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http://dx.doi.org/10.14348/molcells.2018.0341

Ventx1.1 as a Direct Repressor of Early Neural Gene zic3 in Xenopus laevis  

Umair, Zobia (Department of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University)
Kumar, Shiv (Department of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University)
Kim, Daniel H. (Department of Chemical and Biomolecular Engineering, Yonsei University)
Rafiq, Khezina (Department of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University)
Kumar, Vijay (Department of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University)
Kim, SungChan (Department of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University)
Park, Jae-Bong (Department of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University)
Lee, Jae-Yong (Department of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University)
Lee, Unjoo (Department of Electrical Engineering, Hallym University)
Kim, Jaebong (Department of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University)
Abstract
From Xenopus embryo studies, the BMP4/Smad1-targeted gene circuit is a key signaling pathway for specifying the cell fate between the ectoderm and neuro-ectoderm as well as the ventral and dorsal mesoderm. In this context, several BMP4/Smad1 target transcriptional factors have been identified as repressors of the neuro-ectoderm. However, none of these direct target transcription factors in this pathway, including GATA1b, Msx1 and Ventx1.1 have yet been proven as direct repressors of early neuro-ectodermal gene expression. In order to demonstrate that Ventx1.1 is a direct repressor of neuro-ectoderm genes, a genome-wide Xenopus ChIP-Seq of Ventx1.1 was performed. In this study, we demonstrated that Ventx1.1 bound to the Ventx1.1 response cis-acting element 1 and 2 (VRE1 and VRE2) on the promoter for zic3, which is a key early neuro-ectoderm gene, and this Ventx1.1 binding led to repression of zic3 transcription. Site-directed mutagenesis of VRE1 and VRE2 within zic3 promoter completely abolished the repression caused by Ventx1.1. In addition, we found both the positive and negative regulation of zic3 promoter activity by FoxD5b and Xcad2, respectively, and that these occur through the VREs and via modulation of Ventx1.1 levels. Taken together, the results demonstrate that the BMP4/Smad1 target gene, Ventx1.1, is a direct repressor of neuro-ectodermal gene zic3 during early Xenopus embryogenesis.
Keywords
neurogenesis; transcriptional regulation; Ventx1.1; Xenopus; zic3;
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1 Lee, S.Y., Lee, H.S., Moon, J.S., Kim, J.I., Park, J.B., Lee, J.Y., Park, M.J., and Kim, J. (2004). Transcriptional regulation of Zic3 by heterodimeric AP-1(c-Jun/c-Fos) during Xenopus development. Exp. Mol. Med. 36, 468-475.   DOI
2 Levy, V., Marom, K., Zins, S., Koutsia, N., Yelin, R., and Fainsod, A. (2002). The competence of marginal zone cells to become Spemann's organizer is controlled by Xcad2. Dev. Biol. 248, 40-51.   DOI
3 Maeno, M., Mead, P.E., Kelley, C., Xu, R.H., Kung, H.F., Suzuki, A., Ueno, N., and Zon, L.I. (1996). The role of BMP-4 and GATA-2 in the induction and differentiation of hematopoietic mesoderm in Xenopus laevis. Blood 88, 1965-1972.
