Mutually repressive interaction between Brn1/2 and Rorb contributes to the establishment of neocortical layer 2/3 and layer 4

新皮层 生物 祖细胞 祖细胞 心理压抑 细胞生物学 转录因子 电池类型 神经科学 互惠的 图层(电子) 抄写(语言学) 基因 细胞 遗传学 基因表达 干细胞 化学 有机化学 哲学 语言学
作者
Koji Oishi,Michihiko Aramaki,Kazunori Nakajima
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [Proceedings of the National Academy of Sciences]
卷期号:113 (12): 3371-3376 被引量:74
标识
DOI:10.1073/pnas.1515949113
摘要

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.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
明理绝悟发布了新的文献求助30
刚刚
完美世界应助茉莉采纳,获得10
1秒前
明亮的嚣发布了新的文献求助10
1秒前
天天快乐应助小伍同学采纳,获得10
1秒前
1秒前
斯文败类应助糊涂呆采纳,获得10
2秒前
机智的天天完成签到,获得积分10
2秒前
刘一一发布了新的文献求助10
3秒前
juckblack发布了新的文献求助10
3秒前
安晓慧完成签到 ,获得积分10
3秒前
FashionBoy应助李金辉采纳,获得10
4秒前
ruuuu发布了新的文献求助10
5秒前
Akim应助hh采纳,获得10
7秒前
8秒前
宫念波发布了新的文献求助10
8秒前
9秒前
9秒前
10秒前
科研通AI6.1应助dd123采纳,获得10
11秒前
bkagyin应助虚拟的寻绿采纳,获得10
11秒前
11秒前
小罗发布了新的文献求助10
12秒前
Guowei发布了新的文献求助10
13秒前
怼怼发布了新的文献求助10
14秒前
14秒前
wheat发布了新的文献求助10
14秒前
14秒前
zzz发布了新的文献求助10
16秒前
147258完成签到,获得积分20
16秒前
俊逸翠柏完成签到 ,获得积分10
17秒前
17秒前
传奇3应助白斯特采纳,获得10
18秒前
orixero应助hjy采纳,获得10
18秒前
w院士发布了新的文献求助10
19秒前
19秒前
小罗完成签到,获得积分10
19秒前
LIAO完成签到,获得积分10
20秒前
打打应助nini采纳,获得10
21秒前
isonomia发布了新的文献求助10
21秒前
FashionBoy应助ddd杜采纳,获得10
21秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Kinesiophobia : a new view of chronic pain behavior 3000
Les Mantodea de guyane 2500
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 2000
Standard: In-Space Storable Fluid Transfer for Prepared Spacecraft (AIAA S-157-2024) 1000
Signals, Systems, and Signal Processing 510
Discrete-Time Signals and Systems 510
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5949082
求助须知:如何正确求助?哪些是违规求助? 7120594
关于积分的说明 15914729
捐赠科研通 5082178
什么是DOI,文献DOI怎么找? 2732416
邀请新用户注册赠送积分活动 1692882
关于科研通互助平台的介绍 1615563