| ID | Sequence | Length | GC content |
|---|---|---|---|
| AGCAGAACCUCCUCGGACAGCGGCCCCAGCCGGGCCCCAGCAGCUCGCG… | 3399 nt | 0.6231 | |
| AGCAGAACCUCCUCGGACAGCGGCCCCAGCCGGGCCCCAGCAGCUCGCG… | 3160 nt | 0.6244 | |
| AGACUAAUUCGGAGUGAAAUGUUUUAGCAAUGGUGGGCUGAUUCUAUCA… | 3233 nt | 0.5982 | |
| AGCAGAACCUCCUCGGACAGCGGCCCCAGCCGGGCCCCAGCAGCUCGCG… | 3070 nt | 0.6283 | |
| AGCAGAACCUCCUCGGACAGCGGCCCCAGCCGGGCCCCAGCAGCUCGCG… | 2176 nt | 0.6209 | |
| GGAGAGUCCUUGAGUCCAUGGAAGCACAGGGCAAGGCCCUGGGCUCCUG… | 2345 nt | 0.6043 | |
| AGCAGAACCUCCUCGGACAGCGGCCCCAGCCGGGCCCCAGCAGCUCGCG… | 3043 nt | 0.6227 | |
| AGCAGAACCUCCUCGGACAGCGGCCCCAGCCGGGCCCCAGCAGCUCGCG… | 3022 nt | 0.6241 | |
| GGAGAGUCCUUGAGUCCAUGGAAGCACAGGGCAAGGCCCUGGGCUCCUG… | 3191 nt | 0.6117 | |
| AGACUAAUUCGGAGUGAAAUGUUUUAGCAAUGGUGGGCUGAUUCUAUCA… | 3095 nt | 0.5968 |
This gene encodes a member of the RNA-binding FOX protein family which is involved in the regulation of alternative splicing of pre-mRNA. The protein has an N-terminal proline-rich region, an RNA recognition motif (RRM) domain, and a C-terminal alanine-rich region. This gene produces the neuronal nuclei (NeuN) antigen that has been widely used as a marker for post-mitotic neurons. This gene has its highest expression in the central nervous system and plays a prominent role in neural tissue development and regulation of adult brain function. Mutations in this gene have been associated with numerous neurological disorders. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2017]
A study in rats demonstrated that traumatic brain injury (TBI) induced by lateral fluid percussion caused significant neuronal loss in the impacted cerebral cortex by 48 hours post-injury, as evidenced by decreased NeuN-positive neuron counts and shrunken neuronal morphology [Shojo et al. DOI:10.1016/j.neuroscience.2010.10.018]. This histopathological marker of neuronal integrity showed a temporal progression alongside other apoptotic and inflammatory markers, supporting its role in characterizing the extent of TBI-related neurodegeneration within the examined subacute phase. A study in mice demonstrated that the RBFOX3 mRNA was low or absent in magnetically isolated CD31+ endothelial cell fractions, confirming successful enrichment of endothelial cells for subsequent analysis of age-dependent vascular responses to traumatic brain injury [Brickler et al. DOI:10.1523/JNEUROSCI.0914-18.2018].