Anirudhan Jithu, Shen Xueyi, Szemes Tünde, Dieu Marc, Azouz Abdulkader, Conrard Louise, Passon Nicolas, Doumont Gilles, Sitte Maren, Achouri Younes, Kricha Sadia, Salinas Gabriela, Goriely Stanislas, Renard Patricia, Bellefroid Eric J
Laboratory of Developmental Genetics, ULB Neuroscience Institute, Université libre de Bruxelles (ULB), Gosselies B-6041, Belgium.
Mass Spectrometry Facility (MaSUN), University of Namur (UNamur), Namur B-5000, Belgium.
J Neurosci. 2025 Jul 2;45(27):e1789242025. doi: 10.1523/JNEUROSCI.1789-24.2025.
Early dorsal telencephalon development is coordinated by an interplay of transcription factors that exhibit a graded expression pattern in neural progenitors. How they function together to orchestrate cortical development remains largely unknown. The and genes encode transcription factors that are expressed in a similar caudomedial/rostrolateral gradient in the ventricular zone of the developing dorsal telencephalon with, in the medial pallium, but not expressed in the developing choroid plexus (ChP). Their constitutive loss has been shown to impart similar cortical abnormalities, and their combined deletion exacerbates the phenotypes, suggesting possible cooperation during cortex development. In this study, using embryos of both sexes, we utilized molecular and genetic approaches to dissect how Emx2 functions with Dmrta2 during mouse cortical development. Our results show that while they regulate a similar set of genes, their common direct targets are limited but include key regulators of cortical development. The identification of the interaction partners of Emx2 suggests that it coordinates with the LIM domain-binding protein Ldb1 to execute the activation and repression of some of its downstream targets. Finally, while is known to suppress ChP development, we also provide evidence that is, in contrast, required for ChP since in its absence in medial telencephalic progenitors, mice develop hydrocephalus postnatally, a phenotype that appears to be due to a compromised cytoarchitecture. Together, these data indicate that Emx2 and Dmrta2 have similar but also distinct functions in telencephalon development and provide the first insights into Emx2 mechanism of action.
早期背侧端脑发育由转录因子之间的相互作用协调,这些转录因子在神经祖细胞中呈现出梯度表达模式。它们如何共同发挥作用以协调皮质发育在很大程度上仍然未知。Emx2和Dmrta2基因编码的转录因子在发育中的背侧端脑脑室区以类似的尾内侧/嘴外侧梯度表达,在内侧皮质中,Emx2表达而Dmrta2在发育中的脉络丛(ChP)中不表达。它们的组成性缺失已被证明会导致类似的皮质异常,并且它们的联合缺失会加剧表型,这表明在皮质发育过程中可能存在合作。在这项研究中,我们使用两性胚胎,利用分子和遗传方法来剖析Emx2在小鼠皮质发育过程中如何与Dmrta2协同作用。我们的结果表明,虽然它们调节一组相似的基因,但它们的共同直接靶点有限,但包括皮质发育的关键调节因子。Emx2相互作用伙伴的鉴定表明,它与LIM结构域结合蛋白Ldb1协同作用以执行其一些下游靶点的激活和抑制。最后,虽然已知Dmrta2抑制脉络丛发育,但我们也提供证据表明,相反,Emx2是脉络丛发育所必需的,因为在中脑祖细胞中缺乏Emx2时,小鼠出生后会出现脑积水,这种表型似乎是由于细胞结构受损所致。总之,这些数据表明Emx2和Dmrta2在端脑发育中具有相似但也不同的功能,并首次深入了解了Emx2的作用机制。