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From Wikipedia, the free encyclopedia

Death inducer-obliterator 1

PDB rendering based on 1wem.
Available structures
Symbols DIDO1; DIO1; BYE1; C20orf158; DATF1; DIDO2; DIDO3; DIO-1; DKFZp434P1115; FLJ11265; KIAA0333; MGC16140; dJ885L7.8
External IDs OMIM604140 MGI1344352 HomoloGene34139 GeneCards: DIDO1 Gene
RNA expression pattern
PBB GE DIDO1 218325 s at tn.png
More reference expression data
Species Human Mouse
Entrez 11083 23856
Ensembl ENSG00000101191 ENSMUSG00000038914
UniProt Q9BTC0 Q05C59
RefSeq (mRNA) NM_022105 NM_011805
RefSeq (protein) NP_071388 NP_035935
Location (UCSC) Chr 20:
60.98 - 61.04 Mb
Chr 2:
180.59 - 180.64 Mb
PubMed search [1] [2]

Death-inducer obliterator 1 is a protein that in humans is encoded by the DIDO1 gene.[1][2]

Apoptosis, a major form of cell death, is an efficient mechanism for eliminating unwanted cells and is of central importance for development and homeostasis in metazoan animals. In mice, the death inducer-obliterator-1 gene is upregulated by apoptotic signals and encodes a cytoplasmic protein that translocates to the nucleus upon apoptotic signal activation. When overexpressed, the mouse protein induced apoptosis in cell lines growing in vitro. This gene is similar to the mouse gene and therefore is thought to be involved in apoptosis. Alternatively spliced transcripts have been found for this gene, encoding multiple isoforms.[2]


  1. ^ Garcia-Domingo D, Leonardo E, Grandien A, Martinez P, Albar JP, Izpisua-Belmonte JC, Martinez-A C (Aug 1999). "DIO-1 is a gene involved in onset of apoptosis in vitro, whose misexpression disrupts limb development". Proc Natl Acad Sci U S A 96 (14): 7992-7. PMID 10393935.  
  2. ^ a b "Entrez Gene: DIDO1 death inducer-obliterator 1".  

Further reading

  • Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery.". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.  
  • Nagase T, Ishikawa K, Nakajima D, et al. (1997). "Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.". DNA Res. 4 (2): 141–50. doi:10.1093/dnares/4.2.141. PMID 9205841.  
  • Deloukas P, Matthews LH, Ashurst J, et al. (2002). "The DNA sequence and comparative analysis of human chromosome 20.". Nature 414 (6866): 865–71. doi:10.1038/414865a. PMID 11780052.  
  • Gomes I, Sharma TT, Edassery S, et al. (2002). "Novel transcription factors in human CD34 antigen-positive hematopoietic cells.". Blood 100 (1): 107–19. doi:10.1182/blood.V100.1.107. PMID 12070015.  
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.  
  • Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.  
  • Brandenberger R, Wei H, Zhang S, et al. (2005). "Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation.". Nat. Biotechnol. 22 (6): 707–16. doi:10.1038/nbt971. PMID 15146197.  
  • Fu GK, Wang JT, Yang J, et al. (2005). "Circular rapid amplification of cDNA ends for high-throughput extension cloning of partial genes.". Genomics 84 (1): 205–10. doi:10.1016/j.ygeno.2004.01.011. PMID 15203218.  
  • Beausoleil SA, Jedrychowski M, Schwartz D, et al. (2004). "Large-scale characterization of HeLa cell nuclear phosphoproteins.". Proc. Natl. Acad. Sci. U.S.A. 101 (33): 12130–5. doi:10.1073/pnas.0404720101. PMID 15302935.  
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.  
  • Fütterer A, Campanero MR, Leonardo E, et al. (2005). "Dido gene expression alterations are implicated in the induction of hematological myeloid neoplasms.". J. Clin. Invest. 115 (9): 2351–62. doi:10.1172/JCI24177. PMID 16127461.  
  • Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.  
  • Beausoleil SA, Villén J, Gerber SA, et al. (2006). "A probability-based approach for high-throughput protein phosphorylation analysis and site localization.". Nat. Biotechnol. 24 (10): 1285–92. doi:10.1038/nbt1240. PMID 16964243.  
  • Olsen JV, Blagoev B, Gnad F, et al. (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.". Cell 127 (3): 635–48. doi:10.1016/j.cell.2006.09.026. PMID 17081983.  
  • Trachana V, van Wely KH, Guerrero AA, et al. (2007). "Dido disruption leads to centrosome amplification and mitotic checkpoint defects compromising chromosome stability.". Proc. Natl. Acad. Sci. U.S.A. 104 (8): 2691–6. doi:10.1073/pnas.0611132104. PMID 17299043.  

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.



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