Basic Information

Symbol
UBB
RNA class
mRNA
Alias
Ubiquitin B Polyubiquitin B Polyubiquitin-B FLJ25987 MGC8385 Epididymis Secretory Protein Li 50 HEL-S-50
Location (GRCh38)
Forensic tag(s)
Cause of death analysis

MANE select

Transcript ID
NM_018955.4
Sequence length
933.0 nt
GC content
0.5230

Transcripts

ID Sequence Length GC content
AGUGCCGGCGCUGCAAGGAAGUUUCCAGAGCUUUCGAGGAAGGUUUCUU… 1097 nt 0.5132
AGUUUGUGUGGUUUCUGGAAGCCUUUACUUUGGAAUCCCAGUGUGAGAA… 1068 nt 0.5047
GGGCCUUGUUGACCUGAGGGGGGCGAGGGCGGUUGGCGCGCGCGCGCGU… 1028 nt 0.5253
GUGGGGGAGGGGAGGGCGAGGUGACGCGGCGCUGGGCCUUUCCGGGACA… 1026 nt 0.5409
AUUUAGGGGCGGUUGGCUUUGUUGGGUCAAAAUGCAGAUCUUCGUGAAA… 864 nt 0.5208
AUUUAGGGGCGGUUGGCUUUGUUGGGUGAGCUUGUUUGUGUCCCUGUGG… 933 nt 0.5230
Summary

This gene encodes ubiquitin, one of the most conserved proteins known. Ubiquitin has a major role in targeting cellular proteins for degradation by the 26S proteosome. It is also involved in the maintenance of chromatin structure, the regulation of gene expression, and the stress response. Ubiquitin is synthesized as a precursor protein consisting of either polyubiquitin chains or a single ubiquitin moiety fused to an unrelated protein. This gene consists of three direct repeats of the ubiquitin coding sequence with no spacer sequence. Consequently, the protein is expressed as a polyubiquitin precursor with a final amino acid after the last repeat. An aberrant form of this protein has been detected in patients with Alzheimer's disease and Down syndrome. Pseudogenes of this gene are located on chromosomes 1, 2, 13, and 17. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

Forensic Context

A study in humans demonstrated that the UBB is up-regulated in post-mortem blood and is involved in nucleotide-excision repair and DNA damage recognition, with pathway analysis suggesting active processes promoting cell survival and DNA damage repair are the source of early postmortem gene expression changes [Antiga et al. DOI:10.1038/s41598-021-96095-z]. In a separate human study, the UBB was differentially expressed as part of non-canonical NF-kB signalling mediated by Dectin-1 in the heart and colon of sepsis patients [Pinheiro da Silva et al. DOI:10.1111/jcmm.17938].