A single-cell transcriptome atlas of the maturing zebrafish telencephalon
Open accessAbstract
The zebrafish telencephalon is composed of highly specialized subregions that regulate complex behaviors such as learning, memory, and social interactions. The transcriptional signatures of the neuronal cell types in the telencephalon and the timeline of their emergence from larva to adult remain largely undescribed. Using an integrated analysis of single-cell transcriptomes of approximately 64,000 cells obtained from 6-day-postfertilization (dpf), 15-dpf, and adult telencephalon, we delineated nine main neuronal cell types in the pallium and eight in the subpallium and nominated novel marker genes. Comparing zebrafish and mouse neuronal cell types revealed both conserved and absent types and marker genes. Mapping of cell types onto a spatial larval reference atlas created a resource for anatomical and functional studies. Using this multiage approach, we discovered that although most neuronal subtypes are established early in the 6-dpf fish, some emerge or expand in number later in development. Analyzing the samples from each age separately revealed further complexity in the data, including several cell types that expand substantially in the adult forebrain and do not form clusters at the larval stages. Together, our work provides a comprehensive transcriptional analysis of the cell types in the zebrafish telencephalon and a resource for dissecting its development and function.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The telencephalon contains putative analogues to components of the mammalian limbic system (for example, hippocampus).
“a brain region that contains putative analogues to components of the mammalian limbic system (for example, hippocampus)2–4”
From A population code for spatial representation in the zebrafish telencephalon (2024) · cites this paper as [3]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Hafemeister, C., & Satija, R. (2019) · Genome Biology · doi:10.1186/s13059-019-1874-1 · Cited by 4,479 · cited 1× · see citing works
“UMI counts were normalized using SCTransform (Hafemeister and Satija 2019) with the percentage of mitochondrial transcripts used as a variable for regression.”
MethodMolecular Architecture of the Mouse Nervous System
Zeisel, A., Hochgerner, H., Lönnerberg, P., Johnsson, A., Memic, F., van der Zwan, J., Häring, M., Braun, E., Borm, L. E., La Manno, G., et al. (2018) · Cell · doi:10.1016/j.cell.2018.06.021 · Cited by 2,995 · see citing works
Flagged first, then by citations
Research works printed but not linked: 72
- Adolf B, Chapouton P, Lam CS, Topp S, Tannhäuser B, Strähle U, Götz M, Bally-Cuif L. 2006. Conserved and acquired features of adult neurogenesis in the zebrafish telencephalon. Dev Biol 295: 278– 293. 10.1016/j.ydbio.2006.03.023 16828638 · DOI · Paper page
- Adutwum-Ofosu KK, Magnani D, Theil T, Price DJ, Fotaki V. 2016. The molecular and cellular signatures of the mouse eminentia thalami support its role as a signalling centre in the developing forebrain. Brain Struct Funct 221: 3709– 3727. 10.1007/s00429-015-1127-3 26459142 PMC5009181 · DOI
- Aguda V, Chasiotis H, Riadi I, Thiele T. 2021. Identification of subpallial neuronal populations across zebrafish larval stages that express molecular markers for the striatum. bioRxiv 10.1101/2021.08.11.455880 · DOI
- Aoki T, Kinoshita M, Aoki R, Agetsuma M, Aizawa H, Yamazaki M, Takahoko M, Amo R, Arata A, Higashijima S, 2013. Imaging of neural ensemble for the retrieval of a learned behavioral program. Neuron 78: 881– 894. 10.1016/j.neuron.2013.04.009 23684786 · DOI
