C2orf16

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C2orf16
Identifiers
AliasesC2orf16, chromosome 2 open reading frame 16
External IDsHomoloGene: 82476 GeneCards: C2orf16
Orthologs
SpeciesHumanMouse
Entrez

84226

102635566

Ensembl

ENSG00000221843

n/a

UniProt

Q68DN1

n/a

RefSeq (mRNA)

NM_032266

XM_017321194

RefSeq (protein)

NP_115642

n/a

Location (UCSC)Chr 2: 27.54 – 27.58 Mbn/a
PubMed search[2][3]
Wikidata
View/Edit HumanView/Edit Mouse

C2orf16 is a protein that in humans is encoded by the C2orf16 gene. Isoform 2 of this protein (NCBI ID: CAH18189.1[4] henceforth referred to as C2orf16) is 1,984 amino acids long.[5] The gene contains 1 exon and is located at 2p23.3.[6] Aliases for C2orf16 include Open Reading Frame 16 on Chromosome 2 and P-S-E-R-S-H-H-S Repeats Containing Sequence.[7]

68 orthologs are known for this gene, including in mice and sheep, but no paralogs have been found.[8]

Gene[edit]

The C2orf16 isoform 2 is a 6.2 kb, 1 exon gene at locus 2p23.3, and contains P-S-E-R-S-H-H-S repeats on the C-terminal side of the gene from amino acid 1,559 to 1,903. These repeats appear to have arisen from a transposable element. Primates show more P-S-E-R-S-H-H-S repeats than other mammalian orthologs do.[6]

Expression[edit]

C2orf16 is found to be highly expressed in the testes[9] and a retinoic acid and mitogen-treated human embryonic stem cell line,[10] but is not known to be expressed differently in age or disease phenotypes.[11] C2orf16 is also seen to have high expression in the pre-implantation embryo from the 4-cell embryo stage to the blastocyst stage.[12]

C2orf16 is not seen to have rapamycin sensitive expression.[13] C2orf16 is also seen to significantly increase expression in c-MYC knockdown breast cancer cells.[14]

mRNA[edit]

Isoforms[edit]

Two isoforms exist of C2orf16. Isoform 1 is 5,388 amino acids long encoded in 5 exons over 16,401 base pairs. Isoform 2 uses an alternate start site of transcription and is considerably shorter at 1,984 amino acids long encoded in 1 exon over 6,200 base pairs.[8]

Expression Regulation[edit]

One miRNA is predicted to bind to the 3'UTR of C2orf16, accession number MI0005564.[15][16]

Protein[edit]

C2orf16 has a predicted molecular weight of 224kD and a predicted isoelectric point of 10.08,[17] values that are relatively constant between orthologs. The protein includes higher than average composition of serine, histidine, and arginine and a lower than average composition of alanine.[18]

Compositional Features[edit]

A positive charge cluster is found from amino acid residues 1,274 to 1,302.[18]

An arginine rich region is found from amino acids 1,545 to 1,933, a serine rich region is found from amino acids 1,568 to 1,934, and a histidine rich region is found from amino acids 1,630 to 1,853.[18]

A dot matrix analysis[19] reveals a heavily repeated region from approximately residue 1,500 to 1,984, this being the P-S-E-R-S-H-H-S repeat. a small band of dots at approximately amino acid 1,200 denotes a half repeat of the P-S-E-R-S-H-H-S sequence.

Dot matrix analysis of uncharacterized protein C2orf16 isoform 2. The P-S-E-R-S-H-H-S repeat sequence is visualized via the darker area of the matrix from amino acid 1500–1984, and a half P-S-E-R-S-H-H-S repeat sequence is seen as a band near amino acid 1200.

C2orf16 isoform 2 has no transmembrane domains,[20] and is predicted to be localized to the nucleus after translation due to two nuclear localization sequences predicted at residues 1,233 and 1,281.[21] No nuclear export sequence is conserved amongst orthologs,[22] suggesting C2orf16 is not meant to leave the nucleus after import. No N- or C- terminal modifications were predicted.[23][24][25][26]

Sub-cellular Localization[edit]

C2orf16 is predicted to be localized to the nucleus after transcription.[8]

Structure[edit]

C2orf16 Isoform 2 predicted 3D structure showing the three major domains of the protein. Domain 3 contains the P-S-E-R-S-H-H-S repeat sequence.

