Abstract
Loss of the maternal T-box transcription factor VegT has a devastating effect on development. Embryos fail to gastrulate, lack the expression of all early zygotic genes characteristic of the endoderm germ layer and also fail to activate ventral, general and dorsal mesodermal gene expression (Zhang et al. 1998; Kofron et al. 1999; Xanthos et al. 2001, 2002). All activity in the activin receptor/Smad 2 signaling pathway is lost (Lee et al. 2001). Embryos depleted of maternal ß-catenin (and therefore deprived of maternal Wnt signaling) also have severe defects. Gastrulation is delayed, embryos develop without heads, dorsal axes and tails and lack neural, dorsal mesodermal and dorsal endodermal gene expression (Heasman et al. 1994; Wylie et al. 1996; Xanthos et al. 2002). Many early zygotic genes have been shown to be targets of these two signaling pathways (see Xanthos et al. 2002 for the expression profiles of zygotic genes in VegT- and β-catenin-embryos). The challenge now is to understand the networks downstream of VegT and ß-catenin that are responsible for embryonic patterning. In particular, two aspects of patterning will be considered here: cell fate specification in the animal-vegetal axis, and asymmetrical gene expression in the dorso-ventral axis of the embryo during the late blastula to early gastrula stages.
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References
Agius E, Oelgeschlager M, Wessely O, Kemp C, de Robertis EM (2000) Endodermal Nodal-related signals and mesoderm induction in Xenopus. Development 127: 1173–1183
Alexander J, Stainier DY (1999) A molecular pathway leading to endoderm formation in zebra-fish. Curr Biol 9: 1147–1157
Behrens J, von Kries JP, Kuhl M, Bruhn L, Wedlich D, Grosschedl R, Birchmeier W (1996) Functional interaction of beta-catenin with the transcription factor LEF-1. Nature 382: 638–642
Bouwmeester T, Kim S, Sasai Y, Lu B, de Robertis EM (1996) Cerberus is a head-inducing secreted factor expressed in the anterior endoderm of Spemann’s organizer. Nature 382: 595–601
Carnac G, Kodjabachian L, Gurdon JB, Lemaire P (1996) The homeobox gene Siamois is a target of the Wnt dorsalisation pathway and triggers organiser activity in the absence of mesoderm. Development 122: 3055–3065
Chang C, Hemmati-Brivanlou A (2000) A post-mid-blastula transition requirement for TGFbeta signaling in early endodermal specification. Mech Dev 90: 227–235
Crease DJ, Dyson S, Gurdon JB (1998) Cooperation between the activin and Wnt pathways in the spatial control of organizer gene expression. Proc Natl Acad Sci USA 95: 4398–4403
Frank D, Harland RM (1991) Transient expression of XMyoD in non-somitic mesoderm of Xenopus gastrulae. Development 113: 1387–1393
Green JB, Smith JC (1990) Graded changes in dose of a Xenopus activin A homologue elicit stepwise transitions in embryonic cell fate. Nature 347: 391–394
Heasman J, Crawford A, Goldstone K, Garner-Hamrick P, Gumbiner B, McCrea P, Kintner C, Noro CY, Wylie C (1994) Overexpression of cadherins and underexpression of beta-catenin inhibit dorsal mesoderm induction in early Xenopus embryos. Cell 79: 791–803
Henry GL, Melton DA (1998) Mixer, a homeobox gene required for endoderm development. Science 281: 91–96
Horb ME, Thomsen GH (1997) A vegetally localized T-box transcription factor in Xenopus eggs specifies mesoderm and endoderm and is essential for embryonic mesoderm formation. Development 124: 1689–1698
Houston DW, Kofron M, Resnik E, Langland R, Destree O, Wylie C, Heasman J (2002) Repression of organizer genes in dorsal and ventral Xenopus cells mediated by maternal XTcf3. Development 129: 4015–4025
Hudson C, Clements D, Friday RV, Stott D, Woodland HR (1997) Xsoxl7alpha and -beta mediate endoderm formation in Xenopus. Cell 91: 397–405
Hyde CE, Old RW (2000) Regulation of the early expression of the Xenopus nodal-related 1 gene, Xnrl. Development 127: 1221–1229
Jones CM, Broadbent J, Thomas PQ, Smith JC, Beddington RS (1999) An anterior signalling centre in Xenopus revealed by the homeobox gene XHex. Curr Biol 9: 946–954
Kimelman D, Griffin KJ (1998) Mesoderm induction: a postmodern view. Cell 94: 419–421
Kodjabachian L, Karavanov AA, Hikasa H, Hukriede NA, Aoki T, Taira M, Dawid IB (2001) A study of Xliml function in the Spemann-Mangold organizer. Int J Dev Biol 45: 209–218
Kofron M, Demel T, Xanthos J, Lohr J, Sun B, Sive H, Osada S, Wright C, Wylie C, Heasman J (1999) Mesoderm induction in Xenopus is a zygotic event regulated by maternal VegT via TGFbeta growth factors. Development 126: 5759–5770
Larabell CA, Torres M, Rowning BA, Yost C, Miller JR, Wu M, Kimelman D, Moon RT (1997) Establishment of the dorso-ventral axis in Xenopus embryos is presaged by early asymmetries in beta-catenin that are modulated by the Wnt signaling pathway. J Cell Biol 136: 1123–1136
Lee MA, Heasman J, Whitman M (2001) Timing of endogenous activin-like signals and regional specification of the Xenopus embryo. Development 128: 2939–2952
