XB-ART-59235
Front Neuroanat
2022 Jan 01;16:914281. doi: 10.3389/fnana.2022.914281.
Show Gene links
Show Anatomy links
Patterns of tubb2b Promoter-Driven Fluorescence in the Forebrain of Larval Xenopus laevis.
Daume D
,
Offner T
,
Hassenklöver T
,
Manzini I
.
???displayArticle.abstract???
Microtubules are essential components of the cytoskeleton of all eukaryotic cells and consist of α- and β-tubulin heterodimers. Several tissue-specific isotypes of α- and β-tubulins, encoded by distinct genes, have been described in vertebrates. In the African clawed frog (Xenopus laevis), class II β-tubulin (tubb2b) is expressed exclusively in neurons, and its promoter is used to establish different transgenic frog lines. However, a thorough investigation of the expression pattern of tubb2b has not been carried out yet. In this study, we describe the expression of tubb2b-dependent Katushka fluorescence in the forebrain of premetamorphic Xenopus laevis at cellular resolution. To determine the exact location of Katushka-positive neurons in the forebrain nuclei and to verify the extent of neuronal Katushka expression, we used a transgenic frog line and performed several additional antibody stainings. We found tubb2b-dependent fluorescence throughout the Xenopus forebrain, but not in all neurons. In the olfactory bulb, tubb2b-dependent fluorescence is present in axonal projections from the olfactory epithelium, cells in the mitral cell layer, and fibers of the extrabulbar system, but not in interneurons. We also detected tubb2b-dependent fluorescence in parts of the basal ganglia, the amygdaloid complex, the pallium, the optic nerve, the preoptic area, and the hypothalamus. In the diencephalon, tubb2b-dependent fluorescence occurred mainly in the prethalamus and thalamus. As in the olfactory system, not all neurons of these forebrain regions exhibited tubb2b-dependent fluorescence. Together, our results present a detailed overview of the distribution of tubb2b-dependent fluorescence in neurons of the forebrain of larval Xenopus laevis and clearly show that tubb2b-dependent fluorescence cannot be used as a pan-neuronal marker.
???displayArticle.pubmedLink??? 35873659
???displayArticle.link??? Front Neuroanat
Species referenced: Xenopus laevis
Genes referenced: calb2 crygdl.43 fh pax6 pax7 tubb2b
GO keywords: forebrain neuron differentiation [+]
???displayArticle.antibodies??? Calb2 Ab6 GFP Ab25 Pax7 Ab1 RFP Ab2 Th Ab1
???attribute.lit??? ???displayArticles.show???
![]() |
FIGURE 1. tubb2b-dependent fluorescence within the MOE and OB of larval Xenopus laevis. (A) Dorsal view of a single focal plane of the left main olfactory epithelium (MOE). tubb2b-dependent fluorescence (magenta) is present in olfactory receptor neurons. (B) Close-up of tubb2b-positive olfactory receptor neurons of the MOE. (C) Schematic overview of the olfactory organs (magenta). Close-up of the left MOE. (D) Coronal slice of the OB (left and right) of a transgenic NBT-Katushka γ-cry-Venus tadpole. tubb2b-dependent fluorescence (magenta) is present in axons of ORNs terminating in all known axonal projection fields of the OB (projection fields 1â9 and projection fields α, β, γ, and δ; see Gaudin and Gascuel, 2005). (E) Coronal slice of the OB (one side only) of transgenic NBT-Katushka γ-cry-Venus tadpoles and tubb2b-dependent fluorescence in cells of the mitral cell layer of the main and accessory (projection field 8) olfactory bulb. (FâH) Coronal slices of the OB (one side only) of transgenic NBT-Katushka pax6-GFP tadpoles. (F) tubb2b- (magenta) and pax6-dependent fluorescence (green) in cells in the mitral cell layer. (G,H) Close-ups of the mitral cell layer of the main and accessory OB showing tubb2b-dependent fluorescence and pax6-dependent fluorescence. Examples of cells featuring tubb2b-dependent fluorescence only and pax6-dependent fluorescence only, and double-fluorescent cells (*) are encircled. (IâK) Maximum projection of the whole ventral OB of one brain