Basic Information

Symbol
SIRT4
RNA class
mRNA
Alias
Sirtuin 4 SIR2L4 NAD-Dependent Protein Lipoamidase Sirtuin-4, Mitochondrial NAD-Dependent ADP-Ribosyltransferase Sirtuin-4 NAD-Dependent Protein Biotinylase Sirtuin-4 NAD-Dependent Protein Deacetylase Sirtuin-4 Regulatory Protein SIR2 Homolog 4 SIR2-Like Protein 4 Sirtuin (Silent Mating Type Information Regulation 2, S. Cerevisiae, Homolog) 4 Sirtuin (Silent Mating Type Information Regulation 2 Homolog) 4 (S. Cerevisiae) Sirtuin Type 4 EC 2.3.1.286 Sir2-Like 4 EC 2.3.1.- EC 2.4.2.-
Location (GRCh38)
Forensic tag(s)
Sudden cardiac death diagnosis Other applications

MANE select

Transcript ID
NM_012240.3
Sequence length
1217.0 nt
GC content
0.5127

Transcripts

ID Sequence Length GC content
AAAAAUUGCCAAUGCCGACUAUAUUUCAAGUCGUCAUGGCGGGGUAUUG… 2322 nt 0.5108
GCAAAUGCAAUCAGACGGUCCCACUGUGGGGUGUGAAGUGUCCGUAGAG… 944 nt 0.4926
AAAAAUUGCCAAUGCCGACUAUAUUUCAAGUCGUCAUGGCGGGGUAUUG… 2049 nt 0.5012
GCAAAUGCAAUCAGACGGUCCCACUGUGGGGUGUGAAGUGUCCGUAGAG… 1217 nt 0.5127
Summary

This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class IV of the sirtuin family. [provided by RefSeq, Jul 2008]

Forensic Context

A study in humans demonstrated that the SIRT4 mRNA is a predicted target of the upregulated miRNA miR-339-5p and shows anticorrelated expression (Pearson r = -0.78) in left ventricular myocardium following acute ischemia during cardiac surgery [Saddic et al. DOI:10.1152/physiolgenomics.00049.2015]. In a separate human study of monozygotic twins, the SIRT4 expression was undetectable in subcutaneous adipose tissue samples from both heavier and leaner co-twins [Jukarainen et al. DOI:10.1210/jc.2015-3095].