14 research outputs found

    Identification and stable expression of vitellogenin receptor (VTGR) through vitellogenesis in the European eel

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    [EN] In teleosts, vitellogenin (Vtg) is a phospholipoglycoprotein synthesized by the liver, released into the blood circulation and incorporated into the oocytes via endocytosis mediated by the Vtg receptor (VTGR) to form the yolk granules. The VTGR is crucial for oocyte growth in egg-laying animals but is also present in non-oviparous vertebrates, such as human. The VTGR belongs to the low-density lipoprotein receptor superfamily (LDLR) and is also named very-low-density lipoprotein receptor (VLDLR). In this study, we identified and phylogenetically positioned the VTGR of a basal teleost, the European eel, Anguilla anguilla. We developed quantitative real-time PCR (qRT-PCR) and investigated the tissue distribution of vtgr transcripts. We compared by qRT-PCR the ovarian expression levels of vtgr in juvenile yellow eels and pre-pubertal silver eels. We also analyzed the regulation of ovarian vtgr expression throughout vitellogenesis in experimentally matured eels. The Vtg plasma level was measured by homologous ELISA experimental maturation. Our in silico search and phylogenetical analysis revealed a single vtgr in the European eel, orthologous to other vertebrate vtgr. The qRT-PCR studies revealed that vtgr is mainly expressed in the ovary and also detected in various other tissues such as brain, pituitary, gill, fat, heart, and testis, suggesting some extra-ovarian functions of VTGR. We showed that vtgr is expressed in ovaries of juvenile yellow eels with no higher expression in pre-pubertal silver eels nor in experimentally matured eels. This suggests that vtgr transcription already occurs during early pre-vitellogenesis of immature eels and is not further activated in vitellogenic oocytes. European eel Vtg plasma level increased throughout experimental maturation in agreement with previous studies. Taken together, these results suggest that vtgr transcript levels may not be a limiting step for the uptake of Vtg by the oocyte in the European eel.M.M., A.G.L. and S.D. were granted with Short Term Scientific Missions by the COST Office (COST Action FA1205: AQUAGAMETE). S.D. was also awarded with a grant from the UPV's School of Doctorate (Accion para la Internacionalizacion de los Programas de Doctorado) in 2017. We thank E. Feunteun and colleagues, MNHN, Dinard, for the ovarian samples from eels of the Fremur, France.Morini, M.; Lafont, AG.; Maugars, G.; Baloche, S.; Dufour, S.; Asturiano, JF.; Pérez Igualada, LM. (2020). Identification and stable expression of vitellogenin receptor (VTGR) through vitellogenesis in the European eel. Animal. 14(6):1213-1222. https://doi.org/10.1017/S1751731119003355S12131222146Abascal, F., Zardoya, R., & Posada, D. (2005). ProtTest: selection of best-fit models of protein evolution. Bioinformatics, 21(9), 2104-2105. doi:10.1093/bioinformatics/bti263Ali, B. R., Silhavy, J. L., Gleeson, M. J., Gleeson, J. G., & Al-Gazali, L. (2012). A missense founder mutation in VLDLR is associated with Dysequilibrium Syndrome without quadrupedal locomotion. BMC Medical Genetics, 13(1). doi:10.1186/1471-2350-13-80Andersen, Ø., Xu, C., Timmerhaus, G., Kirste, K. H., Naeve, I., Mommens, M., & Tveiten, H. (2017). Resolving the complexity of vitellogenins and their receptors in the tetraploid Atlantic salmon (Salmo salar ): Ancient origin of the phosvitin-less VtgC in chondrichthyean fishes. Molecular Reproduction and Development, 84(11), 1191-1202. doi:10.1002/mrd.22881Bidwell, C., & Carlson, D. (1995). Characterization of vitellogenin from white sturgeon, Acipenser transmontanus. Journal of Molecular Evolution, 