Korean Journal of Poultry Science (한국가금학회지)

The Korean Society of Poultry Science (한국가금학회)
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Application of Animal Biomodel using Poultry: A Review

가금을 이용한 동물 바이오모델: 총설

  • Seo, Dongwon (Division of Animal and Dairy Science, Chungnam National University) ;
  • Lee, Jun Heon (Division of Animal and Dairy Science, Chungnam National University)
  • 서동원 (충남대학교 동물자원과학부) ;
  • 이준헌 (충남대학교 동물자원과학부)
  • Received : 2016.08.29
  • Accepted : 2016.12.05
  • Published : 2016.12.31
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Abstract

Chicken not only serves as a high-protein source to humans, but it is also used as a suitable biomodel for increasing livestock productivity and studying human diseases. Chickens have numerous advantages as model organisms mainly because of they are relatively convenient to manage due to their small body size and short generational interval. In addition, they have a small genome size and numerous genes have biologically similar functions to those of human and livestock animals. In this review, we investigated the chicken biomodel for human disease research and the use of this model for increasing livestock productivity. This summary could provide useful and basic information for further development of strategies for enhancing livestock production and human disease studies.

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References

  1. Agarwal SK, Cogburn LA, Burnside J 1994 Dysfunctional growth hormone receptor in a strain of sex-linked dwarf chicken: Evidence for a mutation in the intracellular domain. J Endocrinol 142:427-434. https://doi.org/10.1677/joe.0.1420427
  2. Akhtar S, Grizenkova J, Wenborn A, Hummerich H, Fernandez de Marco M, Brandner S, Collinge J, Lloyd SE 2013 Sod1 deficiency reduces incubation time in mouse models of prion disease. PLoS ONE 8:e54454. https://doi.org/10.1371/journal.pone.0054454
  3. Anthony NB, Balog JM 2003 Divergent selection for ascites:Development of susceptible and resistant lines. Proceedings of the 52nd Annual National Breeders Roundtable. US Poultry & Egg Association. St. Louis, MO.
  4. Babbs C, Furniss D, Morriss-Kay GM, Wilkie AOM 2008 Polydactyly in the mouse mutant Doublefoot involves altered Gli3 processing and is caused by a large deletion in cis to Indian hedgehog. Mech Dev 125:517-526. https://doi.org/10.1016/j.mod.2008.01.001
  5. Beyer C, Schett G, Distler O, Distler JHW 2010 Animal models of systemic sclerosis: Prospects and limitations. Arthritis Rheum 62:2831-2844. https://doi.org/10.1002/art.27647
  6. Bujo H, Hermann M, Kaderli MO, Jacobsen L, Sugawara S, Nimpf J, Yamamoto T, Schneider WJ 1994 Chicken oocyte growth is mediated by an eight ligand binding repeat member of the LDL receptor family. EMBO J 13:5165-5175.
  7. Cipriani P, Di Benedetto P, Dietrich H, Ruscitti P, Liakouli V, Carubbi F, Pantano I, Berardicurti O, Sgonc R, Giacomelli R 2016 Searching for a good model for systemic sclerosis:The molecular profile and vascular changes occurring in UCD-200 chickens strongly resemble the early phase of human systemic sclerosis. Arch Med Sci 12:828-843.
  8. Clark RM, Marker PC, Kingsley DM 2000 A novel candidate gene for mouse and human preaxial polydactyly with altered expression in limbs of Hemimelic extra-toes mutant mice. Genomics 67:19-27. https://doi.org/10.1006/geno.2000.6225
  9. Crawford RD 1970 Epileptiform seizures in domestic fowl. J Hered 61:185-188. https://doi.org/10.1093/oxfordjournals.jhered.a108078
  10. Dorshorst B, Okimoto R, Ashwell C 2010 Genomic regions associated with dermal hyperpigmentation, polydactyly and other morphological traits in the Silkie chicken. J Hered 101:339-350. https://doi.org/10.1093/jhered/esp120