hemisphere. (I) tubb2b-dependent fluorescence has not been detected in calretinin (CR; green)-positive cells. tubb2b-positive fibers that bypass the OB were found in the intermediate OB (white arrow). (J) tubb2b-dependent fluorescence has not been detected in tyrosine hydroxylase (TH; green)-positive cells. (K) tubb2b-dependent fluorescence and pax6-dependent fluorescence have been detected in cells of the mitral cell layer. tubb2b-dependent fluorescence was also found in the nucleus accumbens (Acc) and pax6-dependent fluorescence in the anterior part of the striatum (Str). (L) Scheme of the larval brain showing the approximate positions (lines) of the sections shown in (AâL). POA, preoptic area; Hyp, hypothalamus; NC, nasal cavity; ON, olfactory nerve; mcl, mitral cell layer; gcl, granule cell layer; V, ventricle; d, dorsal; v, ventral; a, anterior; p, posterior; m, medial; l, lateral. |
![]() |
FIGURE 2. Schematic overview of regions featuring tubb2b-dependent fluorescence in the forebrain of premetamorphic Xenopus laevis. Ventral view of the larval forebrain and transverse sections of the olfactory bulb (OB; AâC), telencephalon (Tel; AâF), diencephalon (Di), and hypothalamus (G). The position and density of the cells shown for each region are presented based on observation and not via quantitative analysis. (A,B) tubb2b-dependent fluorescence is present in projection fields of axons arriving from the olfactory epithelium (1â9 + α, β, γ, δ; Gaudin and Gascuel, 2005). (C,D) tubb2b-dependent fluorescence in cells of the mitral cell layer of the main and accessory olfactory bulbs, the nucleus accumbens (Acc), and pallium. (E) tubb2b-dependent fluorescence in the medial pallium (Mp), lateral pallium (Lp), dorsal pallium (Dp), ventral pallium (Vp), striatum (Str), and septum (S). (F) tubb2b-dependent fluorescence in the anterior commissure (ac), medial amygdala (MeA), optic nerve (OpN), dorsal pallidum (DP), and preoptic area (POA). (G) tubb2b-dependent fluorescence in prosomeres 1â3 (p1â3). Hyp, Hypothalamus; lfb, lateral forebrain bundle; V, ventricle; MOE, main olfactory epithelium; ON, olfactory nerve; a, anterior; p, posterior; d, dorsal; v, ventral; l, lateral; m, medial. |
![]() |
FIGURE 3. Cell density of tubb2b-positive neurons in the OB of premetamorphic Xenopus larvae. (AâC) Ventral view of a single focal plane of the OB of one brain hemisphere. (A) HuC/D-positive cells (green) are present throughout the whole OB. Few HuC/D-positive cells are also tubb2b-positive (magenta). (B) Pattern of HuC/D-positive cells within the OB. (C) tubb2b-positive cells are located in the mitral cell layer (mcl) of the OB. (D) Number of tubb2b-positive cells in comparison to HuC/D-positive cells of the whole OB. Average number of tubb2b-positive cells: 1,588 ± 191 (n = 10). Average number of HuC/D-positive cells: 6,517 ± 210 (n = 3). Cell density of tubb2b-positive cells compared to HuC/D-positive cells: 24,4%. (E) Scheme of the ventral OB showing the position of the images (AâC). ON, olfactory nerve; a, anterior; p, posterior; m, medial; l, lateral. |
![]() |
FIGURE 4. tubb2b-dependent fluorescence in the telencephalon of larval Xenopus laevis. Coronal sections through the telencephalon of NBT-Katushka γ-cry-Venus (A,E,F) and NBT-Katushka pax6-GFP (BâD,G,H) transgenic tadpoles. (A) tubb2b-dependent fluorescence (magenta) in the anterior telencephalon. Stained cells could be detected in the nucleus accumbens (Acc), striatum (Str), accessory OB (projection field 8), and pallium. (BâD) Close-ups of various zones of the anterior telencephalon showing tubb2b-dependent fluorescence in cells of the dorsal pallium (Dp), ventral pallium (Vp), medial pallium (Mp), lateral pallium (Lp), septum (S), and medial amygdala (MeA). (E) Sections through the posterior telencephalon showing tubb2b-dependent fluorescence in cells of the Mp, Lp, Vp, MeA, dorsal pallidum (DP), preoptic area (POA), and optic nerve (OpN). (FâH) Close-ups of various zones of the ventral posterior telencephalon. (F) tubb2b-dependent fluorescence in cells of the POA. (G,H) No overlap was detected between tubb2b- and pax6-dependent fluorescence (green) in the POA, ac, and central amygdala (CeA). (I) Scheme of the larval brain showing the approximate positions (dashed rectangles) of the sections shown in (AâH). Hyp, hypothalamus; OB, olfactory bulb; BST, bed nucleus of the stria terminalis; V, ventricle; d, dorsal; v, ventral; a, anterior; p, posterior; m, medial; l, lateral. |
