|
伍、參考文獻 余靖 核磁共振光譜在結構生物學的應用。 後基因體時代之生物技術。pp. 91-111. 郭光雄、羅竹芳 魚類之品種改良後基因體時代之生物技術。pp. 377- 393. 陳香惠、陳基旺 電腦虛擬篩選。後基因體時代之生物技術。pp. 295- 309. 鄭貽生、蔡麗珠、楊維仁、袁小琀 X-光晶體繞射學與結構生物學。 後基因體時代之生物技術。pp. 81-90. Abrahams, M.V., Sutterlin, A., 1999. The foraging and antipredator behaviour of growth-enhanced transgenic Atlantic salmon. Anim. Behav. 58, 933-942. Bilezikjian, L.M., Blount, A.L., Corrigan, A.Z., Leal, A., Chen, Y., Vale, W.W., 2001. Actions of activins, inhibins and follistatins: Implications in anterior pituitary function. Clin. Exp. Pharmacol. Physiol. 28, 244-248. Bilezikjian, L.M., Corrigan, A.Z., Vale, W., 1990. Activin-A modulates growth hormone secretion from cultures of rat anterior pituitary cells. Endocrinology 126, 2369-2376. Blobe, G.C., Schiemann, W.P., Lodish, H.F., 2000. Role of transforming growth factor in human disease. New Engl. J. Med. 342, 1350–1358. Boesen C.C., Radaev S., Motyka S.A., Patamawenu A., Sun P.D., 2002. The 1.1 Å crystal structure of human TGF-β type II receptor ligand binding domain. Structure 10, 913-919. Braden, T.D., Conn, P.M., 1992. Activin-A stimulates the synthesis of gonadotropin-releasing hormone receptors. Endocrinology 130, 2101-2105. Brown, C.W., Houston-Hawkins, D.E., Woodruff, T.K., Matzuk, M.M., 2000. Insertion of Inhbb into the Inhba locus rescues the Inhba-null phenotype and reveals new activin functions. Nat. Genet. 25, 453-457. Calogero, A.E., Burrello, N., Ossino, A.M., Polosa, P., D'Agata, R., 1998. Activin-A stimulates hypothalamic gonadotropin-releasing hormone release by the explanted male rat hypothalamus: interaction with inhibin and androgens. J. Endocrinol. 156, 269-274. Danilovich, N., Babu, P.S., Xing, W., Gerdes, M., Krishnamurthy, H., Sairam, M.R., 2000. Estrogen deficiency, obesity, and skeletal abnormalities in follicle-stimulating hormone receptor knockout (FORKO) female mice. Endocrinology. 141, 4295-4308. Davis, A.A., Matzuk, M.M., Reh, T.A., 2000. Activin A promotes progenitor differentiation into photoreceptors in rodent retina. Mol. Cell. Neurosci. 15, 11-21. de Caestecker, M., 2004. The transforming growth factor-β superfamily of receptors. Cytokine and Growth Factor Rev. 15, 1–11 de Fays, K., Tibor, A., Lambert, C., Vinals, C., Denoel, P., De Bolle, X., Wouters, J., Letesson, J.J., Depiereux, E.,1999. Structure and function prediction of the Brucella abortus P39 protein by comparative modeling with marginal sequence similarities. Protein Eng. 12, 217–223. Devlin, R.H., Biagi, C.A., Yesaki, T.Y., Smailus, D.E., Byatt, J.C., 2001. Growth of domesticated transgenic fish. Nature 409, 781-782. Devlin, R.H., D'Andradem, M., Uh, M. and Biagi, C.A., 2004. Population effects of growth hormone transgenic coho salmon depend on food availability and genotype by environment interactions. Proc. Natl. Acad. Sci. U. S. A. 101, 9303-9308. Dodd, J.M., 1986. The ovary. In: Pang, P.K.T., Schreibman, M.P. (Eds.), Vertebrate Endocrinology: Fundamentals and Biomedical Implications. Academic Press, San Diego, pp. 351-397. Ethier, J.F., Findlay, J.K., 2001. Roles of activin and its signal transduction mechanisms in reproductive tissues. Reproduction 121, 667-675. Ferguson, C.A., Tucker, A.S., Christensen, L., Lau, A.L., Matzuk, M.M., Sharpe, P.T., 1998. Activin is an essential early mesenchymal signal in tooth development that is required for patterning of the murine dentition. Genes Dev. 12, 2636-2649. Findlay, J.K., Drummond, A.E., 1999. Regulation of the FSH receptor in the ovary. Trends Endocrinol. Metab. 