C9orf91

.[1] C9orf91 I-Tasser Predicted Protein Structure with a score of -2.87

C9orf91 is a protein that in humans is encoded by C9ORF91. The protein is a transmembrane protein of 342 amino acids long with eight alternative splice variants. The protein has been identified in organisms from the common fruit fly to primates. To date, there has been no protein expression found in organisms simpler than insects.

C9orf91
Identifiers
Symbol C9orf91
RefSeq NP_694590.2
UniProt Q5VZI3
Other data
Locus Chr. 9 q32
Chromosome 9 is shown. Area in green is 9q32, where C9ORF91 is found.

Gene

Location

C9ORF91 maps on chromosome 9 at 9q32.[2] The gene neighborhood for C9ORF91 is shown below. The area enclosed by the red circle is C9ORF91's coding region, which is surrounded by neighbors DFNB31 and ATP6V1G1.

C9ORF91 gene neighborhood within chromosome 9.

mRNA

Eight different alternative splice variants for C9ORF91 have been found.[3] The exon Sequence for the combinations shown indicate combined regions. Amino Acid length differs due to variants in nucleotide additions or deletions within exon regions, conferring different splice variants with similar sequence combinations.

Table for Exon and Transcript Variants for C9orf91
Splice variants of C9ORF91 gene.

Protein

General Characteristics

C9orf91 has seven variants. NP_694590.2 is the variant that is the most studied. An ExPasy result indicates C9orf91 has an isoelectric point at 5.19 and a molecular weight around 37.6 kdal.[4] C9orf91 is a member of a domain of unknown function, DUF4481.[5] The region is located within 37 and 328 in the amino acid sequence. BLAST results indicate there are no paralogs within humans, zebra fish, and fruit flies.

C9orf91 Domain and Transmembrane Globe Plot 2.[6]

Transmembrane Characteristics

Transmembrane conformation hypothesis of C9orf91.

Two predicted transmembrane regions are on the polypeptide, located at amino acids 104-125 and 130-152 respectively.[7] The SAPS tool on the San Diego Super Computing Biology Workbench garnered protein structural characteristics.[8]

An hypothesis for transmembrane direction is the N terminus and C terminus to remain within the cell, and the loop to stick out of the membrane into the cytosol, presented in the adjacent image.

Evidence for the transmembrane direction stems from phosphorylation site predictions. Net Phos 2.0 results for C9orf91 indicate regions of phosphorylation that are present present in areas around the transmembrane region. This indicates the N terminus and C terminus are going to be facing into the cell, providing support to the transmembrane direction.

Phosphorylation sites predicted on C9orf91.[9]

Protein Expression

The protein was found to be expressed in numerous different tissues. The ETS Profile for C9orf91 indicates the gene is expressed ubiquitously within the body.[10] In support, there has been experimental evidence using antibody staining to show various tissue types that express C9orf91.[11]

A recent study linked C9orf91 as a lysosome transporter.[12] The exact function within the lysosome and interactions with other molecules, however, is not known.

ETS Profile for C9orf91.

Associated Disease

Due to limited characterization, linkage to associated diseases is not well known. Techniques to view SNPs have been used in numerous diseases to determine loci influence. In spondylocostal dysostosis and spondyloarthritis, both were found to have SNPs that had indicated C9orf91 as a possible factor to the diseases[13][14]

Interacting Proteins

Interacting proteins were found with c-REL(via affinity chromotography and yeast-two hybrid) and ELAV1, via a yeast-two hybrid.[15][16] REL is assosciated to be a proto-oncogene that is from a family of transcription factors. It is assosciated with B-cell proliferation. ELAV1 is associated with binding to mRNA in order to help increase stability of transcripts.

Homology

Ortholog identity and similarity

Identity of orthologous domains within C9orf91 in other species with a 40% identity and above is shown below. The DUFF4481 start shown on the image retains conservation throughout time. Of interest, areas of transmembrane region are not as conserved as thought, indicating that specific amino acids may not be a vital component towards the protein's function.

Alignment of sample of orthologs based on 40% or more identity

Conservation within species

C9orf91 is conserved in many organisms. Orthologs have been found in mammals, birds, reptiles, amphibians, sharks, fish, and a few insects. It was not found within plants, bacteria, or archea. Amino acid length tends to increase within orthologs as divergence from humans goes up based on BLAST search results for similar proteins.

External links

References

  1. ↑ "I-TASSER server for protein structure and function prediction". zhanglab.ccmb.med.umich.edu. Retrieved 2016-05-08.
  2. ↑ [email protected], Danielle Thierry-Mieg and Jean Thierry-Mieg, NCBI/NLM/NIH,. "AceView: Gene:C9orf91, a comprehensive annotation of human, mouse and worm genes with mRNAs or ESTsAceView.". www.ncbi.nlm.nih.gov. Retrieved 2016-04-28.
  3. ↑ "NCBI Gene".
  4. ↑ "ExPASy isoelectric point".
  5. ↑ "transmembrane protein C9orf91 [Homo sapiens] - Protein - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2016-04-28.
  6. ↑ "GlobPlot 2.3 - Predictor of intrinsic protein disorder & globularity". globplot.embl.de. Retrieved 2016-04-28.
  7. ↑ "C9orf91 - Transmembrane protein C9orf91 - Homo sapiens (Human) - C9orf91 gene & protein". www.uniprot.org. Retrieved 2016-04-28.
  8. ↑ "SDSC Biology Workbench". workbench.sdsc.edu. Retrieved 2016-04-28.
  9. ↑ "GlobPlot 2.3 - Predictor of intrinsic protein disorder & globularity". globplot.embl.de. Retrieved 2016-04-28.
  10. ↑ "EST Profile - Hs.522357". www.ncbi.nlm.nih.gov. Retrieved 2016-04-28.
  11. ↑ "Tissue expression of C9orf91 - Summary - The Human Protein Atlas". www.proteinatlas.org. Retrieved 2016-04-28.
  12. ↑ Chapel, A., Kieffer-Jaquinod, S., Sagne, C., Verdon, Q., Ivaldi, C., Mellal, M., . . . Journet, A. (2013). An Extended Proteome Map of the Lysosomal Membrane Reveals Novel Potential Transporters. Molecular & Cellular Proteomics, 12(6), 1572-1588.
  13. ↑ Zinovieva, E., Kadi, A., Letourneur, F., Cagnard, N., Izac, B., Vigier, A., . . . Breban, M. (2011). Systematic candidate gene investigations in the SPA2 locus (9q32) show an association between TNFSF8 and susceptibility to spondylarthritis. Arthritis & Rheumatism, 63(7), 1853-1859.
  14. ↑ Sparrow, D. B., Mcinerney-Leo, A., Gucev, Z. S., Gardiner, B., Marshall, M., Leo, P. J., . . . Dunwoodie, S. L. (2013). Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6. Human Molecular Genetics, 22(8), 1625-1631. Retrieved from http://hmg.oxfordjournals.org/content/22/8/1625.short#cited-by
  15. ↑ Abdelmohsen, K., Srikantan, S., Yang, X., Lal, A., Kim, H. H., Kuwano, Y., . . . Gorospe, M. (2009). Ubiquitin-mediated proteolysis of HuR by heat shock. EMBO J The EMBO Journal, 28(9), 1271-1282. doi:10.1038/emboj.2009.67
  16. ↑ Wang J. et al. . Toward an understanding of the protein interaction network of the human liver. Mol. Syst. Biol. 7, 536 (2011).
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