- Benjamini Y, Hochberg Y. 1995. Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc: Series B (Methodol) 57: 289– 300. 10.1111/j.2517-6161.1995.tb02031.x · DOI · Paper page
- Brüning RS, Tombor L, Schulz MH, Dimmeler S, John D. 2022. Comparative analysis of common alignment tools for single-cell RNA sequencing. GigaScience 11: giac001. 10.1093/gigascience/giac001 35084033 PMC8848315 · DOI
- Bugeon S, Duffield J, Dipoppa M, Ritoux A, Prankerd I, Nicoloutsopoulos D, Orme D, Shinn M, Peng H, Forrest H, 2022. A transcriptomic axis predicts state modulation of cortical interneurons. Nature 607: 330– 338. 10.1038/s41586-022-04915-7 35794483 PMC9279161 · DOI
- Cao J, Spielmann M, Qiu X, Huang X, Ibrahim DM, Hill AJ, Zhang F, Mundlos S, Christiansen L, Steemers FJ, 2019. The single-cell transcriptional landscape of mammalian organogenesis. Nature 566: 496– 502. 10.1038/s41586-019-0969-x 30787437 PMC6434952 · DOI · Paper page
- Carmona SJ, Teichmann SA, Ferreira L, Macaulay IC, Stubbington MJT, Cvejic A, Gfeller D. 2017. Single-cell transcriptome analysis of fish immune cells provides insight into the evolution of vertebrate immune cell types. Genome Res 27: 451– 461. 10.1101/gr.207704.116 28087841 PMC5340972 · DOI
- Castellano JM, Mosher KI, Abbey RJ, McBride AA, James ML, Berdnik D, Shen JC, Zou B, Xie XS, Tingle M, 2017. Human umbilical cord plasma proteins revitalize hippocampal function in aged mice. Nature 544: 488– 492. 10.1038/nature22067 28424512 PMC5586222 · DOI · Paper page
- Castro A, Becerra M, Manso MJ, Anadón R. 2006. Calretinin immunoreactivity in the brain of the zebrafish, Danio rerio: distribution and comparison with some neuropeptides and neurotransmitter-synthesizing enzymes. I. Olfactory organ and forebrain. J Comp Neurol 494: 435– 459. 10.1002/cne.20782 16320255 · DOI
- Cecchi C. 2002. Emx2: a gene responsible for cortical development, regionalization and area specification. Gene 291: 1– 9. 10.1016/S0378-1119(02)00623-6 12095673 · DOI
- Chen J, Poskanzer KE, Freeman MR, Monk KR. 2020. Live-imaging of astrocyte morphogenesis and function in zebrafish neural circuits. Nat Neurosci 23: 1297– 1306. 10.1038/s41593-020-0703-x 32895565 PMC7530038 · DOI
- Cheng R-K, Jesuthasan SJ, Penney TB. 2014. Zebrafish forebrain and temporal conditioning. Philos Trans R Soc Lond B Biol Sci 369: 20120462. 10.1098/rstb.2012.0462 24446496 PMC3895987 · DOI
- Conway JR, Lex A, Gehlenborg N. 2017. UpSetR: an R package for the visualization of intersecting sets and their properties. Bioinformatics 33: 2938– 2940. 10.1093/bioinformatics/btx364 28645171 PMC5870712 · DOI · Paper page
- Cuapio A, Ljunggren H-G. 2021. Activated natural killer cells hit neurogenesis in the aging brain. Neurosci Bull 37: 1072– 1074. 10.1007/s12264-021-00654-3 33779894 PMC8006623 · DOI
- Diotel N, Rodriguez Viales R, Armant O, März M, Ferg M, Rastegar S, Strähle U. 2015. Comprehensive expression map of transcription regulators in the adult zebrafish telencephalon reveals distinct neurogenic niches. J Comp Neurol 523: 1202– 1221. 10.1002/cne.23733 25556858 PMC4418305 · DOI
- Dreosti E, Lopes G, Kampff AR, Wilson SW. 2015. Development of social behavior in young zebrafish. Front Neural Circuits 9: 39. 10.3389/fncir.2015.00039 26347614 PMC4539524 · DOI
- Folgueira M, Bayley P, Navratilova P, Becker TS, Wilson SW, Clarke JDW. 2012. Morphogenesis underlying the development of the everted teleost telencephalon. Neural Dev 7: 32. 10.1186/1749-8104-7-32 22989074 PMC3520737 · DOI · Paper page