10, 183-188. Ge, W., 2002. Roles of the activin regulatory system in fish reproduction. Can. J. Physiol. Pharmacol. 78, 1077-1085. Ge, W., Gallin, W.J., Strobeck, C.,Peter, R.E., 1993. Cloning and sequencing of goldfish activin subunit genes: strong structural conservation during vertebrate evolution. Biochem. Bbiophys. Res. Commun. 193, 711-717. Greenwald, J., Fischer, W.H., Vale, W.W., Choe, S., 1999. Three-finger toxin fold for the extracellular ligand-binding domain of the type II activin receptor serine kinase. Nat. Struct. Biol. 6, 18-22. Greenwald, J., Groppe, J., Gray, P., Wiater, E., Kwiatkowski, W., Vale, W., Choe, S., 2003. The BMP7/ActRII extracellular domain complex provides new insights into the cooperative nature of receptor assembly. Mol. Cell. 11, 605-617. Harrison, C.A., Gray, P.C., Vale, W.W., Robertson, D.M., 2005. Antagonists of activin signaling: mechanisms and potential biological applications. Trends Endocrinol. Metab. 16, 73-78. Hillier, S.G., Miro, F., 1993. Local regulation of primate granulosa cell aromatase activity. J. Steroid Biochem. Mol. Biol. 44, 435-439. Hogan, B.L., 1996. Bone morphogenetic proteins: multifunctional regulators of vertebrate development. Genes Dev. 10,: 1580-1594. Hsueh, A.J., Dahl, K.D., Vaughan, J., Tucker, E., Rivier, J., Bardin, C.W., Vale, W., 1987. Heterodimers and homodimers of inhibin subunits have different paracrine action in the modulation of luteinizing hormone-stimulated androgen biosynthesis. Proc. Natl. Acad. Sci. U. S. A. 84, 5082-5086. Inman, G.J., Nicolas, F.J., Callahan, J.F., Harling, J.D., Gaster, L.M., Reith, A.D., Laping, N.J., Hill, C.S., 2002. SB-431542 is a potent and specific inhibitor of transforming growth factor-beta superfamily type I activin receptor-like kinase (ALK) receptors ALK4, ALK5, and ALK7. Mol. Pharmacol. 62, 65-74. Jhaveri, S., Erzurumlu, R.S., Chiaia, N., Kumar, T.R., Matzuk, M.M., 1998. Defective whisker follicles and altered brainstem patterns in activin and follistatin knockout mice. Mol. Cell. Neurosci. 12: 206-219. Kishi, H., Minegishi, T., Tano, M., Kameda, T., Ibuki, Y., Miyamoto, K., 1998. The effect of activin and FSH on the differentiation of rat granulosa cells. FEBS Lett. 422, 274-278. Knight, P.G., Glister, C., 2003. Local roles of TGF-β superfamily members in the control of ovarian follicle development. Anim. Reprod. Sci. 78, 165-183. Krupa, A., Preethi, G., Srinivasan, N., 2004. Structural modes of stabilization of permissive phosphorylation sites in protein kinases: distinct strategies in Ser/Thr and Tyr kinases. J. Mol. Biol. 339, 1025 -1039 Lin, S.Y., Morrison, J.R., Phillps, D.J., de Kretser, D.M., 2003. Regulation ovarian function by the TGF-β superfamily and follistatin. Reproduction 126, 113-148. Ling, N., Ying, S.Y., Ueno, N., Esch, F., Denoroy, L., Guillemin, R., 1985. Isolation and partial characterization of a Mr 32,000 protein with inhibin activity from porcine follicular fluid. Proc. Natl. Acad. Sci. U. S. A. 82, 7217-7221. Ling, N., Ying, S.Y., Ueno, N., Shimasaki, S., Esch, F., Hotta, M., Guillemin, R., 1986. Pituitary FSH is released by a heterodimer of the beta-subunits from the two forms of inhibin. Nature 321, 779-782. Lipinski, C.A., Lombardo, F., Dominy, B.W., Feeney, P.J., 1997. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Delivery Rev. 23: 3-25. MacConell, L.A., Lawson, M.A., Mellon, P.L., Roberts, V.J., 1999. Activin A regulation of gonadotropin-releasing hormone synthesis and release in vitro. Neuroendocrinology. 70, 246-254. Maggio, E.T., Ramnarayan, K., 2001. Recent Developments in Computational Proteomics. Drug Discov. Today 6: 996-1004. Marshall, J.C., Dalkin, A.C., Haissenleder, D.J., Kirk, S.E., 1997. Inhibin, activin, follistatin, and GnRH: regulators of gonadotropin subunit gene expression. In: Aono, T., Sugino, H., Vale, W.W. (Eds.), Inhibin, activin, and follistatin: regulatory functions in system and cell biology. Springer, New York, pp. 39-50. Mason, A.J., Hayflick, J.S., Ling, N., Esch, F., Ueno, N., Ying, S.Y., Guillemin, R., Niall, H., Seeburg, P.H., 1985. Complementary DNA sequences of ovarian follicular fluid inhibin show precursor structure and homology with transforming growth factor-beta. Nature 318, 659-663. Massagué, J., Cheifetz, S., Laiho, M., Ralph, D.A., Weis, F.M., Zentella, A., 1992. Transforming growth factor-beta. Cancer Surv. 12, 81-103. Mather, J.P., Attie, K.M., Woodruff, T.K., Rice, G.C., Phillips, D.M., 1990. Activin stimulates spermatogonial proliferation in germ-Sertoli cell cocultures from immature rat testis. Endocrinology 127, 3206-3214. Matzuk, M.M., Finegold, M.J., Mather, J.P., Krummen, L., Lu, H., Bradley, A., 1994. Development of cancer cachexia-like syndrome and adrenal tumors in inhibin-deficient mice. Proc. Natl. Acad. Sci. U. S. A. 91, 8817-8821. Matzuk, M.M., Finegold, M.J., Su, J.G., Hsueh, A.J., Bradley, A., 1992. Alpha-inhibin is a tumour-suppressor gene with gonadal specificity in mice. Nature 360, 313-319. Matzuk, M.M, Kumar, T.R., Bradley, A., 1995. Different phenotypes for mice deficient in either activins or activin receptor type II. Nature 374, 356-360. Matzuk, M.M., Kumar, T.R., Shou, W., Coerver, K.A., Lau, A.L., Behringer, R.R., Finegold, M.J., 1996. Transgenic models to study the roles of inhibins and activins in reproduction, oncogenesis, and development. Recent Prog. Horm. Res. 51, 123-154. Mayo, K.E., “Actions and Regulation of Inhibin and Activin in the Ovary http://www.biochem.northwestern.edu/mayo/Reasearch1.html” McPherron, A.C., Lawler, A.M., Lee, S.J., 1997. Regulation of skeletal muscle mass in mice by a new TGF-β superfamily member. Nature 387, 83-90. Miro, F., Hillier, S.G., 1992. Relative effects of activin and inhibin on steroid hormone synthesis in primate granulosa cells. J. Clin. Endocrinol. Metab. 75, 1556-1561 Miura, T., Miura, C., Yamauchi, K., Nagahama, Y., 1995. Human recombinant activin induces proliferation of spermatogonia in vitro in the Japanese eel Anguilla japonica. Fish. Sci. 61, 434-437. Miyamoto, K., Hasegawa, Y., Fukuda, M., Nomura, M., Igarashi, M., Kangawa, K., Matsuo, H., 1985. Isolation of porcine follicular fluid inhibin of 32 kDa. Biochem. Biophys. Res. Commun. 