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SKIDA1

Ski/Dach domain-containing protein 1 is a protein that in humans is encoded by the SKIDA1 gene.[5] It is also known as C10orf140 and DLN-1. It has orthologs in vertebrates. It has two domains: the Ski/Sno/Dac domain and a domain of unknown function, DUF4854. It is associated with multiple types of cancer, like leukemia, ovarian cancer, and colon cancer.[6][7] It's predicted to be a nuclear protein.[8] It may interact with PRC2.[9][10]

SKIDA1
Identifiers
AliasesSKIDA1, C10orf140, DLN-1, SKI/DACH domain containing 1
External IDsMGI: 1919918 HomoloGene: 66327 GeneCards: SKIDA1
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_207371

NM_028317

RefSeq (protein)

NP_997254

NP_082593

Location (UCSC)Chr 10: 21.51 – 21.53 MbChr 2: 18.05 – 18.05 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Homologs Edit

Orthologs Edit

SKIDA1 has orthologs in vertebrate species. The species least related to humans with a SKIDA1 ortholog is the lancelet Branchiostoma belcheri. The clades amphibia and chondrichthyes have at least two species with SKIDA1, but SKIDA1 is not found throughout the clades. No orthologs have been found in lungfish or invertebrate species.[11]

Paralogous Domains Edit

SKIDA1 shares the Ski/Sno/Dac domain with Ski oncogene (Ski), Ski-like protein (Sno), and dachshund (Dac).[12] It shares DUF4584 with Elongin BC Polycomb Repressive Complex 2 associated Protein (EPOP).[5]

Structure Edit

 
Diagram of the SKIDA1 protein.

In humans, SKIDA1 is located on the reverse strand of chromosome 10 at locus 10p12.31. It contains five exons.[5]

Isoforms Edit

There is not a consensus on whether humans have one or two SKIDA1 isoforms. NCBI Gene claims there is one, while UniProt claims there are two.[13][14] It's possible isoform 2 is recorded in NCBI Gene as DLN-1 (accession BAE93016.1). Isoform 1 is 908 amino acids long, while isoform 2 is 827 amino acids long; isoform 2 is missing amino acids 240-318 from isoform 1.[14] Isoform 1 is predicted to weigh 98 kDa and have an isoelectric point of 8.7, while isoform 2 is predicted to weigh 90 kDa and have an isoelectric point of 7.6.[15]

Other mammalian species also have multiple isoforms of SKIDA1, including carnivorans, rodents, and primates. The number of isoforms each species has varies: cheetahs have five recorded isoforms, chimpanzees have three recorded, and brown rats have two recorded.[16]

 
A predicted 3D structure of SKIDA1. The Ski/Sno/Dac domain, DUF4584, and C-Terminal region (amino acids 844-908) are annotated.

Amino Acid Repeats Edit

Human SKIDA1 contains two poly-alanine regions, one poly-histidine region, and one poly-glutamic acid region.[5] It's unknown if they have any function. The poly-alanine and poly-histidine regions are not highly conserved among orthologs; for example, while they are found in the house mouse ortholog, they are not found in the western lowland gorilla ortholog.[17][18] The poly-glutamic acid region shows more conservation, and is found abbreviated in species as distantly related from humans as the tire track eel.[19]

Domains Edit

SKIDA1 contains two domains: Ski/Sno/Dac and DUF4854. The Ski/Sno/Dac domain is at the N-terminus end of the protein. The Ski/Sno/Dac domain is also found in the proteins Ski, Ski-like protein, and dachshund.[12] It is potentially a DNA-binding domain.[20]

The other domain, DUF4854, is also found in EPOP, near its C-terminus. However, the DUF4584 found in EPOP is roughly a fifth the size of that in SKIDA1. The C-termini of SKIDA1 (amino acids 844-908) and EPOP (amino acids 313-379) have 52% identity. The C-terminus of EPOP binds to the SUZ12 subunit of Polycomb Repressive Complex 2 (PRC2), suggesting that of SKIDA1 may as well.[9]

Regulation Edit

Promoter and Transcription Factors Edit

In humans, there are five predicted potential promoters. Two align with the second half of the mRNA transcript, suggesting they are not used or only produce an incomplete polypeptide.[21]

The promoter that aligns best with the start of the mRNA transcript is potentially bound to by many transcription factors, including Transcription factor II B, Nuclear factor Y, Early growth response 1, and Krueppel-like factor 6.[21] It does not contain a TATA box.

