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神经元 KGB-1 JNK MAPK 信号转导调控秀丽隐杆线虫对环境胁迫的 dauer 发育决策。

Neuronal KGB-1 JNK MAPK signaling regulates the dauer developmental decision in response to environmental stress in Caenorhabditis elegans.

机构信息

Division of Infectious Diseases, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115, USA.

Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

出版信息

Genetics. 2022 Jan 4;220(1). doi: 10.1093/genetics/iyab186.

DOI:10.1093/genetics/iyab186
PMID:34726729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8733477/
Abstract

In response to stressful growth conditions of high population density, food scarcity, and elevated temperature, young larvae of nematode Caenorhabditis elegans can enter a developmentally arrested stage called dauer that is characterized by dramatic anatomic and metabolic remodeling. Genetic analysis of dauer formation of C. elegans has served as an experimental paradigm for the identification and characterization of conserved neuroendocrine signaling pathways. Here, we report the identification and characterization of a conserved c-Jun N-terminal Kinase-like mitogen-activated protein kinase (MAPK) pathway that is required for dauer formation in response to environmental stressors. We observed that loss-of-function mutations in the MLK-1-MEK-1-KGB-1 MAPK pathway suppress dauer entry. A loss-of-function mutation in the VHP-1 MAPK phosphatase, a negative regulator of KGB-1 signaling, results in constitutive dauer formation, which is dependent on the presence of dauer pheromone but independent of diminished food levels or elevated temperatures. Our data suggest that the KGB-1 pathway acts in the sensory neurons, in parallel to established insulin and TGF-β signaling pathways, to transduce the dauer-inducing environmental cues of diminished food levels and elevated temperature.

摘要

在应对高密度种群、食物匮乏和温度升高的压力生长条件下,秀丽隐杆线虫的幼体可以进入一种发育停滞的阶段,称为 dauer,其特征是剧烈的解剖和代谢重塑。秀丽隐杆线虫 dauer 形成的遗传分析已成为鉴定和表征保守神经内分泌信号通路的实验范例。在这里,我们报告了一个保守的 c-Jun N 末端激酶样丝裂原活化蛋白激酶(MAPK)途径的鉴定和表征,该途径是对环境胁迫产生 dauer 所必需的。我们观察到 MLK-1-MEK-1-KGB-1 MAPK 途径中的功能丧失突变会抑制 dauer 的进入。VHP-1 MAPK 磷酸酶的功能丧失突变导致 dauer 的组成型形成,这依赖于 dauer 信息素的存在,但与食物水平降低或温度升高无关。我们的数据表明,KGB-1 途径在感觉神经元中与已建立的胰岛素和 TGF-β信号通路平行作用,以转导食物水平降低和温度升高的 dauer 诱导环境线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/f49fd058c961/iyab186f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/f76b490d2195/iyab186f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/24c164b9d802/iyab186f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/55d2e837f9ab/iyab186f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/a7245eed8cfb/iyab186f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/82ee9e0a2d86/iyab186f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/f49fd058c961/iyab186f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/f76b490d2195/iyab186f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/521743f9f9d2/iyab186f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/24c164b9d802/iyab186f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/55d2e837f9ab/iyab186f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/a7245eed8cfb/iyab186f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/82ee9e0a2d86/iyab186f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cec5/8733477/f49fd058c961/iyab186f7.jpg

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