129, 396-403 Muir, W.M., Howard, R.D., 1999. Possible ecological risks of transgenic organism release when transgenes affect mating success: sexual selection and the Trojan gene hypothesis. Proc. Natl. Acad. Sci. U. S. A. 96, 13853-13856. Muttukrishna, S., Knight, P.G., 1991. Inverse effects of activin and inhibin on the synthesis and secretion of FSH and LH by ovine pituitary cells in vitro. J. Mol. Endocrinol. 6, 171-178. Nakamura, K., Nakamura, M., Igarashi, S., Miyamoto, K., Eto, Y., Ibuki, Y., Minegishi, T., 1994. Effect of activin on luteinizing hormone-human chorionic gonadotropin receptor messenger ribonucleic acid in granulosa cells. Endocrinology 134, 2329-2335. Pangas, S.A., Woodruff, T.K., 2000. Activin Signal Transduction Pathways. Trends Endocrinol. Metab. 11, 309-314. Patiño, R., Sullivan, C.V., 2002. Ovarian follicle growth, maturation, and ovulation in teleost fish. Fish Physiol. Biochem. 26, 57-70. Reichhardt, T., 2000. Will souped up salmon sink or swim? Nature 406, 10-12. Rivier, J., Spiess, J., McClintock, R., Vaughan, J., Vale, W., 1985. Purification and partial characterization of inhibin from porcine follicular fluid. Biochem. Biophys. Res. Commun. 133, 120-127. Robertson, D.M., de Vos, F.L., Foulds, L.M., McLachlan, R.I., Burger, H.G., Morgan, F.J., Hear,n M.T., de Kretser, D.M., 1986. Isolation of a 31 kDa form of inhibin from bovine follicular fluid. Mol. Cell. Endocrinol. 44, 271-277. Robertson, D.M., Foulds, L.M., Leversha, L., Morgan, F.J., Hearn, M.T., Burger, H.G., Wettenhall, R.E., de Kretser, D.M., 1985. Isolation of inhibin from bovine follicular fluid. Biochem. Biophys. Res. Commun. 126, 220-226. Rodaway, A., Takeda, H., Koshida, S., Broadbent, J., Price, B., Smith, J.C., Patient, R., Holder, N., 1999. Induction of the mesendoderm in the zebrafish germ ring by yolk cell- derived TGF-beta family signals and discrimination of mesoderm and endoderm by FGF. Development 126, 3067-3078. Rombauts, L., Vanmontfort, D., Decuypere, E., Verhoeven, G., 1996. Inhibin and activin have antagonistic paracrine effects on gonadal steroidogenesis during the development of the chicken embryo. Biol. Reprod. 54, 1229-1237. Sadatsuki, M., Tsutsumi, O., Yamada, R., Muramatsu, M., Taketani, Y., 1993. Local regulatory effects of activin A and follistatin on meiotic maturation of rat oocytes. Biochem. Biophys. Res. Commun.196, 388-395. Sairam, M.R., Krishnamurthy, H., 2001. The role of follicle-stimulating hormone in spermatogenesis: lessons from knockout animal models. Arc. Med. Res. 32, 601-608. Sawchenko, P.E., Plotsky, P.M., Pfeiffer, S.W., Cunningham, E.T., Jr Vaughan, J., Rivier, J., Vale, W., 1988. Inhibin β in central neural pathways involved in the control of oxytocin secretion. Nature 334, 615-617. Shimonaka, M., Inouye, S., Shimasaki, S., Ling, N., 1991. Follistatin binds to both activin and inhibin through the common subunit. Endocrinology 128, 3313-3315. Smith, J.C., Price, B.M., Van Nimmen, K., Huylebroeck, D., 1990. Identification of a potent Xenopus mesoderm-inducing factor as a homologue of activin A. Nature 345, 729-731. Struthers, R.S., Gaddy-Kurten, D., Vale, W.W., 1992. Activin inhibits binding of transcription factor Pit-1 to the growth hormone promoter. Proc. Natl. Acad. Sci. U. S. A. 89, 11451-11455 Swanson, P., 1991. Gonadotropins: Reconciling old and new ideas. In: Scott AP, Sumpter JP, Kime DE and Rolfe MS (Eds.), Proceedings of the fourth international symposium on the reproductive physiology of fish. FishSymp91; 1991 July 7-12. FishSymp91, Sheffield, UK. pp. 2-7. Tada, T., Hirono, I., Aoki, T., Takashima, F., 1998. Structure and expression of activin genes in rainbow trout. Mol. Mar. Biol. Miotechnol. 