Skip to main content
Log in

Polymorphisms and expression of the chicken POU1F1 gene associated with carcass traits

  • Published:
Molecular Biology Reports Aims and scope Submit manuscript

Abstract

POU1F1 is an essential factor that regulates the development and reproduction of animal. The objective of the current research was to screen for polymorphism, expression of POU1F1 and their association with carcass quality traits. A total of 126 Erlang mountainous chickens from two strains (SD02 and SD03) were employed for testing. Seventeen single nucleotide polymorphisms (SNPs) were detected, but only two SNPs (g.96217999 T > C and g.96219442 C > T) were associated with carcass quality traits. In SD03 chicken, g.96217999 T > C genotypes were significantly associated with body weight (BW), carcass weight (CW), eviscerated weight (EW), and semi-eviscerated weight (SEW; P < 0.05), and was highly significantly associated with breast muscle weight (BMW) and abdominal fat weight (AW; P < 0.01). g.96219442 C > T was significantly associated with BW, EW, SEW (P < 0.05). However, these two SNPs were not significantly associated with any carcass traits in SD02 chicken. Diplotypes showed that in SD03 chicken, the haplotype [C: C] was the most favorable haplotype because it was associated with higher BW, CW, SEW, EW, BMW, and AW (P < 0.05). On the contrary, haplotype [T: T] was associated with lower carcass quality traits (P < 0.01). In addition, qRT-PCR revealed that at 13 weeks, the POU1F1 mRNA expression was significantly higher in breast muscle of cock compared to that of hens (P < 0.05), whereas there was no significant correlation between POU1F1 expression and carcass traits. These results suggested that POU1F1 could be a potential candidate gene for carcass traits in chicken.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Chung HO, Kato T, Tomizawa K, Kato Y (1998) Molecular cloning of pit-1 cDNA from porcine anterior pituitary and its involvement in pituitary stimulation by growth hormone-releasing factor. Exp Clin Endocrinol Diabetes 106:203–210

    Article  PubMed  CAS  Google Scholar 

  2. Ingraham HA, Albert VR, Chen RP et al (1990) A family of POU-domain and Pit-1 tissue-specific transcription factors in pituitary and neuroendocrine development. Annu Rev Physiol 52:773–791

    Article  PubMed  CAS  Google Scholar 

  3. Mangalam HJ, Albert VR, Ingraham HA et al (1989) A pituitary POU domain protein, Pit-1, activates both growth hormone and prolactin promoters transcriptionally. Gene Dev 3:946

    Article  PubMed  CAS  Google Scholar 

  4. Nelson C, Albert VR, Elsholtz HP et al (1988) Activation of cell-specific expression of rat growth hormone and prolactin genes by a common transcription factor. Science 239:1400–1405

    Article  PubMed  CAS  Google Scholar 

  5. Steinfelder HJ, Hauser BE, Nakayama Y, Radovick S et al (1991) Thyrotropin-releasing hormone regulation of human TSHβ expression: role of a pituitary-specific transcription factor (Pit-1/GHF-1) and potential interaction with a thyroid hormone-inhibitory element. Proc Nat Acad Sci USA 88:3130–3134

    Article  PubMed  CAS  Google Scholar 

  6. Pfffle R, DiMattia G, Parks J et al (1992) Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia. Science 257:1118–1121

    Article  Google Scholar 

  7. Tatsumi K, Miyai K, Notomi T et al (1992) Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene. Nat Genet 1:56–58

    Article  PubMed  CAS  Google Scholar 

  8. Sun Y, Zhang F, Gao J et al (2006) Positive association between POU1F1 and mental retardation in young females in the Chinese Han population. Hum Mol Genet 15:1237

    Article  PubMed  CAS  Google Scholar 

  9. Yu T, Tuggle C, Schmitz C et al (1995) Association of PIT1 polymorphisms with growth and carcass traits in pigs. J Anim Sci 73:1282–1288

    PubMed  CAS  Google Scholar 

  10. Yu TP, Rothschild MF, Tuggle CK (1993) Rapid communication: a MspI restriction fragment length polymorphism at the swine POU1F1 locus. J Anim Sci 71:2275

