Analyze Diet
Biology of reproduction2010; 83(5); 874-886; doi: 10.1095/biolreprod.110.085233

Microarray analysis of equine endometrium at days 8 and 12 of pregnancy.

Abstract: Establishment and maintenance of pregnancy in equids is only partially understood. To provide new insights into early events of this process, we performed a systematic analysis of transcriptome changes in the endometrium at Days 8 and 12 of pregnancy. Endometrial biopsy samples from pregnant and nonpregnant stages were taken from the same mares. Composition of the collected biopsy samples was analyzed using quantitative stereological techniques to determine proportions of surface and glandular epithelium and blood vessels. Microarray analysis did not reveal detectable changes in gene expression at Day 8, whereas at Day 12 of pregnancy 374 differentially expressed genes were identified, 332 with higher and 42 with lower transcript levels in pregnant endometrium. Expression of selected genes was validated by quantitative real-time RT-PCR. Gene set enrichment analysis, functional annotation clustering, and cocitation analysis were performed to characterize the genes differentially expressed in Day 12 pregnant endometrium. Many known estrogen-induced genes and genes involved in regulation of estrogen signaling were found, but also genes known to be regulated by progesterone and prostaglandin E2. Additionally, differential expression of a number of genes related to angiogenesis and vascular remodeling suggests an important role of this process. Furthermore, genes that probably have conserved functions across species, such as CRYAB, ERRFI1, FGF9, IGFBP2, NR2F2, STC1, and TNFSF10, were identified. This study revealed the potential target genes and pathways of conceptus-derived estrogens, progesterone, and prostaglandin E2 in the equine endometrium probably involved in the early events of establishment and maintenance of pregnancy in the mare.
Publication Date: 2010-07-14 PubMed ID: 20631402DOI: 10.1095/biolreprod.110.085233Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Validation Study

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research investigates how gene expression changes in the endometrium (the lining of the uterus) of mares in the early stages of pregnancy, giving us new insights into horse reproduction and pregnancy.

Research Context and Methodology

  • The study was motivated by the fact that our understanding of how pregnancy happens and is maintained in horses (equids) is still incomplete. Understanding these early stages can help improve breeding and pregnancy success rates.
  • To uncover these early events, the researchers systematically analyzed changes in the transcriptome (all the gene expression activity) in the endometrium on the 8th and 12th days of pregnancy.
  • Endometrial biopsy samples were taken from the same mares when they were pregnant and not pregnant. The composition of these biopsies was analyzed to identify the proportions of different types of cells (surface and glandular epithelium and blood vessels).

Microarray Analysis Findings

  • At Day 8 of pregnancy, no noticeable changes in gene expression were found between pregnant and non-pregnant mares.
  • However, at Day 12 of pregnancy, there were 374 genes expressing differently, with 332 showing higher levels of transcript activity and 42 showing lower levels in the pregnant endometrium.
  • The researchers validated these results with quantitative real-time RT-PCR, a technique that quantifies RNA (gene transcripts) in real time as they are being amplified.

Interpretation of Results

  • The researchers performed gene set enrichment analysis, functional annotation clustering, and cocitation analysis to characterize the genes that expressed differently on Day 12.
  • Many of the identified genes were already known to be induced by estrogen and involved in regulating estrogen signaling. Besides, genes that are regulated by progesterone and prostaglandin E2, other hormones critical for pregnancy, were also identified.
  • There was a differential expression of several genes that relate to angiogenesis and vascular remodeling, suggesting this process might play a critical role in early pregnancy.
  • The study also identified genes that are likely to have conserved, or similar, functions across different species. This includes genes such as CRYAB, ERRFI1, FGF9, IGFBP2, NR2F2, STC1, and TNFSF10.
  • In conclusion, this study identified potential target genes and pathways of conceptus-derived hormones in the equine endometrium, likely involved in the early events of pregnancy establishment and maintenance.