The 3D structure of C2orf16 is predicted to have three major domains. Domain 1 is from amino acids 1 to 662, domain 2 is from amino acids 674 to 1,487, and domain 3 is from amino acids 1,488 to 1,984.[27] Domain 1 and 2 are predicted to be connected via a stretch of 12 amino acids not otherwise organized into a secondary structure allowing flexibility between domains 1 and 2. Domain 2 is predicted to have protein interacting domains for transcription factors.[27] Domain 3 is predicted to follow a "balls on a string" structure[27] and has many sites for possible phosphorylation.[28]

Protein Interactions[edit]

C2orf16 has been shown to have a physical interaction with proto-oncogene Myc by tandem affinity purification.[29]

Ortholog Phylogeny[edit]

68 orthologs are known for C2orf16.[8] The protein seems to have appeared in the mammalian evolutionary history 320 million years ago, around the divergence of mammals from reptiles. This history would explain why orthologs do not exist in amphibians, reptiles, birds, nor other more distantly related species.[30]

Any orthologs from species more distant from humans than other mammals are likely not related in function, however, the P-S-E-R-S-H-H-S repeat is present in bony fishes, crustaceans, stramenopiles including potato blight, plantae, and prokaryotes.[30]

The transposon repeat may have been reintroduced to mammals by a viral vector.

Repeat Sequence[edit]

P-S-E-R-S-H-H-S Repeat Sequence Logo

The P-S-E-R-S-H-H-S repeat sequence is seen to be conserved in orthologs for C2orf16, and is conserved in organisms as distantly related as oomycete slime mold[31] and plants including the chloroplasts of Ashby's Wattle.[32] The S-P-S-E-R portion of the repeat is seen to be the most important for conservation, as seen by alignment with these orthologs and by creation of a Logo.[33]

The conservation analysis of the repeat shows the initial S-P-S is highly conserved, possibly for phosphorylation(S) and structure(P), and the R is almost completely conserved, mutating to a Lysine in some orthologs,[32] implying the positive charge is necessary for the purpose of the repeat.

The 3D shape of the repeat sequence is unclear as it has been predicted to be either balls-on-a-string[34] or an antiparallel beta-sheet[6] structure.

Function[edit]

C2orf16 isoform 2 is predicted to have a possible function in mitosis regulation through its nuclear localization,[8][21] predicted transcription factor binding site,[27] physical association with Myc,[29] and increased expression in c-MYC knockdown breast cancer cells.[14]

Clinical Significance[edit]

There are four patents on record for C2orf16, one each involving: cancerous PPP2RIA and ARID1A mutations,[35] Alzheimer's predisposition,[36] viral vaccine diversity,[37] and copy number variation relation to common variable immunodeficiency.[38] C2orf16 is also shown to have increased expression in some breast cancer lines,[14] as well as being involved with Myc[29] which is a common oncogene, making C2orf16 a possible oncogene to target in cancer treatments.