![]() |
FIGURE 5. Location of tubb2b-dependent fluorescence in the diencephalon of larval Xenopus laevis. Coronal sections through the diencephalon of NBT-Katushka γ-cry-Venus transgenic tadpoles. (A) tubb2b-dependent fluorescence (magenta) in cells of prosomeres 1â3 (p1â3). (B) No tubb2b-dependent fluorescence could be detected in calretinin-positive cell bodies and fibers (CR; green) of the thalamus (Th). (C) tubb2b-dependent fluorescence-positive cell bodies in the area of the Th. CR-positive cells and fibers were not tubb2b-positive. (D) Cells in prosomere 3 (p3) did not show tubb2b-dependent fluorescence but could be stained with an antibody against Pax7 (green). (E) Approximate positions of the sliced regions are shown in a schematic image of the larval brain (lines). OB, olfactory bulb; Hyp, hypothalamus; POA, preoptic area; V, ventricle; d, dorsal; v, ventral; a, anterior; p, posterior; m, medial; l, lateral. |
References [+] :
Agetsuma,
The habenula is crucial for experience-dependent modification of fear responses in zebrafish.
2010, Pubmed
Agetsuma, The habenula is crucial for experience-dependent modification of fear responses in zebrafish. 2010, Pubmed
Bandín, Prepatterning and patterning of the thalamus along embryonic development of Xenopus laevis. 2015, Pubmed , Xenbase
Bandín, Immunohistochemical analysis of Pax6 and Pax7 expression in the CNS of adult Xenopus laevis. 2014, Pubmed , Xenbase
Bandín, Regional expression of Pax7 in the brain of Xenopus laevis during embryonic and larval development. 2013, Pubmed , Xenbase
Bieker, The multiple beta-tubulin genes of Xenopus: isolation and developmental expression of a germ-cell isotype beta-tubulin gene. 1992, Pubmed , Xenbase
Bisbee, Albumin phylogeny for clawed frogs (Xenopus). 1977, Pubmed , Xenbase
Boyd, Tyrosine hydroxylase-immunoreactive interneurons in the olfactory bulb of the frogs Rana pipiens and Xenopus laevis. 2002, Pubmed , Xenbase
Brann, A lifetime of neurogenesis in the olfactory system. 2014, Pubmed
Burd, Development of the olfactory nerve in the African clawed frog, Xenopus laevis: I. Normal development. 1991, Pubmed , Xenbase
Byrd, Development of the olfactory bulb in the clawed frog, Xenopus laevis: a morphological and quantitative analysis. 1991, Pubmed , Xenbase
Calvo-Ochoa, Diving into the streams and waves of constitutive and regenerative olfactory neurogenesis: insights from zebrafish. 2021, Pubmed
Castro, Distribution of calretinin during development of the olfactory system in the brown trout, Salmo trutta fario: Comparison with other immunohistochemical markers. 2008, Pubmed
Cima, Development of the optic nerve in Xenopus laevis. I. Early development and organization. 1982, Pubmed , Xenbase
D'Amico, Proliferation, migration and differentiation in juvenile and adult Xenopus laevis brains. 2011, Pubmed , Xenbase
Demski, The terminal nerve: a new chemosensory system in vertebrates? 1983, Pubmed
Domínguez, Characterization of the hypothalamus of Xenopus laevis during development. II. The basal regions. 2014, Pubmed , Xenbase
Domínguez, Characterization of the hypothalamus of Xenopus laevis during development. I. The alar regions. 2013, Pubmed , Xenbase
Dworkin-Rastl, Localization of specific mRNA sequences in Xenopus laevis embryos by in situ hybridization. 1986, Pubmed , Xenbase
Eddé, One beta-tubulin subunit accumulates during neurite outgrowth in mouse neuroblastoma cells. 1981, Pubmed
Evans, A mitochondrial DNA phylogeny of African clawed frogs: phylogeography and implications for polyploid evolution. 2004, Pubmed , Xenbase