Cite This Article

APA
Merkl M, Ulbrich SE, Otzdorff C, Herbach N, Wanke R, Wolf E, Handler J, Bauersachs S. (2010). Microarray analysis of equine endometrium at days 8 and 12 of pregnancy. Biol Reprod, 83(5), 874-886. https://doi.org/10.1095/biolreprod.110.085233

Publication

ISSN: 1529-7268
NlmUniqueID: 0207224
Country: United States
Language: English
Volume: 83
Issue: 5
Pages: 874-886

Researcher Affiliations

Merkl, M
  • Clinic for Horses, Center for Clinical Veterinary Medicine, and Laboratory for Functional Genome Analysis (LAFUGA), Gene Center, Ludwig-Maximilians University of Munich, Munich, Germany.
Ulbrich, S E
    Otzdorff, C
      Herbach, N
        Wanke, R
          Wolf, E
            Handler, J
              Bauersachs, S

                MeSH Terms

                • Animals
                • Biopsy / veterinary
                • Embryo Implantation / physiology
                • Endometrium / blood supply
                • Endometrium / metabolism
                • Estrogens / metabolism
                • Estrous Cycle / metabolism
                • Female
                • Gene Expression Profiling / veterinary
                • Gene Expression Regulation
                • Gene Regulatory Networks
                • Horses / genetics
                • Horses / metabolism
                • Multigene Family
                • Neovascularization, Physiologic
                • Oligonucleotide Array Sequence Analysis / veterinary
                • Pregnancy
                • Pregnancy Maintenance / physiology
                • Pregnancy, Animal / genetics
                • Pregnancy, Animal / metabolism
                • Progesterone / blood
                • Progesterone / metabolism
                • Prostaglandins / metabolism
                • RNA, Messenger / metabolism
                • Reverse Transcriptase Polymerase Chain Reaction / veterinary
                • Signal Transduction

