Recently, our conception of the two principal myelin protein genes, i.e. the myelin basic protein (MBP) and proteolipid protein (PLP) genes, has begun to change in view of new information about their structure, expression patterns and possible non-myelin related functions of their products. There is a considerable body of evidence to suggest that the PLP/DM20 gene plays roles other than that encoding the major myelin structural proteins in non-myelinating cells. This could occur either through multiple activities of the """"""""classic"""""""" PLP and DM20, or through the existence of other products of the gene that have not yet been identified. We have isolated two new srPLP/DM20 gene products and identified a new exon of the gene. These products are expressed in neurons as well as oligodendrocytes, and they are localized in the somata of oligodendrocytes and neurons and are absent from the myelin sheath. On the basis of these and other preliminary data, we propose the existence of other products of the PLP/DM20 gene in addition to the """"""""classic"""""""" and sr-PLP/DM20 variants. The overall objective of this application is to isolate and identify these other variants of the PLP/DM20 gene and to examine possible non-myelin functions of the """"""""classic"""""""" PLP and DM20 as well as the variant products of the gene. These include: (1) identifying and characterizing novel products of the PLP/DM20 gene and examining their cellular and regional localization in the developing nervous system; (2)[re-] evaluating the hypothesis that cell death in the jimpy mutant is due solely to toxic effects of the mutated protein by prepare cell lines stably transfected with normal and variant/mutant PLP/DM20 cDNAs and comparing levels of expression in conditionally-immortalized OL lines on cell survival; and (3) examining aspects of the non-myelin roles of PLP/DM20 gene products.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS023022-17
Application #
6539641
Study Section
Special Emphasis Panel (ZRG1-MDCN-2 (01))
Program Officer
Behar, Toby
Project Start
1985-09-01
Project End
2004-03-31
Budget Start
2002-04-01
Budget End
2003-03-31
Support Year
17
Fiscal Year
2002
Total Cost
$305,250
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Fulton, Daniel; Paez, Pablo; Spreur, Vilma et al. (2011) Developmental activation of the proteolipid protein promoter transgene in neuronal and oligodendroglial cells of neostriatum in mice. Dev Neurosci 33:170-84
Paez, Pablo M; Fulton, Daniel; Spreuer, Vilma et al. (2011) Modulation of canonical transient receptor potential channel 1 in the proliferation of oligodendrocyte precursor cells by the golli products of the myelin basic protein gene. J Neurosci 31:3625-37
Fisher, Robin; Xie, Yuan-Yun (2010) Growth defects in the dorsal pallium after genetically targeted ablation of principal preplate neurons and neuroblasts: a morphometric analysis. ASN Neuro 2:e00046
Fulton, Daniel; Paez, Pablo M; Fisher, Robin et al. (2010) Regulation of L-type Ca++ currents and process morphology in white matter oligodendrocyte precursor cells by golli-myelin proteins. Glia 58:1292-303
Xie, Yuan-Yun; Jacobs, Erin; Fisher, Robin (2009) Targeted ablation and reorganization of the principal preplate neurons and their neuroblasts identified by golli promoter transgene expression in the neocortex of mice. ASN Neuro 1:
Paez, Pablo M; Fulton, Daniel J; Spreuer, Vilma et al. (2009) Golli myelin basic proteins regulate oligodendroglial progenitor cell migration through voltage-gated Ca2+ influx. J Neurosci 29:6663-76
Martin, Melanie; Reyes, Samuel D; Hiltner, Timothy D et al. (2007) T(2)-weighted microMRI and evoked potential of the visual system measurements during the development of hypomyelinated transgenic mice. Neurochem Res 32:159-65
Paez, Pablo M; Spreuer, Vilma; Handley, Vance et al. (2007) Increased expression of golli myelin basic proteins enhances calcium influx into oligodendroglial cells. J Neurosci 27:12690-9
Feng, Ji-Ming; Hu, Yanhong K; Xie, Lai-Hua et al. (2006) Golli protein negatively regulates store depletion-induced calcium influx in T cells. Immunity 24:717-27
Jacobs, Erin C; Pribyl, Thomas M; Feng, Ji-Ming et al. (2005) Region-specific myelin pathology in mice lacking the golli products of the myelin basic protein gene. J Neurosci 25:7004-13

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