     Document Type: Article

References (34)

1. Ainger K., Avossa D., Morgan F., Hill S.J., Barry C., Barbarese E., Carson J.H. Transport and localization of exogenous myelin basic protein mRNA microinjected into oligodendrocytes. J. Cell Biol. 1993, 123:431-441.
2. Amur-Umarjee S., Schonmann V., Campagnoni A.T. Neuronal regulation of myelin basic protein mRNA translocation in oligodendrocytes is mediated by platelet-derived growth factor. Dev. Neurosci. 1997, 19:143-151.
3. Bardoni B., Schenck A., Mandel J.L. A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein. Hum. Mol. Genet. 1999, 8:2557-2566.
4. Barnea-Goraly N., Eliez S., Hedeus M., Menon V., White C.D., Moseley M., Reiss A.L. White matter tract alterations in fragile X syndrome: preliminary evidence from diffusion tensor imaging. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2003, 118B:81-88.
5. Boggs J.M. Myelin basic protein: a multifunctional protein. Cell. Mol. Life Sci. 2006, 63:1945-1961.
6. Ceman S., O'Donnell W.T., Reed M., Patton S., Pohl J., Warren S.T. Phosphorylation influences the translation state of FMRP-associated polyribosomes. Hum. Mol. Genet. 2003, 12:3295-3305.
7. Colman D.R., Kreibich G., Frey A.B., Sabatini D.D. Synthesis and incorporation of myelin polypeptides into CNS myelin. J. Cell Biol. 1982, 95:598-608.
8. Darnell J.C., Van Driesche S.J., Zhang C., Hung K.Y., Mele A., Fraser C.E., Stone E.F., Chen C., Fak J.J., Chi S.W., Licatalosi D.D., Richter J.D., Darnell R.B. FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism. Cell 2011, 146:247-261.
9. Devys D., Lutz Y., Rouyer N., Bellocq J.P., Mandel J.L. The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation. Nat. Genet. 1993, 4:335-340.
10. Ellegood J., Pacey L.K., Hampson D.R., Lerch J.P., Henkelman R.M. Anatomical phenotyping in a mouse model of fragile X syndrome with magnetic resonance imaging. NeuroImage 2010, 53:1023-1029.
11. Geiser M., Cebe R., Drewello D., Schmitz R. Integration of PCR fragments at any specific site within cloning vectors without the use of restriction enzymes and DNA ligase. Biotechniques 2001, 31(88-90):92.
12. Greenough W.T., Klintsova A.Y., Irwin S.A., Galvez R., Bates K.E., Weiler I.J. Synaptic regulation of protein synthesis and the fragile X protein. Proc. Natl. Acad. Sci. U. S. A. 2001, 98:7101-7106.
13. Haas B.W., Barnea-Goraly N., Lightbody A.A., Patnaik S.S., Hoeft F., Hazlett H., Piven J., Reiss A.L. Early white-matter abnormalities of the ventral frontostriatal pathway in fragile X syndrome. Dev. Med. Child Neurol. 2009, 51:593-599.
14. Hallahan B.P., Craig M.C., Toal F., Daly E.M., Moore C.J., Ambikapathy A., Robertson D., Murphy K.C., Murphy D.G. In vivo brain anatomy of adult males with fragile X syndrome: an MRI study. NeuroImage 2011, 54:16-24.
15. Hinds H.L., Ashley C.T., Sutcliffe J.S., Nelson D.L., Warren S.T., Housman D.E., Schalling M. Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Nat. Genet. 1993, 3:36-43.
16. Hoeft F., Carter J.C., Lightbody A.A., Cody Hazlett H., Piven J., Reiss A.L. Region-specific alterations in brain development in one- to three-year-old boys with fragile X syndrome. Proc. Natl. Acad. Sci. U. S. A. 2010, 107:9335-9339.
17. Hoeft F., Walter E., Lightbody A.A., Hazlett H.C., Chang C., Piven J., Reiss A.L. Neuroanatomical differences in toddler boys with fragile x syndrome and idiopathic autism. Arch. Gen. Psychiatry 2011, 68:295-305.
