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Volume 51 Issue 9
Sep.  2024
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Article Contents

A role for Retinoblastoma 1 in hindbrain morphogenesis by regulating GBX family

doi: 10.1016/j.jgg.2024.03.008
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This work was supported by the National Key R&D Program of China (2018YFA0801000), the Guangdong Basic and Applied Basic Research Foundation (2023A1515010396), and the Science and Technology Program of Guangzhou (202201010156).

  • Received Date: 2024-03-22
  • Accepted Date: 2024-03-26
  • Rev Recd Date: 2024-03-26
  • Available Online: 2025-06-06
  • Publish Date: 2024-04-01
  • The hindbrain, which develops from the anterior end of the neural tube expansion, can differentiate into the metencephalon and myelencephalon, with varying sizes and functions. The midbrain-hindbrain boundary (MHB) and hindbrain myelencephalon/ventral midline (HMVM) are known to be the source of the progenitors for the anterior hindbrain and myelencephalon, respectively. However, the molecular networks regulating hindbrain morphogenesis in these structures remain unclear. In this study, we show that retinoblastoma 1 (rb1) is highly expressed at the MHB and HMVM in zebrafish. Knocking out rb1 in mice and zebrafish results in an enlarged hindbrain due to hindbrain neuronal hyperproliferation. Further study reveals that Rb1 controls the hindbrain morphogenesis by suppressing the expression of Gbx1/Gbx2, essential transcription factors for hindbrain development, through its binding to E2f3/Hdac1, respectively. Interestingly, we find that Gbx1 and Gbx2 are expressed in different types of hindbrain neurons, suggesting distinct roles in hindbrain morphogenesis. In summary, our study clarifies the specific role of RB1 in hindbrain neural cell proliferation and morphogenesis by regulating the E2f3-Gbx1 axis and the Hdac1-Gbx2 axis. These findings provide a research paradigm for exploring the differential proliferation of neurons in various brain regions.
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  • Bae, Y.K., Kani, S., Shimizu, T., Tanabe, K., Nojima, H., Kimura, Y., Higashijima, S., Hibi, M., 2009. Anatomy of zebrafish cerebellum and screen for mutations affecting its development. Dev. Biol. 330, 406-426.
    Beattie, R., Hippenmeyer, S., 2017. Mechanisms of radial glia progenitor cell lineage progression. FEBS Lett. 591, 3993-4008.
    Brend, T., Holley, S.A., 2009. Zebrafish whole mount high-resolution double fluorescent in situ hybridization. J. Vis. Exp. 25, 1229.
    Buckley, D.M., Burroughs-Garcia, J., Lewandoski, M., Waters, S.T., 2013. Characterization of the Gbx1-/- mouse mutant: a requirement for Gbx1 in normal locomotion and sensorimotor circuit development. PLoS ONE 8, e56214.
    Burkhart, D.L., Sage, J., 2008. Cellular mechanisms of tumour suppression by the retinoblastoma gene. Nat. Rev. Cancer 8, 671-682.
    Burroughs-Garcia, J., Sittaramane, V., Chandrasekhar, A., Waters, S.T., 2011. Evolutionarily conserved function of Gbx2 in anterior hindbrain development. Dev. Dyn. 240, 828-838.
    Castro, L.F., Rasmussen, S.L., Holland, P.W., Holland, N.D., Holland, L.Z., 2006. A Gbx homeobox gene in amphioxus: insights into ancestry of the ANTP class and evolution of the midbrain/hindbrain boundary. Dev. Biol. 295, 40-51.
    Clarke, A.R., Maandag, E.R., van Roon, M., van der Lugt, N.M., van der Valk, M., Hooper, M.L., Berns, A., te Riele, H., 1992. Requirement for a functional Rb-1 gene in murine development. Nature 359, 328-330.
    Dahiya, A., Gavin, M.R., Luo, R.X., Dean, D.C., 2000. Role of the LXCXE binding site in Rb function. Mol. Cell. Biol. 20, 6799-6805.
