The basic helix-loop-helix factor Olig2 is essential for the development of motoneuron and oligodendrocyte lineages

被引:415
作者
Takebayashi, H
Nabeshima, Y
Yoshida, S
Chisaka, O
Ikenaka, K
Nabeshima, Y
机构
[1] Kyoto Univ, Dept Pathol & Tumor Biol, Grad Sch Med, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Fac Sci, Sakyo Ku, Kyoto 6068502, Japan
[3] Kyoto Univ, Grad Sch Biostudies, Sakyo Ku, Kyoto 6068502, Japan
[4] Natl Inst Physiol Sci, Lab Neural Informat, Okazaki, Aichi 4448585, Japan
基金
日本学术振兴会;
关键词
D O I
10.1016/S0960-9822(02)00926-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sonic hedgehog (Shh), an organizing signal from ventral midline structures, is essential for the induction and maintenance of many ventral cell types in the embryonic neural tube. Olig1 and Olig2 are related basic helix-loop-helix factors induced by Shh in the ventral neural tube. Although expression analyses and gain-of-function experiments suggested that these factors were involved in motoneuron and oligodendrocyte development, they do not clearly define the functional differences between Olig1 and Olig2. We generated mice with a homozygous inactivation of Olig2. These mice did not feed and died on the day of birth. In the spinal cord of the mutant mice, motoneurons are largely eliminated and oligodendrocytes are not produced. Olig2(-/-) neuroepithelial cells in the ventral spinal cord failed to differentiate into motoneurons or oligodendrocytes and expressed an astrocyte marker, S100beta, at the time of oligodendrogenesis. Olig1 or Olig3, other family members, were expressed in the descendent cells that should have expressed Olig2. We concluded that Olig2 is an essential transcriptional regulator in motoneuron and oligodendrocyte development. Our data provide the first evidence that a single gene mutation leads to the loss of two cell types, motoneuron and oligodendrocyte.
引用
收藏
页码:1157 / 1163
页数:7
相关论文
共 45 条
[1]   Requirement for the homeobox gene Hb9 in the consolidation of motor neuron identity [J].
Arber, S ;
Han, B ;
Mendelsohn, M ;
Smith, M ;
Jessell, TM ;
Sockanathan, S .
NEURON, 1999, 23 (04) :659-674
[2]   Proprioceptor pathway development is dependent on MATH1 [J].
Bermingham, NA ;
Hassan, BA ;
Wang, VY ;
Fernandez, M ;
Banfi, S ;
Bellen, HJ ;
Fritzsch, B ;
Zoghbi, HY .
NEURON, 2001, 30 (02) :411-422
[3]   Spatio-temporally controlled site-specific somatic mutagenesis in the mouse [J].
Brocard, J ;
Warot, X ;
Wendling, O ;
Messaddeq, N ;
Vonesch, JL ;
Chambon, P ;
Metzger, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14559-14563
[4]   Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase [J].
Danielian, PS ;
Muccino, D ;
Rowitch, DH ;
Michael, SK ;
McMahon, AP .
CURRENT BIOLOGY, 1998, 8 (24) :1323-1326
[5]   SPATIAL REGULATION OF AXONAL GLYCOPROTEIN EXPRESSION ON SUBSETS OF EMBRYONIC SPINAL NEURONS [J].
DODD, J ;
MORTON, SB ;
KARAGOGEOS, D ;
YAMAMOTO, M ;
JESSELL, TM .
NEURON, 1988, 1 (02) :105-116
[6]   Pax6 controls progenitor cell identity and neuronal fate in response to graded shh signaling [J].
Ericson, J ;
Rashbass, P ;
Schedl, A ;
BrennerMorton, S ;
Kawakami, A ;
vanHeyningen, V ;
Jessell, TM ;
Briscoe, J .
CELL, 1997, 90 (01) :169-180
[7]   EARLY STAGES OF MOTOR-NEURON DIFFERENTIATION REVEALED BY EXPRESSION OF HOMEOBOX GENE ISLET-1 [J].
ERICSON, J ;
THOR, S ;
EDLUND, T ;
JESSELL, TM ;
YAMADA, T .
SCIENCE, 1992, 256 (5063) :1555-1560
[8]  
Fruttiger M, 1999, DEVELOPMENT, V126, P457
[9]  
Fu H, 2002, DEVELOPMENT, V129, P681
[10]   SPECIFIC AND ARTEFACTUAL CELLULAR-LOCALIZATIONS OF S100 PROTEIN - AN ASTROCYTE MARKER IN RAT CEREBELLUM [J].
GHANDOUR, MS ;
LANGLEY, OK ;
LABOURDETTE, G ;
VINCENDON, G ;
GOMBOS, G .
DEVELOPMENTAL NEUROSCIENCE, 1981, 4 (01) :66-78