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Background
[edit]My name is Justine Nowicki, I am a student in BIO3595 (Advanced Genetics) at Western University. I am an undergraduate student pursuing a Ivey HBA (Honours Business Administration) and Honours Specialization in Genetics.
DOPEY2
[edit]DOPEY2 is a human gene located just above the Down Syndrome chromosomal region (DSCR) located at 21p22.2 sub-band[1][2]. Although the exact function of the this gene is not yet fully understood, it has been proven to play a role in multiple biological processes, and its over-expression (triplication) has been linked to multiple facets of the Down Syndrome phenotype, most notably mental retardation[2].
Gene
[edit]The DOPEY2 gene is located on human chromosome 21, at chromosome band 21q22.12. This band is located in open reading frame 5, hence the alias C21orf5. DOPEY2 gene is composed of 137,493 bases making up 37 exons and 39 distinct gt-ag introns, all located between CBR3 and KIAA0136 genes[1][3].
Transcription produces 10 unique mRNAs, 8 alternatively spliced variants, and 2 unspliced forms. These unique mRNAs differ by varying truncation of the 3’ and 5’ ends, as well as the presence of 3 cassette exons[3]. These mRNA variants range from 7691bp (mRNA variant DOPEY2.aAug10) to 315bp (mRNA variant DOPEY2.jAug10-unspliced) and are further described in the table below[3]:
mRNA
Variant |
Spliced mRNA Length | Protein Length | 5' UTR | 3' UTR | Unspliced pre-mRNA Length | Number of Exons | Tissue-mRNA Expression (no strict specificity implied) |
---|---|---|---|---|---|---|---|
aAug10 | 7691 bp | 2298 aa | 85 bp | 709 bp | 129746 bp | 37 | ubiquitous |
bAug10 | 2173 bp | 332aa | 1174 bp | 15610 bp | 6 | carcinoid, lung, colon, colon tumor, RER+ | |
cAug10 | 742 bp | 222 aa | 74 bp | 49789 bp | 6 | breast, t-lymphocytes | |
dAug10 | 623 bp | 145 aa | 188 bp | 43664 bp | 4 | lung | |
eAug10 | 345 bp | 114 aa | 9925 bp | 3 | spleen | ||
fAug10 | 571 bp | 110 aa | 241 bp | 1322 bp | 2 | thalamus | |
gAug10 | 549 bp | non-coding | 11 bp | 499 bp | 794 bp | 2 | spleen |
hAug- unspliced | 543 bp | non-coding | 377 bp | 543 bp | 1 | stomach | |
iAug10 | 514 bp | non-coding | 205 bp | 204 bp | 7377 bp | 2 | thyroid gland |
jAug10-
unspliced |
315 bp | non-coding | 165 bp | 315 bp | 1 | marrow |
The mRNA expressed and levels of expression differ based on the location and tissue type in the body, but overall has been found to be expressed ubiquitously[1]. The highest expression has been found in differentiating, rather than proliferating tissue zones. Transcript was identified with the highest confidence in the erythroleukemia, placental cells and overall in the brain, and at a medium confidence level in the perirhinal cortex, medial temporal lobe, colon, as well in the salivary and adrenal glands[4].
Protein
[edit]Of the 10 mRNAs produced, 6 of them are translated into viable proteins. Please see table above for more details. The largest, having a molecular weight of 258230 Da, and highest expressed protein, DOPEY2.a, is composed of 2298 amino acids that make up an N-terminal domain, 7 transmembrane domains, and a C-terminal coiled coil stretch that forms a leucine-like zipper domain[3]. Like other leucine zippers domains, DOPEY2's C-terminal is hypothesized to be involved in multiple protein-protein and transcription factor interactions[1]. This indicates that DOPEY2 might act as a transcription co-activator; however, further research must be done to fully understand the precise physiological function[1].
Protein Interactions
[edit]Although very little work has been done on understanding the intricacies of the protein interactions; however, STRING has identified direct links with three proteins: MON2, TRIP12, and HECTD1. DOPEY2 is also indirectly associated with the following proteins: ARL16, ATP9A, ARL1, ATP9B, UBE3A, HERC5, HERC4, HACE1, UBE3C, and UBR5[5].
![](http://upload.wikimedia.org/wikipedia/commons/thumb/8/8e/DOPEY2_protein.interactions.jpg/220px-DOPEY2_protein.interactions.jpg)
Homology
[edit]Phylogenesis suggest that DOPEY2 can be traced back to a common ancestor of animals and fungi due to its highly conserved C-terminal domain DOPEY2 has 84 known orthologs and 158 speciation nodes in the gene tree. The most similar orthologs being in the chimpanzee (Pan troglodytes), dog (Canis familiaris), cow (Bos Taurus), as well as the rat and mouse (Rattus norvegicus and Mus musculus).[6]
The only known paralog is DOPEY1[6].