- Furlan G, Cuccioli V, Vuillemin N, Dirian L, Muntasell AJ, Coolen M, Dray N, Bedu S, Houart C, Beaurepaire E, 2017. Life-long neurogenic activity of individual neural stem cells and continuous growth establish an outside-in architecture in the teleost pallium. Curr Biol 27: 3288– 3301.e3. 10.1016/j.cub.2017.09.052 29107546 PMC5678050 · DOI
- Ganz J, Kaslin J, Freudenreich D, Machate A, Geffarth M, Brand M. 2012. Subdivisions of the adult zebrafish subpallium by molecular marker analysis. J Comp Neurol 520: 633– 655. 10.1002/cne.22757 21858823 · DOI
- Ganz J, Kroehne V, Freudenreich D, Machate A, Geffarth M, Braasch I, Kaslin J, Brand M. 2014. Subdivisions of the adult zebrafish pallium based on molecular marker analysis. F1000Res 3: 308. 10.12688/f1000research.5595.1 25713698 PMC4335597 · DOI
- Gokce O, Stanley GM, Treutlein B, Neff NF, Camp JG, Malenka RC, Rothwell PE, Fuccillo MV, Südhof TC, Quake SR. 2016. Cellular taxonomy of the mouse striatum as revealed by single-cell RNA-seq. Cell Rep 16: 1126– 1137. 10.1016/j.celrep.2016.06.059 27425622 PMC5004635 · DOI · Paper page
- Hashikawa Y, Hashikawa K, Rossi MA, Basiri ML, Liu Y, Johnston NL, Ahmad OR, Stuber GD. 2020. Transcriptional and spatial resolution of cell types in the mammalian habenula. Neuron 106: 743– 758.e5. 10.1016/j.neuron.2020.03.011 32272058 PMC7285796 · DOI · Paper page
- Inoue T, Ota M, Ogawa M, Mikoshiba K, Aruga J. 2007. Zic1 and Zic3 regulate medial forebrain development through expansion of neuronal progenitors. J Neurosci 27: 5461– 5473. 10.1523/JNEUROSCI.4046-06.2007 17507568 PMC6672357 · DOI
- Jie W, Andrade KC, Lin X, Yang X, Yue X, Chang J. 2015. Pathophysiological functions of Rnd3/RhoE. Compr Physiol 6: 169– 186. 10.1002/cphy.c150018 26756630 PMC4842315 · DOI
- Jiménez S, Moreno N. 2022. Analysis of the expression pattern of Cajal–Retzius cell markers in the Xenopus laevis forebrain. Brain Behav Evol 96: 263– 282. 10.1159/000519025 34614492 · DOI
- Jin W-N, Shi K, He W, Sun J-H, Van Kaer L, Shi F-D, Liu Q. 2021. Neuroblast senescence in the aged brain augments natural killer cell cytotoxicity leading to impaired neurogenesis and cognition. Nat Neurosci 24: 61– 73. 10.1038/s41593-020-00745-w 33257875 · DOI · Paper page
- Kaminow B, Yunusov D, Dobin A. 2021. STARsolo: accurate, fast and versatile mapping/quantification of single-cell and single-nucleus RNA-seq data. bioRxiv 10.1101/2021.05.05.442755 · DOI
- Kenney JW, Steadman PE, Young O, Shi MT, Polanco M, Dubaishi S, Covert K, Mueller T, Frankland PW. 2021. A 3D adult zebrafish brain atlas (AZBA) for the digital age. eLife 10: e69988. 10.7554/eLife.69988 34806976 PMC8639146 · DOI
- Kim K, Yang J, Kim E. 2010. Diacylglycerol kinases in the regulation of dendritic spines. J Neurochem 112: 577– 587. 10.1111/j.1471-4159.2009.06499.x 19922438 · DOI
- Kizil C, Kaslin J, Kroehne V, Brand M. 2012. Adult neurogenesis and brain regeneration in zebrafish. Dev Neurobiol 72: 429– 461. 10.1002/dneu.20918 21595047 · DOI
- Korsunsky I, Millard N, Fan J, Slowikowski K, Zhang F, Wei K, Baglaenko Y, Brenner M, Loh P-R, Raychaudhuri S. 2019. Fast, sensitive and accurate integration of single-cell data with Harmony. Nat Methods 16: 1289– 1296. 10.1038/s41592-019-0619-0 31740819 PMC6884693 · DOI · Paper page
- Kutsia M, Takeuchi Y, Ranawat N, Masai I. 2022. Single-cell transcriptome analysis reveals heterogeneity and a dynamic regenerative response of quiescent radial glia in adult zebrafish brain. bioRxiv 10.1101/2022.07.27.501663 · DOI
