| ID | Sequence | Length | GC content |
|---|---|---|---|
| AUAUAGUAACAUAGUGUGGUACUUUGUCUUGAGGAGAUGUCCUGGACUC… | 1386 nt | 0.5938 | |
| AUAGUAGCAGGACCACUAUAGAGAGAACACUCAUGUAGCAGGUCAUGGA… | 1424 nt | 0.5934 | |
| AUUCUCCCCAGACGCCAAGGAUGGUGGUCAUGGCGCCCCGAACCCUCUU… | 1319 nt | 0.6027 | |
| AUAUAGUAACAUAGUGUGGUACUUUGUCUUGAGGAGAUGUCCUGGACUC… | 1489 nt | 0.5910 |
HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placental cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exon 6 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]
A study in humans demonstrated that the HLA-G serves as a stable housekeeping gene for normalizing mRNA levels in post-mortem brain tissue, with its expression used as a reference to quantify the relative amount of m-opiate receptor (MOR1) mRNA via real-time PCR [Becker et al. DOI:10.1016/J.Forsciint.2003.10.012]. The HLA-G is also established as a reference gene for gene expression studies in forensic molecular pathology, including applications for cause of death determination [Madea et al. DOI:10.1016/J.Forsciint.2010.07.017]. A study in humans demonstrated that the HLA-G exhibited the highest relative expression across saliva, blood, menstrual blood, and vaginal secretion stains and was among the highest in semen, showing consistent high expression across individual donors and successful detection in small and environmentally exposed stains, establishing it as an effective reference for mRNA quantity assessment prior to profiling [Moreno et al. DOI:10.1111/j.1556-4029.2012.02086.x]. Subsequent research in humans quantified the degradation state of the HLA-G transcript in dried bloodstains via ΔCq, finding its degradation rate accelerated 5-10 fold at 37°C versus 20°C and continued steadily even in cold, dry conditions, with multivariate regression indicating temperature and relative humidity similarly accelerated degradation for estimating sample age [Heneghan et al. DOI:10.1016/j.fsigen.2020.102456].