Polycomb genes interact with the tumor suppressor genes hippo and warts in the maintenance of Drosophila sensory neuron dendrites

被引:46
作者
Parrish, Jay Z.
Emoto, Kazuo
Jan, Lily Yeh
Jan, Yuh Nung [1 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Physiol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
关键词
Drosophila; neuron; dendrite; polycomb; homeobox; tumor suppressor;
D O I
10.1101/gad.1514507
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dendritic fields are important determinants of neuronal function. However, how neurons establish and then maintain their dendritic fields is not well understood. Here we show that Polycomb group (PcG) genes are required for maintenance of complete and nonoverlapping dendritic coverage of the larval body wall by Drosophila class IV dendrite arborization (da) neurons. In esc, Su(z)12, or Pc mutants, dendritic fields are established normally, but class IV neurons display a gradual loss of dendritic coverage, while axons remain normal in appearance, demonstrating that PcG genes are specifically required for dendrite maintenance. Both multiprotein Polycomb repressor complexes (PRCs) involved in transcriptional silencing are implicated in regulation of dendrite arborization in class IV da neurons, likely through regulation of homeobox (Hox) transcription factors. We further show genetic interactions and association between PcG proteins and the tumor suppressor kinase Warts (Wts), providing evidence for their cooperation in multiple developmental processes including dendrite maintenance.
引用
收藏
页码:956 / 972
页数:17
相关论文
共 52 条
  • [1] Xenopus Enhancer of Zeste (XEZ);: an anteriorly restricted polycomb gene with a role in neural patterning
    Barnett, MW
    Seville, RA
    Nijjar, S
    Old, RW
    Jones, EA
    [J]. MECHANISMS OF DEVELOPMENT, 2001, 102 (1-2) : 157 - 167
  • [2] On dendrties in Down syndrome and DS murine models:: a spiny way to learn
    Benavides-Piccione, R
    Ballesteros-Yáñez, I
    de Lagrán, MM
    Elston, G
    Estivill, X
    Fillat, C
    DeFelipe, J
    Dierssen, M
    [J]. PROGRESS IN NEUROBIOLOGY, 2004, 74 (02) : 111 - 126
  • [3] MORPHOLOGICAL-DIFFERENTIATION OF THE EMBRYONIC PERIPHERAL NEURONS IN DROSOPHILA
    BODMER, R
    JAN, YN
    [J]. ROUXS ARCHIVES OF DEVELOPMENTAL BIOLOGY, 1987, 196 (02): : 69 - 77
  • [4] Polycomb complexes repress developmental regulators in murine embryonic stem cells
    Boyer, LA
    Plath, K
    Zeitlinger, J
    Brambrink, T
    Medeiros, LA
    Lee, TI
    Levine, SS
    Wernig, M
    Tajonar, A
    Ray, MK
    Bell, GW
    Otte, AP
    Vidal, M
    Gifford, DK
    Young, RA
    Jaenisch, R
    [J]. NATURE, 2006, 441 (7091) : 349 - 353
  • [5] Genome-wide mapping of Polycomb target genes unravels their roles in cell fate transitions
    Bracken, AP
    Dietrich, N
    Pasini, D
    Hansen, KH
    Helin, K
    [J]. GENES & DEVELOPMENT, 2006, 20 (09) : 1123 - 1136
  • [6] Sequoia, a tramtrack-related zinc finger protein, functions as a pan-neural regulator for dendrite and axon morphogenesis in Drosophila
    Brenman, JE
    Gao, FB
    Jan, LY
    Jan, YN
    [J]. DEVELOPMENTAL CELL, 2001, 1 (05) : 667 - 677
  • [7] Role of histone H3 lysine 27 methylation in polycomb-group silencing
    Cao, R
    Wang, LJ
    Wang, HB
    Xia, L
    Erdjument-Bromage, H
    Tempst, P
    Jones, RS
    Zhang, Y
    [J]. SCIENCE, 2002, 298 (5595) : 1039 - 1043
  • [8] Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal polycomb sites
    Czermin, B
    Melfi, R
    McCabe, D
    Seitz, V
    Imhof, A
    Pirrotta, V
    [J]. CELL, 2002, 111 (02) : 185 - 196
  • [9] A Hox regulatory network establishes motor neuron pool identity and target-muscle connectivity
    Dasen, JS
    Tice, BC
    Brenner-Morton, S
    Jessell, TM
    [J]. CELL, 2005, 123 (03) : 477 - 491
  • [10] Control of dendritic branching and tiling by the tricornered-kinase/furry signaling pathway in Drosophila sensory neurons
    Emoto, K
    He, Y
    Ye, B
    Grueber, WB
    Adler, PN
    Jan, LY
    Jan, YN
    [J]. CELL, 2004, 119 (02) : 245 - 256