SMDF and GGF neuregulin splice variant isoforms and uses thereof
AssigneeThe UAB Research Foundation
InventorSteven L. Carroll
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AssigneeThe UAB Research Foundation
InventorSteven L. Carroll
Estimating the term…
Distinct cDNAs encoding six cysteine-rich domain-NRGs and four glial growth factor isoforms were identified and sequenced. Additional heterogeneity is found in the EGF-like (α- and β-isoforms) and carboxy terminal (a and b variant) regions of CRD-NRGs. Furthermore, the predicted GGF proteins contain glycosylation domains previously found only in mesenchymal NRGs. GGF mRNAs accumulate in axotomized nerve, a subpopulation of DRG neurons and most spinal cord motoneurons. CRD-NRGs, however, are undetectable in injured nerve except by RT-PCR. In contrast, the majority of DRG and spinal cord motor neurons express CRD-NRGs, with a β1 isoform being most abundant and at least some of these proteins are secreted in a form capable of activating erbB receptors. Thus, GGF and CRD-NRG subfamilies are more structurally diverse than previously appreciated. NRG actions during Wallerian degeneration may be modulated by the action of distinct splice variants.
An isolated splice variant isoform of sensory and motor neuron-derived factor (SMDF) SMDFβ1a protein having an amino acid sequence of SEQ ID No 2.
A method of treating a condition involving nervous system dysfunction, comprising the step of:
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