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呆滞有助于缺口响应的稳健性。

Deadpan contributes to the robustness of the notch response.

机构信息

Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.

出版信息

PLoS One. 2013 Sep 24;8(9):e75632. doi: 10.1371/journal.pone.0075632. eCollection 2013.

DOI:10.1371/journal.pone.0075632
PMID:24086596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3782438/
Abstract

Notch signaling regulates many fundamental events including lateral inhibition and boundary formation to generate very reproducible patterns in developing tissues. Its targets include genes of the bHLH hairy and Enhancer of split [E(spl)] family, which contribute to many of these developmental decisions. One member of this family in Drosophila, deadpan (dpn), was originally found to have functions independent of Notch in promoting neural development. Employing genome-wide chromatin-immunoprecipitation we have identified several Notch responsive enhancers in dpn, demonstrating its direct regulation by Notch in a range of contexts including the Drosophila wing and eye. dpn expression largely overlaps that of several E(spl) genes and the combined knock-down leads to more severe phenotypes than either alone. In addition, Dpn contributes to the establishment of Cut expression at the wing dorsal-ventral (D/V) boundary; in its absence Cut expression is delayed. Furthermore, over-expression of Dpn inhibits expression from E(spl) gene enhancers, but not vice versa, suggesting that dpn contributes to a feed-back mechanism that limits E(spl) gene expression following Notch activation. Thus the combined actions of dpn and E(spl) appear to provide a mechanism that confers an initial rapid output from Notch activity which becomes self-limited via feedback between the targets.

摘要

Notch 信号通路调控着许多基本事件,包括侧向抑制和边界形成,从而在发育组织中产生非常可重复的模式。其靶标包括 bHLH hairy 和 Enhancer of split [E(spl)]家族的基因,这些基因对许多发育决策都有贡献。在果蝇中,这个家族的一个成员 deadpan (dpn)最初被发现具有与 Notch 独立的功能,可促进神经发育。通过全基因组染色质免疫沉淀,我们在 dpn 中鉴定出了几个 Notch 反应性增强子,证明了 Notch 在包括果蝇翅膀和眼睛在内的多种情况下对其进行直接调控。dpn 的表达在很大程度上与几个 E(spl)基因的表达重叠,并且联合敲低比单独敲低导致更严重的表型。此外,Dpn 有助于在翅膀背腹(D/V)边界处建立 Cut 的表达;在其不存在的情况下,Cut 的表达被延迟。此外,Dpn 的过表达抑制了 E(spl)基因增强子的表达,但反之则不然,这表明 dpn 有助于一种反馈机制,该机制在 Notch 激活后限制 E(spl)基因的表达。因此,dpn 和 E(spl)的联合作用似乎提供了一种机制,赋予 Notch 活性初始快速输出,然后通过靶标之间的反馈自我限制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/17ce5756a1a9/pone.0075632.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/1f37699432d0/pone.0075632.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/00bb3b933b89/pone.0075632.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/3feeb6a750b3/pone.0075632.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/d45ca1e10e8f/pone.0075632.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/158cdb8133d5/pone.0075632.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/e117e386b334/pone.0075632.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/17ce5756a1a9/pone.0075632.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/1f37699432d0/pone.0075632.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/00bb3b933b89/pone.0075632.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/3feeb6a750b3/pone.0075632.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/d45ca1e10e8f/pone.0075632.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/158cdb8133d5/pone.0075632.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/e117e386b334/pone.0075632.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf85/3782438/17ce5756a1a9/pone.0075632.g007.jpg

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