Regulation of egg formation in the oviduct of laying hen

References

• ANASTASI, A., BROWN, M.A., KEMBHAVI, A.A., NICKLIN, M.J., SAYERS, C.A., SUNTER, D.C. and BARRETT, A.J. (1983) Cystatin, a protein inhibitor of cysteine proteinases. Improved purification from egg white, characterisation, and detection in chicken serum. The Biochemical Journal 211: 129–138.
   PubMed Web of Science ®Google Scholar
• ARAZI, H., YOSELEWITZ, I., MALKA, Y., KELNER, Y., GENIN, O. and PINES, M. (2009) Osteopontin and calbindin gene expression in the eggshell gland as related to eggshell abnormalities. Poultry Science 88: 647–653.
   PubMed Web of Science ®Google Scholar
• ATIKUZZAMAN, M., ALVAREZ-RODRIGUEZ, M., VICENTE-CARRILLO, A., JOHNSSON, M., WRIGHT, D. and RODRIGUEZ-MARTINEZ, H. (2017) Conserved gene expression in sperm reservoirs between birds and mammals in response to mating. BMC Genomics 18: 98.
   PubMed Web of Science ®Google Scholar
• ATIKUZZAMAN, M., MEHTA BHAI, R., FOGELHOLM, J., WRIGHT, D. and RODRIGUEZ-MARTINEZ, H. (2015) Mating induces the expression of immune- and pH-regulatory genes in the utero-vaginal junction containing mucosal sperm-storage tubuli of hens. Reproduction 150: 473–483.
   PubMed Web of Science ®Google Scholar
• BARON, F., JAN, S., GONNET, F., PASCO, M., JARDIN, J., GIUDICI, B., GAUTIER, M., GUÉRIN-DUBIARD, C. and NAU, F. (2014) Ovotransferrin plays a major role in the strong bactericidal effect of egg white against the bacillus cereus group. Journal of Food Protection 77: 955–962.
   PubMed Web of Science ®Google Scholar
• BOURIN, M., GAUTRON, J., BERGES, M., ATTUCCI, S., LE BLAY, G., LABAS, V., NYS, Y. and REHAULT-GODBERT, S. (2011) Antimicrobial potential of egg yolk ovoinhibitor, a multidomain kazal-like inhibitor of chicken egg. Journal of Agricultural and Food Chemistry 59: 12368–12374.
   PubMed Web of Science ®Google Scholar
• BRIONNE, A., NYS, Y., HENNEQUET-ANTIER, C. and GAUTRON, J. (2014) Hen uterine gene expression profiling during eggshell formation reveals putative proteins involved in the supply of minerals or in the shell mineralisation process. BMC Genomics 15: 220.
   PubMed Web of Science ®Google Scholar
• CHIEN, Y.C., HINCKE, M.T. and MCKEE, M.D. (2008) Avian eggshell structure and osteopontin. In: Cells Tissues Organs, pp. 38–43.
   Google Scholar
• COLBERT, D.A., KNOLL, B.J., WOO, S.L., MACE, M.L., TSAI, M.J. and O'MALLEY, B.W. (1980) Differential hormonal responsiveness of the ovalbumin gene and its pseudogenes in the chick oviduct. Biochemistry 19: 5586–5592.
   PubMed Web of Science ®Google Scholar
• COLELLA, R., JOHNSON, A. and BIRD, J.W. (1991) Steady-state cystatin mRNA levels in chicken tissues in response to estrogen. Biomedica Biochimica Acta 50: 607–611.
   PubMedGoogle Scholar
• CORDEIRO, C.M.M., ESMAILI, H., ANSAH, G. and HINCKE, M.T. (2013) Ovocalyxin-36 is a pattern recognition protein in phicken eggshell membranes. PLoS ONE 8: e84112.
   PubMed Web of Science ®Google Scholar
• CORSON, G.M., CHALBERG, S.C., DIETZ, H.C., CHARBONNEAU, N.L. and SAKAI, L.Y. (1993) Fibrillin binds calcium and is coded by cdnas that reveal a multidomain structure and alternatively spliced exons at the 5′ end. Genomics 17: 476–484.
   PubMed Web of Science ®Google Scholar
• DU, J., HINCKE, M.T., ROSE-MARTEL, M., HENNEQUET-ANTIER, C., BRIONNE, A., COGBURN, L.A., NYS, Y. and GAUTRON, J. (2015) Identifying specific proteins involved in eggshell membrane formation using gene expression analysis and bioinformatics. BMC Genomics 16: 1–13.