  11. Douaud M, Feve K, Pituello F, Gourichon D, Boitard S, Leguern E, Coquerelle G, Vieaud A, Batini C, Naquet R, Vignal A, Tixier-Boichard M, Pitel F 2011 Epilepsy caused by an abnormal alternative splicing with dosage effect of the SV2A gene in a chicken model. PLoS ONE 6:e26932. https://doi.org/10.1371/journal.pone.0026932
  12. Elkin RG, Bauer R, Schneider WJ 2012 The restricted ovulator chicken strain: An oviparous vertebrate model of reproductive dysfunction caused by a gene defect affecting an oocyte-specific receptor. Anim Reprod Sci 136:1-13. https://doi.org/10.1016/j.anireprosci.2012.10.002
  13. Giles JR, Elkin RG, Trevino LS, Urick ME, Ramachandran R, Johnson PA 2010 The restricted ovulator chicken: A unique animal model for investigating the etiology of ovarian cancer. Int J Gynecol Cancer 20:738-744. https://doi.org/10.1111/IGC.0b013e3181da2c49
  14. Hierck BP, Molin DGM, Boot MJ, Poelmann RE, Groot ACGD 2004 A chicken model for DGCR6 as a modifier gene in the DiGeorge critical region. Pediatr Res 56:440-448. https://doi.org/10.1203/01.PDR.0000136151.50127.1C
  15. Ho KJ, Lawrence WD, Lewis LA, Liu LB, Taylor CB 1974 Hereditary hyperlipidemia in nonlaying chickens. Arch Pathol 98:161-172.
  16. International Chicken Genome Sequencing Consortium 2004 Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution. Nature 432:695-716. https://doi.org/10.1038/nature03154
  17. Jang HM, Erf GF, Rowland KC, Kong BW 2014 Genome resequencing and bioinformatic analysis of SNP containing candidate genes in the autoimmune vitiligo Smyth line chicken model. BMC Genomics 15:707. https://doi.org/10.1186/1471-2164-15-707
  18. Jones DG, Briles WE 1975 Mutation restricting ovulation in chickens. Poult Sci 54:1780-1780.
  19. Knizetova H 2007 Effects of the sex linked dwarf gene (dw) on skeletal muscle cellularity in broiler chickens. Brit Poult Sci 34:479-485.
  20. Krishnamoorthy S, Smith CD, Al-Rubaye AA, Erf GF, Wideman RF, Anthony NB, Rhoads DD 2014 A quantitative trait locus for ascites on chromosome 9 in broiler chicken lines. Poult Sci 93:307-317. https://doi.org/10.3382/ps.2013-03359
  21. Laron Z, Pertzelan A, Mannheimer S 1966 Genetic pituitary dwarfism with high serum concentation of growth hormone-a new inborn error of metabolism? Isr J Med Sci 2:152-155.
  22. Li H, Deeb N, Zhou H, Mitchell AD, Ashwell CM, Lamont SJ 2003 Chicken quantitative trait loci for growth and body composition associated with transforming growth factorbeta genes. Poult Sci 82:347-356. https://doi.org/10.1093/ps/82.3.347
  23. Lin S, Li H, Mu H, Luo W, Li Y, Jia X, Wang S, Jia X, Nie Q, Li Y, Zhang X 2012 Let-7b regulates the expression of the growth hormone receptor gene in deletion-type dwarf chickens. BMC Genomics 13:306. https://doi.org/10.1186/1471-2164-13-306
  24. Muir WM, Aggrey SE 2003 Poultry Genetics, Breeding, and Biotechnology. CABI.
  25. Nanda I, Zend-Ajusch E, Shan Z, Grutzner F, Schartl M, Burt DW, Koehler M, Fowler VM, Goodwin G, Schneider WJ, Mizuno S, Dechant G, Haaf T, Schmid M 2000 Conserved synteny between the chicken Z sex chromosome and human chromosome 9 includes the male regulatory gene DMRT1: A comparative (re)view on avian sex determination. Cytogenet Cell Genet 89:67-78. https://doi.org/10.1159/000015567
  26. Naquet R, Batini C 2002 Genetic reflex epilepsy from chicken to man: Relations between genetic reflex epilepsy. Epilepsy Disord 29.
  27. Pinto D, Westland B, de Haan GJ, Rudolf G, da Silva BM, Hirsch E, Lindhout D, Trenite DGAKN, Koeleman BPC 2005 Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: Evidence for linkage on chromosomes 7q32 and 16p13. Hum Mol Genet 14:171-178. https://doi.org/10.1093/hmg/ddi335
  28. Pollock CG, Orosz SE 2002 Avian reproductive anatomy, physiology and endocrinology. Vet Clin N Am Exotic Anim Prac 5:441-474. https://doi.org/10.1016/S1094-9194(02)00010-5
  29. Riddle RD, Johnson RL, Laufer E, Tabin C 1993 Sonic hedgehog mediates the polarizing activity of the ZPA. Cell 75:1401-1416. https://doi.org/10.1016/0092-8674(93)90626-2