7, 72-77. Thompson, D.A., Cronin, C.N., Martin, F., 1994. Genomic cloning and sequence analyses of the bovine alpha-, beta A- and beta B-inhibin/activin genes. Identification of transcription factor AP-2- binding sites in the 5'-flanking regions by DNase I footprinting. Eur. J. Biochem. 226, 751-764. Thompson, T.B., Woodruff, T.K., Jardetzky, T.S., 2003. Structures of an ActRIIB:activin A complex reveal a novel binding mode for TGF-β ligand:receptor interactions. EMBO J. 22, 1555-1566. Tsuchiya, M., Minegishi, T., Kishi, H., Tano, M., Kameda, T., Hirakawa, T., Ibuki, Y., Mizutani, T., Miyamoto, K., 1999. Control of the expression of luteinizing hormone receptor by local factors in rat granulosa cells. Arch. Biochem. Biophys. 367, 185-192. Vale, W., Rivier, J., Vaughan, J., McClintock, R., Corrigan, A., Woo, W., Karr, D., Spiess, J., 1986. Purification and characterization of an FSH releasing protein from porcine ovarian follicular fluid. Nature 321, 776-779. van den Eijnden-Van Raaij, A.J.M., van Zoelent, E.J.J., van Nimmen, K., Koster, C.H., Snoek, G.T., Durston, A.J., Huylebroeck, D., 1990. Activin-like factor from a Xenopus laevis cell line responsible for mesoderm induction. Nature 345, 732-734. Vinals, C., De Bolle, X., Depiereux, E., Feytmans, E., 1995. Knowledge- based modeling of the D-lactate dehydrogenase three-dimensional structure. Proteins 21, 307-318 Wang, Y., Ge, W., 2003. Involvement of cyclic adenosine 3',5'-mono- phosphate in the differential regulation of activin betaA and betaB expression by gonadotropin in the zebrafish ovarian follicle cells. Endocrinology 144, 491-499. Weil, C., Bougoussa-Houadec, M., Gallais, C., Itoh, S., Sekine, S., Valotaire, Y., 1995. Preliminary evidence suggesting variations of GtH 1 and GtH2 mRNA levels at different stages of gonadal development in rainbow trout, Oncorhynchus mykiss. Gen. Comp. Endocrinol. 100, 327-333. Wittbrodt, J., Rosa, F.M., 1994. Disruption of mesoderm and axis formation in fish by ectopic expression of activin variants: the role of maternal activin. Genes Dev. 8, 1448-1462. Xiao, S., Findlay, J.K., 1991. Interactions between activin and follicle- stimulating hormone-suppressing protein and their mechanisms of action on cultured rat granulosa cells. Mol. Cell. Endocrinol. 79, 99-107. Yam, K.M., Yoshiura, Y., Kobayashi, M., Ge, W., 1999. Recombinant goldfish activin B stimulates gonadotropin-Iβ but inhibits gonadotropin-IIβ expression in the goldfish, Carassius auratus. Gen. Comp. Endocrinol. 116, 81-89. Ying, S.Y., 1988. Inhibins, activins, and follistatins: gonadal proteins modulating the secretion of follicle-stimulating hormone. Endocr. Rev. 9, 267-293 Yuen, C.W., Ge, W., 2004. Follistatin suppresses FSHβ but increases LHβ expression in the goldfish - evidence for an activin-mediated autocrine/paracrine system in fish pituitary. Gen. Comp. Endocrinol. 135, 108-115.
|