| ID | Sequence | Length | GC content |
|---|---|---|---|
| GUCCGGAUGCUGCGCCUGCGGUAGAGCGGCCGCCAUGUUGCAACCGGGA… | 1386 nt | 0.5657 | |
| GCUCUCUGCUCCUCCUGUUCGACAGUCAGCCGCAUCUUCUUUUGCGUCG… | 1377 nt | 0.5730 | |
| GCUCUCUGCUCCUCCUGUUCGACAGUCAGCCGCAUCUUCUUUUGCGUCG… | 1525 nt | 0.5908 | |
| GCUCUCUGCUCCUCCUGUUCGACAGUCAGCCGCAUCUUCUUUUGCGUCG… | 1231 nt | 0.5662 | |
| GCUCUCUGCUCCUCCUGUUCGACAGUCAGCCGCAUCUUCUUUUGCGUCG… | 1285 nt | 0.5611 |
This gene encodes a member of the glyceraldehyde-3-phosphate dehydrogenase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. The product of this gene catalyzes an important energy-yielding step in carbohydrate metabolism, the reversible oxidative phosphorylation of glyceraldehyde-3-phosphate in the presence of inorganic phosphate and nicotinamide adenine dinucleotide (NAD). The encoded protein has additionally been identified to have uracil DNA glycosylase activity in the nucleus. Also, this protein contains a peptide that has antimicrobial activity against E. coli, P. aeruginosa, and C. albicans. Studies of a similar protein in mouse have assigned a variety of additional functions including nitrosylation of nuclear proteins, the regulation of mRNA stability, and acting as a transferrin receptor on the cell surface of macrophage. Many pseudogenes similar to this locus are present in the human genome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]
A study in human skeletal muscle demonstrated that the GAPDH mRNA is a reliable marker for time since death (TSD) estimation, as its Ct value increased consistently with the postmortem interval up to 48 hours, showing a strong correlation with TSD and being particularly suitable for the 36 to 48-hour period [Devi et al. DOI:10.1002/ca.70026]. In human forensic autopsy tissues, the GAPDH mRNA degraded gradually postmortem, and its degradation profile was parallel to that of VEGF and HIF1A mRNAs, making it a useful endogenous reference for relative quantification in brain, kidney, and lung samples up to 48 hours postmortem [Zhao et al. DOI:10.1016/j.legalmed.2005.09.001]. A review of forensic methods notes that in experimental studies using porcine skeletal muscle and mouse liver, the GAPDH mRNA showed decreasing transcript levels over a 48-hour postmortem interval, indicating its potential role in PMI estimation through degradation analysis [Nanny Wenzlow et al. DOI:10.1177/10406387231153930].