Embryonic development in the primitive bilaterian Neochildia fusca:: normal morphogenesis and isolation of POU genes Brn-1 and Brn-3

被引:37
|
作者
Ramachandra, NB
Gates, RD
Ladurner, P
Jacobs, DK
Hartenstein, V
机构
[1] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Organism Biol Ecol & Evolut, Los Angeles, CA 90095 USA
[3] Univ Innsbruck, Inst Zool & Limnol, A-6020 Innsbruck, Austria
关键词
acoel; Neochildia; nervous system; development; POU gene;
D O I
10.1007/s00427-001-0207-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neochildia fusca is a member of the taxon Acoela, a group of flatworms that, according to some recent molecular phylogenetic analyses, are distinct from other flatworms and constitute a basal branch with a sister taxon relationship to the rest of the Bilateria. In this paper, we analyze early neural development in this species and report the sequence and expression of two Pit-Oct-Unc (POU) genes, NeocBrn-1 and NeocBrn-3. Homologs of these highly conserved genes play a role in neural fate determination in vertebrates, Drosophila and Caenorhabditis elegans. Acoels, including Neochildia, have a unique invariant pattern of early cleavage called duet spiral cleavage. In subsequent cell divisions descendants of the first three micromere duets form an outer layer of epidermal and neural progenitors surrounding the meso/endoderm progenitors, which are themselves descended from the macromere duet 4A, B and the micromere duet 4a, b. Organ formation begins at mid-embryonic stages with the epidermal primordium adopting a ciliated epithelial shape. Sub-epidermally, a bilaterally symmetric brain primordium can be seen at the anterior pole. Laterally and posteriorly, myoblasts form a thin layer underneath the epidermis. In late embryos and juveniles of Neochildia, the brain is formed by a 3-4 cell-diameter-thick layer of neurons forming a cortex surrounding, a neuropile that is relatively free of cell bodies. A highly regular "orthogonal" array of muscle fibers penetrates the brain. We have isolated and partially sequenced homologs of the vertebrate Brn-1 and Brn-3 genes, which we call NeocBrn-1 and NeocBrn-3, respectively. These sequences contain and span portions of the POU-specific domain and a homeodomain, and are sequence similar to their respective homologs in vertebrates and Drosophila. RT-PCR reveals that NeocBrn-1 and NeocBrn-3 are expressed from mid-embryonic to adult stages. Whole-mount in situ hybridization shows expression of both genes in distinct subsets of nerve cells in juvenile and adult worms. NeocBrn-1 also appears in a subset of intra-epidermal gland cells. These observations are an initial step towards reconstructing the neural development of a key group of bilaterians, the Acoela. These flatworms, by virtue of their distinct morphology, development and phylogenetically basal placement, are likely to provide key insights into the interpretation of the evolution of metazoan neural architecture.
引用
收藏
页码:55 / 69
页数:15
相关论文
共 10 条
  • [1] Embryonic development in the primitive bilaterian Neochildia fusca: normal morphogenesis and isolation of POU genes Brn-1 and Brn-3
    Nallur B. Ramachandra
    Ruth D. Gates
    Peter Ladurner
    David K. Jacobs
    Volker Hartenstein
    Development Genes and Evolution, 2002, 212 : 55 - 69
  • [2] Role of the Brn-3 family of POU-domain genes in the development of the auditory/nestibular, somatosensory, and visual systems
    Xiang, M
    Gan, L
    Li, D
    Zhou, L
    Chen, ZY
    Wagner, D
    O'Malley, BW
    Klein, W
    Nathans, J
    COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1997, 62 : 325 - 336
  • [3] Differential regulation of genes encoding synaptic proteins by members of the Brn-3 subfamily of POU transcription factors
    Morris, PJ
    Lakin, ND
    Dawson, SJ
    Ryabinin, AE
    Kilimann, MW
    Wilson, MC
    Latchman, DS
    MOLECULAR BRAIN RESEARCH, 1996, 43 (1-2): : 279 - 285
  • [4] Expression of Pou3f3/Brn-1 and Its Genomic Methylation in Developing Auditory Epithelium
    Mutai, Hideki
    Nagashima, Reiko
    Sugitani, Yoshinobu
    Noda, Tetsuo
    Fujii, Masato
    Matsunaga, Tatsuo
    DEVELOPMENTAL NEUROBIOLOGY, 2009, 69 (14) : 913 - 930
  • [5] Combinatorial expression of zebrafish Brn-1- and Brn-2-related POU genes in the embryonic brain, pronephric primordium, and pharyngeal arches
    Hauptmann, G
    Gerster, T
    DEVELOPMENTAL DYNAMICS, 2000, 218 (02) : 345 - 358
  • [6] Direct inhibition of the DNA-binding activity of POU transcription factors Pit-1 and Brn-3 by selective binding of a phenyl-furan-benzimidazole dication
    Peixoto, Paul
    Liu, Yang
    Depauw, Sabine
    Hildebrand, Marie-Paule
    Boykin, David W.
    Bailly, Christian
    Wilson, W. David
    David-Cordonnier, Marie-Helene
    NUCLEIC ACIDS RESEARCH, 2008, 36 (10) : 3341 - 3353
  • [7] Pou4f1/Brn3a regulates neurite- and synapse-associated genes during Retinal Ganglion Cell development
    Muzyka, Vladimir
    Badea, Tudor C.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2017, 58 (08)
  • [8] The Ath5 proneural genes function upstream of Brn3 POU domain transcription factor genes to promote retinal ganglion cell development
    Liu, W
    Mo, ZQ
    Xiang, MQ
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (04) : 1649 - 1654
  • [9] Postnatal developmental dynamics of cell type specification genes in Brn3a/Pou4f1 Retinal Ganglion Cells
    Muzyka, Vladimir Vladimirovich
    Brooks, Matthew
    Badea, Tudor Constantin
    NEURAL DEVELOPMENT, 2018, 13
  • [10] Postnatal developmental dynamics of cell type specification genes in Brn3a/Pou4f1 Retinal Ganglion Cells
    Vladimir Vladimirovich Muzyka
    Matthew Brooks
    Tudor Constantin Badea
    Neural Development, 13