Hox Genes are Differentially Expressed during Mouse Placentation

  • Park, Sung-Joo (Department of Anatomy, Embryology Laboratory, Yonsei University College of Medicine) ;
  • Lee, Ji-Yeon (Department of Anatomy, Embryology Laboratory, Yonsei University College of Medicine) ;
  • Ma, Ji-Hyun (Department of Anatomy, Embryology Laboratory, Yonsei University College of Medicine) ;
  • Kim, Helena Hye-Soo (Department of Anatomy, Embryology Laboratory, Yonsei University College of Medicine) ;
  • Kim, Myoung-Hee (Department of Anatomy, Embryology Laboratory, Yonsei University College of Medicine)
  • Received : 2012.05.23
  • Accepted : 2012.06.01
  • Published : 2012.06.30

Abstract

The placenta is an extraembryonic tissue that is formed between mother and fetus and mediates delivery of nutrients and oxygen from the mother to the fetus. Because of its essential role in sustaining the growth of the fetus during gestation, defects in its development and function frequently result in fetal growth retardation or intrauterine death, depending on its severity. Vertebrate Hox genes are well known transcription factors that are essential for the proper organization of the body plan during embryogenesis. However, certain Hox genes have been known to be expressed in placenta, implying that Hox genes not only play a crucial role during embryonic patterning but also play an important role in placental development. So far, there has been no report that shows the expression pattern of the whole Hox genes during placentation. In this study, therefore, we investigated the Hox gene expression pattern in mouse placenta, from day 10.5 to 18.5 of gestation using real-time RT-PCR method. In general, the 5' posterior Hox genes were expressed more in the developing placenta compared to the 3' Hox genes. Statistical analysis revealed that the expression of 15 Hox genes (Hoxa9, -a11, -a13/ -b8, -b9/ -c6, -c9, -c13/ -d1, -d3, -d8, -d9, -d10, -d11, -d12) were significantly changed in the course of gestation. The majority of these genes showed highest expression at gestational day 10.5, suggesting their possible role in the early stage during placental development.

Keywords

References

  1. Amesse LS, Moulton R, Zhang YM, Pfaff-Amesse T. Expression of HOX gene products in normal and abnormal trophoblastic tissue. Gynecol Oncol. 2003. 90: 512-518. https://doi.org/10.1016/S0090-8258(03)00357-3
  2. Cross JC. How to make a placenta: mechanisms of trophoblast cell differentiation in mice. Placenta. 2005. 26; A: S3-S9. https://doi.org/10.1016/j.placenta.2005.01.015
  3. Duboule D. Temporal colinearity and the phylotypic progression: a basis for the stability of a vertebrate Bauplan and the evolution of morphologies through heterochrony. Dev Suppl. 1994. 135-142.
  4. Gehring WJ, Hiromi Y. Homeotic genes and the homeobox. Annu Rev Genet. 1986. 20: 147-173. https://doi.org/10.1146/annurev.ge.20.120186.001051
  5. Kim SH, Lee JY, Park SJ, Kim MH. Effect of dexamethasone on embryo development and Hox gene expression patterns in mice. J Exp Biomed Sci. 2011. 17: 231-238.
  6. Murasawa H, Takashima R, Yamanouchi K, Tojo H, Tachi C. Comparative analysis of HOXC-9 gene expression in murine hemochorial and caprine synepitheliochorial placentae by in situ hybridization. Anat Rec. 2000. 259: 383-394. https://doi.org/10.1002/1097-0185(20000801)259:4<383::AID-AR20>3.0.CO;2-N
  7. Rossant J, Cross JC. Placental development: lessons from mouse mutants. Nat Rev Genet. 2001. 2: 538-548.
  8. Ruthala K, Gadi J, Lee JY, Yoon H, Chung HJ, Kim MH. Hoxc8 downregulates Mgl1 tumor suppressor gene expression and reduces its concomitant function on cell adhesion. Mol Cells. 2011. 32: 273-279. https://doi.org/10.1007/s10059-011-0069-8
  9. Shaut CA, Keene DR, Sorensen LK, Li DY, Stadler HS. HOXA13 is essential for placental vascular patterning and labyrinth endothelial specification. PLoS Genet. 2008. 16; 4: e1000073.
  10. Taylor HS, Vanden Heuvel GB, Igarashi P. A conserved Hox axis in the mouse and human female reproductive system: late establishment and persistent adult expression of the Hoxa cluster genes. Biol Reprod. 1997. 57: 1338-1345. https://doi.org/10.1095/biolreprod57.6.1338
  11. Watson ED, Cross JC. Development of structures and transport functions in the mouse placenta. Physiology. 2005. 20: 180 -193.
  12. Yu SJ, Lee JY, Kim SH, Deocaris CC, Kim MH. Synthetic maternal stress hormone can modulate the expression of Hox Genes. J. Exp. Biomed. Sci. 2009. 15: 249-255.
  13. Zanatta A, Rocha AM, Carvalho FM, Pereira RM, Taylor HS, Motta EL, Baracat EC, Serafini PC. The role of the Hoxa10/ HOXA10 gene in the etiology of endometriosis and its related infertility: a review. J Assist Reprod Genet. 2010. 27: 701-710. https://doi.org/10.1007/s10815-010-9471-y