   PubMed Web of Science ®Google Scholar
• EBERS, K.L., ZHANG, C.Y., ZHANG, M.Z., BAILEY, R.H. and ZHANG, S. (2009) Transcriptional profiling avian beta-defensins in chicken oviduct epithelial cells before and after infection with Salmonella enterica serovar Enteritidis. BMC Microbiology 9: 153.
   PubMed Web of Science ®Google Scholar
• EK-RYLANDER, B., FLORES, M., WENDEL, M., HEINEGARD, D. and ANDERSSON, G. (1994) Dephosphorylation of osteopontin and bone sialoprotein by osteoclastic tartrate-resistant acid phosphatase. Modulation of osteoclast adhesion in vitro. Journal of Biological Chemistry 269: 14853–14856.
   PubMed Web of Science ®Google Scholar
• FEENEY, R.E., STEVENS, F.C. and OSUGA, D.T. (1963) The specificities of chicken ovomucoid and ovoinhibitor. The Journal of Biological Chemistry 238: 1415–1418.
   PubMed Web of Science ®Google Scholar
• FREEMAN, C.L., HARDING, J.H., QUIGLEY, D. and RODGER, P.M. (2010) Structural control of crystal nuclei by an eggshell protein. Angewandte Chemie International Edition 49: 5135–5137.
   PubMed Web of Science ®Google Scholar
• GAUTRON, J., HINCKE, M.T., PANHELEUX, M., GARCIA-RUIZ, J.M., BOLDICKE, T., NYS, Y. (2001) Ovotransferrin is a matrix protein of the hen eggshell membranes and basal calcified layer. Connective Tissue Research 42: 255–267.
   PubMed Web of Science ®Google Scholar
• GIANSANTI, F., LEBOFFE, L. and ANTONINI, G. (2012) Antiviral Activity of Lactoferrin and Ovotransferrin Derived Peptides Towards Herpesviridae. Herpesviridae - A Look Into This Unique Family of Viruses, pp. 295–320 (InTech).
   Google Scholar
• GONG, D., WILSON, P.W., BAIN, M.M., MCDADE, K., KALINA, J., HERVÉ-GRÉPINET, V., NYS, Y. and DUNN, I.C. (2010) Gallin; an antimicrobial peptide member of a new avian defensin family, the ovodefensins, has been subject to recent gene duplication. BMC Immunology 11: 12.
   PubMed Web of Science ®Google Scholar
• HARRIS, E.D., BLOUNT, J.E. and LEACH, R.M. (1980) Localisation of lysyl oxidase in hen oviduct: implications in eggshell membrane formation and composition. Science 208: 55–56.
   PubMed Web of Science ®Google Scholar
• HERNÁNDEZ-HERNÁNDEZ, A., GÓMEZ-MORALES, J., RODRÍGUEZ-NAVARRO, A.B., GAUTRON, J., NYS, Y. and GARCÍA-RUIZ, J.M. (2008) Identification of some active proteins in the process of hen eggshell formation. In: Crystal Growth and Design. 2008, pp. 4330–4339.
   Google Scholar
• HINCKE, M.T., GAUTRON, J., TSANG, C.P., MCKEE, M.D. and NYS, Y. (1999) Molecular cloning and ultrastructural localisation of the core protein of an eggshell matrix proteoglycan, ovocleidin-116. The Journal of Biological Chemistry 274: 32915–32923.
   PubMed Web of Science ®Google Scholar
• HINCKE, M.T., TSANG, C.P., COURTNEY, M., HILL, V. and NARBAITZ, R. (1995) Purification and immunochemistry of a soluble matrix protein of the chicken eggshell (ovocleidin 17). Calcified Tissue International 56: 578–583.
   PubMed Web of Science ®Google Scholar
• HOUSLEY, P.R., GRIPPO, J.F., DAHMER, M.K. and PRATT, W.B. (1984) Chapter 12 - Inactivation, Activation, and Stabilisation of Glucocorticoid Receptors. Biochemical Actions of Hormones. pp. 347–376.
   Google Scholar
• HRABIA, A., LEŚNIAK-WALENTYN, A., SECHMAN, A. and GERTLER, A. (2014) Chicken oviduct - The target tissue for growth hormone action: Effect on cell proliferation and apoptosis and on the gene expression of some oviduct-specific proteins. Cell and Tissue Research 357: 363–372.
   PubMed Web of Science ®Google Scholar
• JEONG, W., LIM, W., KIM, J., AHN, S.E., LEE, H.C., JEONG, J.-W., HAN, J.Y., SONG, G. and BAZER, F.W. (2012) Cell-specific and temporal aspects of gene expression in the chicken oviduct at different stages of the laying cycle. Biology of Reproduction 86: 172.