    PubMed  CAS  Google Scholar 

  11. Song C, Gao B, Teng Y et al (2005) MspI polymorphisms in the 3rd intron of the swine POU1F1 gene and their associations with growth performance. J Appl Genet 46:285–289

    PubMed  Google Scholar 

  12. Song CY, Gao B, Teng SH et al (2007) Polymorphisms in intron 1 of the porcine POU1F1 gene. J Appl Genet 48:371–374

    Article  PubMed  Google Scholar 

  13. Fang H, Zheng YM, Li HB et al (2009) Relationship of single nucleotide polymorphism of intrion 1 in porcine POU1F1 and the growth trait. Sci Agric Sin 42:283–289

    CAS  Google Scholar 

  14. Song CY, Zhao Q, Gao B et al (2011) Polymorphism analysis of POU1F1 promoter region and its association with growth traits. Sci Agric Sin 44:5067–5072

    CAS  Google Scholar 

  15. Hu Z (2008) The advanced progress of POU1F1 gene in bovine and caprine. China Cattle Sci 34:56–60

    Google Scholar 

  16. Jia XJ, Qin J, Li QL et al (2011) Research progress of single nucleotide polymorphism of bovine POU1F1 gene and the relationship with milk production traits. China Anim Hus Vet Med 38:138–142

    CAS  Google Scholar 

  17. Jia XJ, Wang CF, Yang GW, Huang JM et al (2011) Polymorphism of POU1F1 gene and PRL gene and their combined effects on milk performance traits in Chinese Holstein cattle. Hereditas (Beijing) 33:1359–1365

    Article  CAS  Google Scholar 

  18. Lin JP, He SG, Bai J et al (2009) Correlations between POU1F1 polymorphism and milk yield in Xinjiang brown breed and Chinese Holstein. China Cattle Sci 35:1–4

    CAS  Google Scholar 

  19. Zhang C, Liu B, Chen H et al (2009) Associations of a Hinf I PCR-RFLP of POU1F1 gene with growth traits in Qinchuan cattle. Anim Biotech 20:71–74

    Article  CAS  Google Scholar 

  20. Niu ZG, Shi HC, Liu MJ et al (2011) Polymorphism of POU1F1 Gene and Fitting of Early Growth Curve in Xinjiang Brown Cattle. Acta Agriculturae Boreali-Occidentalis Sinica 20(11):1–5

    CAS  Google Scholar 

  21. Zhao JW, Wu HG, Sun GQ et al (2010) Association study of POU1F1–exon 6 polymorphisms with growth traits in cattle. Heilong Jiang Anim Sci Vet Med 12:4–6

    Google Scholar 

  22. Mura MC, Daga C, Paludo M et al (2012) Analysis of polymorphism within POU1F1 gene in relation to milk production traits in dairy Sarda sheep breed. Mol Biol Rep 39(6):6975–6979

    Article  PubMed  CAS  Google Scholar 

  23. Zhang ZR, Liu YP, Yao YG et al (2009) Identification and association of the single nucleotide polymorphisms in calpain3 (CAPN3) gene with carcass traits in chickens. BMC Genet 10:10

    Article  PubMed  CAS  Google Scholar 

  24. Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2-∆∆CT method. Methods 25:402–408

    Article  PubMed  CAS  Google Scholar 

  25. Chung H, Kato T, Tomizawa K et al (1998) Molecular cloning of pit-1 cDNA from porcine anterior pituitary and its involvement in pituitary stimulation by growth hormone-releasing factor. Exp Clin Endocrinol Diab 106:203–210

    Article  CAS  Google Scholar 

  26. Cohen LE, Wondisford FE, Radovick S (1996) Role of Pit-1 in the gene expression of growth hormone, prolactin, and thyrotropin. Endocrinol Metab Clin North Am 25:523–540

    Article  PubMed  CAS  Google Scholar 

  27. Staneková K, Vaíek D, Pekoviová D et al (1999) Effect of genetic variability of the porcine pituitary-specific transcription factor (PIT-1) on carcas traits in pigs. Anim Genet 30:313–315