Transcript Regulation Edit

SKIDA1 is regulated by microRNAs. miR-93 binds to the SKIDA1 3'-UTR.[22] Multiple microRNAs are predicted to bind to the SKIDA1 3'-UTR, including miR-130, miR-301, miR-454, and miR-494.[23]

Polypeptide Modification Edit

SKIDA1 is SUMOylated at five sites.[24] Additional sites are predicted to be SUMOylated.[25][26] SKIDA1 is also predicted to be phosphorylated and O-GlcNAcylated.[27][28]

Expression Edit

Subcellular Localization Edit

SKIDA1 is predicted to be localized primarily in the nucleus and less so in the cytosol.[8]

 
SKIDA1 is highly expressed in Purkinje cells in the cerebellum.

Tissue Expression Edit

SKIDA1 is expressed at high levels in the brain, thyroid, and testes. It's expressed at medium to low levels in adipose tissue, lymph nodes, and skeletal muscle.[29][30][31][32] In mice, it's noted to have medium-to-high expression in the olfactory bulb, retina, and salivary gland.[29]

Developmental Expression Edit

 
Expression of SKIDA1 in the house mouse fetal heart increases, then decreases with age.

SKIDA1 expression changes during organism development. Expression is low in the zygote, peaks during embryonic development, and is low post-birth. In the house mouse, it's expressed most during organogenesis.[33] In the fetus, its expression is low in the liver but not other organs.[34] Expression in the adult liver is much higher. In contrast, SKIDA1 expression in the fetal brain is higher than in the adult brain.[32]

SKIDA1 in the African clawed frog is expressed faintly in the marginal zone of gastrulae. During neurulation, it's expressed in the brain and cranial neural crest. During tailbud, SKIDA1 expression increases in sensory placodes. By the end of tailbud, neural expression has faded except in the olfactory organ.[35]

Function Edit

SKIDA1 is predicted to function primarily in the nucleus and also in the cytosol.[8]

SKIDA1 knockouts in mice have significant differences from wild-type mice in the skeletal, neurological, reproductive, and immune systems. Other significant differences include effected hearing, an enlarged thymus, and increased pre-weaning mortality.[36] Some, but not all, of these effects were found in heterozygous knockouts.

Clinical significance Edit

SKIDA1 expression is associated with multiple types of cancer. It is over-expressed in epithelial ovarian cancer cells.[37] Its expression is altered by various cancer-treatment compounds: human alpha-lactalbumin made lethal to tumor cells; oleate salts; metformin; and aspirin.[citation needed] In cell lines of cancerous cells, altered expression is associated with resistance to dasatinib and docetaxel, which are used to treat cancer.[38][39]

Altered methylation of SKIDA1 is associated with human pancreatic cancer, rheumatoid arthritis, and lupus erythematosus.[40][41] Additionally, SKIDA1 is expressed less in women with Down syndrome compared to their identical twins without Down syndrome.[42] Its expression is dramatically reduced in brains affected by untreated HIV1-associated neurocognitive disorders (HAND) in comparison to healthy brains and brains affected by HAND but treated with antiretrovirals.[43]