  30. Schaeffel F, Feldkaemper M 2015 Animal models in myopia research. Clin Exp Optom 98:507-517. https://doi.org/10.1111/cxo.12312
  31. Semple-Rowland SL, Cheng KM 1999 Rd and rc chickens carry the same GC1 null allele (GUCY1*). Exp Eye Res 69:579-581. https://doi.org/10.1006/exer.1999.0743
  32. Semple-Rowland SL, Lee NR, Van Hooser JP, Palczewski K, Baehr W 1998 A null mutation in the photoreceptor guanylate cyclase gene causes the retinal degeneration chicken phenotype. Proc Natl Acad Sci USA 95:1271-1276. https://doi.org/10.1073/pnas.95.3.1271
  33. Sgonc R, Wick G 2008 Pro-and anti-fibrotic effects of TGFbeta in scleroderma. Rheumatology 47:5-7. https://doi.org/10.1093/rheumatology/ken275
  34. Shi F, Kong BW, Song JJ, Lee JY, Dienglewicz RL, Erf GF 2012 Understanding mechanisms of vitiligo development in Smyth line of chickens by transcriptomic microarray analysis of evolving autoimmune lesions. BMC Immuno logy 13:18. https://doi.org/10.1186/1471-2172-13-18
  35. Song G, Han JY 2011 Avian biomodels for use as pharmaceutical bioreactors and for studying human disease. Annuals of the New York Academy of Sciences 1229:69-75. https://doi.org/10.1111/j.1749-6632.2011.06087.x
  36. Spritz RA 2012 Six decades of vitiligo genetics: genome-wide studies provide insights into autoimmune pathogenesis. J Invest Dermatol 132:268-273. https://doi.org/10.1038/jid.2011.321
  37. Stern CD 2004 The chick embryo-past, present and future as a model system in developmental biology. Mech dev 12:1011-1013.
  38. Tanaka M, Hayashida Y, Wakita M, Hoshino S, Nakashima K 1995 Expression of aberrantly spliced growth hormone receptor mRNA in the sex-linked dwarf chicken, Gifu 20. Growth Regul 5:218-223.
  39. Tauer U, Lorenz S, Lenzen KP, Heils A, Muhle H, Gresch M, Neubauer BA, Waltz S, Rudolf G, Mattheisen M, Strauch K, Nurnberg P, Schmitz B, Stephani U, Sander T 2005 Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy. Ann Neurol 57:866-873. https://doi.org/10.1002/ana.20500
  40. Trojanowska M 2008 Role of PDGF in fibrotic diseases and systemic sclerosis. Rheumatology 47:2-4. https://doi.org/10.1093/rheumatology/ken265
  41. Valdez DJ, Nieto PS, Diaz NM, Garbarino-Pico E, Guido ME 2013 Differential regulation of feeding rhythms through a multiple-photoreceptor system in an avian model of blindness. FASEB J 27:2702-2712. https://doi.org/10.1096/fj.12-222885
  42. Vondell, JH 1948 Detection of chickens laying "Fishy Eggs." Poult Sci 27:244-245. https://doi.org/10.3382/ps.0270244
  43. Wang J, Wu SG, Zhang HJ, Yue HY, Xu L, Ji F, Qi GH 2013 Trimethylamine deposition in the egg yolk from laying hens with different FMO3 genotypes. Poult Sci 92:746-752. https://doi.org/10.3382/ps.2012-02313
  44. Warren DC 1944 Inheritance of polydactylism in the fowl. Genetics 29:217-231.
  45. Wick G, Andersson L, Hala K, Gershwin ME, Selmi C, Erf GF, Lamont SJ, Sgonc R 2006 Avian models with spontaneous autoimmune diseases. Adv Immunol 92:71-117. https://doi.org/10.1016/S0065-2776(06)92002-1
  46. Wideman RF, Chapman ME, Hamal KR, Bowen OT, Lorenzoni AG, Erf GF, Anthony NB 2007 An inadequate pulmonary vascular capacity and susceptibility to pulmonary arterial hypertension in broilers. Poult Sci 86:984-998. https://doi.org/10.1093/ps/86.5.984
  47. Wilkinson JM 2011 Re-defining efficiency of feed use by livestock. Animal 5:1014-1022. https://doi.org/10.1017/S175173111100005X
  48. Yeung CK, Adman ET, Rettie AE, 2007 Functional characterization of genetic variants of human FMO3 associated with trimethylaminuria. Arch Biochem Biophys 464:251-259. https://doi.org/10.1016/j.abb.2007.04.014
  49. Zhang Z, Nie C, Jia Y, Jiang R, Xia H, Lv X, Chen Y, Li J, Li X, Ning Z, Xu G, Chen J, Yang N, Qu L 2016 Parallel evolution of polydactyly traits in Chinese and European chickens. PLoS ONE 11:e0149010. https://doi.org/10.1371/journal.pone.0149010