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DCC1

Introduction

Sister chromatid cohesion protein DCC1 is a protein that in humans is encoded by the DSCC1 gene.[1][2]

Model organisms

Model organisms

Model organisms have been used in the study of DSCC1 function. A conditional knockout mouse line, called Dscc1tm1a(KOMP)Wtsi[8][9] was generated at the Wellcome Trust Sanger Institute as part of the International Knockout Mouse Consortium program β€” a high-throughput mutagenesis project to generate and distribute animal models of disease to interested scientists.[10][11][12]

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[6][13] Twenty four tests were carried out on mutant mice and four significant abnormalities were observed.[6] Few homozygous mutant embryos were identified during gestation, and some displayed oedema, therefore less than expected survived until weaning. Those that did survive had increased chromosomal instability in a micronucleus test and numerous skeletal abnormalities by radiography.[6]

Interactions

Interactions

DCC1 has been shown to interact with CHTF18.[14][15]

References

References

  1. ↑ Merkle CJ, Karnitz LM, Henry-SΓ‘nchez JT, Chen J (Aug 2003). “Cloning and characterization of hCTF18, hCTF8, and hDCC1. Human homologs of a Saccharomyces cerevisiae complex involved in sister chromatid cohesion establishment”. The Journal of Biological Chemistry. 278 (32): 30051–6. doi:10.1074/jbc.M211591200. PMIDΒ 12766176.
  2. ↑ “Entrez Gene: DCC1 defective in sister chromatid cohesion homolog 1 (S. cerevisiae)”.
  3. ↑ “Radiography data for Dscc1”. Wellcome Trust Sanger Institute.
  4. ↑ “Salmonella infection data for Dscc1″. Wellcome Trust Sanger Institute.
  5. ↑ “Citrobacter infection data for Dscc1″. Wellcome Trust Sanger Institute.
  6. ↑ 6.0 6.1 6.2 6.3 White JK, Gerdin AK, Karp NA, Ryder E, Buljan M, Bussell JN, Salisbury J, Clare S, Ingham NJ, Podrini C, Houghton R, Estabel J, Bottomley JR, Melvin DG, Sunter D, Adams NC, Tannahill D, Logan DW, Macarthur DG, Flint J, Mahajan VB, Tsang SH, Smyth I, Watt FM, Skarnes WC, Dougan G, Adams DJ, Ramirez-Solis R, Bradley A, Steel KP (Jul 2013). “Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes”. Cell. 154 (2): 452–64. doi:10.1016/j.cell.2013.06.022. PMCΒ 3717207. PMIDΒ 23870131.
  7. ↑ Mouse Resources Portal, Wellcome Trust Sanger Institute.
  8. ↑ “International Knockout Mouse Consortium”.
  9. ↑ “Mouse Genome Informatics”.
  10. ↑ Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF, Bradley A (Jun 2011). “A conditional knockout resource for the genome-wide study of mouse gene function”. Nature. 474 (7351): 337–42. doi:10.1038/nature10163. PMCΒ 3572410. PMIDΒ 21677750.
  11. ↑ Dolgin E (Jun 2011). “Mouse library set to be knockout”. Nature. 474 (7351): 262–3. doi:10.1038/474262a. PMIDΒ 21677718.
  12. ↑ Collins FS, Rossant J, Wurst W (Jan 2007). “A mouse for all reasons”. Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMIDΒ 17218247.
  13. ↑ van der Weyden L, White JK, Adams DJ, Logan DW (2011). “The mouse genetics toolkit: revealing function and mechanism”. Genome Biology. 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMCΒ 3218837. PMIDΒ 21722353.
  14. ↑ Merkle CJ, Karnitz LM, Henry-SΓ‘nchez JT, Chen J (Aug 2003). “Cloning and characterization of hCTF18, hCTF8, and hDCC1. Human homologs of a Saccharomyces cerevisiae complex involved in sister chromatid cohesion establishment”. The Journal of Biological Chemistry. 278 (32): 30051–6. doi:10.1074/jbc.M211591200. PMIDΒ 12766176.
  15. ↑ Bermudez VP, Maniwa Y, Tappin I, Ozato K, Yokomori K, Hurwitz J (Sep 2003). “The alternative Ctf18-Dcc1-Ctf8-replication factor C complex required for sister chromatid cohesion loads proliferating cell nuclear antigen onto DNA”. Proceedings of the National Academy of Sciences of the United States of America. 100 (18): 10237–42. doi:10.1073/pnas.1434308100. PMCΒ 193545. PMIDΒ 12930902.
Further reading

Further reading