2023
DOI: 10.1101/2023.03.15.531610
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Differentiation trajectories of theHydranervous system reveal transcriptional regulators of neuronal fate

Abstract: The small freshwater cnidarian polyp Hydra vulgaris uses adult stem cells (interstitial stem cells) to continually replace neurons throughout its life. This feature, combined with the ability to image the entire nervous system (Badhiwala et al., 2021; Dupre & Yuste, 2017) and availability of gene knockdown techniques (Juliano, Reich, et al., 2014; Lohmann et al., 1999; Vogg et al., 2022), makes Hydra a tractable model for studying nervous system development and regeneration at the whole-organism level. In … Show more

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Cited by 14 publications
(10 citation statements)
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“…Generation of Tg(hym176c:tdTomato,tba1c:GCAMP7s) cj1-in transgenic strain Hydra transgenic line Tg(hym176c:tdTomato,tba1c:GCAMP7s) cj1-in was created by microinjecting a single plasmid containing two promoters and two transgenes. Nuclear tdTomato was driven by a 2022 bp section of the hym176c regulatory region, which should be specifically expressed in ec5 neurons found in the peduncle (Fig 1H,26), and GCaMP7s was driven by a 1901 bp section of the tba1c regulatory region, which was validated in Primack et al (2023) to be a pan-neuronal promoter. The plasmid injection solution was injected into Hydra vulgaris AEP 1-cell stage embryos using an Eppendorf FemtoJet 4x and Eppendorf InjectMan NI 2 microinjector (Eppendorf; Hamburg, Germany) under a Leica M165 C stereo microscope (Leica Microscopes, Inc; Buffalo Grove, Il).…”
Section: Methodsmentioning
confidence: 88%
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“…Generation of Tg(hym176c:tdTomato,tba1c:GCAMP7s) cj1-in transgenic strain Hydra transgenic line Tg(hym176c:tdTomato,tba1c:GCAMP7s) cj1-in was created by microinjecting a single plasmid containing two promoters and two transgenes. Nuclear tdTomato was driven by a 2022 bp section of the hym176c regulatory region, which should be specifically expressed in ec5 neurons found in the peduncle (Fig 1H,26), and GCaMP7s was driven by a 1901 bp section of the tba1c regulatory region, which was validated in Primack et al (2023) to be a pan-neuronal promoter. The plasmid injection solution was injected into Hydra vulgaris AEP 1-cell stage embryos using an Eppendorf FemtoJet 4x and Eppendorf InjectMan NI 2 microinjector (Eppendorf; Hamburg, Germany) under a Leica M165 C stereo microscope (Leica Microscopes, Inc; Buffalo Grove, Il).…”
Section: Methodsmentioning
confidence: 88%
“…The transcriptional state of all eleven Hydra neuron subtypes has been profiled using single cell RNA-sequencing [1,47]. Similar to findings in C. elegans [20], the Hydra neurons are best defined by unique combinatorial expression of specific genes, including transcription factors and neuropeptides [21,22].…”
Section: Introductionmentioning
confidence: 93%
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“…One transgenic strain uses the promoter of an alpha-tubulin gene driving expression of NeonGreen. This transgene has been demonstrated to be strongly expressed in all differentiated nerve cells in Hydra , and correspondingly the entire nervous system is brightly NeonGreen-positive (Primak et al 2023). Fixed polyps of this strain were stained with PNab and transgenic NeonGreen expressing nerve cells were scored for PNab staining (see Materials and Methods).…”
Section: Resultsmentioning
confidence: 99%
“…To approach the nature of the neuronal control of satiety in Hydra , we conducted a systematic screening of different neuronal populations by using previously established calcium imaging lines. In a first step, we took the advantage of a pan-neuronal Hydra line (alpha-tubulin promotor 15 ) and investigated neuronal activity in the body column ( Fig. 3A ).…”
Section: Resultsmentioning
confidence: 99%