Gaudin, 3D atlas describing the ontogenic evolution of the primary olfactory projections in the olfactory bulb of Xenopus laevis. 2005, Pubmed , Xenbase
González, Ontogeny of catecholamine systems in the central nervous system of anuran amphibians: an immunohistochemical study with antibodies against tyrosine hydroxylase and dopamine. 1994, Pubmed , Xenbase
Graziadei, Neuronal regeneration in frog olfactory system. 1973, Pubmed
Graziadei, Regeneration in the olfactory system of vertebrates. 1983, Pubmed
Guo, The distribution of β-tubulin isotypes in cultured neurons from embryonic, newborn, and adult mouse brains. 2011, Pubmed
Hartley, Transgenic Xenopus embryos reveal that anterior neural development requires continued suppression of BMP signaling after gastrulation. 2001, Pubmed , Xenbase
Hawkins, Functional Reintegration of Sensory Neurons and Transitional Dendritic Reduction of Mitral/Tufted Cells during Injury-Induced Recovery of the Larval Xenopus Olfactory Circuit. 2017, Pubmed , Xenbase
Higgs, Neuronal turnover in the Xenopus laevis olfactory epithelium during metamorphosis. 2001, Pubmed , Xenbase
HOFFMAN, The olfactory bulb, accessory olfactory bulb, and hemisphere of some anurans. 1963, Pubmed
Hofmann, Central projections of the nervus terminalis in four species of amphibians. 1989, Pubmed , Xenbase
Hoke, Functional coupling between substantia nigra and basal ganglia homologues in amphibians. 2007, Pubmed , Xenbase
Horb, Xenopus Resources: Transgenic, Inbred and Mutant Animals, Training Opportunities, and Web-Based Support. 2019, Pubmed , Xenbase
Jolkkonen, Intrinsic connections of the rat amygdaloid complex: projections originating in the central nucleus. 1998, Pubmed
Joshi, Differential utilization of beta-tubulin isotypes in differentiating neurites. 1989, Pubmed
Kapitein, Building the Neuronal Microtubule Cytoskeleton. 2015, Pubmed
Katsetos, Differential localization of class III, beta-tubulin isotype and calbindin-D28k defines distinct neuronal types in the developing human cerebellar cortex. 1993, Pubmed
Katsetos, Class III beta-tubulin in human development and cancer. 2003, Pubmed
Kludt, Integrating temperature with odor processing in the olfactory bulb. 2015, Pubmed , Xenbase
Knossow, The Mechanism of Tubulin Assembly into Microtubules: Insights from Structural Studies. 2020, Pubmed
Kosaka, Neuronal organization of the main olfactory bulb revisited. 2016, Pubmed
Lasser, The Role of the Microtubule Cytoskeleton in Neurodevelopmental Disorders. 2018, Pubmed
Latremoliere, Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon Regeneration. 2018, Pubmed
Lee, The habenula prevents helpless behavior in larval zebrafish. 2010, Pubmed
Lee, Posttranslational modification of class III beta-tubulin. 1990, Pubmed
Lee, The expression and posttranslational modification of a neuron-specific beta-tubulin isotype during chick embryogenesis. 1990, Pubmed
Lewis, Free intermingling of mammalian beta-tubulin isotypes among functionally distinct microtubules. 1987, Pubmed
Love, pTransgenesis: a cross-species, modular transgenesis resource. 2011, Pubmed , Xenbase
Ludueńa, Structure of the tubulin dimer. 1977, Pubmed
Ludueña, Multiple forms of tubulin: different gene products and covalent modifications. 1998, Pubmed
Manzini, Principles of odor coding in vertebrates and artificial chemosensory systems. 2022, Pubmed
Marín, Basal ganglia organization in amphibians: catecholaminergic innervation of the striatum and the nucleus accumbens. 1997, Pubmed , Xenbase
Marín, Basal ganglia organization in amphibians: afferent connections to the striatum and the nucleus accumbens. 1997, Pubmed , Xenbase
Menini, Olfactory Coding in Larvae of the African Clawed Frog Xenopus laevis 2010, Pubmed
Miyasaka, Olfactory projectome in the zebrafish forebrain revealed by genetic single-neuron labelling. 2014, Pubmed