- Lal P, Tanabe H, Suster ML, Ailani D, Kotani Y, Muto A, Itoh M, Iwasaki M, Wada H, Yaksi E, 2018. Identification of a neuronal population in the telencephalon essential for fear conditioning in zebrafish. BMC Biol 16: 45. 10.1186/s12915-018-0502-y 29690872 PMC5978991 · DOI
- Lange C, Rost F, Machate A, Reinhardt S, Lesche M, Weber A, Kuscha V, Dahl A, Rulands S, Brand M. 2020. Single cell sequencing of radial glia progeny reveals the diversity of newborn neurons in the adult zebrafish brain. Development 147: 1855951. 10.1242/dev.185595 PMC6983714 31908317 · DOI
- Law CW, Chen Y, Shi W, Smyth GK. 2014. voom: Precision weights unlock linear model analysis tools for RNA-seq read counts. Genome Biol 15: R29. 10.1186/gb-2014-15-2-r29 24485249 PMC4053721 · DOI · Paper page
- Lawson ND, Li R, Shin M, Grosse A, Yukselen O, Stone OA, Kucukural A, Zhu L. 2020. An improved zebrafish transcriptome annotation for sensitive and comprehensive detection of cell type-specific genes. eLife 9: e55792. 10.7554/eLife.55792 32831172 PMC7486121 · DOI
- Lex A, Gehlenborg N, Strobelt H, Vuillemot R, Pfister H. 2014. UpSet: visualization of intersecting sets. IEEE Trans Vis Comput Graph 20: 1983– 1992. 10.1109/TVCG.2014.2346248 26356912 PMC4720993 · DOI
- Liu R-Z, Denovan-Wright EM, Degrave A, Thisse C, Thisse B, Wright JM. 2004. Differential expression of duplicated genes for brain-type fatty acid-binding proteins (fabp7a and fabp7b) during early development of the CNS in zebrafish (Danio rerio). Gene Expr Patterns 4: 379– 387. 10.1016/j.modgep.2004.01.010 15183304 · DOI
- Lozano D, López JM, Morona R, Jiménez S, Moreno N. 2022. Expression of Satb2 in adult brain of key non-mammalian vertebrates: insights from evolution. Research Square 10.21203/rs.3.rs-1828516/v3 · DOI
- Mueller T, Wullimann MF, Guo S. 2008. Early teleostean basal ganglia development visualized by zebrafish Dlx2a, Lhx6, Lhx7, Tbr2 (eomesa), and GAD67 gene expression. J Comp Neurol 507: 1245– 1257. 10.1002/cne.21604 18181142 · DOI
- Mueller T, Dong Z, Berberoglu MA, Guo S. 2011. The dorsal pallium in zebrafish, Danio rerio (Cyprinidae, Teleostei). Brain Res 1381: 95– 105. 10.1016/j.brainres.2010.12.089 21219890 PMC3052766 · DOI
- Ncube D, Tallafuss A, Serafin J, Bruckner J, Farnsworth DR, Miller AC, Eisen JS, Washbourne P. 2022. A conserved transcriptional fingerprint of multi-neurotransmitter neurons necessary for social behavior. BMC Genomics 23: 675. 10.1186/s12864-022-08879-w 36175871 PMC9523972 · DOI
- Otani T, Marchetto MC, Gage FH, Simons BD, Livesey FJ. 2016. 2D and 3D stem cell models of primate cortical development identify species-specific differences in progenitor behavior contributing to brain size. Cell Stem Cell 18: 467– 480. 10.1016/j.stem.2016.03.003 27049876 PMC4826446 · DOI · Paper page
- Palumbo F, Serneels B, Pelgrims R, Yaksi E. 2020. The zebrafish dorsolateral habenula is required for updating learned behaviors. Cell Rep 32: 108054. 10.1016/j.celrep.2020.108054 32846116 PMC7479510 · DOI
- Pandey S, Shekhar K, Regev A, Schier AF. 2018. Comprehensive identification and spatial mapping of habenular neuronal types using single-cell RNA-seq. Curr Biol 28: 1052– 1065.e7. 10.1016/j.cub.2018.02.040 29576475 PMC6042852 · DOI
- Pérez-Martínez L, Jaworski DM. 2005. Tissue inhibitor of metalloproteinase-2 promotes neuronal differentiation by acting as an anti-mitogenic signal. J Neurosci 25: 4917– 4929. 10.1523/JNEUROSCI.5066-04.2005 15901773 PMC1282460 · DOI
- Peris B, Gonzalez-Granero S, Ballester-Lurbe B, García-Verdugo J-M, Pérez-Roger I, Guerri C, Terrado J, Guasch RM. 2012. Neuronal polarization is impaired in mice lacking RhoE expression. J Neurochem 121: 903– 914. 10.1111/j.1471-4159.2012.07733.x 22428561 · DOI