4 Munoz-Sanjuan, I., and Brivanlou, A.H. (2002). Neural induction, the default model and embryonic stem cells. Nat. Rev. Neurosci. 3, 271-280.   DOI
5 Nakata, K., Nagai, T., Aruga, J., and Mikoshiba, K. (1998). Xenopus Zic family and its role in neural and neural crest development. Mech. Dev. 75, 43-51.   DOI
6 Pillemer, G., Yelin, R., Epstein, M., Gont, L., Frumkin, Y., Yisraeli, J.K., Steinbeisser, H., and Fainsod, A. (1998). The Xcad-2 gene can provide a ventral signal independent of BMP-4. Mech. Dev. 74, 133-143.   DOI
7 Rogers, C.D., Moody, S.A., and Casey, E.S. (2009). Neural induction and factors that stabilize a neural fate. Birth Defects Res. C Embryo Today 87, 249-262.   DOI
8 Sasai, Y. (1998). Identifying the missing links: genes that connect neural induction and primary neurogenesis in vertebrate embryos. Neuron 21, 455-458.   DOI
9 Sasai, Y., Lu, B., Steinbeisser, H., and De Robertis, E.M. (1995). Regulation of neural induction by the Chd and Bmp-4 antagonistic patterning signals in Xenopus. Nature 376, 333-336.   DOI
10 Session, A.M., Uno, Y., Kwon, T., Chapman, J.A., Toyoda, A., Takahashi, S., Fukui, A., Hikosaka, A., Suzuki, A., Kondo, M., et al. (2016). Genome evolution in the allotetraploid frog Xenopus laevis. Nature 538, 336-343.   DOI
11 Shim, S., Bae, N., Park, S.Y., Kim, W.S., and Han, J.K. (2005). Isolation of Xenopus FGF-8b and comparison with FGF-8a. Mol. Cells 19, 310-317.
12 Xu, R.H., Kim, J., Taira, M., Lin, J.J., Zhang, C.H., Sredni, D., Evans, T., and Kung, H.F. (1997). Differential regulation of neurogenesis by the two Xenopus GATA-1 genes. Mol. Cell Biol. 17, 436-443.   DOI
13 Suzuki, A., Kaneko, E., Maeda, J., and Ueno, N. (1997a). Mesoderm induction by BMP-4 and -7 heterodimers. Biochem Biophys Res Commun. 232, 153-156.   DOI
14 Suzuki, A., Ueno, N., and Hemmati-Brivanlou, A. (1997b). Xenopus msx1 mediates epidermal induction and neural inhibition by BMP4. Development 124, 3037-3044.
15 Wilson, P.A., Lagna, G., Suzuki, A., and Hemmati-Brivanlou, A. (1997). Concentration-dependent patterning of the Xenopus ectoderm by BMP4 and its signal transducer Smad1. Development 124, 3177-3184.
16 Xu, R.H., Kim, J., Taira, M., Zhan, S., Sredni, D., and Kung, H.F. (1995). A dominant negative bone morphogenetic protein 4 receptor causes neuralization in Xenopus ectoderm. Biochem. Biophys. Res. Commun. 212, 212-219.   DOI
17 Yan, B., Neilson, K.M., and Moody, S.A. (2010). Microarray identification of novel downstream targets of FoxD4L1/D5, a critical component of the neural ectodermal transcriptional network. Dev. Dyn. 239, 3467-3480.   DOI
18 Yoon, J., Kim, J.H., Kim, S.C., Park, J.B., Lee, J.Y., and Kim, J. (2014a). PV.1 suppresses the expression of FoxD5b during neural induction in Xenopus embryos. Mol. Cells 37, 220-225.   DOI
19 Blythe, S.A., Reid, C.D., Kessler, D.S., and Klein, P.S. (2009). Chromatin immunoprecipitation in early Xenopus laevis embryos. Dev. Dyn. 238, 1422-1432.   DOI
20 Ault, K.T., Dirksen, M.L., and Jamrich, M. (1996). A novel homeobox gene PV.1 mediates induction of ventral mesoderm in Xenopus embryos. Proc. Natl. Acad. Sci. USA 93, 6415-6420.   DOI
21 Delaune, E., Lemaire, P., and Kodjabachian, L. (2005). Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition. Development 132, 299-310.   DOI
