{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"institution":[{"name":"bioRxiv"}],"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T15:57:58Z","timestamp":1785427078354,"version":"3.56.0"},"posted":{"date-parts":[[2025,7,13]]},"group-title":"Molecular Biology","reference-count":46,"publisher":"openRxiv","license":[{"start":{"date-parts":[[2025,7,13]],"date-time":"2025-07-13T00:00:00Z","timestamp":1752364800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.biorxiv.org\/about\/FAQ#license"}],"funder":[{"award":["EDUC4-12812"],"award-info":[{"award-number":["EDUC4-12812"]}],"id":[{"id":"https:\/\/ror.org\/033m8b439","id-type":"ROR","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"accepted":{"date-parts":[[2025,7,13]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                <jats:p>\n                  METTL5 is a conserved methyltransferase responsible for catalyzing N6-methyladenosine (m\n                  <jats:sup>6<\/jats:sup>\n                  A) modification on 18S ribosomal RNA. Human patients with mutations in\n                  <jats:italic>METTL5<\/jats:italic>\n                  show severe microcephaly and intellectual disability, which has not been fully recapitulated in animal models. Given its emerging role in neurodevelopment, we sought to investigate METTL5 function in a human-specific context using cortical forebrain organoids derived from human induced pluripotent stem cells. We generated\n                  <jats:italic>METTL5<\/jats:italic>\n                  knockout organoids and observed a marked delay in neural stem cell proliferation and the timing of neuronal differentiation, suggesting a critical role for METTL5 in the temporal regulation of neurogenesis. Though METTL5 methylates rRNA near the decoding center, the mechanism of this methylation remains highly contested. In our cortical organoids, broad translational changes mirror stress response rather than transcript-specific regulation of translation. Transcriptomic analysis further revealed a significant downregulation of\n                  <jats:italic>CHCHD2<\/jats:italic>\n                  , a nuclear-encoded mitochondrial gene linked to cellular energy metabolism and neurodevelopmental processes. Overexpression of CHCHD2 rescued proliferation defects of\n                  <jats:italic>METTL5<\/jats:italic>\n                  -KO neural progenitor cells, suggesting dysregulation of CHCHD2 is heavily involved in the phenotypes of\n                  <jats:italic>METTL5<\/jats:italic>\n                  mutant patient brains. These findings highlight a previously uncharacterized link between METTL5, ribosomal RNA modification, and cellular metabolism essential for proper human brain development.\n                <\/jats:p>","DOI":"10.1101\/2025.07.13.664555","type":"posted-content","created":{"date-parts":[[2025,7,14]],"date-time":"2025-07-14T04:05:12Z","timestamp":1752465912000},"source":"Crossref","is-referenced-by-count":1,"title":["Cortical organoids reveal human-specific roles of METTL5 in neurodevelopment via regulation of CHCHD2"],"prefix":"10.64898","author":[{"given":"Elena M","family":"Turkalj","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mariami","family":"Kuljanishvili","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gugene","family":"Kang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Isabelle","family":"Liu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chloe","family":"Ghent","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carlo","family":"Waltier Soriano","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Neda","family":"Keyhanvar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Daniel","family":"Brody","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael","family":"Oldham","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Caroline","family":"Vissers","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"54368","reference":[{"key":"2025071515250540000_2025.07.13.664555v1.1","doi-asserted-by":"publisher","DOI":"10.1093\/nar\/gkz619"},{"key":"2025071515250540000_2025.07.13.664555v1.2","doi-asserted-by":"publisher","DOI":"10.1038\/s12276-022-00869-y"},{"key":"2025071515250540000_2025.07.13.664555v1.3","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2019.09.007"},{"key":"2025071515250540000_2025.07.13.664555v1.4","doi-asserted-by":"crossref","first-page":"956","DOI":"10.24953\/turkjped.2020.3992","article-title":"Three Afghani siblings with a novel homozygous variant and further delineation of the clinical features of METTL5 related intellectual disability syndrome","volume":"64","year":"2022","journal-title":"Turk J Pediatr"},{"key":"2025071515250540000_2025.07.13.664555v1.5","doi-asserted-by":"crossref","unstructured":"F. 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