References Edit

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000180592 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000054074 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b c d "SKI/DACH domain-containing protein 1 [Homo sapiens]". NCBI. Retrieved 11 February 2019.
  6. ^ Pharoah PD, Tsai YY, Ramus SJ, Phelan CM, Goode EL, Lawrenson K, et al. (April 2013). "GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer". Nature Genetics. 45 (4): 362–70, 370e1-2. doi:10.1038/ng.2564. PMC 3693183. PMID 23535730.
  7. ^ Cortes-Ciriano I, Lee S, Park WY, Kim TM, Park PJ (June 2017). "A molecular portrait of microsatellite instability across multiple cancers". Nature Communications. 8: 15180. Bibcode:2017NatCo...815180C. doi:10.1038/ncomms15180. PMC 5467167. PMID 28585546.
  8. ^ a b c "PSORT II". PSORT II. 24 November 1999. Retrieved 12 April 2019.
  9. ^ a b Liefke R, Shi Y (2015-04-28). "The PRC2-associated factor C17orf96 is a novel CpG island regulator in mouse ES cells". Cell Discovery. 1: 15008. doi:10.1038/celldisc.2015.8. PMC 4860827. PMID 27462409.
  10. ^ Hauri S, Comoglio F, Seimiya M, Gerstung M, Glatter T, Hansen K, et al. (October 2016). "A High-Density Map for Navigating the Human Polycomb Complexome". Cell Reports. 17 (2): 583–595. doi:10.1016/j.celrep.2016.08.096. PMID 27705803.
  11. ^ "NCBI Protein". NCBI. Retrieved 10 February 2019.
  12. ^ a b "NCBI CDD CDD Conserved Protein Domain Ski_Sno". www.ncbi.nlm.nih.gov. Retrieved 2019-02-11.
  13. ^ "SKIDA1 SKI/DACH domain containing 1 [Homo sapiens (human)]". NCBI. 13 February 2019. Retrieved 1 May 2019.
  14. ^ a b "SKIDA1 - SKI/DACH domain-containing protein 1". UniProt. 10 April 2019. Retrieved 1 May 2019.
  15. ^ "Compute pI/Mw". ExPASy. Retrieved 2 April 2019.
  16. ^ Protein [Internet]. Bethesda (MD): National Library of Medicine (US), National Center for Biotechnology Information; 2004 – [cited 2019 March 2]. Available from: https://www.ncbi.nlm.nih.gov/protein/
  17. ^ "SKI/DACH domain-containing protein 1 [Mus musculus]". NCBI. 15 August 2018. Retrieved 26 February 2019.
  18. ^ "PREDICTED: SKI/DACH domain-containing protein 1[Gorilla gorilla gorilla]". NCBI. 4 November 2016. Retrieved 26 February 2019.
  19. ^ "SKI/Dach domain-containing protein 1 [Mastacembelus armatus]". NCBI. 6 September 2018. Retrieved 26 February 2019.
  20. ^ Kim SS, Zhang RG, Braunstein SE, Joachimiak A, Cvekl A, Hegde RS (June 2002). "Structure of the retinal determination protein Dachshund reveals a DNA binding motif". Structure. 10 (6): 787–95. doi:10.1016/S0969-2126(02)00769-4. PMID 12057194.
  21. ^ a b "Genome Annotation and Browser". Genomatix. December 2017. Retrieved 31 March 2019.
  22. ^ Saito K (2011). "The mechanism of inflammation in autoimmune response during the acute phase of Kawasaki disease". KAKEN. Retrieved 5 May 2019.
  23. ^ "TargetScanHuman 7.2 predicted targeting of Human SKIDA1". TargetScan. March 2018. Retrieved 31 March 2019.
  24. ^ Hendriks IA, Lyon D, Young C, Jensen LJ, Vertegaal AC, Nielsen ML (March 2017). "Site-specific mapping of the human SUMO proteome reveals co-modification with phosphorylation". Nature Structural & Molecular Biology. 24 (3): 325–336. doi:10.1038/nsmb.3366. PMID 28112733. S2CID 2651164.
  25. ^ "SUMOplot". Abgent. 2013. Retrieved 19 April 2019.
  26. ^ "GPS-SUMO: Prediction of SUMOylation Sites & SUMO-interaction Motifs". The CUCKOO Workshop. 2014. Retrieved 19 April 2019.
  27. ^ "GPS 3.0 - Kinase-specific Phosphorylation Site Prediction". The CUCKOO Workshop. Retrieved 19 April 2016.
  28. ^ "YinOYang 1.2 Server". DTU Bioinformatics. 2 January 2017. Retrieved 19 April 2019.