Moody, Developmental expression of a neuron-specific beta-tubulin in frog (Xenopus laevis): a marker for growing axons during the embryonic period. 1996, Pubmed , Xenbase
Moody, Quantitative lineage analysis of the origin of frog primary motor and sensory neurons from cleavage stage blastomeres. 1989, Pubmed , Xenbase
Moreno, Localization and connectivity of the lateral amygdala in anuran amphibians. 2004, Pubmed , Xenbase
Moreno, Hodological characterization of the medial amygdala in anuran amphibians. 2003, Pubmed , Xenbase
Moreno, Central amygdala in anuran amphibians: neurochemical organization and connectivity. 2005, Pubmed , Xenbase
Moreno, Characterization of the bed nucleus of the stria terminalis in the forebrain of anuran amphibians. 2012, Pubmed , Xenbase
Moreno, Lateral and medial amygdala of anuran amphibians and their relation to olfactory and vomeronasal information. 2005, Pubmed , Xenbase
Moreno, Spatio-temporal expression of Pax6 in Xenopus forebrain. 2008, Pubmed , Xenbase
Morona, Pattern of calbindin-D28k and calretinin immunoreactivity in the brain of Xenopus laevis during embryonic and larval development. 2013, Pubmed , Xenbase
Moura Neto, Microheterogeneity of tubulin proteins in neuronal and glial cells from the mouse brain in culture. 1983, Pubmed
Muroyama, Microtubule organization, dynamics and functions in differentiated cells. 2017, Pubmed
Nagayama, Neuronal organization of olfactory bulb circuits. 2014, Pubmed
Nezlin, Structure of the olfactory bulb in tadpoles of Xenopus laevis. 2000, Pubmed , Xenbase
Nogales, Structural insights into microtubule function. 2000, Pubmed
Oehlmann, Zebrafish beta tubulin 1 expression is limited to the nervous system throughout development, and in the adult brain is restricted to a subset of proliferative regions. 2004, Pubmed
Offner, Erratum: Whole-Brain Calcium Imaging in Larval Xenopus. 2020, Pubmed , Xenbase
Oschwald, Localization of a nervous system-specific class II beta-tubulin gene in Xenopus laevis embryos by whole-mount in situ hybridization. 1991, Pubmed , Xenbase
Pinelli, Extrabulbar olfactory system and nervus terminalis FMRFamide immunoreactive components in Xenopus laevis ontogenesis. 2004, Pubmed , Xenbase
Porteros, Calretinin immunoreactivity in the developing olfactory system of the rainbow trout. 1997, Pubmed
Preibisch, Globally optimal stitching of tiled 3D microscopic image acquisitions. 2009, Pubmed
Puelles, Pallial and subpallial derivatives in the embryonic chick and mouse telencephalon, traced by the expression of the genes Dlx-2, Emx-1, Nkx-2.1, Pax-6, and Tbr-1. 2000, Pubmed
Richter, Gene expression in the embryonic nervous system of Xenopus laevis. 1988, Pubmed , Xenbase
Scalia, A note on the organization of the amphibian olfactory bulb. 1991, Pubmed
Schindelin, Fiji: an open-source platform for biological-image analysis. 2012, Pubmed
Schwob, Neural regeneration and the peripheral olfactory system. 2002, Pubmed
Session, Genome evolution in the allotetraploid frog Xenopus laevis. 2016, Pubmed , Xenbase
Steuer, Using the olfactory system as an in vivo model to study traumatic brain injury and repair. 2014, Pubmed
Stoykova, Roles of Pax-genes in developing and adult brain as suggested by expression patterns. 1994, Pubmed
Sullivan, Structure and utilization of tubulin isotypes. 1988, Pubmed
Sullivan, Identification of conserved isotype-defining variable region sequences for four vertebrate beta tubulin polypeptide classes. 1986, Pubmed
Swanson, What is the amygdala? 1998, Pubmed
von Bartheld, Central projections of the nervus terminalis in lampreys, lungfishes, and bichirs. 1988, Pubmed
Wade, On and around microtubules: an overview. 2009, Pubmed
Weiss, Conservation of Glomerular Organization in the Main Olfactory Bulb of Anuran Larvae. 2020, Pubmed , Xenbase
Weiss, Olfaction across the water-air interface in anuran amphibians. 2021, Pubmed
Wullimann, Teleostean and mammalian forebrains contrasted: Evidence from genes to behavior. 2004, Pubmed
Yu, Regeneration and rewiring of rodent olfactory sensory neurons. 2017, Pubmed