4.7 Article

Mllt11 Regulates Migration and Neurite Outgrowth of Cortical Projection Neurons during Development

期刊

JOURNAL OF NEUROSCIENCE
卷 42, 期 19, 页码 3931-3948

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0124-22.2022

关键词

axonogenesis; callosal projection neurons; microtubules; Mllt11; Af1q; neuritogenesis; neurodevelopmental disorders

资金

  1. Canadian Institutes of Health Research (CIHR) [PJT-388914]
  2. CIHR [PJT-159738]

向作者/读者索取更多资源

The role of Mllt11 in the migration and neurite outgrowth of callosal projection neurons during mouse brain formation is highlighted in this study. Mllt11 is expressed exclusively in developing neurons, particularly in the formation of the superficial cortical layers. Mllt11 is crucial for the morphogenesis and connectivity of upper layer projection neurons.
The formation of connections within the mammalian neocortex is highly regulated by both extracellular guidance mechanisms and intrinsic gene expression programs. There are two types of cortical projection neurons (CPNs): those that project locally and interhemispherically and those that project to subcerebral structures such as the thalamus, hindbrain, and spinal cord. The regulation of cortical projection morphologies is not yet fully understood at the molecular level. Here, we report a role for Mllt11 (Myeloid/lymphoid or mixed-lineage leukemia; translocated to chromosome 11/All1 Fused Gene From Chromosome 1q) in the migration and neurite outgrowth of callosal projection neurons during mouse brain formation. We show that Mllt11 expression is exclusive to developing neurons and is enriched in the developing cortical plate (CP) during the formation of the superficial cortical layers. In cultured primary cortical neurons, Mllt11 is detected in varicosities and growth cones as well as the soma. Using conditional loss-of-function and gainof-function analysis we show that Mllt11 is required for neuritogenesis and proper migration of upper layer CPNs. Loss of Mllt11 in the superficial cortex of male and female neonates leads to a severe reduction in fibers crossing the corpus callosum (CC), a progressive loss in the maintenance of upper layer projection neuron gene expression, and reduced complexity of dendritic arborization. Proteomic analysis revealed that Mllt11 associates with stabilized microtubules, and Mllt11 loss affected microtubule staining in callosal axons. Taken together, our findings support a role for Mllt11 in promoting the formation of mature upper-layer neuron morphologies and connectivity in the cerebral cortex.

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