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BOR - Papers in Press, published online ahead of print May 28, 2003.
Biol Reprod 2003, 10.1095/biolreprod.102.015065
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BIOLOGY OF REPRODUCTION 69, 1002–1012 (2003)
DOI: 10.1095/biolreprod.102.015065
© 2003 by the Society for the Study of Reproduction, Inc.


Embryo

Increased Messenger RNA for Allograft Inflammatory Factor-1, LERK-5, and a Novel Gene in 17.5-Day Relative to 15.5-Day Bovine Embryos1

Michelle D. Glover, and George E. Seidel, Jr2

Animal Reproduction and Biotechnology Laboratory, Colorado State University, Fort Collins, Colorado 80523

Considerable embryonic loss occurs between Gestation Days 15 and 18 in cattle when critical cellular and molecular events occur, including maternal recognition of pregnancy. To gain insight into these events, mRNA differential display analysis was used to identify eight unique cDNA fragments present in greater abundance in 17.5-day than in 15.5-day bovine embryos. Four cDNA fragments, confirmed to be upregulated in 17.5-day embryos using Northern analysis, were cloned and sequenced. Three cDNA fragments shared sequence identities with known homologs: human allograft inflammatory factor-1 (AIF-1), human LERK-5, and bovine interferon-{tau}. One novel cDNA fragment did not share sequence identity to previously reported genes, except for a similar DNA sequence in the human genome. AIF-1 mRNA was present in developing placenta through Gestation Day 36, and abundant levels were observed in adult bovine spleen and lung. The novel gene, which we have named periattachment factor (PAF), was not detected in adult tissues using Northern analysis or in conceptuses between Days 30 and 36 of pregnancy. Additional sequence information for bPAF was obtained from a cDNA library constructed from a 25-day bovine embryo. The protein corresponding to the open reading frame has four protein kinase C phosphorylation sites, two casein kinase II phosphorylation sites, a nuclear targeting sequence, but no obvious DNA or RNA binding motifs. Abundant expression of this gene during a narrow but critical window of embryonic development makes it worthy of further study.

1 This work was supported by NIH Grant R01-HD-27938 and the Colorado State University Experiment Station through Regional Project W-171. M.D.G. was supported in part by a Colorado Institute for Research in Biotechnology Fellowship.

2 Correspondence: G.E. Seidel, Jr., ARBL, Colorado State University, Fort Collins, CO 80523. FAX: 970 491 3557; gseidel{at}colostate.edu




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