    Doyle, E.L., Booher, N.J., Standage, D.S., Voytas, D.F., Brendel, V.P., Vandyk, J.K., Bogdanove, A.J., 2012. TAL Effector-Nucleotide Targeter (TALE-NT) 2.0: tools for TAL effector design and target prediction. Nucleic Acids Res. 40, W117-W122.
    Duan, N., Hu, X., Qiu, H., Zhou, R., Li, Y., Lu, W., Zhu, Y., Shen, S., Wu, W., Yang, F., et al., 2023. Targeting the E2F1/Rb/HDAC1 axis with the small molecule HR488B effectively inhibits colorectal cancer growth. Cell Death Dis. 14, 801.
    Engeland, K., 2022. Cell cycle regulation: p53-p21-RB signaling. Cell Death Differ. 29, 946-960.
    Fishilevich, S., Nudel, R., Rappaport, N., Hadar, R., Plaschkes, I., Iny Stein, T., Rosen, N., Kohn, A., Twik, M., Safran, M., et al., 2017. GeneHancer: genome-wide integration of enhancers and target genes in GeneCards. Database (Oxford) 2017.
    Flores, M., Goodrich, D.W., 2022. Retinoblastoma Protein Paralogs and Tumor Suppression. Front. Genet. 13, 818719.
    Gibbs, H.C., Chang-Gonzalez, A., Hwang, W., Yeh, A.T., Lekven, A.C., 2017. Midbrain-Hindbrain Boundary Morphogenesis: At the Intersection of Wnt and Fgf Signaling. Front. in Neuroanat. 11, 64.
    Gyda, M., Wolman, M., Lorent, K., Granato, M., 2012. The tumor suppressor gene retinoblastoma-1 is required for retinotectal development and visual function in zebrafish. PLoS Genet. 8, e1003106.
    Harada, H., Sato, T., Nakamura, H., 2016. Fgf8 signaling for development of the midbrain and hindbrain. Dev. Growth Differ. 58, 437-445.
    Harbour, J.W., Dean, D.C., 2000. The Rb/E2F pathway: expanding roles and emerging paradigms. Genes Dev. 14, 2393-2409.
    Harrison, M.R., Georgiou, A.S., Spaink, H.P., Cunliffe, V.T., 2011. The epigenetic regulator Histone Deacetylase 1 promotes transcription of a core neurogenic programme in zebrafish embryos. BMC Genomics 12, 24.
    Higashijima, S., Hotta, Y., Okamoto, H., 2000. Visualization of cranial motor neurons in live transgenic zebrafish expressing green fluorescent protein under the control of the islet-1 promoter/enhancer. J. Neurosci. 20, 206-218.
    Hoang, C.Q., Duong, H.-Q., Nguyen, N.T., Nguyen, S.A.H., Nguyen, C., Nguyen, B.D., Phung, L.T., Nguyen, D.T., Pham, C.T.M., Le Doan, T., et al., 2021. Clinical evaluation of RB1 genetic testing reveals novel mutations in Vietnamese patients with retinoblastoma. Mol. Clin. Oncol. 15, 182-182.
    Hu, H., Miao, Y.R., Jia, L.H., Yu, Q.Y., Zhang, Q., Guo, A.Y., 2019. AnimalTFDB 3.0: a comprehensive resource for annotation and prediction of animal transcription factors. Nucleic Acids Res. 47, D33-D38.
    Ishikawa, Y., Yamamoto, N., Yoshimoto, M., Ito, H., 2012. The primary brain vesicles revisited: are the three primary vesicles (forebrain/midbrain/hindbrain) universal in vertebrates? Brain Behav. Evol. 79, 75-83.
    Jacks, T., Fazeli, A., Schmitt, E.M., Bronson, R.T., Goodell, M.A., Weinberg, R.A., 1992. Effects of an Rb mutation in the mouse. Nature 359, 295-300.