Sub-cellular localization
[edit]Gene Ontology (GO) has traced the DOPEY2 protein to 5 main areas: the Golgi membrane, endosomes, the trans-Golgi network, cytosol, and extracellular endosome. COMPARTMENTS localization data places the highest confidence of localization to the extracellular exosome and the Golgi membrane.
Function
[edit]AS mentioned previously, the specific function and however, its function can be largely inferred through the study of similar genes. DOPEY2 has been found to be involved in the following processes: multicellular organism development in cell differentiation and developmental patterning, cognition, as well as endoplasmic reticulum organization and Golgi to endosome transport.
Cell Differentiation and Patterning
[edit]The DOPEY2 ortholog, pad-1, in C. elegans was found to have a role in cell differentiation and patterning. In an experiment where the pad-1 was silenced using RNA-mediated interference. The phenotype of the injected worm's offspring was fetal lethality, as most of the embryonic tissues did not undergo appropriate cell patterning during gastrulation. Abnormally positioned cells lead to misinformation of organs; the failed morphogenesis of embryo. A similar observation was made in the inactivation of the DOP1 gene in S. cerevisiae. The inactivation lead to abnormal cell positioning and subsequent death. Overexpression of the N-terminal in S. cerevisiae also resulted in a loss of proper growth polarity and abnormal asexual reproductive patterning. This function was further supported by the function of the ortholog DopA in A. nidulans, which similarly codes for a 207kDa protein that also contains leucine zipper-like domains. Its inactivation revealed its role directing alternations in cell division timing, growth polarity, as well as cell-specific gene expression, ultimately affecting organogenesis and cell differentiation.
Cognition
[edit]DOPEY2 has been identified as a CNV region in Alzheimer's Disease subjects, and its triplication has been tied to various phenotypic aspects of Down Syndrome.
Endoplasmic Reticulum and Golgi Transport
[edit]Dop1, an ortholog of DOPEY2, in S. cerevisiae was found to play a essential role in membrane organization. It was found that it forms a complex with another protein, Mon2, which recruits the pool of Dop1 from the Golgi. In a Mon2 knockout model, Dop1 was mislocalized, and in turn resulted in defective cycling between endosomes and the Golgi. In a Dop1 knockout model, severe defects in the endoplasmic reticulum organization. This Dop1 and Mon2 complex was also linked to traffic in the enocytic pathway.
Clinical Relevance
[edit]DOPEY2 has been linked to the Down Syndrome phenotype. When DOPEY2 was overexpressed in mice, abnormal lamination patterns of cortical cells was observed, as well as altered cortical, hippocampal, and cerebellar cells, regions that play key roles in memory and learning. These changes are similar to those observed in Down Syndrome patients. It is because of this that C21orf15 is now being studied as a new candidate gene for the mental retardation phenotype in Down Syndrome.
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- ^ a b c d e Rachidi, Mohammed; Lopes, Carmela; Costantine, Maher; Delabar, Jean-Maurice (2005-01-01). "C21orf5, a New Member of Dopey Family Involved in Morphogenesis, Could Participate in Neurological Alterations and Mental Retardation in Down Syndrome". DNA Research. 12 (3): 203–210. doi:10.1093/dnares/dsi004. ISSN 1340-2838.
- ^ a b Guipponi, M.; Brunschwig, K.; Chamoun, Z.; Scott, H. S.; Shibuya, K.; Kudoh, J.; Delezoide, A. L.; El Samadi, S.; Chettouh, Z. (2000-08-15). "C21orf5, a novel human chromosome 21 gene, has a Caenorhabditis elegans ortholog (pad-1) required for embryonic patterning". Genomics. 68 (1): 30–40. doi:10.1006/geno.2000.6250. ISSN 0888-7543. PMID 10950924.
- ^ a b c d Consortium, Gene Ontology. "AmiGO 2: Term Details for "molecular_function" (GO:0003674)". amigo.geneontology.org. Retrieved 2017-11-29.
- ^ "COMPARTMENTS - DOPEY2". compartments.jensenlab.org. Retrieved 2017-11-29.
- ^ a b "26 items (Homo sapiens) - STRING network view". string-db.org. Retrieved 2017-11-29.
- ^ a b "Gene: DOPEY2 (ENSG00000142197) - Gene tree - Homo sapiens - Ensembl genome browser 90". www.ensembl.org. Retrieved 2017-11-29.