  29. ^ a b Su AI, Wiltshire T, Batalov S, Lapp H, Ching KA, Block D, et al. (April 2004). "A gene atlas of the mouse and human protein-encoding transcriptomes". Proceedings of the National Academy of Sciences of the United States of America. 101 (16): 6062–7. Bibcode:2004PNAS..101.6062S. doi:10.1073/pnas.0400782101. PMC 395923. PMID 15075390.
  30. ^ She X, Rohl CA, Castle JC, Kulkarni AV, Johnson JM, Chen R (June 2009). "Definition, conservation and epigenetics of housekeeping and tissue-enriched genes". BMC Genomics. 10 (1): 269. doi:10.1186/1471-2164-10-269. PMC 2706266. PMID 19534766.
  31. ^ Fagerberg L, Hallström BM, Oksvold P, Kampf C, Djureinovic D, Odeberg J, et al. (February 2014). "Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics". Molecular & Cellular Proteomics. 13 (2): 397–406. doi:10.1074/mcp.M113.035600. PMC 3916642. PMID 24309898.
  32. ^ a b Duff MO, Olson S, Wei X, Garrett SC, Osman A, Bolisetty M, et al. (May 2015). "Genome-wide identification of zero nucleotide recursive splicing in Drosophila". Nature. 521 (7552): 376–9. Bibcode:2015Natur.521..376D. doi:10.1038/nature14475. PMC 4529404. PMID 25970244.
  33. ^ "EST Profile - Mm.102183". NCBI Unigene. Retrieved 3 May 2019.
  34. ^ "GenePaint". GenePaint. Retrieved 29 March 2019.
  35. ^ Seufert DW, Hegde RS, Nekkalapudi S, Kelly LE, El-Hodiri HM (December 2005). "Expression of a novel Ski-like gene in Xenopus development". Gene Expression Patterns. 6 (1): 22–8. doi:10.1016/j.modgep.2005.05.004. PMID 16169285.
  36. ^ Dickinson ME, Flenniken AM, Ji X, Teboul L, Wong MD, White JK, et al. (September 2016). "High-throughput discovery of novel developmental phenotypes". Nature. 537 (7621): 508–514. Bibcode:2016Natur.537..508.. doi:10.1038/nature19356. PMC 5295821. PMID 27626380.
  37. ^ Pharoah PD, Tsai YY, Ramus SJ, Phelan CM, Goode EL, Lawrenson K, et al. (April 2013). "GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer". Nature Genetics. 45 (4): 362–70, 370e1-2. doi:10.1038/ng.2564. PMC 3693183. PMID 23535730.
  38. ^ Chien W, Sun QY, Lee KL, Ding LW, Wuensche P, Torres-Fernandez LA, Tan SZ, Tokatly I, Zaiden N, Poellinger L, Mori S, Yang H, Tyner JW, Koeffler HP (April 2015). "Activation of protein phosphatase 2A tumor suppressor as potential treatment of pancreatic cancer". Molecular Oncology. 9 (4): 889–905. doi:10.1016/j.molonc.2015.01.002. PMC 4387089. PMID 25637283.
  39. ^ Marín-Aguilera M, Codony-Servat J, Kalko SG, Fernández PL, Bermudo R, Buxo E, Ribal MJ, Gascón P, Mellado B (February 2012). "Identification of docetaxel resistance genes in castration-resistant prostate cancer". Molecular Cancer Therapeutics. 11 (2): 329–39. doi:10.1158/1535-7163.MCT-11-0289. PMID 22027694.
  40. ^ US 9994911, Ahlquist DA, Kisiel JB, Taylor WR, Yab TC, Mahoney DW, Lidgard GP, Allawi HT, "Detecting Neoplasm", issued 12 June 2018, assigned to Mayo Foundation for Medical Education and Research Exact Sciences Development Company LLC 
  41. ^ Julià A, Absher D, López-Lasanta M, Palau N, Pluma A, Waite Jones L, Glossop JR, Farrell WE, Myers RM, Marsal S (July 2017). "Epigenome-wide association study of rheumatoid arthritis identifies differentially methylated loci in B cells". Human Molecular Genetics. 26 (14): 2803–2811. doi:10.1093/hmg/ddx177. PMID 28475762.
  42. ^ Hibaoui Y, Grad I, Letourneau A, Santoni FA, Antonarakis SE, Feki A (December 2014). "Data in brief: Transcriptome analysis of induced pluripotent stem cells from monozygotic twins discordant for trisomy 21". Genomics Data. 2: 226–9. doi:10.1016/j.gdata.2014.07.006. PMC 4535757. PMID 26484098.
  43. ^ Borjabad A, Morgello S, Chao W, Kim SY, Brooks AI, Murray J, Potash MJ, Volsky DJ (September 2011). Desrosiers RC (ed.). "Significant effects of antiretroviral therapy on global gene expression in brain tissues of patients with HIV-1-associated neurocognitive disorders". PLOS Pathogens. 7 (9): e1002213. doi:10.1371/journal.ppat.1002213. PMC 3164642. PMID 21909266.