    Jowett, T., Lettice, L., 1994. Whole-mount in situ hybridizations on zebrafish embryos using a mixture of digoxigenin- and fluorescein-labelled probes. Trends Genet. 10, 73-74.
    Joyner, A.L., Liu, A., Millet, S., 2000. Otx2, Gbx2 and Fgf8 interact to position and maintain a mid-hindbrain organizer. Curr. Opin. Cell Biol. 12, 736-741.
    Katahira, T., Sato, T., Sugiyama, S., Okafuji, T., Araki, I., Funahashi, J., Nakamura, H., 2000. Interaction between Otx2 and Gbx2 defines the organizing center for the optic tectum. Mech. Dev. 91, 43-52.
    Kent, B., Magnani, E., Walsh, M.J., Sadler, K.C., 2016. UHRF1 regulation of Dnmt1 is required for pre-gastrula zebrafish development. Dev. Biol. 412, 99-113.
    Kikuta, H., Kanai, M., Ito, Y., Yamasu, K., 2003. gbx2 Homeobox gene is required for the maintenance of the isthmic region in the zebrafish embryonic brain. Dev. Dyn. 228, 433-450.
    Lalonde, R., Botez, M.I., 1990. The cerebellum and learning processes in animals. Brain Res. Brain Res. Rev. 15, 325-332.
    Lauter, G., Soll, I., Hauptmann, G., 2011. Multicolor fluorescent in situ hybridization to define abutting and overlapping gene expression in the embryonic zebrafish brain. Neural Dev. 6, 10.
    Lee, E.Y., Chang, C.Y., Hu, N., Wang, Y.C., Lai, C.C., Herrup, K., Lee, W.H., Bradley, A., 1992. Mice deficient for Rb are nonviable and show defects in neurogenesis and haematopoiesis. Nature 359, 288-294.
    Leucht, C., Stigloher, C., Wizenmann, A., Klafke, R., Folchert, A., Bally-Cuif, L., 2008. MicroRNA-9 directs late organizer activity of the midbrain-hindbrain boundary. Nat. Neurosci. 11, 641-648.
    Liao, Y., Du, W., 2017. Rb-independent E2F3 promotes cell proliferation and alters expression of genes involved in metabolism and inflammation. FEBS Open Bio 7, 1611-1621.
    Liu, F., Kambakam, S., Almeida, M.P., Ming, Z., Welker, J.M., Wierson, W.A., Schultz-Rogers, L.E., Ekker, S.C., Clark, K.J., Essner, J.J., et al., 2022. Cre/lox regulated conditional rescue and inactivation with zebrafish UFlip alleles generated by CRISPR-Cas9 targeted integration. Elife 11, e71478.
    Liu, J., Li, C., Yu, Z., Huang, P., Wu, H., Wei, C., Zhu, N., Shen, Y., Chen, Y., Zhang, B., et al., 2012. Efficient and specific modifications of the Drosophila genome by means of an easy TALEN strategy. J. Genet. Genomics 39, 209-215.
    Liu, L.Y., Lin, M.H., Lai, Z.Y., Jiang, J.P., Huang, Y.C., Jao, L.E., Chuang, Y.J., 2016. Motor neuron-derived Thsd7a is essential for zebrafish vascular development via the Notch-dll4 signaling pathway. J. Biomed. Sci. 23, 59.
    Lowery, L.A., Sive, H., 2005. Initial formation of zebrafish brain ventricles occurs independently of circulation and requires the nagie oko and snakehead/atp1a1a.1 gene products. Development 132, 2057-2067.
    MacPherson, D., Sage, J., Crowley, D., Trumpp, A., Bronson, R.T., Jacks, T., 2003. Conditional mutation of Rb causes cell cycle defects without apoptosis in the central nervous system. Mol. Cell. Biol. 23, 1044-1053.
    Marino, S., Hoogervoorst, D., Brandner, S., Berns, A., 2003. Rb and p107 are required for normal cerebellar development and granule cell survival but not for Purkinje cell persistence. Development 130, 3359-3368.
