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C6orf58 is a human gene located at locus 6q22.33 of chromosome 6 and encodes for UPF0762, a protein which is subsequently secreted after cleavage of a signal peptide.[1] DUF781, which is the singular identifiable domain in UPF0762, is tied to liver development in an orthologous protein in zebrafish.[2] The function of the human UPF0762 remains unknown.[3]
Gene and mRNA
[edit]Genomic DNA Length (base pairs) | Exons | Mature mRNA Length (base pairs) | Splice variants | Signal peptide CDS (base pair) | Mature Peptide CDS (base pair) | 5'-UTR (base pair) | 3'-UTR (base pair) |
---|---|---|---|---|---|---|---|
14644[1] | 6[1] | 1200[1] | 3 [3] | 13-72[1] | 73-1002[1] | 1-12[1] | 1003-1200[1] |
Expression
[edit]While there are 3 splice variants of C6orf58, only one encodes a good protein.[3] In humans, C6orf58 expressed sequence tags were primarily detected in the larynx and trachea.[4] Transcripts were only detected during the adult stage of development.[4] Experimental microarray data, however, reveals additional regions of C6orf58 expression, namely in the salivary gland, thyroid, and small intestine.[5] Arsenic may also regulate expression as it increases methylation of the C6orf58 promoter.[6]
![Tissue expression profile of C6orf58](http://upload.wikimedia.org/wikipedia/commons/thumb/c/cd/GEO_Profiles_Tissue_Expression_Graph.png/600px-GEO_Profiles_Tissue_Expression_Graph.png)
Gene Neighborhood
[edit]Genes within 500 Kilobases of C6orf58 include RSPO3, C6orf174, KIAA0408, RPL17P23, ECHDC1, RPL5P18, YWHAZP4, LOC100420743, LOC100421513, MRPS17P5, and THEMIS.
Homology
[edit]A selected set of homologous sequences are listed below, with sequence identity being calculated in comparison to the human reference sequence.
Species | Common Name | Accession Number | Sequence Length (base pairs) | Sequence Identity |
---|---|---|---|---|
Nomascus leucogenys | Northern white-cheeked gibbon | XM_003255689.1 | 1190 | .97 |
Macaca mulatta | Rhesus monkey | NM_001194318.1 | 1190 | .95 |
Oryctolagus cuniculus | European rabbit | XM_002714721.1 | 1014 | .79 |
Loxodonta africana | African bush elephant | XM_003404026.1 | 1020 | .78 |
Cavia porcellus | Guinea pig | XM_003468475.1 | 1017 | .76 |
Equus caballus | Horse | XM_001917090.1 | 990 | .77 |
Protein
[edit]Properties
[edit]Amino acid length (amino acids) | Signal Peptide Length (amino acids) | Molecular Weight of Precursor Protein | Molecular Weight of Signal Peptide (Predicted) | Molecular Weight of Mature Peptide(predicted) | Molecular Weight(observed) | Isoelectric Point (Predicted) | N-linked glycosylation Site |
---|---|---|---|---|---|---|---|
330[1] | 20[1] | 37.9 kDa[7] | 2.1 kDa[7] | 35.8 kDa[7] | 32 kDa[8] | 5.78[7] | Amino acid 69 |
Mass spectrometry has shown that the observed molecular weight of UPF0762 is 32kDa.[8] It remains unclear why the observed molecular weight is less than predicted, even after accounting for cleavage of the signal peptide. Attachment of a sugar at the site of N-linked glycosylation would also increase the molecular weight.
Homology
[edit]UPF0762 shows high homology in primates and orthologous proteins can be traced back as far as trichoplax adhaerens. The list of proteins below is not a comprehensive listing of UPF0762 orthologs. Sequence identity and similarity were determined using BLAST[9] with the reference human sequence as the query.