skida1, dach, domain, containing, protein, protein, that, humans, encoded, gene, also, known, c10orf140, orthologs, vertebrates, domains, domain, domain, unknown, function, duf4854, associated, with, multiple, types, cancer, like, leukemia, ovarian, cancer, co. Ski Dach domain containing protein 1 is a protein that in humans is encoded by the SKIDA1 gene 5 It is also known as C10orf140 and DLN 1 It has orthologs in vertebrates It has two domains the Ski Sno Dac domain and a domain of unknown function DUF4854 It is associated with multiple types of cancer like leukemia ovarian cancer and colon cancer 6 7 It s predicted to be a nuclear protein 8 It may interact with PRC2 9 10 SKIDA1IdentifiersAliasesSKIDA1 C10orf140 DLN 1 SKI DACH domain containing 1External IDsMGI 1919918 HomoloGene 66327 GeneCards SKIDA1Gene location Human Chr Chromosome 10 human 1 Band10p12 31Start21 513 475 bp 1 End21 526 368 bp 1 Gene location Mouse Chr Chromosome 2 mouse 2 Band2 2 A3Start18 045 487 bp 2 End18 053 862 bp 2 RNA expression patternBgeeHumanMouse ortholog Top expressed inendothelial cellganglionic eminenceBrodmann area 23middle temporal gyrusright lobe of thyroid glandleft lobe of thyroid glandprefrontal cortexright lobe of liverplacentaright adrenal glandTop expressed inganglionic eminenceneural tubeyolk sacmirrorproximal tubulesuperior frontal gyrusblastocystesophagusmorulastomachMore reference expression dataBioGPSn aOrthologsSpeciesHumanMouseEntrez38764072668EnsemblENSG00000180592ENSMUSG00000054074UniProtQ1XH10Q80YR3RefSeq mRNA NM 207371NM 028317RefSeq protein NP 997254NP 082593Location UCSC Chr 10 21 51 21 53 MbChr 2 18 05 18 05 MbPubMed search 3 4 WikidataView Edit HumanView Edit Mouse Contents 1 Homologs 1 1 Orthologs 1 2 Paralogous Domains 2 Structure 2 1 Isoforms 2 2 Amino Acid Repeats 2 3 Domains 3 Regulation 3 1 Promoter and Transcription Factors 3 2 Transcript Regulation 3 3 Polypeptide Modification 4 Expression 4 1 Subcellular Localization 4 2 Tissue Expression 4 3 Developmental Expression 5 Function 6 Clinical significance 7 ReferencesHomologs EditOrthologs Edit SKIDA1 has orthologs in vertebrate species The species least related to humans with a SKIDA1 ortholog is the lancelet Branchiostoma belcheri The clades amphibia and chondrichthyes have at least two species with SKIDA1 but SKIDA1 is not found throughout the clades No orthologs have been found in lungfish or invertebrate species 11 Paralogous Domains Edit SKIDA1 shares the Ski Sno Dac domain with Ski oncogene Ski Ski like protein Sno and dachshund Dac 12 It shares DUF4584 with Elongin BC Polycomb Repressive Complex 2 associated Protein EPOP 5 Structure Edit nbsp Diagram of the SKIDA1 protein In humans SKIDA1 is located on the reverse strand of chromosome 10 at locus 10p12 31 It contains five exons 5 Isoforms Edit There is not a consensus on whether humans have one or two SKIDA1 isoforms NCBI Gene claims there is one while UniProt claims there are two 13 14 It s possible isoform 2 is recorded in NCBI Gene as DLN 1 accession BAE93016 1 Isoform 1 is 908 amino acids long while isoform 2 is 827 amino acids long isoform 2 is missing amino acids 240 318 from isoform 1 14 Isoform 1 is predicted to weigh 98 kDa and have an isoelectric point of 8 7 while isoform 2 is predicted to weigh 90 kDa and have an isoelectric point of 7 6 15 Other mammalian species also have multiple isoforms of SKIDA1 including carnivorans rodents and primates The number of isoforms each species has varies cheetahs have five recorded isoforms chimpanzees have three recorded and brown