                Citations

                This article has been cited 27 times.
                1. Newcombe JR, Cuervo-Arango J, Wilsher S. The Timing of the Maternal Recognition of Pregnancy Is Specific to Individual Mares.. Animals (Basel) 2023 May 22;13(10).
                  doi: 10.3390/ani13101718pubmed: 37238148google scholar: lookup
                2. Vegas AR, Podico G, Canisso IF, Bollwein H, Fröhlich T, Bauersachs S, Almiñana C. Dynamic regulation of the transcriptome and proteome of the equine embryo during maternal recognition of pregnancy.. FASEB Bioadv 2022 Dec;4(12):775-797.
                  doi: 10.1096/fba.2022-00063pubmed: 36479207google scholar: lookup
                3. Gibson C, de Ruijter-Villani M, Stout TAE. Insulin-like growth factor system components expressed at the conceptus-maternal interface during the establishment of equine pregnancy.. Front Vet Sci 2022;9:912721.
                  doi: 10.3389/fvets.2022.912721pubmed: 36176700google scholar: lookup
                4. Rudolf Vegas A, Hamdi M, Podico G, Bollwein H, Fröhlich T, Canisso IF, Bauersachs S, Almiñana C. Uterine extracellular vesicles as multi-signal messengers during maternal recognition of pregnancy in the mare.. Sci Rep 2022 Sep 16;12(1):15616.
                  doi: 10.1038/s41598-022-19958-zpubmed: 36114358google scholar: lookup
                5. Segabinazzi LGTM, Roberts BN, Peterson EW, Ambrosia R, Bergfelt D, Samper J, French H, Gilbert RO. Early Pregnancy in Jennies in the Caribbean: Corpus Luteum Development and Progesterone Production, Uterine and Embryo Dynamics, Conceptus Growth and Maturation.. Animals (Basel) 2022 Jan 6;12(2).
                  doi: 10.3390/ani12020127pubmed: 35049751google scholar: lookup
                6. Rivera Del Alamo MM, Reilas T, Lukasik K, Galvão AM, Yeste M, Katila T. Inflammatory Markers in Uterine Lavage Fluids of Pregnant, Non-Pregnant, and Intrauterine Device Implanted Mares on Days 10 and 15 Post Ovulation.. Animals (Basel) 2021 Dec 8;11(12).
                  doi: 10.3390/ani11123493pubmed: 34944269google scholar: lookup
                7. Rudolf Vegas A, Podico G, Canisso IF, Bollwein H, Almiñana C, Bauersachs S. Spatiotemporal endometrial transcriptome analysis revealed the luminal epithelium as key player during initial maternal recognition of pregnancy in the mare.. Sci Rep 2021 Nov 16;11(1):22293.
                  doi: 10.1038/s41598-021-01785-3pubmed: 34785745google scholar: lookup
                8. Klein C, Bruce P, Hammermueller J, Hayes T, Lillie B, Betteridge K. Transcriptional profiling of equine endometrium before, during and after capsule disintegration during normal pregnancy and after oxytocin-induced luteostasis in non-pregnant mares.. PLoS One 2021;16(10):e0257161.
                  doi: 10.1371/journal.pone.0257161pubmed: 34614002google scholar: lookup
                9. Camacho CA, Santos GO, Caballeros JE, Cazales N, Ramirez CJ, Vidigal PMP, Ramos HJO, Barros E, Mattos RC. Uterine infusion of conceptus fragments changes the protein profile from cyclic mares.. Anim Reprod 2020 Nov 25;17(4):e20200552.
                  doi: 10.1590/1984-3143-AR2020-0552pubmed: 33791032google scholar: lookup
                10. Almiñana C, Rudolf Vegas A, Tekin M, Hassan M, Uzbekov R, Fröhlich T, Bollwein H, Bauersachs S. Isolation and Characterization of Equine Uterine Extracellular Vesicles: A Comparative Methodological Study.. Int J Mol Sci 2021 Jan 19;22(2).
                  doi: 10.3390/ijms22020979pubmed: 33478136google scholar: lookup
                11. Camacho CA, Estradé MJ, Cazales N, Caballeros JE, Fiala-Rechsteiner SM, Neves AP, Mattos RC. Histomorphometric and vascular changes in equine endometrium after the infusion of conceptus fragments.. Anim Reprod 2020 Jun 29;17(2):e20200006.
                  doi: 10.1590/1984-3143-AR2020-0006pubmed: 32714458google scholar: lookup
                12. Bauersachs S, Almiñana C. Embryo-Maternal Interactions Underlying Reproduction in Mammals.. Int J Mol Sci 2020 Jul 10;21(14).
                  doi: 10.3390/ijms21144872pubmed: 32664189google scholar: lookup
                13. Gibson C, de Ruijter-Villani M, Bauersachs S, Stout TAE. Asynchronous Embryo Transfer Followed by Comparative Transcriptomic Analysis of Conceptus Membranes and Endometrium Identifies Processes Important to the Establishment of Equine Pregnancy.. Int J Mol Sci 2020 Apr 7;21(7).
                  doi: 10.3390/ijms21072562pubmed: 32272720google scholar: lookup