    Marino, S., Vooijs, M., van Der Gulden, H., Jonkers, J., Berns, A., 2000. Induction of medulloblastomas in p53-null mutant mice by somatic inactivation of Rb in the external granular layer cells of the cerebellum. Genes Dev. 14, 994-1004.
    Millet, S., Campbell, K., Epstein, D.J., Losos, K., Harris, E., Joyner, A.L., 1999. A role for Gbx2 in repression of Otx2 and positioning the mid/hindbrain organizer. Nature 401, 161-164.
    Moens, C.B., Prince, V.E., 2002. Constructing the hindbrain: insights from the zebrafish. Dev. Dyn. 224, 1-17.
    Mueller, T., Vernier, P., Wullimann, M.F., 2006. A phylotypic stage in vertebrate brain development: GABA cell patterns in zebrafish compared with mouse. J. Comp. Neurol. 494, 620-634.
    Nakamura, H., Katahira, T., Matsunaga, E., Sato, T., 2005. Isthmus organizer for midbrain and hindbrain development. Brain Re.s Brain Res. Rev. 49, 120-126.
    Nakayama, Y., Inomata, C., Yuikawa, T., Tsuda, S., Yamasu, K., 2017. Comprehensive analysis of target genes in zebrafish embryos reveals gbx2 involvement in neurogenesis. Dev. Biol. 430, 237-248.
    Oxtoby, E., Jowett, T., 1993. Cloning of the zebrafish krox-20 gene (krx-20) and its expression during hindbrain development. Nucleic Acids Res. 21, 1087-1095.
    Peri, F., Nusslein-Volhard, C., 2008. Live imaging of neuronal degradation by microglia reveals a role for v0-ATPase a1 in phagosomal fusion in vivo. Cell 133, 916-927.
    Rakic, P., 1972. Mode of cell migration to the superficial layers of fetal monkey neocortex. J. Comp. Neurol. 145, 61-83.
    Rhinn, M., Lun, K., Ahrendt, R., Geffarth, M., Brand, M., 2009. Zebrafish gbx1 refines the midbrain-hindbrain boundary border and mediates the Wnt8 posteriorization signal. Neural Dev. 4, 12.
    Rhinn, M., Lun, K., Amores, A., Yan, Y.L., Postlethwait, J.H., Brand, M., 2003. Cloning, expression and relationship of zebrafish gbx1 and gbx2 genes to Fgf signaling. Mech. Dev. 120, 919-936.
    Rodriguez, F., Duran, E., Gomez, A., Ocana, F.M., Alvarez, E., Jimenez-Moya, F., Broglio, C., Salas, C., 2005. Cognitive and emotional functions of the teleost fish cerebellum. Brain Res. Bull. 66, 365-370.
    Roeseler, D.A., Sachdev, S., Buckley, D.M., Joshi, T., Wu, D.K., Xu, D., Hannink, M., Waters, S.T., 2012. Elongation factor 1 alpha1 and genes associated with Usher syndromes are downstream targets of GBX2. PLoS ONE 7, e47366.
    Rowitch, D.H., 2004. Glial specification in the vertebrate neural tube. Nat Rev Neurosci 5, 409-419.
    Sachdeva, U.M., O'Brien, J.M., 2012. Understanding pRb: toward the necessary development of targeted treatments for retinoblastoma. J. Clin. Invest. 122, 425-434.
    Sawada, M., Sawamoto, K., 2020. Chapter 21 - Neuronal migration in the postnatal brain, in: Rubenstein, J., Rakic, P., Chen, B., Kwan, K.Y., Kolodkin, A., Anton, E. (Eds.), Cellular Migration and Formation of Axons and Dendrites (Second Edition). Academic Press, pp. 465-478.
    Schredelseker, T., Driever, W., 2020. Conserved Genoarchitecture of the Basal Hypothalamus in Zebrafish Embryos. Front. Neuroanat. 14, 3.
