{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,26]],"date-time":"2026-02-26T19:32:44Z","timestamp":1772134364956,"version":"3.50.1"},"reference-count":124,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2020,12,18]],"date-time":"2020-12-18T00:00:00Z","timestamp":1608249600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Neurosci."],"abstract":"<jats:p>An expanded cortex is a hallmark of human neurodevelopment and endows increased cognitive capabilities. Recent work has shown that the cell cycle-related gene <jats:italic>NDE1<\/jats:italic> is essential for proper cortical development. Patients who have mutations in <jats:italic>NDE1<\/jats:italic> exhibit congenital microcephaly as a primary phenotype. At the cellular level, <jats:italic>NDE1<\/jats:italic> is essential for interkinetic nuclear migration and mitosis of radial glial cells, which translates to an indispensable role in neurodevelopment. The nuclear migration function of <jats:italic>NDE1<\/jats:italic> is well conserved across Opisthokonta. In mammals, multiple isoforms containing alternate terminal exons, which influence the functionality of <jats:italic>NDE1<\/jats:italic>, have been reported. It has been noted that the pattern of terminal exon usage mirrors patterns of cortical complexity in mammals. To provide context to these findings, here, we provide a comprehensive review of the literature regarding <jats:italic>NDE1<\/jats:italic>, its molecular biology and physiological relevance at the cellular and organismal levels. In particular, we outline the potential roles of <jats:italic>NDE1<\/jats:italic> in progenitor cell behavior and explore the spectrum of <jats:italic>NDE1<\/jats:italic> pathogenic variants. Moreover, we assessed the evolutionary conservation of <jats:italic>NDE1<\/jats:italic> and interrogated whether the usage of alternative terminal exons is characteristic of species with gyrencephalic cortices. We found that gyrencephalic species are more likely to express transcripts that use the human-associated terminal exon, whereas lissencephalic species tend to express transcripts that use the mouse-associated terminal exon. Among gyrencephalic species, the human-associated terminal exon was preferentially expressed by those with a high order of gyrification. These findings underscore phylogenetic relationships between the preferential usage of <jats:italic>NDE1<\/jats:italic> terminal exon and high-order gyrification, which provide insight into cortical evolution underlying high-order brain functions.<\/jats:p>","DOI":"10.3389\/fnins.2020.617513","type":"journal-article","created":{"date-parts":[[2020,12,18]],"date-time":"2020-12-18T06:19:23Z","timestamp":1608272363000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":16,"title":["Role of NDE1 in the Development and Evolution of the Gyrified Cortex"],"prefix":"10.3389","volume":"14","author":[{"given":"Jaseph","family":"Soto-Perez","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marybeth","family":"Baumgartner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rahul N.","family":"Kanadia","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1965","published-online":{"date-parts":[[2020,12,18]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","first-page":"494","DOI":"10.1002\/ajmg.a.61035","article-title":"Phenotypic spectrum of NDE1-related disorders: from microlissencephaly to microhydranencephaly.","volume":"179","author":"Abdel-Hamid","year":"2019","journal-title":"Am. 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