                14. Bauersachs S, Mermillod P, Almiñana C. The Oviductal Extracellular Vesicles' RNA Cargo Regulates the Bovine Embryonic Transcriptome.. Int J Mol Sci 2020 Feb 14;21(4).
                  doi: 10.3390/ijms21041303pubmed: 32075098google scholar: lookup
                15. Smits K, Gansemans Y, Tilleman L, Van Nieuwerburgh F, Van De Velde M, Gerits I, Ververs C, Roels K, Govaere J, Peelman L, Deforce D, Van Soom A. Maternal Recognition of Pregnancy in the Horse: Are MicroRNAs the Secret Messengers?. Int J Mol Sci 2020 Jan 9;21(2).
                  doi: 10.3390/ijms21020419pubmed: 31936511google scholar: lookup
                16. Zeng S, Ulbrich SE, Bauersachs S. Spatial organization of endometrial gene expression at the onset of embryo attachment in pigs.. BMC Genomics 2019 Nov 21;20(1):895.
                  doi: 10.1186/s12864-019-6264-2pubmed: 31752681google scholar: lookup
                17. Loux SC, Dini P, El-Sheikh Ali H, Kalbfleisch T, Ball BA. Characterization of the placental transcriptome through mid to late gestation in the mare.. PLoS One 2019;14(11):e0224497.
                  doi: 10.1371/journal.pone.0224497pubmed: 31725741google scholar: lookup
                18. Boakari YL, Ali HE, Dini P, Loux S, Fernandes CB, Scoggin K, Esteller-Vico A, Lawrence L, Ball B. A High Protein Model Alters the Endometrial Transcriptome of Mares.. Genes (Basel) 2019 Jul 30;10(8).
                  doi: 10.3390/genes10080576pubmed: 31366166google scholar: lookup
                19. Zeng S, Bick J, Ulbrich SE, Bauersachs S. Cell type-specific analysis of transcriptome changes in the porcine endometrium on Day 12 of pregnancy.. BMC Genomics 2018 Jun 14;19(1):459.
                  doi: 10.1186/s12864-018-4855-ypubmed: 29898663google scholar: lookup
                20. Smits K, Willems S, Van Steendam K, Van De Velde M, De Lange V, Ververs C, Roels K, Govaere J, Van Nieuwerburgh F, Peelman L, Deforce D, Van Soom A. Proteins involved in embryo-maternal interaction around the signalling of maternal recognition of pregnancy in the horse.. Sci Rep 2018 Mar 27;8(1):5249.
                  doi: 10.1038/s41598-018-23537-6pubmed: 29588480google scholar: lookup
                21. Graubner FR, Gram A, Kautz E, Bauersachs S, Aslan S, Agaoglu AR, Boos A, Kowalewski MP. Uterine responses to early pre-attachment embryos in the domestic dog and comparisons with other domestic animal species.. Biol Reprod 2017 Aug 1;97(2):197-216.
                  doi: 10.1093/biolre/iox063pubmed: 28651344google scholar: lookup
                22. Haneda S, Nagaoka K, Nambo Y, Kikuchi M, Nakano Y, Li J, Matsui M, Miyake YI, Imakawa K. Expression of uterine lipocalin 2 and its receptor during early- to mid-pregnancy period in mares.. J Reprod Dev 2017 Apr 21;63(2):127-133.
                  doi: 10.1262/jrd.2016-096pubmed: 27980236google scholar: lookup
                23. Aurich C, Budik S. Early pregnancy in the horse revisited - does exception prove the rule?. J Anim Sci Biotechnol 2015;6:50.
                  doi: 10.1186/s40104-015-0048-6pubmed: 26635959google scholar: lookup
                24. Soleilhavoup C, Riou C, Tsikis G, Labas V, Harichaux G, Kohnke P, Reynaud K, de Graaf SP, Gerard N, Druart X. Proteomes of the Female Genital Tract During the Oestrous Cycle.. Mol Cell Proteomics 2016 Jan;15(1):93-108.
                  doi: 10.1074/mcp.M115.052332pubmed: 26518761google scholar: lookup
                25. Ma X, Gu L, Li H, Gao Y, Li X, Shen D, Gong H, Li S, Niu S, Zhang Y, Fan Y, Huang Q, Lyu X, Zhang X. Hypoxia-induced overexpression of stanniocalcin-1 is associated with the metastasis of early stage clear cell renal cell carcinoma.. J Transl Med 2015 Feb 12;13:56.
                  doi: 10.1186/s12967-015-0421-4pubmed: 25740019google scholar: lookup
                26. Fleuren WW, Toonen EJ, Verhoeven S, Frijters R, Hulsen T, Rullmann T, van Schaik R, de Vlieg J, Alkema W. Identification of new biomarker candidates for glucocorticoid induced insulin resistance using literature mining.. BioData Min 2013 Feb 4;6(1):2.
                  doi: 10.1186/1756-0381-6-2pubmed: 23379763google scholar: lookup
                27. Fleuren WW, Verhoeven S, Frijters R, Heupers B, Polman J, van Schaik R, de Vlieg J, Alkema W. CoPub update: CoPub 5.0 a text mining system to answer biological questions.. Nucleic Acids Res 2011 Jul;39(Web Server issue):W450-4.
                  doi: 10.1093/nar/gkr310pubmed: 21622961google scholar: lookup