    Schultz-Rogers, L.E., Thayer, M.L., Kambakam, S., Wierson, W.A., Helmer, J.A., Wishman, M.D., Wall, K.A., Greig, J.L., Forsman, J.L., Puchhalapalli, K., et al., 2022. Rbbp4 loss disrupts neural progenitor cell cycle regulation independent of Rb and leads to Tp53 acetylation and apoptosis. Dev. Dyn. 251, 1267-1290.
    Schultz, L.E., Haltom, J.A., Almeida, M.P., Wierson, W.A., Solin, S.L., Weiss, T.J., Helmer, J.A., Sandquist, E.J., Shive, H.R., McGrail, M., 2018. Epigenetic regulators Rbbp4 and Hdac1 are overexpressed in a zebrafish model of RB1 embryonal brain tumor, and are required for neural progenitor survival and proliferation. Dis. Model Mech. 11, dmm034124.
    Shimada, Y., Kuninaga, S., Ariyoshi, M., Zhang, B., Shiina, Y., Takahashi, Y., Umemoto, N., Nishimura, Y., Enari, H., Tanaka, T., 2015. E2F8 promotes hepatic steatosis through FABP3 expression in diet-induced obesity in zebrafish. Nutr. Metab. (Lond) 12, 17.
    Singh, J., Murata, K., Itahana, Y., Desprez, P.Y., 2002. Constitutive expression of the Id-1 promoter in human metastatic breast cancer cells is linked with the loss of NF-1/Rb/HDAC-1 transcription repressor complex. Oncogene 21, 1812-1822.
    Solin, S.L., Shive, H.R., Woolard, K.D., Essner, J.J., McGrail, M., 2015. Rapid tumor induction in zebrafish by TALEN-mediated somatic inactivation of the retinoblastoma1 tumor suppressor rb1. Sci. Rep. 5, 13745.
    Strahle, U., Blader, P., Adam, J., Ingham, P.W., 1994. A simple and efficient procedure for non-isotopic in situ hybridization to sectioned material. Trends Genet. 10, 75-76.
    Wassarman, K.M., Lewandoski, M., Campbell, K., Joyner, A.L., Rubenstein, J.L., Martinez, S., Martin, G.R., 1997. Specification of the anterior hindbrain and establishment of a normal mid/hindbrain organizer is dependent on Gbx2 gene function. Development 124, 2923-2934.
    Wurst, W., Bally-Cuif, L., 2001. Neural plate patterning: upstream and downstream of the isthmic organizer. Nat. Rev. Neurosci. 2, 99-108.
    Xiao, A., Wang, Z., Hu, Y., Wu, Y., Luo, Z., Yang, Z., Zu, Y., Li, W., Huang, P., Tong, X., et al., 2013. Chromosomal deletions and inversions mediated by TALENs and CRISPR/Cas in zebrafish. Nucleic Acids Res. 41, e141.
    Yu, Z., Deng, P., Chen, Y., Lin, D., Liu, S., Hong, J., Guan, P., Chen, J., Zhong, M.E., Chen, J., et al., 2024. Pharmacological modulation of RB1 activity mitigates resistance to neoadjuvant chemotherapy in locally advanced rectal cancer. Proc. Natl. Acad. Sci. U. S. A. 121, e2304619121.
    Zannino, D.A., Appel, B., 2009. Olig2+ precursors produce abducens motor neurons and oligodendrocytes in the zebrafish hindbrain. J. Neurosci. 29, 2322-2333.
    Zhang, H., Wang, H., Shen, X., Jia, X., Yu, S., Qiu, X., Wang, Y., Du, J., Yan, J., He, J., 2021. The landscape of regulatory genes in brain-wide neuronal phenotypes of a vertebrate brain. Elife 10.
    Zhang, Z., Liu, W., Zhao, L., Huang, Z., Chen, X., Ma, N., Xu, J., Zhang, W., Zhang, Y., 2018. Retinoblastoma 1 protects T cell maturation from premature apoptosis by inhibiting E2F1. Development 145, dev158139.
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