41(1). doi:10.1007/bf00174046Bujo, H., Hermann, M., Kaderli, M. O., Jacobsen, L., Sugawara, S., Nimpf, J., … Schneider, W. J. (1994). Chicken oocyte growth is mediated by an eight ligand binding repeat member of the LDL receptor family. The EMBO Journal, 13(21), 5165-5175. doi:10.1002/j.1460-2075.1994.tb06847.xBurzawa-Gerard, E., & Dumas-Vidal, A. (1991). Effects of 17β-estradiol and carp gonadotropin on vitellogenesis in normal and hypophysectomized European silver female eel (Anguilla anguilla L.) employing a homologous radioimmunoassay for vitellogenin. General and Comparative Endocrinology, 84(2), 264-276. doi:10.1016/0016-6480(91)90049-cChen, J.-N., López, J. A., Lavoué, S., Miya, M., & Chen, W.-J. (2014). Phylogeny of the Elopomorpha (Teleostei): Evidence from six nuclear and mitochondrial markers. Molecular Phylogenetics and Evolution, 70, 152-161. doi:10.1016/j.ympev.2013.09.002Clelland, E. S., & Kelly, S. P. (2010). Tight junction proteins in zebrafish ovarian follicles: Stage specific mRNA abundance and response to 17β-estradiol, human chorionic gonadotropin, and maturation inducing hormone. General and Comparative Endocrinology, 168(3), 388-400. doi:10.1016/j.ygcen.2010.05.011Damsteegt, E. L., Mizuta, H., Hiramatsu, N., & Lokman, P. M. (2015). How do eggs get fat? Insights into ovarian fatty acid accumulation in the shortfinned eel, Anguilla australis. General and Comparative Endocrinology, 221, 94-100. doi:10.1016/j.ygcen.2014.12.019Dufour S, Burzawa-Gerard E, Le Belle N, Sbaihi M and Vidal B 2003. Reproductive endocrinology of the European eel, Anguilla anguilla. In Eel biology (eds. K Aida, K Tsukamoto and K Yamauchi ), pp 373–383. Springer-Verlag, Tokyo, Japan.Dufour, S., Lopez, E., Le Menn, F., Le Belle, N., Baloche, S., & Fontaine, Y. A. (1988). Stimulation of gonadotropin release and of ovarian development, by the administration of a gonadoliberin agonist and of dopamine antagonists, in female silver eel pretreated with estradiol. General and Comparative Endocrinology, 70(1), 20-30. doi:10.1016/0016-6480(88)90090-1Henkel, C. V., Burgerhout, E., de Wijze, D. L., Dirks, R. P., Minegishi, Y., Jansen, H. J., … van den Thillart, G. E. E. J. M. (2012). Primitive Duplicate Hox Clusters in the European Eel’s Genome. PLoS ONE, 7(2), e32231. doi:10.1371/journal.pone.0032231Henkel, C. V., Dirks, R. P., de Wijze, D. L., Minegishi, Y., Aoyama, J., Jansen, H. J., … van den Thillart, G. E. E. J. M. (2012). First draft genome sequence of the Japanese eel, Anguilla japonica. Gene, 511(2), 195-201. doi:10.1016/j.gene.2012.09.064Herz, J., & Bock, H. H. (2002). Lipoprotein Receptors in the Nervous System. Annual Review of Biochemistry, 71(1), 405-434. doi:10.1146/annurev.biochem.71.110601.135342Hiramatsu, N., Luo, W., Reading, B. J., Sullivan, C. V., Mizuta, H., Ryu, Y.-W., … Hara, A. (2012). Multiple ovarian lipoprotein receptors in teleosts. Fish Physiology and Biochemistry, 39(1), 29-32. doi:10.1007/s10695-012-9612-6Hiramatsu, N., Todo, T., Sullivan, C. V., Schilling, J., Reading, B. J., Matsubara, T., … Hara, A. (2015). Ovarian yolk formation in fishes: Molecular mechanisms underlying formation of lipid droplets and vitellogenin-derived yolk proteins. General and Comparative Endocrinology, 221, 9-15. doi:10.1016/j.ygcen.2015.01.025Hummel, S., Lynn, E. G., Osanger, A., Hirayama, S., Nimpf, J., & Schneider, W. J. (2003). Molecular characterization of the first avian LDL receptor. Journal of Lipid Research, 44(9), 1633-1642. doi:10.1194/jlr.m300014-jlr200Jéhannet P, Kruijt L, Damsteegt EL, Swinkels W, Heinsbroek LTN, Lokman PM and Palstra AP. A mechanistic model for studying the initiation of anguillid vitellogenesis by comparing the European eel (Anguilla anguilla) and the shortfinned eel (A. australis). General and Comparative Endocrinology (in press). https://doi.org/10.1016/j.ygcen.2019.02.018Lafont, A.