22 Cha, S.W., Lee, J.W., Hwang, Y.S., Chae, J.P., Park, K.M., Cho, H.J., Kim, D.S., Bae, Y.C., and Park, M.J. (2008). Spatiotemporal regulation of fibroblast growth factor signal blocking for endoderm formation in Xenopus laevis. Exp. Mol. Med. 40, 550-557.   DOI
23 Dale, L., and Jones, C.M. (1999). BMP signalling in early Xenopus development. Bioessays 21, 751-760.   DOI
24 De Robertis, E.M., and Kuroda, H. (2004). Dorsal-ventral patterning and neural induction in Xenopus embryos. Annu. Rev. Cell Dev. Biol. 20, 285-308.   DOI
25 Houtmeyers, R., Souopgui, J., Tejpar, S., and Arkell, R. (2013). The ZIC gene family encodes multi-functional proteins essential for patterning and morphogenesis. Cell Mol. life Sci. 70, 3791-3811.   DOI
26 Yoon, J., Kim, J.H., Lee, O.J., Lee, S.Y., Lee, S.H., Park, J.B., Lee, J.Y., Kim, S.C., and Kim, J. (2013). AP-1(c-Jun/FosB) mediates xFoxD5b expression in Xenopus early developmental neurogenesis. Int. J. Dev. Biol. 57, 865-872.   DOI
27 Yoon, J., Kim, J.H., Lee, S.Y., Kim, S., Park, J.B., Lee, J.Y., and Kim, J. (2014b). PV.1 induced by FGF-Xbra functions as a repressor of neurogenesis in Xenopus embryos. BMB Rep. 47, 673-678.   DOI
28 Yu, S.B., Umair, Z., Kumar, S., Lee, U., Lee, S.H., Kim, J.I., Kim, S., Park, J.B., Lee, J.Y., and Kim, J. (2016). xCyp26c induced by inhibition of BMP signaling is involved in anterior-posterior neural patterning of Xenopus laevis. Mol. Cells 39, 352-357.   DOI
29 Feledy, J.A., Beanan, M.J., Sandoval, J.J., Goodrich, J.S., Lim, J.H., Matsuo-Takasaki, M., Sato, S.M., and Sargent, T.D. (1999). Inhibitory patterning of the anterior neural plate in Xenopus by homeodomain factors Dlx3 and Msx1. Dev. Biol. 212, 455-464.   DOI
30 Henningfeld, K.A., Friedle, H., Rastegar, S., and Knochel, W. (2002). Autoregulation of Xvent-2B; direct interaction and functional cooperation of Xvent-2 and Smad1. J. Biol. Chem. 277, 2097-2103.   DOI
31 Hwang, Y.S., Lee, H.S., Roh, D.H., Cha, S., Lee, S.Y., Seo, J.J., Kim, J., and Park, M.J. (2003). Active repression of organizer genes by Cterminal domain of PV.1. Biochem. Biophys. Res. Commun. 308, 79-86.   DOI
32 Lee, H.S., Park, M.J., Lee, S.Y., Hwang, Y.S., Lee, H., Roh, D.H., Kim, J.I., Park, J.B., Lee, J.Y., Kung, H.F., et al. (2002). Transcriptional regulation of Xbr-1a/Xvent-2 homeobox gene: analysis of its promoter region. Biochem. Biophys. Res. Commun. 298, 815-823.   DOI
33 Hwang, Y.S., Seo, J.J., Cha, S.W., Lee, H.S., Lee, S.Y., Roh, D.H., Kung Hf, H.F., Kim, J., and Ja Park, M. (2002). Antimorphic PV.1 causes secondary axis by inducing ectopic organizer. Biochem. Biophys. Res. Commun. 292, 1081-1086.   DOI
34 Kumar, S., Umair, Z., Yoon, J., Lee, U., Kim, S.C., Park, J.B., Lee, J.Y., and Kim, J. (2018). Xbra and Smad-1 cooperate to activate the transcription of neural repressor ventx1.1 in Xenopus embryos. Sci. Rep. 8, 11391.   DOI
35 Lee, H.S., Lee, S.Y., Lee, H., Hwang, Y.S., Cha, S.W., Park, S., Lee, J.Y., Park, J.B., Kim, S., Park, M.J., et al. (2011). Direct response elements of BMP within the PV.1A promoter are essential for its transcriptional regulation during early Xenopus development. PloS one 6, e22621.   DOI