| ID | Sequence | Length | GC content |
|---|---|---|---|
| AGCGCGCCAGCGCCGGCUAGCCGGACGCCCUAGGCUUCCGCGAGAUCUU… | 1523 nt | 0.4412 | |
| AGCGCGCCAGCGCCGGCUAGCCGGACGCCCUAGGCUUCCGCGAGAUCUU… | 1280 nt | 0.4227 | |
| AGCGCGCCAGCGCCGGCUAGCCGGACGCCCUAGGCUUCCGCGAGAUCUU… | 4378 nt | 0.3840 | |
| AGCGCGCCAGCGCCGGCUAGCCGGACGCCCUAGGCUUCCGCGAGAUCUU… | 2394 nt | 0.4098 | |
| AGCGCGCCAGCGCCGGCUAGCCGGACGCCCUAGGCUUCCGCGAGAUCUU… | 4621 nt | 0.3921 |
The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with CDK7 kinase and ring finger protein MAT1. The kinase complex is able to phosphorylate CDK2 and CDC2 kinases, thus functions as a CDK-activating kinase (CAK). This cyclin and its kinase partner are components of TFIIH, as well as RNA polymerase II protein complexes. They participate in two different transcriptional regulation processes, suggesting an important link between basal transcription control and the cell cycle machinery. A pseudogene of this gene is found on chromosome 4. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Nov 2010]
A study in human skin tissue demonstrated that burn injury significantly alters the T cell landscape, with a lower proportion of CD8+ T cells compared to non-burn skin [Labuz et al. DOI:10.7554/eLife.82626]. These burn-infiltrating CD8+ T cells exhibited a pro-inflammatory, circulating phenotype characterized by significantly higher production of IFN-γ and TNF-α upon stimulation, lower expression of the tissue residency marker CD69, and higher transcriptional expression of homing receptors CCR7, S1PR1, and SELL compared to their counterparts in non-burn tissue.