Cysteine Proteinase-1 and Cut Protein Isoform Control Dendritic Innervation of Two Distinct Sensory Fields by a Single Neuron

Dendrites often exhibit structural changes in response to local inputs. Although mechanisms that pattern and maintain dendritic arbors are becoming clearer, processes regulating regrowth, during context-dependent plasticity or after injury, remain poorly understood. We found that a class of Drosophi...

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Main Authors: Gray R. Lyons, Ryan O. Andersen, Khadar Abdi, Won-Seok Song, Chay T. Kuo
Format: Article
Language:English
Published: Elsevier 2014-03-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124714000825
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spelling doaj-25046ed14972416cbbf18d3ef341e9212020-11-24T21:47:27ZengElsevierCell Reports2211-12472014-03-016578379110.1016/j.celrep.2014.02.003Cysteine Proteinase-1 and Cut Protein Isoform Control Dendritic Innervation of Two Distinct Sensory Fields by a Single NeuronGray R. Lyons0Ryan O. Andersen1Khadar Abdi2Won-Seok Song3Chay T. Kuo4Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USADepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USADepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USADepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USADepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USADendrites often exhibit structural changes in response to local inputs. Although mechanisms that pattern and maintain dendritic arbors are becoming clearer, processes regulating regrowth, during context-dependent plasticity or after injury, remain poorly understood. We found that a class of Drosophila sensory neurons, through complete pruning and regeneration, can elaborate two distinct dendritic trees, innervating independent sensory fields. An expression screen identified Cysteine proteinase-1 (Cp1) as a critical regulator of this process. Unlike known ecdysone effectors, Cp1-mutant ddaC neurons pruned larval dendrites normally but failed to regrow adult dendrites. Cp1 expression was upregulated/concentrated in the nucleus during metamorphosis, controlling production of a truncated Cut homeodomain transcription factor. This truncated Cut, but not the full-length protein, allowed Cp1-mutant ddaC neurons to regenerate higher-order adult dendrites. These results identify a molecular pathway needed for dendrite regrowth after pruning, which allows the same neuron to innervate distinct sensory fields.http://www.sciencedirect.com/science/article/pii/S2211124714000825
collection DOAJ
language English
format Article
sources DOAJ
author Gray R. Lyons
Ryan O. Andersen
Khadar Abdi
Won-Seok Song
Chay T. Kuo
spellingShingle Gray R. Lyons
Ryan O. Andersen
Khadar Abdi
Won-Seok Song
Chay T. Kuo
Cysteine Proteinase-1 and Cut Protein Isoform Control Dendritic Innervation of Two Distinct Sensory Fields by a Single Neuron
Cell Reports
author_facet Gray R. Lyons
Ryan O. Andersen
Khadar Abdi
Won-Seok Song
Chay T. Kuo
author_sort Gray R. Lyons
title Cysteine Proteinase-1 and Cut Protein Isoform Control Dendritic Innervation of Two Distinct Sensory Fields by a Single Neuron
title_short Cysteine Proteinase-1 and Cut Protein Isoform Control Dendritic Innervation of Two Distinct Sensory Fields by a Single Neuron
title_full Cysteine Proteinase-1 and Cut Protein Isoform Control Dendritic Innervation of Two Distinct Sensory Fields by a Single Neuron
title_fullStr Cysteine Proteinase-1 and Cut Protein Isoform Control Dendritic Innervation of Two Distinct Sensory Fields by a Single Neuron
title_full_unstemmed Cysteine Proteinase-1 and Cut Protein Isoform Control Dendritic Innervation of Two Distinct Sensory Fields by a Single Neuron
title_sort cysteine proteinase-1 and cut protein isoform control dendritic innervation of two distinct sensory fields by a single neuron
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2014-03-01
description Dendrites often exhibit structural changes in response to local inputs. Although mechanisms that pattern and maintain dendritic arbors are becoming clearer, processes regulating regrowth, during context-dependent plasticity or after injury, remain poorly understood. We found that a class of Drosophila sensory neurons, through complete pruning and regeneration, can elaborate two distinct dendritic trees, innervating independent sensory fields. An expression screen identified Cysteine proteinase-1 (Cp1) as a critical regulator of this process. Unlike known ecdysone effectors, Cp1-mutant ddaC neurons pruned larval dendrites normally but failed to regrow adult dendrites. Cp1 expression was upregulated/concentrated in the nucleus during metamorphosis, controlling production of a truncated Cut homeodomain transcription factor. This truncated Cut, but not the full-length protein, allowed Cp1-mutant ddaC neurons to regenerate higher-order adult dendrites. These results identify a molecular pathway needed for dendrite regrowth after pruning, which allows the same neuron to innervate distinct sensory fields.
url http://www.sciencedirect.com/science/article/pii/S2211124714000825
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