Abstract

BackgroundOvulation and luteinization of follicles are complex biological processes initiated by the preovulatory luteinizing hormone surge. The objective of this study was to identify genes that are differentially expressed in bovine granulosa cells (GC) of ovulatory follicles.MethodsGranulosa cells were collected during the first follicular wave of the bovine estrous cycle from dominant follicles (DF) and from ovulatory follicles (OF) obtained 24 h following injection of human chorionic gonadotropin (hCG). A granulosa cell subtracted cDNA library (OF-DF) was generated using suppression subtractive hybridization and screened.ResultsDetection of genes known to be upregulated in bovine GC during ovulation, such as ADAMTS1, CAV1, EGR1, MMP1, PLAT, PLA2G4A, PTGES, PTGS2, RGS2, TIMP1, TNFAIP6 and VNN2 validated the physiological model and analytical techniques used. For a subset of genes that were identified for the first time, gene expression profiles were further compared by semiquantitative RT-PCR in follicles obtained at different developmental stages. Results confirmed an induction or upregulation of the respective mRNAs in GC of OF 24 h after hCG-injection compared with those of DF for the following genes: ADAMTS9, ARAF, CAPN2, CRISPLD2, FKBP5, GFPT2, KIT, KITLG, L3MBLT3, MRO, NUDT10, NUDT11, P4HA3, POSTN, PSAP, RBP1, SAT1, SDC4, TIMP2, TNC and USP53. In bovine GC, CRISPLD2 and POSTN mRNA were found as full-length transcript whereas L3MBLT3 mRNA was alternatively spliced resulting in a truncated protein missing the carboxy-terminal end amino acids, 774KNSHNEL780. Conversely, L3MBLT3 is expressed as a full-length mRNA in a bovine endometrial cell line. The 774KNSHNEL780 sequence is well conserved in all mammalian species and follows a SAM domain known to confer protein/protein interactions, which suggest a key function for these amino acids in the epigenetic control of gene expression.ConclusionsWe conclude that we have identified novel genes that are upregulated by hCG in bovine GC of OF, thereby providing novel insight into peri-ovulatory regulation of genes that contribute to ovulation and/or luteinization processes.

Highlights

  • Ovulation and luteinization of follicles are complex biological processes initiated by the preovulatory luteinizing hormone surge

  • Reverse subtraction was performed as a control and consisted of ovulatory follicle (OF) cDNAs subtracted from dominant follicle (DF) cDNAs (DF-OF)

  • In the OF-DF subtracted sample, the PCRamplified prostaglandin-endoperoxide synthase 2 (PTGS2) fragment was detected after 13 cycles, revealing that PTGS2 cDNA had been efficiently enriched in the subtracted OF-DF sample when compared with unsubtracted OF sample, confirming the effectiveness of the subtraction

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Summary

Introduction

Ovulation and luteinization of follicles are complex biological processes initiated by the preovulatory luteinizing hormone surge. Activation of the LHCGR induces a developmental program in different compartments of the DF to ensure the release of a competent oocyte via changes in formation/organization of hyaluronan-rich cumulus extracellular matrix followed by rupture of follicular wall, and by formation of the corpus luteum through differentiation of granulosa and theca cells into luteal cells. These processes are controlled by the expression of many genes that are either up- or downregulated in a temporally and spatially distinct fashion. This information is essential to advance our understanding of the cascade of events leading to ovulation and luteinization of the follicle, which may be further applied to enhance fertility

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