- Porter BA, Mueller T. 2020. The zebrafish amygdaloid complex: functional ground plan, molecular delineation, and everted topology. Front Neurosci 14: 608. 10.3389/fnins.2020.00608 32765204 PMC7378821 · DOI · Paper page
- Raj B, Wagner DE, McKenna A, Pandey S, Klein AM, Shendure J, Gagnon JA, Schier AF. 2018. Simultaneous single-cell profiling of lineages and cell types in the vertebrate brain. Nat Biotechnol 36: 442– 450. 10.1038/nbt.4103 29608178 PMC5938111 · DOI
- Raj B, Farrell JA, Liu J, El Kholtei J, Carte AN, Navajas Acedo J, Du LY, McKenna A, Relić Đ, Leslie JM, 2020. Emergence of neuronal diversity during vertebrate brain development. Neuron 108: 1058– 1074.e6. 10.1016/j.neuron.2020.09.023 33068532 PMC8286448 · DOI
- Randlett O, Wee CL, Naumann EA, Nnaemeka O, Schoppik D, Fitzgerald JE, Portugues R, Lacoste AMB, Riegler C, Engert F, 2015. Whole-brain activity mapping onto a zebrafish brain atlas. Nat Methods 12: 1039– 1046. 10.1038/nmeth.3581 26778924 PMC4710481 · DOI · Paper page
- Robinson MD, McCarthy DJ, Smyth GK. 2010. edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics 26: 139– 140. 10.1093/bioinformatics/btp616 19910308 PMC2796818 · DOI · Paper page
- Rohlfing T, Maurer CR. 2003. Nonrigid image registration in shared-memory multiprocessor environments with application to brains, breasts, and bees. IEEE Trans Inf Technol Biomed 7: 16– 25. 10.1109/TITB.2003.808506 12670015 · DOI
- Ronneberger O, Liu K, Rath M, Rueβ D, Mueller T, Skibbe H, Drayer B, Schmidt T, Filippi A, Nitschke R, 2012. ViBE-Z: a framework for 3D virtual colocalization analysis in zebrafish larval brains. Nat Methods 9: 735– 742. 10.1038/nmeth.2076 22706672 · DOI
- Sandberg M, Flandin P, Silberberg S, Su-Feher L, Price JD, Hu JS, Kim C, Visel A, Nord AS, Rubenstein JLR. 2016. Transcriptional networks controlled by NKX2-1 in the development of forebrain GABAergic neurons. Neuron 91: 1260– 1275. 10.1016/j.neuron.2016.08.020 27657450 PMC5319854 · DOI · Paper page
- Satija R, Farrell JA, Gennert D, Schier AF, Regev A. 2015. Spatial reconstruction of single-cell gene expression data. Nat Biotechnol 33: 495– 502. 10.1038/nbt.3192 25867923 PMC4430369 · DOI · Paper page
- Stednitz SJ, Washbourne P. 2020. Rapid progressive social development of zebrafish. Zebrafish 17: 11– 17. 10.1089/zeb.2019.1815 31930951 PMC6987732 · DOI
- Stednitz SJ, McDermott EM, Ncube D, Tallafuss A, Eisen JS, Washbourne P. 2018. Forebrain control of behaviorally driven social orienting in zebrafish. Curr Biol 28: 2445– 2451.e3. 10.1016/j.cub.2018.06.016 30057306 PMC6082377 · DOI
- Sticco MJ, Peña Palomino PA, Lukacsovich D, Thompson BL, Földy C, Ressl S, Martinelli DC. 2021. C1QL3 promotes cell-cell adhesion by mediating complex formation between ADGRB3/BAI3 and neuronal pentraxins. FASEB J 35: e21194. 10.1096/fj.202000351RR 33337553 PMC11565477 · DOI
- Stuart T, Butler A, Hoffman P, Hafemeister C, Papalexi E, Mauck WM, Hao Y, Stoeckius M, Smibert P, Satija R. 2019. Comprehensive integration of single-cell data. Cell 177: 1888– 1902.e21. 10.1016/j.cell.2019.05.031 31178118 PMC6687398 · DOI · Paper page
- Thyme SB, Pieper LM, Li EH, Pandey S, Wang Y, Morris NS, Sha C, Choi JW, Herrera KJ, Soucy ER, 2019. Phenotypic landscape of schizophrenia-associated genes defines candidates and their shared functions. Cell 177: 478– 491.e20. 10.1016/j.cell.2019.01.048 30929901 PMC6494450 · DOI