18. Huber K.M., Gallagher S.M., Warren S.T., Bear M.F. Altered synaptic plasticity in a mouse model of fragile X mental retardation. Proc. Natl. Acad. Sci. U. S. A. 2002, 99:7746-7750.
19. Irwin S.A., Patel B., Idupulapati M., Harris J.B., Crisostomo R.A., Larsen B.P., Kooy F., Willems P.J., Cras P., Kozlowski P.B., Swain R.A., Weiler I.J., Greenough W.T. Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination. Am. J. Med. Genet. 2001, 98:161-167.
20. Jacobs S., Nathwani M., Doering L.C. Fragile X astrocytes induce developmental delays in dendrite maturation and synaptic protein expression. BMC Neurosci. 2010, 11:132. (2202-11-132).
21. Laggerbauer B., Ostareck D., Keidel E.M., Ostareck-Lederer A., Fischer U. Evidence that fragile X mental retardation protein is a negative regulator of translation. Hum. Mol. Genet. 2001, 10:329-338.
22. Li Z., Zhang Y., Ku L., Wilkinson K.D., Warren S.T., Feng Y. The fragile X mental retardation protein inhibits translation via interacting with mRNA. Nucleic Acids Res. 2001, 29:2276-2283.
23. Martin M., Hiltner T.D., Wood J.C., Fraser S.E., Jacobs R.E., Readhead C. Myelin deficiencies visualized in vivo: visually evoked potentials and T2-weighted magnetic resonance images of shiverer mutant and wild-type mice. J. Neurosci. Res. 2006, 84:1716-1726.
24. McCarthy K.D., de Vellis J. Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue. J. Cell Biol. 1980, 85:890-902.
25. Morgan F., Barbarese E., Carson J.H. Visualizing cells in three dimensions using confocal microscopy, image reconstruction and isosurface rendering: application to glial cells in mouse central nervous system. Scanning Microsc. 1992, 6:345-356. discussion 356-7.
26. Narayanan U., Nalavadi V., Nakamoto M., Pallas D.C., Ceman S., Bassell G.J., Warren S.T. FMRP phosphorylation reveals an immediate-early signaling pathway triggered by group I mGluR and mediated by PP2A. J. Neurosci. 2007, 27:14349-14357.
27. O'Meara R.W., Ryan S.D., Colognato H., Kothary R. Derivation of enriched oligodendrocyte cultures and oligodendrocyte/neuron myelinating co-cultures from post-natal murine tissues. J. Vis. Exp. 2011, (54). (pii: 3324). 10.3791/3324.
28. Pacey L.K., Doering L.C. Developmental expression of FMRP in the astrocyte lineage: implications for fragile X syndrome. Glia 2007, 55:1601-1609.
29. Rich R.L., Myszka D.G. Higher-throughput, label-free, real-time molecular interaction analysis. Anal. Biochem. 2007, 361:1-6.
30. Schapiro M.B., Murphy D.G., Hagerman R.J., Azari N.P., Alexander G.E., Miezejeski C.M., Hinton V.J., Horwitz B., Haxby J.V., Kumar A. Adult fragile X syndrome: neuropsychology, brain anatomy, and metabolism. Am. J. Med. Genet. 1995, 60:480-493.
31. Strait K.A., Carlson D.J., Schwartz H.L., Oppenheimer J.H. Transient stimulation of myelin basic protein gene expression in differentiating cultured oligodendrocytes: a model for 3,5,3'-triiodothyronine-induced brain development. Endocrinology 1997, 138:635-641.
32. Tatavarty V., Ifrim M.F., Levin M., Korza G., Barbarese E., Yu J., Carson J.H. Single-molecule imaging of translational output from individual RNA granules in neurons. Mol. Biol. Cell. 2012, 23:918-929.
33. The Dutch-Belgian Fragile X Consortium Fmr1 knockout mice: a model to study fragile X mental retardation. Cell 1994, 78:23-33.
34. Wang H., Ku L., Osterhout D.J., Li W., Ahmadian A., Liang Z., Feng Y. Developmentally-programmed FMRP expression in oligodendrocytes: a potential role of FMRP in regulating translation in oligodendroglia progenitors. Hum. Mol. Genet. 2004, 13:79-89.