TY - JOUR
T1 - Mutually repressive interaction between Brn1/2 and Rorb contributes to the establishment of neocortical layer 2/3 and layer 4
AU - Oishi, Koji
AU - Aramaki, Michihiko
AU - Nakajima, Kazunori
N1 - Funding Information:
ACKNOWLEDGMENTS. We thank J. Miyazaki, H. Kondoh, H. Hamada, C. Cepko, A. Sakakibara, T. Miyata, I. Ajioka, and R. Hevner for reagents and advice. This work was supported by the Strategic Research Program for Brain Sciences ("Understanding of molecular and environmental bases for brain health") of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), KAKENHI Grants (22111004, 25640039, 15H02355, 15H01586, 19700295, 21700356) of MEXT/Japan Society for the Promotion of Science (JSPS), Takeda Science Foundation, Naito Foundation, Terumo Life Science Foundation, Life Science Foundation of Japan, Keio Gijuku Academic Development Funds, and Fukuzawa Memorial Fund for the Advancement of Education and Research.
PY - 2016/3/22
Y1 - 2016/3/22
N2 - Although several molecules have been shown to play important roles in subtype specification of neocortical neurons, the entire mechanism involved in the specification, in particular, of upper cortical plate (UCP) neurons still remains unclear. The UCP, which is responsible for intracortical connections in the neocortex, comprises histologically, functionally, and molecularly different layer 2/3 (L2/3) and L4. Here, we report the essential interactions between two types of transcription factors, Rorb (RAR-related orphan receptor beta) and Brn1/2 (Brain-1/Brain-2), for UCP specification. We found that Brn2 expression was detected in all upper layers in the immature UCP, but was subsequently restricted to L2/3, accompanied by up-regulation of Rorb in L4, suggesting demarcation of L2/3 and L4 during cortical maturation. Rorb indeed inhibited Brn2 expression and the expression of other L2/3 characteristics, revealed by ectopic expression and knockdown studies. Moreover, this inhibition occurred through direct binding of Rorb to the Brn2 locus. Conversely, Brn1/2 also inhibited Rorb expression and the expression of several L4 characteristics. Together, these results suggest that a mutually repressive mechanism exists between Brn1/2 and Rorb expression and that the established expression of Brn1/2 and Rorb further specifies those neurons into L2/3 and L4, respectively, during UCP maturation.
AB - Although several molecules have been shown to play important roles in subtype specification of neocortical neurons, the entire mechanism involved in the specification, in particular, of upper cortical plate (UCP) neurons still remains unclear. The UCP, which is responsible for intracortical connections in the neocortex, comprises histologically, functionally, and molecularly different layer 2/3 (L2/3) and L4. Here, we report the essential interactions between two types of transcription factors, Rorb (RAR-related orphan receptor beta) and Brn1/2 (Brain-1/Brain-2), for UCP specification. We found that Brn2 expression was detected in all upper layers in the immature UCP, but was subsequently restricted to L2/3, accompanied by up-regulation of Rorb in L4, suggesting demarcation of L2/3 and L4 during cortical maturation. Rorb indeed inhibited Brn2 expression and the expression of other L2/3 characteristics, revealed by ectopic expression and knockdown studies. Moreover, this inhibition occurred through direct binding of Rorb to the Brn2 locus. Conversely, Brn1/2 also inhibited Rorb expression and the expression of several L4 characteristics. Together, these results suggest that a mutually repressive mechanism exists between Brn1/2 and Rorb expression and that the established expression of Brn1/2 and Rorb further specifies those neurons into L2/3 and L4, respectively, during UCP maturation.
KW - Cell fate
KW - Cerebral cortex
KW - Layer formation
KW - Transcription factor
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U2 - 10.1073/pnas.1515949113
DO - 10.1073/pnas.1515949113
M3 - Article
C2 - 26951672
AN - SCOPUS:84962241765
SN - 0027-8424
VL - 113
SP - 3371
EP - 3376
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 12
ER -