Insulinoma-Associated 1 Has a Panneurogenic Role and Promotes the Generation and Expansion of Basal Progenitors in the Developing Mouse Neocortex

被引:129
作者
Farkas, Lilla M. [1 ]
Haffner, Christiane [1 ]
Giger, Thomas [2 ]
Khaitovich, Philipp [2 ]
Nowick, Katja [2 ]
Birchmeier, Carmen [3 ]
Paeaebo, Svante [2 ]
Huttner, Wieland B. [1 ]
机构
[1] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
[2] Max Planck Inst Evolutionary Anthropol, D-04103 Leipzig, Germany
[3] Max Delbruck Ctr Mol Med, D-13125 Berlin, Germany
关键词
D O I
10.1016/j.neuron.2008.09.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Basal (intermediate) progenitors are the major source of neurons in the mammalian neocortex. The molecular machinery governing basal progenitor biogenesis is unknown. Here, we show that the zinc-finger transcription factor Insm1 (insulinoma-associated 1) is expressed specifically in progenitors undergoing neurogenic divisions, has a panneurogenic role throughout the brain, and promotes basal progenitor formation in the neocortex. Mouse embryos lacking Insm1 contained half the number of basal progenitors and showed a marked reduction in cortical plate radial thickness. Forced premature expression of Insm1 in neuroepithelial cells resulted in their mitosis occurring at the basal (rather than apical) side of the ventricular zone and induced expression of the basal progenitor marker Tbr2. Remarkably, these cells remained negative for Tis21, a marker of neurogenic progenitors, and did not generate neurons but underwent self-amplification. Our data imply that Insm1 is involved in the generation and expansion of basal progenitors, a hallmark of neocortex evolution.
引用
收藏
页码:40 / 55
页数:16
相关论文
共 51 条
[21]   Cellular and molecular control of neurogenesis in the mammalian telencephalon [J].
Guillemot, F .
CURRENT OPINION IN CELL BIOLOGY, 2005, 17 (06) :639-647
[22]   Hes genes regulate size, shape and histogenesis of the nervous system by control of the timing of neural stem cell differentiation [J].
Hatakeyama, J ;
Bessho, Y ;
Katoh, K ;
Ookawara, S ;
Fujioka, M ;
Guillemot, F ;
Kageyama, R .
DEVELOPMENT, 2004, 131 (22) :5539-5550
[23]   Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: A major site of neurogenesis [J].
Haubensak, W ;
Attardo, A ;
Denk, W ;
Huttner, WB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :3196-3201
[24]   Symmetric versus asymmetric cell division during neurogenesis in the developing vertebrate central nervous system [J].
Huttner, WB ;
Kosodo, Y .
CURRENT OPINION IN CELL BIOLOGY, 2005, 17 (06) :648-657
[25]   Expression of the antiproliferative gene TIS21 at the onset of neurogenesis identifies single neuroepithelial cells that switch from proliferative to neuron-generating division [J].
Iacopetti, P ;
Michelini, M ;
Stuckmann, I ;
Oback, B ;
Aaku-Saraste, E ;
Huttner, WB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4639-4644
[26]   Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis [J].
Konno, Daijiro ;
Shioi, Go ;
Shitamukai, Atsunori ;
Mori, Asako ;
Kiyonari, Hiroshi ;
Miyata, Takaki ;
Matsuzaki, Fumio .
NATURE CELL BIOLOGY, 2008, 10 (01) :93-U78
[27]   Asymmetric distribution of the apical plasma membrane during neurogenic divisions of mammalian neuroepithelial cells [J].
Kosodo, Y ;
Röper, K ;
Haubensak, W ;
Marzesco, AM ;
Corbeil, D ;
Huttner, WB .
EMBO JOURNAL, 2004, 23 (11) :2314-2324
[28]   Radial glia diversity:: A matter of cell fate [J].
Kriegstein, AR ;
Götz, M .
GLIA, 2003, 43 (01) :37-43
[29]   Patterns of neural stem and progenitor cell division may underlie evolutionary cortical expansion [J].
Kriegstein, Arnold ;
Noctor, Stephen ;
Martinez-Cerdeno, Veronica .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (11) :883-890
[30]   Nerfin-1 is required for early axon guidance decisions in the developing Drosophila CNS [J].
Kuzin, A ;
Brody, T ;
Moore, AW ;
Odenwald, WF .
DEVELOPMENTAL BIOLOGY, 2005, 277 (02) :347-365