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OSER1
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OSER1

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OSER1
Identifiers
Aliases OSER1, C20orf111, HSPC207, Osr1, Perit1, dJ1183I21.1, oxidative stress responsive serine rich 1
External IDs MGI: 1913930 HomoloGene: 9521 GeneCards: OSER1
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_016470

NM_025699

RefSeq (protein)

NP_057554

NP_079975

Location (UCSC) Chr 20: 44.2 – 44.21 Mb Chr 2: 163.25 – 163.27 Mb
PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Chromosome 20 open reading frame 111, or C20orf111, is the hypothetical protein that in humans is encoded by the C20orf111 gene. C20orf111 is also known as Perit1 (peroxide inducible transcript 1), HSPC207, and dJ1183I21.1. It was originally located using genomic sequencing of chromosome 20. The National Center for Biotechnology Information, or NCBI, shows that it is located at q13.11 on chromosome 20, however the genome browser at the University of California-Santa Cruz (UCSC) website shows that it is at location q13.12, and within a million base pairs of the adenosine deaminase locus. It was also found to have an increase in expression in cells undergoing hydrogen peroxide(H
2
O
2
)-induced apoptosis. After analyzing the amino acid content of C20orf111, it was found to be rich in serine residues.

Gene

C20orf111 a valid, protein coding gene that is found on the minus strand of chromosome 20 at q13.12 by searching the UCSC Genome Browser, but q13.11 according to Refseq on NCBI.


Gene neighborhood

A few of the known genes near C20orf111 are given in the box below with their known function.

Gene Chromosomal Location Strand Function
Junctophilin 2 (JPH2) 20q13.12 Minus Help facilitate the assembly of DHPR with other proteins of the excitation-contraction coupling machinery. Loss of function leads to cardiac-specific JPH2 deficiency and results in lower cardiac contractility
TOX high mobility group box family member 2 (Tox2) 20q13.12 Plus Shown to play a large role in transcription activation
Adenosine deaminase (ADA) 20q13.12 Minus Encodes an enzyme that catalyzes the hydrolysis of adenosine to inosine. Deficiency in this enzyme causes a form of severe combined immunodeficiency disease (SCID), in which there is dysfunction of both B and T lymphocytes with impaired cellular immunity and decreased production of immunoglobulins.

Transcript

General properties

Transcript variants

Transcript Variants of C20orf111

10 splice isoforms that encode good proteins, altogether 8 different isoforms, 2 of which are complete isoforms. The image below shows the 10 isoforms that are predicted. Of these 10 splice isoforms, 8 have varying peptide lengths, however all of these proteins are only hypothetical with no extensive research done on them.

Transcription regulation

When looking at the predicted promoter sequence, there are no RNA Polymerase II binding sites, however there is a binding site for core promoter element for TATA-less promoters. In this same region of the promoter, there is also a TATA-binding factor sequence, which helps in the positioning of RNA polymerase II for transcription.

Protein

General properties

Function

The function of C20orf111 is not well understood by the scientific community. It does contain a domain of unknown function, DUF776, which has a large segment that is conserved well conserved through Xenopus tropicalus. It is also shown to have an increase in expression in rat cardiomyocytes undergoing hydrogen peroxide induced apoptosis.

Expression

When looking at the EST Profiles in humans, normal tissue (non-cancerous), expresses at a level of 82 transcripts per million. C20orf111 has been shown to increase in expression in rat cardiac myocytes undergoing |H|2|O|2|-induced apoptosis, suggesting a role in cell death. In bladder, cervical, head and neck, non-neoplasia, pancreatic, and prostate cancer cells, there are expression levels lower than normal.

Expression of Perit1 in cancerous cells according to NCBI Geo Profiles.

Homology

C20orf111 gene has no clear paralogs in the human genome. However, it has many orthologs in other organisms, and is conserved highly in organisms such as Xenopus tropicalis and is semi-conserved in the proto-animal Trichoplax adherens at the C-terminus.

The following table presents a select number of the orthologs found.

Scientific name Common Name Accession Number Sequence Length(aa) Percent Identity Percent Similarity
Homo sapiens Human NP_057554.4 292 - -
Pan troglodytes Chimpanzee NP_001151026.1 292 99.7 99
Ailuropoda melanoleuca Giant Panda XP_002917406 292 92 96
Equus caballus Horse XP_001503005.1 292 91 96
Mus musculus Mouse NP_079975 291 87 92
Ornithorhynchus anatinus Platypus XP_001513001 293 66 73
Gallus gallus Chicken NP_001025152 294 66 75
Xenopus tropicalis W.Clawed Frog NP_988917 291 58 69
Danio rerio Zebrafish XP_956651 300 45 59
Nasonia vitripennis Jewel Wasp XP_003424720 271 58 14
Drosophila melanogaster Fruit Fly NP_609391 287 47 18
Trichoplax adhaerens Trichoplax XP_002114376 237 46 13

Conservation

The image below is a multiple sequence alignment comparing the conservation of the C20orf111 protein amongst other organisms. The protein is highly conserved in the DUF776 region amongst vertebrates, and also at the C-terminus in eukaryotes.

MSA of the orthologs of C20orf111 protein

Predicted post-translational modification

C20orf111 protein schematic showing predicted secondary structure and post-translational modifications.

Using tools at ExPASy the following are predicted post-translational modifications for C20orf111.

  • Predicted propeptide cleavage site in protein between position R81 and S82.
  • 30 predicted Serine phosphorylation sites
  • 5 predicted Threonine phosphorylation sites
  • 3 predicted Tyrosine phosphorylation sites

Predicted secondary structure

PELE (Protein Secondary Structure Prediction) was used to predict the secondary structure of C20orf111. There is little in the way of β-strand or α-helix secondary structure, but a large part of the protein appears to exist as random coils. This is shown on the image of the C20orf111 images to the right.

External links


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