| ID | Sequence | Length | GC content |
|---|---|---|---|
| GAGGUCAGAGACUUAAGUCUAAGGCACUGAGCGUAUCAUGUUAAAGAUG… | 1081 nt | 0.4903 | |
| GAGGUCAGAGACUUAAGUCUAAGGCACUGAGCGUAUCAUGUUAAAGAUG… | 1028 nt | 0.4961 | |
| GAGGUCAGAGACUUAAGUCUAAGGCACUGAGCGUAUCAUGUUAAAGAUG… | 1005 nt | 0.5005 | |
| GAGGUCAGAGACUUAAGUCUAAGGCACUGAGCGUAUCAUGUUAAAGAUG… | 1191 nt | 0.4786 | |
| GAGGUCAGAGACUUAAGUCUAAGGCACUGAGCGUAUCAUGUUAAAGAUG… | 910 nt | 0.5000 | |
| GUCAGAGACUUAAGUCUAAGGCACUGAGCGUAUCAUGUUAAAGAUGAGC… | 924 nt | 0.5065 | |
| GUCAGAGACUUAAGUCUAAGGCACUGAGCGUAUCAUGUUAAAGAUGAGC… | 876 nt | 0.5114 | |
| GUCAGAGACUUAAGUCUAAGGCACUGAGCGUAUCAUGUUAAAGAUGAGC… | 903 nt | 0.5050 |
This gene encodes a member of the CCAAT/enhancer-binding protein (C/EBP) family of transcription factors. The protein functions as a dominant-negative inhibitor by forming heterodimers with other C/EBP members, such as C/EBP and LAP (liver activator protein), and preventing their DNA binding activity. The protein is implicated in adipogenesis and erythropoiesis, is activated by endoplasmic reticulum stress, and promotes apoptosis. Fusion of this gene and FUS on chromosome 16 or EWSR1 on chromosome 22 induced by translocation generates chimeric proteins in myxoid liposarcomas or Ewing sarcoma. Multiple alternatively spliced transcript variants encoding two isoforms with different length have been identified. [provided by RefSeq, Aug 2010]
A study in humans demonstrated that the DDIT3 was significantly down-regulated in subcutaneous adipose tissue of heavier co-twins in BMI-discordant monozygotic twin pairs and was negatively correlated with adiposity and inflammation, while positively correlated with insulin sensitivity [Jukarainen et al. DOI:10.1210/jc.2015-3095]. Research in zebrafish showed that the DDIT3 transcript abundance significantly increased at 12 hours postmortem, classifying it among apoptosis and cancer-related genes with altered expression after death [Pozhitkov et al. DOI:10.1098/rsob.160267]. A study in human HT-29 colorectal adenocarcinoma cells demonstrated that arsenic trioxide exposure induced the DDIT3 protein, as shown by immunoblotting, indicating an unusual endoplasmic reticulum stress response [Kazuta et al. DOI:10.1016/J.Legalmed.2026.102774]. In a rat model, research in Wistar rats showed that the DDIT3 protein, an ER stress-induced apoptosis marker, was increased in the midbrain of saline-pretreated animals after a neurotoxic high-dose methamphetamine challenge, and this induction was inhibited by protective low-dose methamphetamine pretreatment [Takeichi et al. DOI:10.1016/J.Legalmed.2011.12.004].