Identification of Pax2-regulated genes by expression profiling of the mid-hindbrain organizer region

被引:55
作者
Bouchard, M
Grote, D
Craven, SE
Sun, G
Steinlein, P
Busslinger, M
机构
[1] Vienna Bioctr, Res Inst Mol Pathol, A-1030 Vienna, Austria
[2] McGill Univ, McGill Canc Ctr, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[3] Genentech Inc, Dept Biol Mol, San Francisco, CA 94080 USA
来源
DEVELOPMENT | 2005年 / 132卷 / 11期
关键词
mid-hindbrain development; Pax2-regulated genes; Sef; Tapp1; Ncrms; En2; Brn1; Fgf8; regulation; mouse;
D O I
10.1242/dev.01833
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The paired domain transcription factor Pax2 is required for the formation of the isthmic organizer (IsO) at the midbrain-hindbrain boundary, where it initiates expression of the IsO signal Fgf8. To gain further insight into the role of Pax2 in mid-hindbrain patterning, we searched for novel Pax2-regulated genes by cDNA microarray analysis of FACS-sorted GFP(+) mid-hindbrain cells from wild-type and Pax2(-/-) embryos carrying a Pax2(GFP) BAC transgene. Here, we report the identification of five genes that depend on Pax2 function for their expression in the mid-hindbrain boundary region. These genes code for the transcription factors En2 and Brn1 (Pou3f3), the intracellular signaling modifiers Sef and Tapp1, and the non-coding RNA Ncrms. The Brn1 gene was further identified as a direct target of Pax2, as two functional Pax2-binding sites in the promoter and in an upstream regulatory element of Brn1 were essential for lacZ transgene expression at the mid-hindbrain boundary. Moreover, ectopic expression of a dominant-negative Brn1 protein in chick embryos implicated Brn1 in Fgf8 gene regulation. Together, these data defined novel functions of Pax2 in the establishment of distinct transcriptional programs and in the control of intracellular signaling during mid-hindbrain development.
引用
收藏
页码:2633 / 2643
页数:11
相关论文
共 60 条
  • [1] CpG islands as genomic footprints of promoters that are associated with replication origins
    Antequera, F
    Bird, A
    [J]. CURRENT BIOLOGY, 1999, 9 (17) : R661 - R667
  • [2] Bouchard M, 2000, DEVELOPMENT, V127, P3703
  • [3] Brand M, 1996, DEVELOPMENT, V123, P179
  • [4] Bürglin TR, 2001, DEVELOPMENT, V128, P779
  • [5] Unbiased mapping of transcription factor binding sites along human chromosomes 21 and 22 points to widespread regulation of noncoding RNAs
    Cawley, S
    Bekiranov, S
    Ng, HH
    Kapranov, P
    Sekinger, EA
    Kampa, D
    Piccolboni, A
    Sementchenko, V
    Cheng, J
    Williams, AJ
    Wheeler, R
    Wong, B
    Drenkow, J
    Yamanaka, M
    Patel, S
    Brubaker, S
    Tammana, H
    Helt, G
    Struhl, K
    Gingeras, TR
    [J]. CELL, 2004, 116 (04) : 499 - 509
  • [6] Identification of a novel gene NCRMS on chromosome 12q21 with differential expression between Rhabdomyosarcoma subtypes
    Chan, AS
    Thorner, PS
    Squire, JA
    Zielenska, M
    [J]. ONCOGENE, 2002, 21 (19) : 3029 - 3037
  • [7] Making and reading microarrays
    Cheung, VG
    Morley, M
    Aguilar, F
    Massimi, A
    Kucherlapati, R
    Childs, G
    [J]. NATURE GENETICS, 1999, 21 (Suppl 1) : 15 - 19
  • [8] The isthmic organizer signal FGF8 is required for cell survival in the prospective midbrain and cerebellum
    Chi, CL
    Martinez, S
    Wurst, W
    Martin, GR
    [J]. DEVELOPMENT, 2003, 130 (12): : 2633 - 2644
  • [9] Spatial and temporal patterns of ERK signaling during mouse embryogenesis
    Corson, LB
    Yamanaka, Y
    Lai, KMV
    Rossant, J
    [J]. DEVELOPMENT, 2003, 130 (19): : 4527 - 4537
  • [10] Midbrain development induced by FGF8 in the chick embryo
    Crossley, PH
    Martinez, S
    Martin, GR
    [J]. NATURE, 1996, 380 (6569) : 66 - 68