rats have two recorded 16 nbsp A predicted 3D structure of SKIDA1 The Ski Sno Dac domain DUF4584 and C Terminal region amino acids 844 908 are annotated Amino Acid Repeats Edit Human SKIDA1 contains two poly alanine regions one poly histidine region and one poly glutamic acid region 5 It s unknown if they have any function The poly alanine and poly histidine regions are not highly conserved among orthologs for example while they are found in the house mouse ortholog they are not found in the western lowland gorilla ortholog 17 18 The poly glutamic acid region shows more conservation and is found abbreviated in species as distantly related from humans as the tire track eel 19 Domains Edit SKIDA1 contains two domains Ski Sno Dac and DUF4854 The Ski Sno Dac domain is at the N terminus end of the protein The Ski Sno Dac domain is also found in the proteins Ski Ski like protein and dachshund 12 It is potentially a DNA binding domain 20 The other domain DUF4854 is also found in EPOP near its C terminus However the DUF4584 found in EPOP is roughly a fifth the size of that in SKIDA1 The C termini of SKIDA1 amino acids 844 908 and EPOP amino acids 313 379 have 52 identity The C terminus of EPOP binds to the SUZ12 subunit of Polycomb Repressive Complex 2 PRC2 suggesting that of SKIDA1 may as well 9 Regulation EditPromoter and Transcription Factors Edit In humans there are five predicted potential promoters Two align with the second half of the mRNA transcript suggesting they are not used or only produce an incomplete polypeptide 21 The promoter that aligns best with the start of the mRNA transcript is potentially bound to by many transcription factors including Transcription factor II B Nuclear factor Y Early growth response 1 and Krueppel like factor 6 21 It does not contain a TATA box Transcript Regulation Edit SKIDA1 is regulated by microRNAs miR 93 binds to the SKIDA1 3 UTR 22 Multiple microRNAs are predicted to bind to the SKIDA1 3 UTR including miR 130 miR 301 miR 454 and miR 494 23 Polypeptide Modification Edit SKIDA1 is SUMOylated at five sites 24 Additional sites are predicted to be SUMOylated 25 26 SKIDA1 is also predicted to be phosphorylated and O GlcNAcylated 27 28 Expression EditSubcellular Localization Edit SKIDA1 is predicted to be localized primarily in the nucleus and less so in the cytosol 8 nbsp SKIDA1 is highly expressed in Purkinje cells in the cerebellum Tissue Expression Edit SKIDA1 is expressed at high levels in the brain thyroid and testes It s expressed at medium to low levels in adipose tissue lymph nodes and skeletal muscle 29 30 31 32 In mice it s noted to have medium to high expression in the olfactory bulb retina and salivary gland 29 Developmental Expression Edit nbsp Expression of SKIDA1 in the house mouse fetal heart increases then decreases with age SKIDA1 expression changes during organism development Expression is low in the zygote peaks during embryonic development and is low post birth In the house mouse it s expressed most during organogenesis 33 In the fetus its expression is low in the liver but not other organs 34 Expression in the adult liver is much higher In contrast SKIDA1 expression in the fetal brain is higher than in the adult brain 32 SKIDA1 in the African clawed frog is expressed faintly in the marginal zone of gastrulae During neurulation it s expressed in the brain and cranial neural crest During tailbud SKIDA1 expression increases in sensory placodes By the end of tailbud neural expression has faded except in the olfactory organ 35 Function EditSKIDA1 is