Id4 regulates neural progenitor proliferation and differentiation in vivo

被引:101
作者
Yun, K
Mantani, A
Garel, S
Rubenstein, J
Israel, MA
机构
[1] Dartmouth Hitchcock Med Ctr, Dartmouth Med Sch, Dept Pediat & Genet, Lebanon, NH 03756 USA
[2] Dartmouth Hitchcock Med Ctr, Dartmouth Med Sch, Norris Cotton Canc Ctr, Lebanon, NH 03756 USA
[3] Univ Calif San Francisco, LPPI, Dept Psychiat, Nina Ireland Lab Dev Neurobiol, San Francisco, CA 94143 USA
来源
DEVELOPMENT | 2004年 / 131卷 / 21期
关键词
Id4; Id2; cortex; hippocampus; GI-S; cell cycle; neurogenesis; CNS development;
D O I
10.1242/dev.01430
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mechanisms that determine whether a precursor cell re-enters the cell cycle or exits and differentiates are crucial in determining the types and numbers of cells that constitute a particular organ. Here, we report that Id4 is required for normal brain size, and regulates lateral expansion of the proliferative zone in the developing cortex and hippocampus. In its absence, proliferation of stem cells in the ventricular zone (VZ) is compromised. In early cortical progenitors, Id4 is required for the normal G1-S transition. By contrast, at later ages, ectopically positioned proliferating cells are found in the mantle zone of the Id4(-/-) cortex. These observations, together with evidence for the premature differentiation of early cortical stem cells, indicate that Id4 has a unique and complex function in regulating neural stem cell proliferation and differentiation.
引用
收藏
页码:5441 / 5448
页数:8
相关论文
共 44 条
[1]   Id1 regulation of cellular senescence through transcriptional repression of p16/Ink4a [J].
Alani, RM ;
Young, AZ ;
Shifflett, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (14) :7812-7816
[2]  
Andres-Barquin PJ, 2000, HISTOL HISTOPATHOL, V15, P603, DOI 10.14670/HH-15.603
[3]   THE PROTEIN ID - A NEGATIVE REGULATOR OF HELIX-LOOP-HELIX DNA-BINDING PROTEINS [J].
BENEZRA, R ;
DAVIS, RL ;
LOCKSHON, D ;
TURNER, DL ;
WEINTRAUB, H .
CELL, 1990, 61 (01) :49-59
[4]   Expression pattern of the Tbr2 (Eomesodermin) gene during mouse and chick brain development [J].
Bulfone, A ;
Martinez, S ;
Marigo, V ;
Campanella, M ;
Basile, A ;
Quaderi, N ;
Gattuso, C ;
Rubenstein, JLR ;
Ballabio, A .
MECHANISMS OF DEVELOPMENT, 1999, 84 (1-2) :133-138
[5]   Cell output, cell cycle duration and neuronal specification: a model of integrated mechanisms of the neocortical proliferative process [J].
Caviness, VS ;
Goto, T ;
Tarui, T ;
Takahashi, T ;
Bhide, PG ;
Nowakowski, RS .
CEREBRAL CORTEX, 2003, 13 (06) :592-598
[6]   AN ID-RELATED HELIX LOOP HELIX PROTEIN ENCODED BY A GROWTH FACTOR-INDUCIBLE GENE [J].
CHRISTY, BA ;
SANDERS, LK ;
LAU, LF ;
COPELAND, NG ;
JENKINS, NA ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (05) :1815-1819
[7]   REQUIREMENT FOR A FUNCTIONAL RB-1 GENE IN MURINE DEVELOPMENT [J].
CLARKE, AR ;
MAANDAG, ER ;
VANROON, M ;
VANDERLUGT, NMT ;
VANDERVALK, M ;
HOOPER, ML ;
BERNS, A ;
RIELE, HT .
NATURE, 1992, 359 (6393) :328-330
[8]  
Fode C, 2000, GENE DEV, V14, P67
[9]   Restricted expression of a novel murine atonal-related bHLH protein in undifferentiated neural precursors [J].
Gradwohl, G ;
Fode, C ;
Guillemot, F .
DEVELOPMENTAL BIOLOGY, 1996, 180 (01) :227-241
[10]   Vertebrate bHLH genes and the determination of neuronal fates [J].
Guillemot, F .
EXPERIMENTAL CELL RESEARCH, 1999, 253 (02) :357-364