<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hu Y</submitter><funding>International School of Medicine</funding><funding>University of Toronto Open Fellowships</funding><funding>Canadian Institutes of Health Research</funding><funding>Zhejiang University</funding><funding>CIHR</funding><pagination>iyaf015</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11912871</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>229(3)</volume><pubmed_abstract>The Drosophila TRIM-NHL RNA-binding protein (RBP), MEI-P26, has previously been shown to suppress tumor formation in the germline. Here we show that, in the Drosophila larval central brain, cell-type-specific expression of MEI-P26 plays a vital role in regulating neural development. MEI-P26 and another TRIM-NHL RBP, Brain tumor (BRAT), have distinct expression patterns in Type I neuroblast (NB) lineages: While both proteins are expressed in NBs, BRAT is expressed in ganglion mother cells (GMCs) but not neurons, whereas MEI-P26 is expressed in neurons but not GMCs. Knockdown of MEI-P26 leads to re-expression of the stem cell marker Deadpan (DPN) and over-production of neurons. In contrast, ectopically expressed MEI-P26 reduces NB lineage size by repressing division of GMCs, resulting in red</pubmed_abstract><journal>Genetics</journal><pubmed_title>The TRIM-NHL RNA-binding protein MEI-P26 modulates the size of Drosophila Type I neuroblast lineages.</pubmed_title><pmcid>PMC11912871</pmcid><funding_grant_id>PJT-190124</funding_grant_id><funding_grant_id>Q23019</funding_grant_id><funding_grant_id>PJT-159702</funding_grant_id><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Hu Y</pubmed_authors><pubmed_authors>Lipshitz HD</pubmed_authors></additional><is_claimable>false</is_claimable><name>The TRIM-NHL RNA-binding protein MEI-P26 modulates the size of Drosophila Type I neuroblast lineages.</name><description>The Drosophila TRIM-NHL RNA-binding protein (RBP), MEI-P26, has previously been shown to suppress tumor formation in the germline. Here we show that, in the Drosophila larval central brain, cell-type-specific expression of MEI-P26 plays a vital role in regulating neural development. MEI-P26 and another TRIM-NHL RBP, Brain tumor (BRAT), have distinct expression patterns in Type I neuroblast (NB) lineages: While both proteins are expressed in NBs, BRAT is expressed in ganglion mother cells (GMCs) but not neurons, whereas MEI-P26 is expressed in neurons but not GMCs. Knockdown of MEI-P26 leads to re-expression of the stem cell marker Deadpan (DPN) and over-production of neurons. In contrast, ectopically expressed MEI-P26 reduces NB lineage size by repressing division of GMCs, resulting in red</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-07-07T03:17:25.897Z</modification><creation>2025-04-05T12:38:56.954Z</creation></dates><accession>S-EPMC11912871</accession><cross_references><pubmed>39854267</pubmed><doi>10.1093/genetics/iyaf015</doi></cross_references></HashMap>