predicted to function primarily in the nucleus and also in the cytosol 8 SKIDA1 knockouts in mice have significant differences from wild type mice in the skeletal neurological reproductive and immune systems Other significant differences include effected hearing an enlarged thymus and increased pre weaning mortality 36 Some but not all of these effects were found in heterozygous knockouts Clinical significance EditSKIDA1 expression is associated with multiple types of cancer It is over expressed in epithelial ovarian cancer cells 37 Its expression is altered by various cancer treatment compounds human alpha lactalbumin made lethal to tumor cells oleate salts metformin and aspirin citation needed In cell lines of cancerous cells altered expression is associated with resistance to dasatinib and docetaxel which are used to treat cancer 38 39 Altered methylation of SKIDA1 is associated with human pancreatic cancer rheumatoid arthritis and lupus erythematosus 40 41 Additionally SKIDA1 is expressed less in women with Down syndrome compared to their identical twins without Down syndrome 42 Its expression is dramatically reduced in brains affected by untreated HIV1 associated neurocognitive disorders HAND in comparison to healthy brains and brains affected by HAND but treated with antiretrovirals 43 References Edit a b c GRCh38 Ensembl release 89 ENSG00000180592 Ensembl May 2017 a b c GRCm38 Ensembl release 89 ENSMUSG00000054074 Ensembl May 2017 Human PubMed Reference National Center for Biotechnology Information U S National Library of Medicine Mouse PubMed Reference National Center for Biotechnology Information U S National Library of Medicine a b c d SKI DACH domain containing protein 1 Homo sapiens NCBI Retrieved 11 February 2019 Pharoah PD Tsai YY Ramus SJ Phelan CM Goode EL Lawrenson K et al April 2013 GWAS meta analysis and replication identifies three new susceptibility loci for ovarian cancer Nature Genetics 45 4 362 70 370e1 2 doi 10 1038 ng 2564 PMC 3693183 PMID 23535730 Cortes Ciriano I Lee S Park WY Kim TM Park PJ June 2017 A molecular portrait of microsatellite instability across multiple cancers Nature Communications 8 15180 Bibcode 2017NatCo 815180C doi 10 1038 ncomms15180 PMC 5467167 PMID 28585546 a b c PSORT II PSORT II 24 November 1999 Retrieved 12 April 2019 a b Liefke R Shi Y 2015 04 28 The PRC2 associated factor C17orf96 is a novel CpG island regulator in mouse ES cells Cell Discovery 1 15008 doi 10 1038 celldisc 2015 8 PMC 4860827 PMID 27462409 Hauri S Comoglio F Seimiya M Gerstung M Glatter T Hansen K et al October 2016 A High Density Map for Navigating the Human Polycomb Complexome Cell Reports 17 2 583 595 doi 10 1016 j celrep 2016 08 096 PMID 27705803 NCBI Protein NCBI Retrieved 10 February 2019 a b NCBI CDD CDD Conserved Protein Domain Ski Sno www ncbi nlm nih gov Retrieved 2019 02 11 SKIDA1 SKI DACH domain containing 1 Homo sapiens human NCBI 13 February 2019 Retrieved 1 May 2019 a b SKIDA1 SKI DACH domain containing protein 1 UniProt 10 April 2019 Retrieved 1 May 2019 Compute pI Mw ExPASy Retrieved 2 April 2019 Protein Internet Bethesda MD National Library of Medicine US National Center for Biotechnology Information 2004 cited 2019 March 2 Available from https www ncbi nlm nih gov protein SKI DACH domain containing protein 1 Mus musculus NCBI 15 August 2018 Retrieved 26 February 2019 PREDICTED SKI DACH domain containing protein 1 Gorilla gorilla gorilla NCBI 4 November 2016 Retrieved 26 February 2019 SKI Dach domain containing protein 1 Mastacembelus armatus NCBI 6 September 2018 