ABHD18 explained

Chromosome 4 open reading frame 29
Symbol:C4orf29
Entrezgene:80167
Hgncid:26111
Refseq:NP_001034806.1
Uniprot:Q0P651
Chromosome:4
Arm:q
Band:28.2

ABHD18 is a protein that in Homo sapiens is encoded by the ABHD18 gene.[1]

Gene

ABHD18 is found on the positive strand of the human genome at 4q28.2. It is 74.4 kbp. The gene contains 17 exons.[2] The longest mRNA transcript is composed of 13 exons and is 2200 base pairs.

Homology

Orthologs

Many orthologs to human ABHD18 have been discovered, with the most distant ortholog with high (over 90%) coverage is found in rice Oryza sativa.[3] The protein is not found in fungi. Bacteria of the order Myxobacteria and genus Chitinimonas contain orthologous regions to the C4orf29 protein. The few bacterial homologs indicate a horizontal gene transfer event. The domain of unknown function, DUF2048, is conserved throughout orthologs.

Organism NCBI Accession Number Divergence from Humans (Million Years) Protein Length (Amino Acids) Sequence Identity to HumanSequence Similarity to Human
NP_001034806.1 0 414 100% 100%
XP_005631879.1 94.2 484 87% 89%
Canary XP_009094557.1 296 414 75% 87%
XP_005282815.1 296 464 73% 83%
XP_011141314.1 782 468 46% 64%
NP_492206.1 937 378 33% 50%
NP_001046183.1 1369 366 31% 47%
WP_043404439.1 2535 321 31% 52%

Protein

ABHD18 codes a 414 amino acid sequence of 46.9 kDa in humans. The predicted isoelectric point is 9.37.[4] The domain of unknown function, DUF2048, is found from amino acid residues 25 to 414 in the precursor C4orf29 protein.[5] This domain is part of the alpha/beta hydrolase superfamily, which comprises enzymes that catalyze fat metabolism. Predicted post-translational modifications include glycosylation at residues Ser287 and Ser319 [6] and sumoylation[7] at the motifs Phe240 to Gly243, Ala377 to Asp340, and Phe408 to Gly411.

Expression

The protein product of ABHD18 in humans is predicted to be a secreted product. It is ubiquitously expressed at low to moderate levels.[8] In humans, the protein is found at high levels the digestive tract and parathyroid gland.[9] The homologous mouse protein 3110057O12Rik is expressed at high levels in the granule layer of the cerebellum.[10]

Clinical significance

ABHD18 contains highly variable numbers of Alu repeats.[11] A low number of Alu repeats in the human ABHD18 protein is associated with increase prevalence of hepatocellular carcinoma (HCC) in Asian populations. This information is used as a genetic marker to determine genetic risk of HCC.[12] Swine muscle transcriptome analysis indicates high expression of ABHD18 in swine with extreme low levels of fatty acid composition.[13]

Notes and References

  1. Web site: C4orf29. NCBI Gene. NCBI. 5 May 2015.
  2. Web site: C4orf29. NCBI AceView. 2015-05-05.
  3. Web site: NP_001034806. NCBI Protein BLAST.
  4. Web site: C4orf29 (human). Phosphosite.org. 2015-05-05.
  5. Web site: uncharacterized protein C4orf29 precursor [Homo sapiens]]. NCBI Protein.
  6. Web site: NetOGlyc4.0 C4orf29. CBS Prediction Servers.
  7. Web site: C4orf29 Sumoylation. ABGENT.
  8. Web site: Large-scale analysis of the human transcriptome GDS596. NCBI GeoProfile. 2015-05-05.
  9. Web site: C4orf29. The Human Protein Atlas. 2015-05-05.
  10. Web site: 3110057O12Rik. Allen Brain Atlas. 2015-05-05.
  11. Osenberg S, Paz Yaacov N, Safran M, Moshkovitz S, Shtrichman R, Sherf O, Jacob-Hirsch J, Keshet G, Amariglio N, Itskovitz-Eldor J, Rechavi G . Alu sequences in undifferentiated human embryonic stem cells display high levels of A-to-I RNA editing . PLOS ONE . 5 . 6 . e11173 . June 2010 . 20574523 . 2888580 . 10.1371/journal.pone.0011173 . 2010PLoSO...511173O . free .
  12. Clifford RJ, Zhang J, Meerzaman DM, Lyu MS, Hu Y, Cultraro CM, Finney RP, Kelley JM, Efroni S, Greenblum SI, Nguyen CV, Rowe WL, Sharma S, Wu G, Yan C, Zhang H, Chung YH, Kim JA, Park NH, Song IH, Buetow KH . Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma . Hepatology . 52 . 6 . 2034–43 . December 2010 . 21105107 . 10.1002/hep.23943 . 8259333 . 5286278 . free .
  13. Puig-Oliveras A, Ramayo-Caldas Y, Corominas J, Estellé J, Pérez-Montarelo D, Hudson NJ, Casellas J, Folch JM, Ballester M . Differences in muscle transcriptome among pigs phenotypically extreme for fatty acid composition . PLOS ONE . 9 . 6 . e99720 . June 2014 . 24926690 . 4057286 . 10.1371/journal.pone.0099720 . 2014PLoSO...999720P . free .