Volume 11, Issue 2 (4-2013)                   IJRM 2013, 11(2): 139-0 | Back to browse issues page

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Hai-Xia L, Xin-Yu G, Yan X, Qi-Long Y, Ming-Xiao G, Jin-Yu Z. Study of the dynamic expression of Meis1 in mice. IJRM 2013; 11 (2) :139-0
URL: http://ijrm.ir/article-1-385-en.html
1- Reproductive Medicine Center, Department of Obstetrics and Gynecology, Guangzhou General Hospital of Guangzhou Military Region, Guangzhou 510010, Guangdong, China
2- Reproductive Medicine Center, Department of Obstetrics and Gynecology, Guangzhou General Hospital of Guangzhou Military Region, Guangzhou 510010, Guangdong, China , haixiatj2006@yahoo.com.cn
Abstract:   (2282 Views)
Background: Aggressive embryo and receptive endometrium are necessary for successful implantation. On this time endometrium transformates to receptive state, which permits embryonic implantation. Studies about embryonic implantation and endometrial receptivity are always a hot spot in the field of reproductive medicine.
Objective: To investigate the expression pattern of Meis1 during peri-implantation in mice endometrium.
Materials and Methods: Mice for experiment were raised in SPF environment. The mice were mated with a female/male ratio of 2:1. The female mice with detected plugs were regarded as pregnant day 1 (pd1). Endometrial tissues were collected respectively on pd1, pd2, pd4, pd5 and pd6. Immunohistochemistry was used to detect the location of Meis1 in mice endometrium. The expression level of mRNA and protein of Meis1 were further detected using Quantitative PCR and Western blotting, respectively.
Results: We found that Meis1 is located in the cytoplasm and membrane of endometrial glandual epithelium cells and the nucleus of endometrial stromal and decidual cells. Both Quantitative RT-PCR and western blotting showed that Meis1 expressed regularly in mice endometrium. Meis1 mRNA expressed weakly on pd1, then significantly increased on pd4 (p=0.018), and achieved to a peak on pd5 (p=0.0012), it showed a decrease trend on pd6. Meis1 protein expressed weakly on pd1 and pd2, then significantly increased on pd4 and pd5 (p=0.0019), it showed a decrease trend on pd6.
Conclusion: Meis1 is dynamically expressed in mice endometrium during peri-implantation. The time that Meis1 expression reaches its peak value is coincident with the implantation window, which implied that Meis1 is closely related with embryonic implantation.
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References
1. Diedrich K, Fauser BC, Devroey P, Griesinger G; Evian Annual Reproduction (EVAR) Workshop Group.The role of the endometrium and embryo in human implantation. Hum Reprod Update 2007; 13: 365-377. [DOI:10.1093/humupd/dmm011]
2. Innis JW. Role of HOX genes in human development. Curr Opin Pediatr 1997; 9: 617-622. [DOI:10.1097/00008480-199712000-00011]
3. Krumlauf R. Hox genes in vertabrate development. Cell 1994; 78: 191-201. [DOI:10.1016/0092-8674(94)90290-9]
4. Yong W, Pei Jun Z. On structure and function of homeodomain. Devel Reprod Biol 1997; 6: 81-89.
5. Taylor HS, Arici A, Olive D, Igarashi P. HOXA10 is response to sex steroid at the time of implantation in the human endometrium. J Glin Invest 1998; 101: 1397-1384.
6. Holland PW, Booth HA, Bruford EA. Classification and nomenclature of all human homeobox genes. BMC Biol 2007; 5: 47-74. [DOI:10.1186/1741-7007-5-47]
7. Xu B, Geerts D, Qian K, Zhang H, Zhu G. Myeloid ecotropic viral integration site1 (MEIS) 1 involvement in embryonic implantation. Hum Reprod 2008; 6: 1394-1406. [DOI:10.1093/humrep/den082]
8. Carson DD, Bagchi I, Dey SK, Enders AC, Fazleabas AT, Lessey BA, et al. Embryo implantation. Dev Biol 2000; 223: 217-237. [DOI:10.1006/dbio.2000.9767]
9. Wong P, Iwasaki M, Somervaille TC, So CW, Cleary ML. Meis1 is an essential and rate-limiting regulator of MLL leukemia stem cell potential. Genes Dev 2007; 21: 2762-2774. [DOI:10.1101/gad.1602107]
10. Stankunas K, Shang C, Twu KY, Kao SC, Jenkins NA, Copeland NG, et al. Pbx/Meis Deficiencies Demonstrate Multigenetic Origins of Congenital Heart Disease. Circ Res 2008; 103: 702-709. [DOI:10.1161/CIRCRESAHA.108.175489]
11. Orlovsky K, Kalinkovich A, Rozovskaia T, Shezen E, Itkin T, Alder H, et al. Down-regulation of homeobox genes MEIS1 and HOXA in MLL-rearranged acute leukemia impairs engraftment and reduces proliferation. Proc Natl Acad Sci USA 2011; 108: 7956-7961. [DOI:10.1073/pnas.1103154108]
12. Benson GV, Lim H, Paria BC, Satokata I, Dey SK, Maas RL. Mechanisms of reduced fertility in Hoxa-10 mutant mice: uterine homeosis and loss of maternal Hoxa-10 expression. Development 1996; 122: 2687-2696.
13. Pillay LM, Forrester AM, Erickson T, Berman JN, Waskiewicz AJ. The Hox cofactors Meis1 and Pbx act upstream of gata1 to regulate primitive hematopoiesis. Dev Biol 2010; 340: 306-317. [DOI:10.1016/j.ydbio.2010.01.033]
14. Sarno JL, Kliman HJ, Taylor HS. HOXA10, Pbx2, and Meis1 Protein Expression in the Human Endometrium: Formation of Multimeric Complexes on HOXA10 Target Genes. J Clin Endocrinol Metab 2005; 90: 522-528. [DOI:10.1210/jc.2004-0817]
15. Ota T, Asahina H, Park SH, Huang Q, Minegishi T, Auersperg N, et al. HOX cofactors expression and regulation in the human ovary. Reprod Biol Endocrinol 2008; 6: 49-57. [DOI:10.1186/1477-7827-6-49]
16. Dintilhac A, Bihan R, Guerrier D, Deschamps S, Bougerie H, Watrin T, et al. PBX1 intracellular localization is independent of MEIS1 in epithelial cells of the developing female genital tract. Int J Dev Biol 2005; 49: 851-858. [DOI:10.1387/ijdb.052013ad]
17. Taylor HS, Arici A, Olive D, Igarashi P. HOXA10 is response to sex steroid at the time of implantation in the human endometrium. Glin Invest 1998; 101: 1397-1384.

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