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ARS Home » Plains Area » Clay Center, Nebraska » U.S. Meat Animal Research Center » Livestock Bio-Systems » Research » Publications at this Location » Publication #412768
Research Project: Applying Nutritional Strategies to Improve Early Embryonic Development and Progeny Performance in Beef Cows

Location: Livestock Bio-Systems

Title: Transcriptomic analysis of luteal tissue supports the delayed timing of luteolysis in heifers with greater ovarian reserve

Author
item KAPS, M - University Of Nebraska
item Snider, Alexandria - Alex
item QUAIL, L - Texas Agrilife
item PERRY, G - Texas Agrilife
item Miles, Jeremy
item Cushman, Robert - Bob

Submitted to: Society for the Study of Reproduction Annual Meeting
Publication Type: Abstract Only
Publication Acceptance Date: 4/24/2024
Publication Date: N/A
Citation: N/A

Interpretive Summary:

Technical Abstract: Antral follicle count (AFC) is reflective of ovarian reserve and linked to reproductive performance in mammalian females. We previously demonstrated a delayed upregulation of endometrial oxytocin receptors in heifers with greater ovarian reserve, indicating delayed induction of luteolysis. Luteal abundance of selected genes of the luteolytic cascade were investigated to further support these findings. We hypothesized that in response to luteolytic signals, mRNA transcript abundance of thrombospondin-1 (THBS1) will be increased and luteinizing hormone/choriogonadotropin receptor (LH/CG-R) will be decreased in the corpus luteum (CL) of open heifers, with a pronounced effect in heifers with diminished ovarian reserve. Furthermore, we hypothesized that the increase of luteal interferon-stimulated gene 15 (ISG15) and interferon-induced GTP-binding protein Mx1 (MX1) transcript abundance in pregnant heifers is greater in animals with increased ovarian reserve. Based on rectal ultrasonography, beef heifers were chosen from the top 10% (high AFC, 33.5±8.4, n=40) and bottom 10% (low AFC, 14.4±2.9, n=40) of the population distribution. All heifers were inseminated (d0) following a 7d-CO-Synch protocol. On day 15 or 16 after insemination, reproductive tracts were collected and flushed. Pregnancy status was defined by presence or absence of a conceptus. Corpora lutea were isolated, weighed and snap-frozen. Transcript abundance of ISG15, MX1, THBS1 and LH/CG-R was determined by RT-qPCR from heifers with a single CL. Circulating progesterone concentrations were determined via radioimmunoassay. Data were analyzed using the MIXED procedure of SAS with AFC group, pregnancy status and their interaction as fixed effects and day as a covariate, followed by Tukey’s test. Progesterone concentrations tended to be greater in high vs low AFC heifers (9.3±1.1 vs 6.5±1.2 ng/ml, P<0.09) and pregnant vs open heifers (9.5±1.1 vs 6.4±1.2 ng/ml, P<0.06), but were not influenced by their interaction. Luteal weights and transcript abundance of ISG15 and MX1 were not affected by pregnancy status, AFC group or their interaction. Transcript abundance of THBS1 was upregulated in open vs pregnant animals (8.4±1.2 vs 3.7±0.5-fold, P<0.0001) and showed greater abundance in low vs high AFC heifers (7.3±1.1 vs 4.3±0.6-fold, P<0.01). THBS1 expression was not influenced by the interaction of AFC group and pregnancy status. An interaction of AFC group and pregnancy status was identified (P<0.05) for LH/CG-R abundance, with greater transcript abundance in pregnant vs open (228.5±39.0 vs 88.5±16.2-fold) and in high vs low AFC heifers (199.5±33.5-fold vs 101.3±18.7-fold). Open low AFC heifers showed the lowest LH/CG-R transcript abundance (46.7±13.5-fold, P<0.01).