The COP9 Signalosome Converts Temporal Hormone Signaling to Spatial Restriction on Neural Competence

博士 === 國防醫學院 === 生命科學研究所 === 103 === During development, neural competence is conferred and maintained by integrating spatial and temporal regulations. The Drosophila sensory bristles that detect mechanical and chemical stimulations are arranged in stereotypical positions. The anterior wing margin (...

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Main Authors: Yi-Chun Huang, 黃亦君
Other Authors: Cheng-Ting Chien
Format: Others
Language:en_US
Published: 2014
Online Access:http://ndltd.ncl.edu.tw/handle/53134084600333522757
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spelling ndltd-TW-103NDMC01050052017-02-19T04:30:31Z http://ndltd.ncl.edu.tw/handle/53134084600333522757 The COP9 Signalosome Converts Temporal Hormone Signaling to Spatial Restriction on Neural Competence 探討 COP 9 複雜亞單位將果蠅蛻皮激素時間軸訊號轉化為果蠅神神經發育位置決定的機制 Yi-Chun Huang 黃亦君 博士 國防醫學院 生命科學研究所 103 During development, neural competence is conferred and maintained by integrating spatial and temporal regulations. The Drosophila sensory bristles that detect mechanical and chemical stimulations are arranged in stereotypical positions. The anterior wing margin (AWM) is arrayed with neuron-innervated sensory bristles while posterior wing margin (PWM) bristles are non-innervated. We found that the COP9 signalosome (CSN) suppresses the neural competence of non-innervated bristles at the PWM. In CSN mutants, PWM bristles are transformed into neuron-innervated, which is attributed to sustained expression of the neural-determining factor Senseless (Sens). The CSN suppresses Sens through repression of the ecdysone signaling target gene broad (br) that encodes the BR-Z1 transcription factor to activate sens expression. Strikingly, CSN suppression of BR-Z1 is initiated at the prepupa-to-pupa transition, leading to Sens downregulation, and termination of the neural competence of PWM bristles. The role of ecdysone signaling to repress br after the prepupa-to-pupa transition is distinct from its conventional role in activation, and requires CSN deneddylating activity and multiple cullins, the major substrates of deneddylation. Several CSN subunits physically associate with ecdysone receptors to represses br at the transcriptional level. We propose a model in which nuclear hormone receptors cooperate with the deneddylation machinery to temporally shutdown downstream target gene expression, conferring a spatial restriction on neural competence at the PWM. Cheng-Ting Chien Haiwei Pi 簡正鼎 皮海薇 2014 學位論文 ; thesis 81 en_US
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description 博士 === 國防醫學院 === 生命科學研究所 === 103 === During development, neural competence is conferred and maintained by integrating spatial and temporal regulations. The Drosophila sensory bristles that detect mechanical and chemical stimulations are arranged in stereotypical positions. The anterior wing margin (AWM) is arrayed with neuron-innervated sensory bristles while posterior wing margin (PWM) bristles are non-innervated. We found that the COP9 signalosome (CSN) suppresses the neural competence of non-innervated bristles at the PWM. In CSN mutants, PWM bristles are transformed into neuron-innervated, which is attributed to sustained expression of the neural-determining factor Senseless (Sens). The CSN suppresses Sens through repression of the ecdysone signaling target gene broad (br) that encodes the BR-Z1 transcription factor to activate sens expression. Strikingly, CSN suppression of BR-Z1 is initiated at the prepupa-to-pupa transition, leading to Sens downregulation, and termination of the neural competence of PWM bristles. The role of ecdysone signaling to repress br after the prepupa-to-pupa transition is distinct from its conventional role in activation, and requires CSN deneddylating activity and multiple cullins, the major substrates of deneddylation. Several CSN subunits physically associate with ecdysone receptors to represses br at the transcriptional level. We propose a model in which nuclear hormone receptors cooperate with the deneddylation machinery to temporally shutdown downstream target gene expression, conferring a spatial restriction on neural competence at the PWM.
author2 Cheng-Ting Chien
author_facet Cheng-Ting Chien
Yi-Chun Huang
黃亦君
author Yi-Chun Huang
黃亦君
spellingShingle Yi-Chun Huang
黃亦君
The COP9 Signalosome Converts Temporal Hormone Signaling to Spatial Restriction on Neural Competence
author_sort Yi-Chun Huang
title The COP9 Signalosome Converts Temporal Hormone Signaling to Spatial Restriction on Neural Competence
title_short The COP9 Signalosome Converts Temporal Hormone Signaling to Spatial Restriction on Neural Competence
title_full The COP9 Signalosome Converts Temporal Hormone Signaling to Spatial Restriction on Neural Competence
title_fullStr The COP9 Signalosome Converts Temporal Hormone Signaling to Spatial Restriction on Neural Competence
title_full_unstemmed The COP9 Signalosome Converts Temporal Hormone Signaling to Spatial Restriction on Neural Competence
title_sort cop9 signalosome converts temporal hormone signaling to spatial restriction on neural competence
publishDate 2014
url http://ndltd.ncl.edu.tw/handle/53134084600333522757
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