   PubMed Web of Science ®Google Scholar
• JOENSUU, T., TUOHIMAA, P. and VILJA, P. (1991) Avidin and ovalbumin induction by progesterone in chicken oviduct detected by sensitive immunoenzymometric assays. The Journal of Endocrinology 130: 191–197.
   PubMed Web of Science ®Google Scholar
• JOHNSON, A.L. and BRIDGHAM, J.T. (2001) Regulation of steroidogenic acute regulatory protein and luteinizing hormone receptor messenger ribonucleic acid in hen granulosa cells. Endocrinology 142: 3116–3124.
   PubMed Web of Science ®Google Scholar
• JONCHERE, V., REHAULT-GODBERT, S., HENNEQUET-ANTIER, C., CABAU, C., SIBUT, V., COGBURN, L.A., NYS, Y. and GAUTRON, J. (2010) Gene expression profiling to identify eggshell proteins involved in physical defense of the chicken egg. BMC Genomics 11: 57.
   PubMed Web of Science ®Google Scholar
• JUNG, J.G., LIM, W., PARK, T.S., KIM, J.N., HAN, B.K., SONG, G. and HAN, J.Y. (2011) Structural and histological characterisation of oviduct magnum and lectin-binding patterns in Gallus domesticus. Reproductive Biology and Endocrinology 9: 62.
   PubMed Web of Science ®Google Scholar
• KAWASHIMA, M., TAKAHASHI, T., KAMIYOSHI, M. and TANAKA, K. (1996) Effects of progesterone, estrogen, and androgen on progesterone receptor binding in hen oviduct uterus (shell gland). Poultry Science 75: 257–260.
   PubMed Web of Science ®Google Scholar
• KIM, J. and CHOI, Y.H. (2014) Differential abundance of egg white proteins in laying hens treated with corticosterone. Journal of Agricultural and Food Chemistry 62: 12346–12359.
   PubMed Web of Science ®Google Scholar
• KITAMOTO, T., NAKASHIMA, M. and IKAI, A. (1982) Hen egg white ovomacroglobulin has a protease inhibitory activity. Journal of Biochemistry 92: 1679–1682.
   PubMed Web of Science ®Google Scholar
• KOBAYASHI, K., HATTORI, M., HARA-KUDO, Y., OKUBO, T., YAMAMOTO, S., TAKITA, T. and SUGITA-KONISHI, Y. (2004) Glycopeptide derived from hen egg ovomucin has the ability to bind enterohemorrhagic Escherichia coli O157:H7. Journal of Agricultural and Food Chemistry 52: 5740–5746.
   PubMed Web of Science ®Google Scholar
• KODALI, V.K., GANNON, S.A., PARAMASIVAM, S., RAJE, S., POLENOVA, T. and THORPE, C. (2011) A novel disulfide-rich protein motif from avian eggshell membranes. PLoS ONE 6: e18187.
   PubMed Web of Science ®Google Scholar
• KOLACZKOWSKA, A., KOLACZKOWSKI, M., SOKOLOWSKA, A., MIECZNIKOWSKA, H., KUBIAK, A., ROLKA, K. and POLANOWSKI, A. (2010) The antifungal properties of chicken egg cystatin against candida yeast isolates showing different levels of azole resistance. Mycoses 53: 314–320.
   PubMed Web of Science ®Google Scholar
• LAVELIN, I., YARDEN, N., BEN-BASSAT, S., BAR, A. and PINES, M. (1998) Regulation of osteopontin gene expression during eggshell formation in the laying hen by mechanical strain. Matrix Biology 17: 615–623.
   PubMed Web of Science ®Google Scholar
• LEE, J.-Y., JEONG, W., LIM, W., KIM, J., BAZER, F.W., HAN, J.Y. and SONG, G. (2012) Chicken pleiotrophin: regulation of tissue specific expression by estrogen in the oviduct and distinct expression pattern in the ovarian carcinomas. PloS one 7: e34215.
   PubMed Web of Science ®Google Scholar
• LEŚNIAK-WALENTYN, A. and HRABIA, A. (2016a) Expression and localisation of matrix metalloproteinases (MMP-2, -7, -9) and their tissue inhibitors (TIMP-2, -3) in the chicken oviduct during maturation. Cell and Tissue Research 364: 185–197.
   PubMed Web of Science ®Google Scholar
• LEŚNIAK-WALENTYN, A. and HRABIA, A. (2016b) Involvement of matrix metalloproteinases (MMP-2, -7, -9) and their tissue inhibitors (TIMP-2, -3) in the chicken oviduct regression and recrudescence. Cell and Tissue Research 366: 443–454.