-G., Rousseau, K., Tomkiewicz, J., & Dufour, S. (2016). Three nuclear and two membrane estrogen receptors in basal teleosts, Anguilla sp.: Identification, evolutionary history and differential expression regulation. General and Comparative Endocrinology, 235, 177-191. doi:10.1016/j.ygcen.2015.11.021Mazzeo, I., Peñaranda, D. S., Gallego, V., Baloche, S., Nourizadeh-Lillabadi, R., Tveiten, H., … Pérez, L. (2014). Temperature modulates the progression of vitellogenesis in the European eel. Aquaculture, 434, 38-47. doi:10.1016/j.aquaculture.2014.07.020Mizuta, H., Luo, W., Ito, Y., Mushirobira, Y., Todo, T., Hara, A., … Hiramatsu, N. (2013). Ovarian expression and localization of a vitellogenin receptor with eight ligand binding repeats in the cutthroat trout (Oncorhynchus clarki). Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 166(1), 81-90. doi:10.1016/j.cbpb.2013.07.005Mizuta, H., Mushirobira, Y., Nagata, J., Todo, T., Hara, A., Reading, B. J., … Hiramatsu, N. (2017). Ovarian expression and localization of clathrin (Cltc) components in cutthroat trout, Oncorhynchus clarki: Evidence for Cltc involvement in endocytosis of vitellogenin during oocyte growth. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 212, 24-34. doi:10.1016/j.cbpa.2017.06.021Morini, M., Peñaranda, D. S., Vílchez, M. C., Gallego, V., Nourizadeh-Lillabadi, R., Asturiano, J. F., … Pérez, L. (2015). Transcript levels of the soluble sperm factor protein phospholipase C zeta 1 (PLCζ1) increase through induced spermatogenesis in European eel. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 187, 168-176. doi:10.1016/j.cbpa.2015.05.028Morini, M., Peñaranda, D. S., Vílchez, M. C., Nourizadeh-Lillabadi, R., Lafont, A.-G., Dufour, S., … Pérez, L. (2017). Nuclear and membrane progestin receptors in the European eel: Characterization and expression in vivo through spermatogenesis. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 207, 79-92. doi:10.1016/j.cbpa.2017.02.009Nader, N., Dib, M., Courjaret, R., Hodeify, R., Machaca, R., Graumann, J., & Machaca, K. (2018). VLDL receptor regulates membrane progesterone receptor trafficking and non-genomic signaling. Journal of Cell Science. doi:10.1242/jcs.212522Okabayashi, K., Shoji, H., Nakamura, T., Hashimoto, O., Asashima, M., & Sugino, H. (1996). cDNA Cloning and Expression of theXenopus laevisVitellogenin Receptor. Biochemical and Biophysical Research Communications, 224(2), 406-413. doi:10.1006/bbrc.1996.1040Palstra, A. P., & van den Thillart, G. E. E. J. M. (2010). Swimming physiology of European silver eels (Anguilla anguilla L.): energetic costs and effects on sexual maturation and reproduction. Fish Physiology and Biochemistry, 36(3), 297-322. doi:10.1007/s10695-010-9397-4Pankhurst, N. W. (1982). Relation of visual changes to the onset of sexual maturation in the European eel Anguilla anguilla (L.). Journal of Fish Biology, 21(2), 127-140. doi:10.1111/j.1095-8649.1982.tb03994.xPasquier, J., Lafont, A.-G., Jeng, S.-R., Morini, M., Dirks, R., van den Thillart, G., … Dufour, S. (2012). Multiple Kisspeptin Receptors in Early Osteichthyans Provide New Insights into the Evolution of This Receptor Family. PLoS ONE, 7(11), e48931. doi:10.1371/journal.pone.0048931Perez, L., Aturiano, J. F., Tomas, A., Zegrari, S., Barrera, R., Espinos, F. J., … Jover, M. (2000). Induction of maturation and spermiation in the male European eel: assessment of sperm quality throughout treatment. Journal of Fish Biology, 57(6), 1488-1504. doi:10.1111/j.1095-8649.2000.tb02227.xPérez L, Vílchez MC, Gallego V, Mazzeo I, Peñaranda DS, Weltzien FA, Dufour S and Asturiano JF 2012. Trying to reproduce the European eel (Anguilla anguilla) under captivity: experiments with females. In Proceeding of the