| ID | Sequence | Length | GC content |
|---|---|---|---|
| AUUGAUUUUGAGACUGCCCUUUGUACCGAAUUCACUCGGGUCCCGUCAG… | 4132 nt | 0.4177 | |
| CACCAUUCCUUUCUCACCUGGCACAAUCUCAGAUUUUUAGACUCUGAGG… | 3685 nt | 0.3927 | |
| AGAGAUCGAGGUGACAGGCGAGCUGGCUGGACUCGGAGCGCGGUCGAGG… | 3861 nt | 0.4084 |
This gene encodes a member of the poly(ADP-ribose) polymerase superfamily. Studies of the mouse ortholog have shown that the encoded protein catalyzes histone poly(ADP-ribosyl)ation and may be involved in T-cell function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]
A study in mice demonstrated that the TIPARP gene was upregulated in common in spleen leukocytes across all three injury models of trauma/hemorrhage, burn, and LPS infusion, indicating its role as part of a common early transcriptional response to systemic inflammation [Brownstein et al. DOI:10.1152/physiolgenomics.00213.2005]. Furthermore, a review consolidating research across multiple species noted that the TIPARP is a target gene derepressed by specific circRNAs, such as circTLK1 and circHECTD1, following ischemic stroke, where its upregulation is associated with worsening injury and astrocyte activation [Mehta et al. DOI:10.1016/j.pneurobio.2020.101746].