Lemaire P, Garrett N, Gurdon JB (1995) Expression cloning of Siamois, a Xenopus homeobox gene expressed in dorsal-vegetal cells of blastulae and able to induce a complete secondary axis. Cell 81: 85–94
Lerchner W, Latinkic BV, Remade JE, Huylebroeck D, Smith JC (2000) Region-specific activation of the Xenopus brachyury promoter involves active repression in ectoderm and endoderm: a study using transgenic frog embryos. Development 127: 2729–2739
Lustig KD, Kroll KL, Sun EE, Kirschner MW (1996) Expression cloning of a Xenopus T-related gene ( Xombi) involved in mesodermal patterning and blastopore lip formation. Development 122: 4001–4012
Molenaar M, van de Wetering M, Oosterwegel M, Peterson-Maduro J, Godsave S, Korinek V, Roose J, Destree O, Clevers H (1996) XTcf-3 transcription factor mediates beta-catenin-induced axis formation in Xenopus embryos. Cell 86: 391–399
Nishita M, Hashimoto MK, Ogata S, Laurent MN, Ueno N, Shibuya H, Cho KW (2000) Interaction between Wnt and TGF-beta signalling pathways during formation of Spemann’s organizer. Nature 403: 781–785
Osada SI, Saijoh Y, Frisch A, Yeo CY, Adachi H, Watanabe M, Whitman M, Hamada H, Wright CV (2000) Activin/nodal responsiveness and asymmetric expression of a Xenopus nodal-related gene converge on a FAST-regulated module in intron 1. Development 127: 2503–2514
Rex M, Hilton E, Old R (2002) Multiple interactions between maternally-activated signalling pathways control Xenopus nodal-related genes. Int J Dev Biol 46: 217–226
Rupp RA, Weintraub H (1991) Ubiquitous MyoD transcription at the midblastula transition precedes induction-dependent MyoD expression in presumptive mesoderm of X. laevis. Cell 65: 927–937
Schneider S, Steinbeisser H, Warga RM, Hausen P (1996) Beta-catenin translocation into nuclei demarcates the dorsalizing centers in frog and fish embryos. Mech Dev 57: 191–198
Schohl A, Fagotto F (2002) Beta-catenin, MAPK and Smad signaling during early Xenopus development. Development 129: 37–52
Smith WC, McKendry R, Ribisi S, Harland RM (1995) A nodal-related gene defines a physical and functional domain within the Spemann organizer. Cell 82: 37–46
Stainier DY (2002) A glimpse into the molecular entrails of endoderm formation. Genes Dev 16: 893–907
Steinbeisser H, de Robertis EM (1993) Xenopus goosecoid: a gene expressed in the prechordal plate that has dorsalizing activity. C R Acad Sci III 316:959–971
Steinbeisser H, de Robertis EM, Ku M, Kessler DS, Melton DA (1993) Xenopus axis formation: induction of goosecoid by injected Xwnt-8 and activin mRNAs. Development 118: 499–507
Stennard F, Carnac G, Gurdon JB (1996) The Xenopus T-box gene, Antipodean, encodes a vegetally localised maternal mRNA and can trigger mesoderm formation. Development 122: 41794188
Stennard F, Zorn AM, Ryan K, Garrett N, Gurdon JB (1999) Differential expression of VegT and Antipodean protein isoforms in Xenopus. Mech Dev 86: 87–98
Takahashi S, Yokota C, Takano K, Tanegashima K, Onuma Y, Goto J, Asashima M (2000) Two novel nodal-related genes initiate early inductive events in Xenopus Nieuwkoop center. Development 127: 5319–5329
Watabe T, Kim S, Candia A, Rothbacher U, Hashimoto C, Inoue K, Cho KW (1995) Molecular mechanisms of Spemann’s organizer formation: conserved growth factor synergy between Xenopus and mouse. Genes Dev 9: 3038–3050
Weber H, Symes CE, Walmsley ME, Rodaway AR, Patient RK (2000) A role for GATA5 in Xenopus endoderm specification. Development 127: 4345–4360
White RJ, Sun BI, Sive HL, Smith JC (2002) Direct and indirect regulation of derriere, a Xenopus mesoderm-inducing factor, by VegT. Development 129: 4867–4876
Wylie C, Kofron M, Payne C, Anderson R, Hosobuchi M, Joseph E, Heasman J (1996) Maternal betacatenin establishes a ‘dorsal signal’ in early Xenopus embryos. Development 122: 2987–2996
Xanthos JB, Kofron M, Wylie C, Heasman J (2001) Maternal VegT is the initiator of a molecular network specifying endoderm in Xenopus laevis. Development 128: 167–180
Xanthos JB, Kofron M, Tao Q, Schaible K, Wylie C, Heasman J (2002) The roles of three signaling pathways in the formation and function of the Spemann organizer. Development 129: 4027–4043
Zhang J, King ML (1996) Xenopus VegT RNA is localized to the vegetal cortex during oogenesis and encodes a novel T-box transcription factor involved in mesodermal patterning. Development 122: 4119–4129
Zhang J, Houston DW, King ML, Payne C, Wylie C, Heasman J (1998) The role of maternal VegT in establishing the primary germ layers in Xenopus embryos. Cell 94: 515–524
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Kofron, M., Xanthos, J., Heasman, J. (2004). Maternal VegT and ß-Catenin: Patterning the Xenopus Blastula. In: Grunz, H. (eds) The Vertebrate Organizer. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-10416-3_1
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DOI: https://doi.org/10.1007/978-3-662-10416-3_1
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-05732-8
Online ISBN: 978-3-662-10416-3
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