Domestication in Finfish Aquaculture, October 2012, Olsztyn, Poland, pp. 11–15.Prat, F., Coward, K., Sumpter, J. P., & Tyler, C. R. (1998). Molecular Characterization and Expression of two Ovarian Lipoprotein Receptors in the Rainbow Trout, Oncorhynchus mykiss 1. Biology of Reproduction, 58(5), 1146-1153. doi:10.1095/biolreprod58.5.1146Reading, B. J., Hiramatsu, N., Schilling, J., Molloy, K. T., Glassbrook, N., Mizuta, H., … Sullivan, C. V. (2014). Lrp13 is a novel vertebrate lipoprotein receptor that binds vitellogenins in teleost fishes. Journal of Lipid Research, 55(11), 2287-2295. doi:10.1194/jlr.m050286Stamatakis, A. (2014). RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics, 30(9), 1312-1313. doi:10.1093/bioinformatics/btu033Takahashi, S., Kawarabayasi, Y., Nakai, T., Sakai, J., & Yamamoto, T. (1992). Rabbit very low density lipoprotein receptor: a low density lipoprotein receptor-like protein with distinct ligand specificity. Proceedings of the National Academy of Sciences, 89(19), 9252-9256. doi:10.1073/pnas.89.19.9252Thompson, J. D., Higgins, D. G., & Gibson, T. J. (1994). CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Research, 22(22), 4673-4680. doi:10.1093/nar/22.22.4673Trommsdorff, M., Gotthardt, M., Hiesberger, T., Shelton, J., Stockinger, W., Nimpf, J., … Herz, J. (1999). Reeler/Disabled-like Disruption of Neuronal Migration in Knockout Mice Lacking the VLDL Receptor and ApoE Receptor 2. Cell, 97(6), 689-701. doi:10.1016/s0092-8674(00)80782-5Tyler, C. R., Pottinger, T. G., Coward, K., Prat, F., Beresford, N., & Maddix, S. (1997). Salmonid Follicle-Stimulating Hormone (GtH I) Mediates Vitellogenic Development of Oocytes in the Rainbow Trout, Oncorhynchus mykiss 1. Biology of Reproduction, 57(5), 1238-1244. doi:10.1095/biolreprod57.5.1238Weltzien, F.-A., Pasqualini, C., Vernier, P., & Dufour, S. (2005). A quantitative real-time RT-PCR assay for European eel tyrosine hydroxylase. General and Comparative Endocrinology, 142(1-2), 134-142. doi:10.1016/j.ygcen.2004.12.01

    Genomic selection in the French Lacaune dairy sheep breed

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    Genomic selection aims to increase accuracy and to decrease generation intervals, thus increasing genetic gains in animal breeding. Using real data of the French Lacaune dairy sheep breed, the purpose of this study was to compare the observed accuracies of genomic estimated breeding values using different models (infinitesimal only, markers only, and joint estimation of infinitesimal and marker effects) and methods [BLUP, Bayes Cp, partial least squares (PLS), and sparse PLS]. The training data set included results of progeny tests of 1,886 rams born from 1998 to 2006, whereas the validation set had results of 681 rams born in 2007 and 2008. The 3 lactation traits studied (milk yield, fat content, and somatic cell scores) had heritabilities varying from 0.14 to 0.41. The inclusion of molecular information, as compared with traditional schemes, increased accuracies of estimated breeding values of young males at birth from 18 up to 25%, according to the trait. Accuracies of genomic methods varied from 0.4 to 0.6, according to the traits, with minor differences among genomic approaches. In Bayes Cp, the joint estimation of marker and infinitesimal effects had a slightly favorable effect on the accuracies of genomic estimated breeding values, and were especially beneficial for somatic cell counts, the less heritable trait. Inclusion of infinitesimal effects also improved slopes of predictive regression equations. Methods that select markers implicitly (Bayes Cp and sparse PLS) were advantageous for some models and traits, and are of interest for further quantitative trait loci studies
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