   PubMed Web of Science ®Google Scholar
• LIM, C.H., JEONG, W., LIM, W., KIM, J., SONG, G. and BAZER, F.W. (2012a) Differential expression of select members of the SLC family of genes and regulation of expression by microRNAs in the chicken oviduct. Biology of Reproduction 87: 145.
   PubMed Web of Science ®Google Scholar
• LIM, W., JEONG, W., KIM, J., KA, H., BAZER, F.W., HAN, J.Y. and SONG, G. (2012b) Differential expression of secreted phosphoprotein 1 in response to estradiol-17beta and in ovarian tumors in chickens. Biochemical and Biophysical Research Communications 422: 494–500.
   PubMed Web of Science ®Google Scholar
• LIM, W., JEONG, W., KIM, J.-H., LEE, J.-Y., KIM, J., BAZER, F.W., HAN, J.Y. and SONG, G. (2011) Differential expression of alpha 2 macroglobulin in response to dietylstilbestrol and in ovarian carcinomas in chickens. Reproductive Biology and Endocrinology 9: 137.
   PubMed Web of Science ®Google Scholar
• MAGEED, A.M.A., ISOBE, N. and YOSHIMURA, Y. (2008) Expression of avian beta-defensins in the oviduct and effects of lipopolysaccharide on their expression in the vagina of hens. Poultry Science 87: 979–984.
   PubMed Web of Science ®Google Scholar
• MAGEED, A.M., ISOBE, N. and YOSHIMURA, Y. (2009) Immunolocalisation of avian beta-defensins in the hen oviduct and their changes in the uterus during eggshell formation. Reproduction 138: 971–978.
   PubMed Web of Science ®Google Scholar
• MANN, K. (2008) Proteomic analysis of the chicken egg vitelline membrane. Proteomics 8: 2322–2332.
   PubMed Web of Science ®Google Scholar
• MATSUSHIMA, I. (1958) An undescribed trypsin inhibitor in egg white. Science 127: 1178–1179.
   PubMed Web of Science ®Google Scholar
• MIKŠÍK, I., SEDLÁKOVÁ, P., LACINOVÁ, K., PATARIDIS, S. and ECKHARDT, A. (2010) Determination of insoluble avian eggshell matrix proteins, in: Analytical and Bioanalytical Chemistry, pp. 205–214.
   Google Scholar
• MINAMI, T., HORIUCHI, K., MIURA, M., ABID, M.R., TAKABE, W., NOGUCHI, N., KOHRO, T., GE, X., ABURATANI, H., HAMAKUBO, T., KODAMA, T. and AIRD, W.C. (2004) Vascular endothelial growth factor- and thrombin-induced termination factor, down syndrome critical region-1, attenuates endothelial cell proliferation and angiogenesis. Journal of Biological Chemistry 279: 50537–50554.
   PubMed Web of Science ®Google Scholar
• MISHRA, B., KIZAKI, K., SATO, T., ITO, A. and HASHIZUME, K. (2012) The role of extracellular matrix metalloproteinase inducer (EMMPRIN) in the regulation of bovine endometrial cell functions. Biology of Reproduction 87: 149.
   PubMed Web of Science ®Google Scholar
• MURAMATSU, T., HIRAMOTO, K. and OKUMURA, J-I. (1991) Changes in ovalbumin and protein synthesis in vivo in the magnum of laying hens during the egg formation cycle. Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 99: 141–146.
   PubMed Web of Science ®Google Scholar
• NYS, Y., BAKER, K. and LAWSON, D.E.M. (1992) Estrogen and a calcium flux dependent factor modulate the calbindin gene expression in the uterus of laying hens. General and Comparative Endocrinology 87: 87–94.
   PubMed Web of Science ®Google Scholar
• PINES, M., KNOPOV, V. and BAR, A. (1995) Involvement of osteopontin in eggshell formation in the laying chicken. Matrix Biology 14: 765–771.
   PubMed Web of Science ®Google Scholar
• RATH, N. C., LIYANAGE, R., MAKKAR, S.K. and LAY, J.O. (2017) Protein profiles of hatchery eggshell membrane. Proteome Science 15: 9.
   PubMed Web of Science ®Google Scholar
• RÉHAULT-GODBERT, S., LABAS, V., HELLOIN, E., HERVÉ-GRÉPINET, V., SLUGOCKI, C., BERGES, M., BOURIN, M.C., BRIONNE, A., POIRIER, J.C., GAUTRON, J., COSTE, F. and NYS, Y. (2013) Ovalbumin-related protein X is a heparin-binding ov-serpin exhibiting antimicrobial activities. Journal of Biological Chemistry 288: 17285–17295.
