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dc.contributor.authorYu, Hung-Hsiang
dc.contributor.authorChen, Chun-Hong
dc.contributor.authorShi, Lei
dc.contributor.authorHuang, Yaling
dc.contributor.authorLee, Tzumin
dc.date2022-08-11T08:08:54.000
dc.date.accessioned2022-08-23T16:11:30Z
dc.date.available2022-08-23T16:11:30Z
dc.date.issued2009-07-01
dc.date.submitted2011-05-20
dc.identifier.citationNat Neurosci. 2009 Jul;12(7):947-53. Epub 2009 Jun 14. <a href="http://dx.doi.org/10.1038/nn.2345">Link to article on publisher's site</a>
dc.identifier.issn1097-6256 (Linking)
dc.identifier.doi10.1038/nn.2345
dc.identifier.pmid19525942
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33182
dc.description.abstractA comprehensive understanding of the brain requires the analysis of individual neurons. We used twin-spot mosaic analysis with repressible cell markers (twin-spot MARCM) to trace cell lineages at high resolution by independently labeling paired sister clones. We determined patterns of neurogenesis and the influences of lineage on neuron-type specification. Notably, neural progenitors were able to yield intermediate precursors that create one, two or more neurons. Furthermore, neurons acquired stereotyped projections according to their temporal position in various brain sublineages. Twin-spot MARCM also permitted birth dating of mutant clones, enabling us to detect a single temporal fate that required chinmo in a sublineage of six Drosophila central complex neurons. In sum, twin-spot MARCM can reveal the developmental origins of neurons and the mechanisms that underlie cell fate.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=19525942&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2701974/pdf/nihms-111998.pdf
dc.subjectAnimals; Animals, Genetically Modified; Brain; *Cell Lineage; Central Nervous System; Drosophila; Drosophila Proteins; Gene Knockout Techniques; Genetic Techniques; Mushroom Bodies; Nerve Tissue Proteins; *Neurogenesis; Neurons; RNA Interference; Time Factors
dc.subjectNeuroscience and Neurobiology
dc.titleTwin-spot MARCM to reveal the developmental origin and identity of neurons
dc.typeJournal Article
dc.source.journaltitleNature neuroscience
dc.source.volume12
dc.source.issue7
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1720
dc.identifier.contextkey2022731
html.description.abstract<p>A comprehensive understanding of the brain requires the analysis of individual neurons. We used twin-spot mosaic analysis with repressible cell markers (twin-spot MARCM) to trace cell lineages at high resolution by independently labeling paired sister clones. We determined patterns of neurogenesis and the influences of lineage on neuron-type specification. Notably, neural progenitors were able to yield intermediate precursors that create one, two or more neurons. Furthermore, neurons acquired stereotyped projections according to their temporal position in various brain sublineages. Twin-spot MARCM also permitted birth dating of mutant clones, enabling us to detect a single temporal fate that required chinmo in a sublineage of six Drosophila central complex neurons. In sum, twin-spot MARCM can reveal the developmental origins of neurons and the mechanisms that underlie cell fate.</p>
dc.identifier.submissionpathgsbs_sp/1720
dc.contributor.departmentMorningside Graduate School of Biomedical Sciences
dc.contributor.departmentLee Lab
dc.contributor.departmentNeurobiology
dc.source.pages947-53
dc.contributor.studentLei Shi
dc.description.thesisprogramNeuroscience


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