    Article  Google Scholar 

  28. Yu T, Sun H, Wahls S et al (2001) Cloning of the full length pig PIT1 (POU1F1) CDNA and a novel alternative PIT1 transcript, and functional studies of their encoded proteins. Anim Biotech 12:1

    Article  CAS  Google Scholar 

  29. Renaville R, Gengler N, Vrech E et al (1997) Pit-1 gene polymorphism, milk yield, and conformation traits for Italian Holstein-Friesian bulls. J Dairy Sci 80:3431–3438

    Article  PubMed  CAS  Google Scholar 

  30. Xue K, Chen H, Wang S et al (2006) Effect of genetic variations of the POU1F1 gene on growth traits of Nanyang cattle. Acta Genetica Sinica 33(10):901–907

    Article  PubMed  CAS  Google Scholar 

  31. Zwierzchowski L, Krzyzewski J, Strzalkowska N et al (2002) Effects of polymorphism of growth hormone (GH), Pit-1, and leptin (LEP) genes, cow’s age, lactation stage and somatic cell count on milk yield and composition of Polish Black-and-White cows. Anim Sci Papers Rep 20(2):213–227

    CAS  Google Scholar 

  32. Brunsch C, Sternstein I, Reinecke P et al (2002) Analysis of associations of PIT1 genotypes with growth, meat quality and carcass composition traits in pigs. J Appl Genet 43:85–92

    PubMed  Google Scholar 

  33. Moody D, Pomp D, Newman S et al (1996) Characterization of DNA polymorphisms in three populations of Hereford cattle and their associations with growth and maternal EPD in line 1 Herefords. J Anim Sci 74:1784

    PubMed  CAS  Google Scholar 

  34. Nie Q, Fang M, Xie L et al (2008) The PIT1 gene polymorphisms were associated with chicken growth traits. BMC Genet 9(20):1–5

    Google Scholar 

  35. Qiu FF, Nie QH, Jin WG et al (2006) Association of a 57 bp Indel in chicken PIT-1 gene with growth and carcass traits. Acta Agri Uni Jiangxi Ensis (China) 28:284–288

    Google Scholar 

  36. Luo WX, Wang XQ et al (2011) Relationship between polymorphism of POU1F1 gene and slaughter traits of goat. Chinese J Anim Sci 47(9):5–9

    CAS  Google Scholar 

  37. Capon F, Allen MH, Ameen M et al (2004) A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups. Hum Mol Genet 13:2361–2368

    Article  PubMed  CAS  Google Scholar 

  38. Grindflek E, Hoen N, Sundvold H et al (2004) Investigation of a peroxisome proliferator-activated receptor gamma haplotype effect on meat quality and carcass traits in pigs. Anim Genet 35:238–241

    Article  PubMed  CAS  Google Scholar 

  39. Stephens JC, Schneider JA, Tanguay DA et al (2001) Haplotype variation and linkage disequilibrium in 313 human genes. Science 293:489–493

    Article  PubMed  CAS  Google Scholar 

  40. Fang H (2006) Studies on the relationship between polymorphism of porcine POU1F1 gene and the mRNA express of interrelated gene. Chinese Academy of Agriculture Sciences, Beijing

    Google Scholar 

  41. Liu L (2008) Studies on the polymorphism of sixth exon of POU1F1 gene and the expression of mRNA in Xinjiang brown cattle. Xinjiang Agricultural University

Download references

Acknowledgments

The authors gratefully acknowledge Yao Zhang for help in managing the birds and collecting the data. This work was financially supported by the Chinese national key technologies R & D programme (Grant no: 2008BADB2B01), the Science Fund for Young Scholars in Sichuan Province (Grant no: ZQ 026-017), the Research Fund for Doctoral Program of Higher Education of China (Grant no: 20105103120006), the Scientific Research Fund of Sichuan Provincial Education Department (Grant no: 10ZB033).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Qing Zhu.

Additional information

Heng-Yong Xu and Yan Wang contributed equally to this work.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Xu, HY., Wang, Y., Liu, YP. et al. Polymorphisms and expression of the chicken POU1F1 gene associated with carcass traits. Mol Biol Rep 39, 8363–8371 (2012). https://doi.org/10.1007/s11033-012-1686-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11033-012-1686-9

Keywords

Navigation