The transcriptional repressor RP58 is crucial for cell-division patterning and neuronal survival in the developing cortex

被引:54
作者
Okado, Haruo [1 ]
Ohtaka-Maruyama, Chiaki [1 ]
Sugitani, Yoshinobu [2 ]
Fukuda, Yuko [3 ]
Ishida, Reiko [3 ]
Hirai, Shinobu [1 ]
Miwa, Akiko [1 ]
Takahashi, Akiyo [1 ]
Aoki, Katsunori [4 ]
Mochida, Keiji [5 ]
Suzuki, Osamu [6 ]
Honda, Takao [7 ]
Nakajima, Kazunori [7 ]
Ogawa, Masaharu [2 ]
Terashima, Toshio [8 ]
Matsuda, Junichiro [6 ]
Kawano, Hitoshi [9 ]
Kasai, Masataka [3 ]
机构
[1] Tokyo Metropolitan Inst Neurosci, Dept Mol Physiol, Tokyo 1838526, Japan
[2] RIKEN, Brain Sci Inst, Neurodev Disorder Res Grp, Ogawa Res Unit, Wako, Saitama 3510198, Japan
[3] Natl Inst Infect Dis, Dept Immunol, Shinjuku Ku, Tokyo 1628640, Japan
[4] Univ Tokyo, Dept Hematol Internal Med, Bunkyo Ku, Tokyo 1138655, Japan
[5] RIKEN, Bioresource Ctr, Tsukuba, Ibaraki 3050074, Japan
[6] Natl Inst Infect Dis, Dept Vet Sci, Shinjuku Ku, Tokyo 1628640, Japan
[7] Keio Univ, Sch Med, Dept Anat, Tokyo 1608582, Japan
[8] Kobe Univ, Grad Sch Med, Dept Neurosci, Div Anat & Dev Neurobiol, Kobe, Hyogo 6500017, Japan
[9] Tokyo Metropolitan Inst Neurosci, Dept Dev Morphol, Tokyo 1838526, Japan
关键词
RP58; Transcriptional repressor; Cerebral cortex; Apoptosis; Cell-cycle exit; Progenitor cell; CEREBRAL-CORTEX; CORTICAL-NEURONS; DENTATE GYRUS; THALAMOCORTICAL PATHWAY; DEVELOPING NEOCORTEX; POSTMITOTIC NEURONS; SUBVENTRICULAR ZONE; SEQUENTIAL STAGES; PROGENITOR CELLS; GENE-EXPRESSION;
D O I
10.1016/j.ydbio.2009.04.030
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The neocortex and the hippocampus comprise several specific layers containing distinct neurons that originate from progenitors at specific development times, under the control of an adequate cell-division patterning mechanism. Although many molecules are known to regulate this cell-division patterning process, its details are not well understood. Here, we show that, in the developing cerebral cortex, the RP58 transcription repressor protein was expressed both in postmitotic glutamatergic projection neurons and in their progenitor cells, but not in GABAergic interneurons. Targeted deletion of the RP58 gene led to dysplasia of the neocortex and of the hippocampus, reduction of the number of mature cortical neurons, and defects of laminar organization, which reflect abnormal neuronal migration within the cortical plate. We demonstrate an impairment of the cell-division patterning during the late embryonic stage and an enhancement of apoptosis of the postmitotic neurons in the RP58-deficient cortex. These results suggest that RP58 controls cell division of progenitor cells and regulates the survival of postmitotic cortical neurons. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:140 / 151
页数:12
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