   PubMed Web of Science ®Google Scholar
• REYES-GRAJEDA, J.P., MORENO, A. and ROMERO, A. (2004) Crystal structure of ovocleidin-17, a major protein of the calcified Gallus gallus eggshell: implications in the calcite mineral growth pattern. The Journal of Biological Chemistry 279: 40876–40881.
   PubMed Web of Science ®Google Scholar
• SOCHA, J.K., SECHMAN, A., MIKA, M. and HRABIA, A. (2017) Effect of growth hormone on steroid concentrations and mRNA expression of their receptor, and selected egg-specific protein genes in the chicken oviduct during pause in laying induced by fasting. Domestic Animal Endocrinology 61: 1–10.
   PubMed Web of Science ®Google Scholar
• SUN, C., XU, G. and YANG, N. (2013) Differential label-free quantitative proteomic analysis of avian eggshell matrix and uterine fluid proteins associated with eggshell mechanical property. Proteomics 13: 3523–3536.
   PubMed Web of Science ®Google Scholar
• TSUGE, Y., SHIMOYAMADA, M. and WATANABE, K. (1997) Structural features of newcastle disease virus- and anti-ovomucin antibody-binding glycopeptides from pronase-treated ovomucin. Journal of Agricultural and Food Chemistry 45: 2393–2398.
   Web of Science ®Google Scholar
• VU, T.H. and WERB, Z. (2000) Matrix metalloproteinases: effectors of development and normal physiology. Genes & Development 14: 2123–2133.
   PubMed Web of Science ®Google Scholar
• WANG, X., FORD, B.C., PRAUL, C.A. and LEACH, R.M. (2002) Collagen X expression in oviduct tissue during the different stages of the egg laying cycle. Poultry Science 81: 805–808.
   PubMed Web of Science ®Google Scholar
• WHITE, H.B. and WHITEHEAD, C.C. (1987) Role of avidin and other biotin-binding proteins in the deposition and distribution of biotin in chicken eggs. Discovery of a new biotin-binding protein. The Biochemical Journal 241: 677–684.
   PubMed Web of Science ®Google Scholar
• WILLEMS, E., DECUYPERE, E., BUYSE, J. and EVERAERT, N. (2014) Importance of albumen during embryonic development in avian species, with emphasis on domestic chicken. World's Poultry Science Journal 70: 503–518.
   Web of Science ®Google Scholar
• WOOD-GUSH, D.G.M. and GILBERT, A.B. (1970) The rate of egg loss through internal laying. British Poultry Science 11: 161–163.
   Web of Science ®Google Scholar
• YACOUB, H.A., ELAZZAZY, A.M., ABUZINADAH, O.A.H., AL-HEJIN, A.M., MAHMOUD, M.M. and HARAKEH, S.M. (2015) Antimicrobial activities of chicken β-defensin (4 and 10) peptides against pathogenic bacteria and fungi. Frontiers in Cellular and Infection Microbiology 5: 36.
   PubMed Web of Science ®Google Scholar
• YOSEFI, S., BRAW-TAL, R. and BAR, A. (2003) Intestinal and eggshell calbindin, and bone ash of laying hens as influenced by age and molting. Comparative Biochemistry and Physiology - A Molecular and Integrative Physiology 136: 673–682.
   PubMed Web of Science ®Google Scholar
• YOSHIMURA, Y., OHASHI, H., SUBEDI, K., NISHIBORI, M. and ISOBE, N. (2006) Effects of age, egg-laying activity, and salmonella-inoculation on the expression of gallinacin mRNA in the vagina of the hen oviduct. Journal of Reproduction and Development 52: 211–218.
   PubMed Web of Science ®Google Scholar
• ZHAO, J.P., ZHANG, Q., JIAO, H.C., WANG, X.J., JIANG, M.J., LUO, H. and LIN, H. (2016) Ovalbumin expression in the oviduct magnum of hens is related to the rate of egg laying and shows distinct stress-type-specific responses. Journal of Animal Physiology and Animal Nutrition 100: 876–883.
   PubMed Web of Science ®Google Scholar
• ZHAO, R., XU, G.Y., LIU, Z.Z., LI, J.Y. and YANG, N. (2006) A study on eggshell pigmentation: biliverdin in blue-shelled chickens. Poultry Science 85: 546–549.
   PubMed Web of Science ®Google Scholar