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秀丽隐杆线虫中参与信息素诱导的 dauer 形成的分子的正向遗传学筛选

A Forward Genetic Screen for Molecules Involved in Pheromone-Induced Dauer Formation in Caenorhabditis elegans.

作者信息

Neal Scott J, Park JiSoo, DiTirro Danielle, Yoon Jason, Shibuya Mayumi, Choi Woochan, Schroeder Frank C, Butcher Rebecca A, Kim Kyuhyung, Sengupta Piali

机构信息

Department of Biology, Brandeis University, Waltham, Massachusetts 02454 National Center for Behavioral Genomics, Brandeis University, Waltham, Massachusetts 02454.

Department of Brain and Cognitive Sciences, DGIST, Daegu 711-873, Republic of Korea.

出版信息

G3 (Bethesda). 2016 May 3;6(5):1475-87. doi: 10.1534/g3.115.026450.

Abstract

Animals must constantly assess their surroundings and integrate sensory cues to make appropriate behavioral and developmental decisions. Pheromones produced by conspecific individuals provide critical information regarding environmental conditions. Ascaroside pheromone concentration and composition are instructive in the decision of Caenorhabditis elegans to either develop into a reproductive adult or enter into the stress-resistant alternate dauer developmental stage. Pheromones are sensed by a small set of sensory neurons, and integrated with additional environmental cues, to regulate neuroendocrine signaling and dauer formation. To identify molecules required for pheromone-induced dauer formation, we performed an unbiased forward genetic screen and identified phd (pheromone response-defective dauer) mutants. Here, we describe new roles in dauer formation for previously identified neuronal molecules such as the WD40 domain protein QUI-1 and MACO-1 Macoilin, report new roles for nociceptive neurons in modulating pheromone-induced dauer formation, and identify tau tubulin kinases as new genes involved in dauer formation. Thus, phd mutants define loci required for the detection, transmission, or integration of pheromone signals in the regulation of dauer formation.

摘要

动物必须不断评估其周围环境并整合感官线索,以做出适当的行为和发育决策。同种个体产生的信息素提供了有关环境条件的关键信息。在秀丽隐杆线虫决定发育为有生殖能力的成虫还是进入抗逆性的替代滞育发育阶段的过程中,ascaroside信息素的浓度和组成具有指导作用。一小部分感觉神经元能感知信息素,并与其他环境线索整合,以调节神经内分泌信号传导和滞育形成。为了鉴定信息素诱导滞育形成所需的分子,我们进行了一项无偏向的正向遗传筛选,并鉴定出了phd(信息素反应缺陷型滞育)突变体。在此,我们描述了先前鉴定出的神经元分子(如WD40结构域蛋白QUI-1和MACO-1麦考林)在滞育形成中的新作用,报道了伤害感受神经元在调节信息素诱导的滞育形成中的新作用,并鉴定出tau微管蛋白激酶是参与滞育形成的新基因。因此,phd突变体定义了在滞育形成调节中信息素信号检测、传递或整合所需的基因座。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69a9/4856098/394e90024a97/1475f1.jpg

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本文引用的文献

1
Crescerin uses a TOG domain array to regulate microtubules in the primary cilium.
Mol Biol Cell. 2015 Nov 15;26(23):4248-64. doi: 10.1091/mbc.E15-08-0603. Epub 2015 Sep 16.
2
A gene-expression-based neural code for food abundance that modulates lifespan.
Elife. 2015 May 12;4:e06259. doi: 10.7554/eLife.06259.
3
TTBK2: a tau protein kinase beyond tau phosphorylation.
Biomed Res Int. 2015;2015:575170. doi: 10.1155/2015/575170. Epub 2015 Apr 9.
5
The Multifunctions of WD40 Proteins in Genome Integrity and Cell Cycle Progression.
J Genomics. 2015 Feb 5;3:40-50. doi: 10.7150/jgen.11015. eCollection 2015.
7
The tau tubulin kinases TTBK1/2 promote accumulation of pathological TDP-43.
PLoS Genet. 2014 Dec 4;10(12):e1004803. doi: 10.1371/journal.pgen.1004803. eCollection 2014 Dec.
8
A model of the effect of uncertainty on the C elegans L2/L2d decision.
PLoS One. 2014 Jul 16;9(7):e100580. doi: 10.1371/journal.pone.0100580. eCollection 2014.
9
Tau-tubulin kinase.
Front Mol Neurosci. 2014 Apr 28;7:33. doi: 10.3389/fnmol.2014.00033. eCollection 2014.

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