| ID | Sequence | Length | GC content |
|---|---|---|---|
| GAACGUAGCUAGCUGCAAGCAGAGGCCGGCAUGACCACCGAGCAGCGAC… | 4622 nt | 0.3992 | |
| GAACGUAGCUAGCUGCAAGCAGAGGCCGGCAUGACCACCGAGCAGCGAC… | 4457 nt | 0.3976 | |
| GAACGUAGCUAGCUGCAAGCAGAGGCCGGCAUGACCACCGAGCAGCGAC… | 4641 nt | 0.3991 | |
| GAACGUAGCUAGCUGCAAGCAGAGGCCGGCAUGACCACCGAGCAGCGAC… | 4480 nt | 0.3982 | |
| GAACGUAGCUAGCUGCAAGCAGAGGCCGGCAUGACCACCGAGCAGCGAC… | 4613 nt | 0.3993 | |
| GAACGUAGCUAGCUGCAAGCAGAGGCCGGCAUGACCACCGAGCAGCGAC… | 4638 nt | 0.3991 | |
| GAACGUAGCUAGCUGCAAGCAGAGGCCGGCAUGACCACCGAGCAGCGAC… | 4628 nt | 0.3991 |
DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases which are implicated in a number of cellular processes involving RNA binding and alteration of RNA secondary structure. This gene encodes a protein containing RNA helicase-DEAD box protein motifs and a caspase recruitment domain (CARD). It is involved in viral double-stranded (ds) RNA recognition and the regulation of the antiviral innate immune response. Mutations in this gene are associated with Singleton-Merten syndrome 2. [provided by RefSeq, Aug 2020]
A study in rats demonstrated that the RIGI (DEXD/H-box helicase 58) was core-enriched in downregulated immune-associated datasets in fetal cardiac fibroblasts compared with neonatal cardiac fibroblasts, identifying it as an innate immune response receptor whose expression is developmentally regulated [Perreault et al. DOI:10.1152/physiolgenomics.00074.2021]. A study in diverse RNA constructs demonstrated that computational models developed via a dual-crowdsourcing approach could predict RNA degradation patterns with high accuracy, with 41% of nucleotide-level predictions from the winning model within experimental error [Wayment-Steele et al. DOI:10.1038/s42256-022-00571-8].