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CDNA Microarray Analysis of Bovine Embryo Gene Expression Profiles During the Pre-implantation Period

Abstract

Background: After fertilization, embryo development involves differentiation, as well as development of the fetal body and extra-embryonic tissues until the moment of implantation. During this period various cellular and molecular changes take place with a genetic origin, e.g. the elongation of embryonic tissues, cell-cell contact between the mother and the embryo and placentation. To identify genetic profiles and search for new candidate molecules involved during this period, embryonic gene expression was analyzed with a custom designed utero-placental complementary DNA (cDNA) microarray.

Methods: Bovine embryos on days 7, 14 and 21, extra-embryonic membranes on day 28 and fetuses on days 28 were collected to represent early embryo, elongating embryo, pre-implantation embryo, post-implantation extra-embryonic membrane and fetus, respectively. Gene expression at these different time points was analyzed using our cDNA microarray. Two clustering algorithms such as k-means and hierarchical clustering methods identified the expression patterns of differentially expressed genes across pre-implantation period. Novel candidate genes were confirmed by real-time RT-PCR.

Results: In total, 1,773 individual genes were analyzed by complete k-means clustering. Comparison of day 7 and day 14 revealed most genes increased during this period, and a small number of genes exhibiting altered expression decreased as gestation progressed. Clustering analysis demonstrated that trophoblast-cell-specific molecules such as placental lactogens (PLs), prolactin-related proteins (PRPs), interferon-tau, and adhesion molecules apparently all play pivotal roles in the preparation needed for implantation, since their expression was remarkably enhanced during the pre-implantation period. The hierarchical clustering analysis and RT-PCR data revealed new functional roles for certain known genes (dickkopf-1, NPM, etc) as well as novel candidate genes (AW464053, AW465434, AW462349, AW485575) related to already established trophoblast-specific genes such as PLs and PRPs.

Conclusions: A large number of genes in extra-embryonic membrane increased up to implantation and these profiles provide information fundamental to an understanding of extra-embryonic membrane differentiation and development. Genes in significant expression suggest novel molecules in trophoblast differentiation.

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References
1.
Putney D, Malayer J, Gross T, Thatcher W, Hansen P, Drost M . Heat stress-induced alterations in the synthesis and secretion of proteins and prostaglandins by cultured bovine conceptuses and uterine endometrium. Biol Reprod. 1988; 39(3):717-28. DOI: 10.1095/biolreprod39.3.717. View

2.
Patel O, Yamada O, Kizaki K, Takahashi T, Imai K, Hashizume K . Quantitative analysis throughout pregnancy of placentomal and interplacentomal expression of pregnancy-associated glycoproteins-1 and -9 in the cow. Mol Reprod Dev. 2004; 67(3):257-63. DOI: 10.1002/mrd.20017. View

3.
Salamonsen L . Role of proteases in implantation. Rev Reprod. 1999; 4(1):11-22. DOI: 10.1530/ror.0.0040011. View

4.
Soukas A, Cohen P, Socci N, Friedman J . Leptin-specific patterns of gene expression in white adipose tissue. Genes Dev. 2000; 14(8):963-80. PMC: 316534. View

5.
Mullins R, Pollard T . Structure and function of the Arp2/3 complex. Curr Opin Struct Biol. 1999; 9(2):244-9. DOI: 10.1016/s0959-440x(99)80034-7. View