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dc.contributor.authorRunko, Alexander Peter
dc.contributor.authorSagerstrom, Charles G.
dc.date2022-08-11T08:08:47.000
dc.date.accessioned2022-08-23T16:08:35Z
dc.date.available2022-08-23T16:08:35Z
dc.date.issued2003-10-11
dc.date.submitted2008-12-09
dc.identifier.citation<p>Dev Biol. 2003 Oct 15;262(2):254-67.</p>
dc.identifier.issn0012-1606 (Print)
dc.identifier.doi10.1016/S0012-1606(03)00388-9
dc.identifier.pmid14550789
dc.identifier.urihttp://hdl.handle.net/20.500.14038/32485
dc.description.abstractThe zebrafish nlz gene has a rostral expression limit at the presumptive rhombomere (r) 3/r4 boundary during gastrula stages, and its expression progressively expands rostrally to encompass both r3 and r2 by segmentation stages, suggesting a role for nlz in hindbrain development. We find that Nlz is a nuclear protein that associates with the corepressor Groucho, suggesting that Nlz acts to repress transcription. Consistent with a role as a repressor, misexpression of nlz causes a loss of gene expression in the rostral hindbrain, likely due to ectopic nlz acting prematurely in this domain, and this repression is accompanied by a partial expansion in the expression domains of r4-specific genes. To interfere with endogenous nlz function, we generated a form of nlz that lacks the Groucho binding site and demonstrate that this construct has a dominant negative effect. We find that interfering with endogenous Nlz function promotes the expansion of r5 and, to a lesser extent, r3 gene expression into r4, leading to a reduction in the size of r4. We conclude that Nlz is a transcriptional repressor that controls segmental gene expression in the hindbrain. Lastly, we identify additional nlz-related genes, suggesting that Nlz belongs to a family of zinc-finger proteins.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=14550789&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1016/S0012-1606(03)00388-9
dc.subjectAnimals; Basic Helix-Loop-Helix Transcription Factors; Binding Sites; DNA-Binding Proteins; Gene Expression Regulation, Developmental; Humans; Mice; Phylogeny; Recombinant Fusion Proteins; Repressor Proteins; Rhombencephalon; Zebrafish; Zinc Fingers
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleNlz belongs to a family of zinc-finger-containing repressors and controls segmental gene expression in the zebrafish hindbrain
dc.typeJournal Article
dc.source.journaltitleDevelopmental biology
dc.source.volume262
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1054
dc.identifier.contextkey678819
html.description.abstract<p>The zebrafish nlz gene has a rostral expression limit at the presumptive rhombomere (r) 3/r4 boundary during gastrula stages, and its expression progressively expands rostrally to encompass both r3 and r2 by segmentation stages, suggesting a role for nlz in hindbrain development. We find that Nlz is a nuclear protein that associates with the corepressor Groucho, suggesting that Nlz acts to repress transcription. Consistent with a role as a repressor, misexpression of nlz causes a loss of gene expression in the rostral hindbrain, likely due to ectopic nlz acting prematurely in this domain, and this repression is accompanied by a partial expansion in the expression domains of r4-specific genes. To interfere with endogenous nlz function, we generated a form of nlz that lacks the Groucho binding site and demonstrate that this construct has a dominant negative effect. We find that interfering with endogenous Nlz function promotes the expansion of r5 and, to a lesser extent, r3 gene expression into r4, leading to a reduction in the size of r4. We conclude that Nlz is a transcriptional repressor that controls segmental gene expression in the hindbrain. Lastly, we identify additional nlz-related genes, suggesting that Nlz belongs to a family of zinc-finger proteins.</p>
dc.identifier.submissionpathgsbs_sp/1054
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages254-67


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