Species | Common Name | Accession Number | Sequence Length (amino acids) | Sequence Identity (%) | Sequence Similarity (%) |
---|---|---|---|---|---|
Pan troglodytes | Chimpanzee | XP_518733.2 | 330 | 1 | 1 |
Pongo abelii | Sumatran orangutan | XP_002817388.1 | 330 | .98 | .99 |
Callithrix jacchus | Marmoset | XP_002746989.1 | 330 | .87 | .93 |
Canis lupus | Gray wolf | XP_851589.1 | 310 | .7 | .82 |
Taeniopygia guttata | Zebra finch | XP_002190886.1 | 364 | .43 | .63 |
Gallus gallus | Red junglefowl | XP_419749.3 | 371 | .42 | .6 |
Xenopus tropicalis | Western clawed frog | XP_002940437.1 | 178 | 0.29 | 0.51 |
Trichoplax adhaerens | N/A | XP_002111384 | 381 | .34 | .49 |
Conserved domains
[edit]DUF781 is the singular domain of the protein and spans 318 of the protein's 330 amino acids. DUF781 has been linked to liver development in zebrafish.[2]
Post-translational modifications
[edit]Observed post-translational modifications include N-linked glycosylation at amino acid 69.[10] A signal peptide, which is predicted to direct the protein to the endoplasmic reticulum for secretion[11], is cleaved from the first 20 amino acids of the peptide sequence[1] . The missense mutation S18F detected in hepatocellular carcinoma[12] significantly reduces the predicted cleavage score of the signal peptide.[13]
![Annotated protein structure of UPF0762 indicating amino acids subject to modification post-translationally](http://upload.wikimedia.org/wikipedia/commons/thumb/2/26/C6orf58_protein_structure.png/300px-C6orf58_protein_structure.png)
Interactions
[edit]Human C6orf58 has been reported to interact with the enzyme ribonucleotide reductase as encoded by the vaccinia virus through a yeast two-hybrid screen.[14]
Pathology
[edit]Statistical analysis has shown C6orf58 to be associated with pancreatic cancer survival time.[15] In addition, a missense mutation at amino acid 18 has been observed in liver cancer cells where serine becomes phenylalanine.[12] Analysis of the mutated protein sequence for a signal peptide shows cleavability at the regular amino acid 20 is lost.[13] DUF781's association with liver development and the missense mutation's association with liver cancer is a correlation that remains to be investigated.
References
[edit]- ^ a b c d e f g h i j k "Homo sapiens chromosome 6 open reading frame 58 (C6orf58), mRNA". National Center for Biotechnology Information. Retrieved 26 April 2012.
- ^ a b Chang C, Hu M, Zhu Z, Lo LJ, Chen J, Peng J (2011). "liver-enriched gene 1a and 1b encode novel secretory proteins essential for normal liver development in zebrafish". PLoS ONE. 6 (8): e22910. doi:10.1371/journal.pone.0022910. PMC 3153479. PMID 21857963.
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: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link) - ^ a b c Thierry-Mieg, Danielle. "AceView: integrative annotation of cDNA-supported genes in human, mouse, rat, worm and Arabidopsis". NCBI. Retrieved 30 April 2012.
- ^ a b "EST Profile Hs.226268". NCBI. Retrieved 30 April 2012.
- ^ Dezso, Z (2008 Nov 12). "A comprehensive functional analysis of tissue specificity of human gene expression". BMC biology. 6: 49. PMID 19014478.
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ignored (help)CS1 maint: multiple names: authors list (link) - ^ Altschul, SF (1990 Oct 5). [BLAST "Basic local alignment search tool"]. Journal of molecular biology. 215 (3): 403–10. PMID 2231712. Retrieved 8 May 2012.
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ignored (help)CS1 maint: multiple names: authors list (link) - ^ Caboche, Michel. "Predotar". Predotar. Retrieved 7 May 2012.
- ^ a b Li, M (2011 Aug 7). "Inactivating mutations of the chromatin remodeling gene ARID2 in hepatocellular carcinoma". Nature genetics. 43 (9): 828–9. PMID 21822264.
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suggested) (help) - ^ a b Petersen, TN (2011 Sep 29). "SignalP 4.0: discriminating signal peptides from transmembrane regions". Nature methods. 8 (10): 785–6. PMID 21959131.
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suggested) (help) - ^ Wu, TT (2011 Dec). "A transcriptome analysis by lasso penalized Cox regression for pancreatic cancer survival". Journal of bioinformatics and computational biology. 9 Suppl 1: 63–73. PMID 22144254.
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