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An evolutionarily acquired microRNA shapes development of mammalian cortical projections. | LitMetric

AI Article Synopsis

  • The corticospinal tract and corpus callosum are specialized structures in mammals that contribute to advanced motor and cognitive abilities.
  • Researchers have identified 17 specific microRNAs (miRNAs) that are enriched in corticospinal motor neurons, 15 of which originate from a unique genomic cluster found only in placental mammals.
  • One particular miRNA, miR-409-3p, plays a crucial role in determining the identity of corticospinal motor neurons by inhibiting a gene involved in developing another type of neuron, showcasing how evolution has influenced neuronal diversity in mammals.

Article Abstract

The corticospinal tract is unique to mammals and the corpus callosum is unique to placental mammals (eutherians). The emergence of these structures is thought to underpin the evolutionary acquisition of complex motor and cognitive skills. Corticospinal motor neurons (CSMN) and callosal projection neurons (CPN) are the archetypal projection neurons of the corticospinal tract and corpus callosum, respectively. Although a number of conserved transcriptional regulators of CSMN and CPN development have been identified in vertebrates, none are unique to mammals and most are coexpressed across multiple projection neuron subtypes. Here, we discover 17 CSMN-enriched microRNAs (miRNAs), 15 of which map to a single genomic cluster that is exclusive to eutherians. One of these, miR-409-3p, promotes CSMN subtype identity in part via repression of LMO4, a key transcriptional regulator of CPN development. In vivo, miR-409-3p is sufficient to convert deep-layer CPN into CSMN. This is a demonstration of an evolutionarily acquired miRNA in eutherians that refines cortical projection neuron subtype development. Our findings implicate miRNAs in the eutherians' increase in neuronal subtype and projection diversity, the anatomic underpinnings of their complex behavior.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682328PMC
http://dx.doi.org/10.1073/pnas.2006700117DOI Listing

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