Retrieved 26 February 2019 Kim SS Zhang RG Braunstein SE Joachimiak A Cvekl A Hegde RS June 2002 Structure of the retinal determination protein Dachshund reveals a DNA binding motif Structure 10 6 787 95 doi 10 1016 S0969 2126 02 00769 4 PMID 12057194 a b Genome Annotation and Browser Genomatix December 2017 Retrieved 31 March 2019 Saito K 2011 The mechanism of inflammation in autoimmune response during the acute phase of Kawasaki disease KAKEN Retrieved 5 May 2019 TargetScanHuman 7 2 predicted targeting of Human SKIDA1 TargetScan March 2018 Retrieved 31 March 2019 Hendriks IA Lyon D Young C Jensen LJ Vertegaal AC Nielsen ML March 2017 Site specific mapping of the human SUMO proteome reveals co modification with phosphorylation Nature Structural amp Molecular Biology 24 3 325 336 doi 10 1038 nsmb 3366 PMID 28112733 S2CID 2651164 SUMOplot Abgent 2013 Retrieved 19 April 2019 GPS SUMO Prediction of SUMOylation Sites amp SUMO interaction Motifs The CUCKOO Workshop 2014 Retrieved 19 April 2019 GPS 3 0 Kinase specific Phosphorylation Site Prediction The CUCKOO Workshop Retrieved 19 April 2016 YinOYang 1 2 Server DTU Bioinformatics 2 January 2017 Retrieved 19 April 2019 a b Su AI Wiltshire T Batalov S Lapp H Ching KA Block D et al April 2004 A gene atlas of the mouse and human protein encoding transcriptomes Proceedings of the National Academy of Sciences of the United States of America 101 16 6062 7 Bibcode 2004PNAS 101 6062S doi 10 1073 pnas 0400782101 PMC 395923 PMID 15075390 She X Rohl CA Castle JC Kulkarni AV Johnson JM Chen R June 2009 Definition conservation and epigenetics of housekeeping and tissue enriched genes BMC Genomics 10 1 269 doi 10 1186 1471 2164 10 269 PMC 2706266 PMID 19534766 Fagerberg L Hallstrom BM Oksvold P Kampf C Djureinovic D Odeberg J et al February 2014 Analysis of the human tissue specific expression by genome wide integration of transcriptomics and antibody based proteomics Molecular amp Cellular Proteomics 13 2 397 406 doi 10 1074 mcp M113 035600 PMC 3916642 PMID 24309898 a b Duff MO Olson S Wei X Garrett SC Osman A Bolisetty M et al May 2015 Genome wide identification of zero nucleotide recursive splicing in Drosophila Nature 521 7552 376 9 Bibcode 2015Natur 521 376D doi 10 1038 nature14475 PMC 4529404 PMID 25970244 EST Profile Mm 102183 NCBI Unigene Retrieved 3 May 2019 GenePaint GenePaint Retrieved 29 March 2019 Seufert DW Hegde RS Nekkalapudi S Kelly LE El Hodiri HM December 2005 Expression of a novel Ski like gene in Xenopus development Gene Expression Patterns 6 1 22 8 doi 10 1016 j modgep 2005 05 004 PMID 16169285 Dickinson ME Flenniken AM Ji X Teboul L Wong MD White JK et al September 2016 High throughput discovery of novel developmental phenotypes Nature 537 7621 508 514 Bibcode 2016Natur 537 508 doi 10 1038 nature19356 PMC 5295821 PMID 27626380 Pharoah PD Tsai YY Ramus SJ Phelan CM Goode EL Lawrenson K et al April 2013 GWAS meta analysis and replication identifies three new susceptibility loci for ovarian cancer Nature Genetics 45 4 362 70 370e1 2 doi 10 1038 ng 2564 PMC 3693183 PMID 23535730 Chien W Sun QY Lee KL Ding LW Wuensche P Torres Fernandez LA Tan SZ Tokatly I Zaiden N Poellinger L Mori S Yang H Tyner JW Koeffler HP April 2015 Activation of protein phosphatase 2A tumor suppressor as potential treatment of pancreatic cancer Molecular Oncology 9 4 889 905 doi 10 1016 j molonc 2015 01 002 PMC 4387089 PMID 25637283 Marin Aguilera M Codony Servat J Kalko SG Fernandez PL Bermudo R Buxo E Ribal MJ Gascon P Mellado B 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