- Trapnell C, Cacchiarelli D, Grimsby J, Pokharel P, Li S, Morse M, Lennon NJ, Livak KJ, Mikkelsen TS, Rinn JL. 2014. The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells. Nat Biotechnol 32: 381– 386. 10.1038/nbt.2859 24658644 PMC4122333 · DOI · Paper page
- Turner KJ, Hawkins TA, Yáñez J, Anadón R, Wilson SW, Folgueira M. 2016. Afferent connectivity of the zebrafish habenulae. Front Neural Circuits 10: 30. 10.3389/fncir.2016.00030 27199671 PMC4844923 · DOI
- Valente A, Huang K-H, Portugues R, Engert F. 2012. Ontogeny of classical and operant learning behaviors in zebrafish. Learn Mem 19: 170– 177. 10.1101/lm.025668.112 22434824 PMC3312620 · DOI
- Woych J, Ortega Gurrola A, Deryckere A, Jaeger ECB, Gumnit E, Merello G, Gu J, Joven Araus A, Leigh ND, Yun M, 2022. Cell-type profiling in salamanders identifies innovations in vertebrate forebrain evolution. Science 377: eabp9186. 10.1126/science.abp9186 36048957 PMC10024926 · DOI
- Wu S, Nguyen LTM, Pan H, Hassan S, Dai Y, Xu J, Wen Z. 2020. Two phenotypically and functionally distinct microglial populations in adult zebrafish. Sci Adv 6: eabd1160. 10.1126/sciadv.abd1160 33208372 PMC7673811 · DOI
- Wullimann MF, Mueller T. 2004. Identification and morphogenesis of the eminentia thalami in the zebrafish. J Comp Neurol 471: 37– 48. 10.1002/cne.20011 14983474 · DOI
- Zappia L, Oshlack A. 2018. Clustering trees: a visualization for evaluating clusterings at multiple resolutions. GigaScience 7: giy083. 10.1093/gigascience/giy083 30010766 PMC6057528 · DOI · Paper page
- Zeisel A, Muñoz-Manchado AB, Codeluppi S, Lönnerberg P, La Manno G, Juréus A, Marques S, Munguba H, He L, Betsholtz C, 2015. Brain structure: cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq. Science 347: 1138– 1142. 10.1126/science.aaa1934 25700174 · DOI · Paper page
- Zhao Y, Marín O, Hermesz E, Powell A, Flames N, Palkovits M, Rubenstein JLR, Westphal H. 2003. The LIM-homeobox gene Lhx8 is required for the development of many cholinergic neurons in the mouse forebrain. Proc Natl Acad Sci 100: 9005– 9010. 10.1073/pnas.1537759100 12855770 PMC166428 · DOI · Paper page
Cited by
Sorted by citations
A population code for spatial representation in the zebrafish telencephalon
Yang, C., Mammen, L., Kim, B., Li, M., Robson, D. N., & Li, J. M. (2024) · Nature · doi:10.1038/s41586-024-07867-2 · Cited by 38 · see citing works
“%) of cells in the telencephalon, a region hypothesized to contain the functional analogue of the mammalian hippocampus 1–3 , 19 .”
- Authors
- Pandey, S., Moyer, A. J., & Thyme, S. B.
- Affiliations
- Harvard University (US)
- University of Alabama at Birmingham (US)
- Corresponding author
- Pandey, Shristi
- Thyme, Summer B.
- Venue
- Genome Research
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2023-04
- Volume
- 33
- Issue
- 4
- Pages
- 658-671
- ISSN
- 1088-9051 (ISSN-L)
- 1549-5469
- PMC
- PMC10234298
- OpenAlex
- W4366249037
- Cited by
- 44
- References
- 2
- Citations by year
- 2026: 19 · 2025: 11 · 2024: 8 · 2023: 6
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genome Research (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (DP1HD094764, R00MH110603)
- Allen Discovery Center
- McKnight Foundation
- Klingenstein-Simons (T32HG008961)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Zebrafish Biomedical Research Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- forebrain development, neuronal cell types, pallium, subpallium, cell type markers, larval to adult transition, single-cell transcriptomics
- MeSH terms
- Animals, Neurons, Telencephalon, Zebrafish, Zebrafish Proteins, Mice, Transcriptome
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review