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000221843 – Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "hypothetical protein [Homo sapiens] – Protein – NCBI". www.ncbi.nlm.nih.gov. Retrieved 2019-05-02.
  5. ^ "C2orf16 Gene". GeneCards Human Gene Database. Weizmann Institute of Science, Life Map Sciences. Retrieved Feb 5, 2019.
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  13. ^ Petrich AM, Leshchenko V, Kuo PY, Xia B, Thirukonda VK, Ulahannan N, Gordon S, Fazzari MJ, Ye BH, Sparano JA, Parekh S (May 2012). "Akt inhibitors MK-2206 and nelfinavir overcome mTOR inhibitor resistance in diffuse large B-cell lymphoma". Clinical Cancer Research. 18 (9): 2534–44. doi:10.1158/1078-0432.CCR-11-1407. PMC 3889476. PMID 22338016.
  14. ^ a b c Cappellen D, Schlange T, Bauer M, Maurer F, Hynes NE (January 2007). "Novel c-MYC target genes mediate differential effects on cell proliferation and migration". EMBO Reports. 8 (1): 70–6. doi:10.1038/sj.embor.7400849. PMC 1796762. PMID 17159920.
  15. ^ Agarwal V, Bell GW, Nam JW, Bartel DP (August 2015). Izaurralde E (ed.). "Predicting effective microRNA target sites in mammalian mRNAs". eLife. 4: e05005. doi:10.7554/eLife.05005. PMC 4532895. PMID 26267216.
  16. ^ "miRNA Entry for MI0005564". www.mirbase.org. Archived from the original on 2020-09-23. Retrieved 2019-05-05.
  17. ^ "ExPASy – Compute pI/Mw tool". web.expasy.org. Retrieved 2019-05-02.
  18. ^ a b c Madeira F, Park YM, Lee J, Buso N, Gur T, Madhusoodanan N, Basutkar P, Tivey AR, Potter SC, Finn RD, Lopez R (April 2019). "The EMBL-EBI search and sequence analysis tools APIs in 2019". Nucleic Acids Research. 47 (W1): W636–W641. doi:10.1093/nar/gkz268. PMC 6602479. PMID 30976793.
  19. ^ "EMBOSS: dotmatcher". www.bioinformatics.nl. Retrieved 2019-05-02.
  20. ^ Cserzö M, Eisenhaber F, Eisenhaber B, Simon I (September 2002). "On filtering false positive transmembrane protein predictions". Protein Engineering. 15 (9): 745–52. doi:10.1093/protein/15.9.745. PMID 12456873.
  21. ^ a b Sigrist CJ, Cerutti L, de Castro E, Langendijk-Genevaux PS, Bulliard V, Bairoch A, Hulo N (January 2010). "PROSITE, a protein domain database for functional characterization and annotation". Nucleic Acids Research. 38 (Database issue): D161-6. doi:10.1093/nar/gkp885. PMC 2808866. PMID 19858104.
  22. ^ la Cour T, Kiemer L, Mølgaard A, Gupta R, Skriver K, Brunak S (June 2004). "Analysis and prediction of leucine-rich nuclear export signals". Protein Engineering, Design & Selection. 17 (6): 527–36. doi:10.1093/protein/gzh062. PMID 15314210.
  23. ^ Kiemer L, Bendtsen JD, Blom N (April 2005). "NetAcet: prediction of N-terminal acetylation sites". Bioinformatics. 21 (7): 1269–70. doi:10.1093/bioinformatics/bti130. PMID 15539450.
  24. ^ Bologna G, Yvon C, Duvaud S, Veuthey AL (June 2004). "N-Terminal myristoylation predictions by ensembles of neural networks". Proteomics. 4 (6): 1626–32. doi:10.1002/pmic.200300783. PMID 15174132. S2CID 20289352.
  25. ^ Chuang GY, Boyington JC, Joyce MG, Zhu J, Nabel GJ, Kwong PD, Georgiev I (September 2012). "Computational prediction of N-linked glycosylation incorporating structural properties and patterns". Bioinformatics. 28 (17): 2249–55. doi:10.1093/bioinformatics/bts426. PMC 3426846. PMID 22782545.
  26. ^ Julenius K (August 2007). "NetCGlyc 1.0: prediction of mammalian C-mannosylation sites". Glycobiology. 17 (8): 868–76. doi:10.1093/glycob/cwm050. PMID 17494086.
  27. ^ a b c d Yang J, Zhang Y (July 2015). "I-TASSER server: new development for protein structure and function predictions". Nucleic Acids Research. 43 (W1): W174-81. doi:10.1093/nar/gkv342. PMC 4489253. PMID 25883148.
  28. ^ Blom N, Gammeltoft S, Brunak S (December 1999). "Sequence and structure-based prediction of eukaryotic protein phosphorylation sites". Journal of Molecular Biology. 294 (5): 1351–62. doi:10.1006/jmbi.1999.3310. PMID 10600390.
  29. ^ a b c "PSICQUIC View". www.ebi.ac.uk. Retrieved 2019-05-02.
  30. ^ a b Madden, Tom (2003-08-13). The BLAST Sequence Analysis Tool. National Center for Biotechnology Information (US).
  31. ^ "cyst germination specific acidic repeat protein precursor [Phytophthora infestans]". NCBI. Retrieved 2019-05-02.
  32. ^ a b "accD (chloroplast) [Acacia ashbyae] – Protein – NCBI". www.ncbi.nlm.nih.gov. Retrieved 2019-05-02.
  33. ^ "WebLogo – Create Sequence Logos". weblogo.berkeley.edu. Retrieved 2019-05-02.
  34. ^ Zhang Y (January 2008). "I-TASSER server for protein 3D structure prediction". BMC Bioinformatics. 9 (1): 40. doi:10.1186/1471-2105-9-40. PMC 2245901. PMID 18215316.
  35. ^ Vogelstein B, Kinzler KW, Velculescu V, Papadopoulous N, Jones S (May 31, 2012). "US Patent 9,982,304" (US 20130210900 A1). Retrieved Feb 5, 2019. {{cite journal}}: Cite journal requires |journal= (help)[permanent dead link]
  36. ^ Nagy, Zsuzsanna (Jan 16, 2014). "US Patent 9,944,986" (US 20150141491 A1). Retrieved Feb 5, 2019. {{cite journal}}: Cite journal requires |journal= (help)[permanent dead link]
  37. ^ Shenk T, Wang D (April 16, 2009). "US Patent 9,439,960" (US 20100285059 A1). Retrieved Feb 5, 2019. {{cite journal}}: Cite journal requires |journal= (help)[permanent dead link]
  38. ^ Hakonarson H, Glessner J, Orange J (Nov 28, 2013). "US Patent 9,109,254" (US 20130315858 A1). Retrieved Feb 5, 2019. {{cite journal}}: Cite journal requires |journal= (help)[permanent dead link]
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