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Cell Mol Life Sci. 2020 Nov;77(22):4523-4551. doi: 10.1007/s00018-020-03547-2. Epub 2020 May 24.
2
Nutritional control of body size through FoxO-Ultraspiracle mediated ecdysone biosynthesis.通过FoxO-超气门蛋白介导的蜕皮激素生物合成实现对体型的营养控制。
Elife. 2014 Nov 25;3:e03091. doi: 10.7554/eLife.03091.
3
The ontogeny and evolution of sex-biased gene expression in Drosophila melanogaster.果蝇中性别偏向基因表达的个体发生和进化。
Mol Biol Evol. 2014 May;31(5):1206-19. doi: 10.1093/molbev/msu072. Epub 2014 Feb 12.
4
Sex-specific weight loss mediates sexual size dimorphism in Drosophila melanogaster.性别特异性体重减轻介导果蝇的性二型大小。
PLoS One. 2013;8(3):e58936. doi: 10.1371/journal.pone.0058936. Epub 2013 Mar 28.
5
Discrete pulses of molting hormone, 20-hydroxyecdysone, during late larval development of Drosophila melanogaster: correlations with changes in gene activity.在黑腹果蝇幼虫后期发育过程中蜕皮激素(20-羟基蜕皮酮)的离散脉冲:与基因活性变化的相关性
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6
A role for betaFTZ-F1 in regulating ecdysteroid titers during post-embryonic development in Drosophila melanogaster.βFTZ-F1在调节黑腹果蝇胚胎后期发育过程中蜕皮甾体滴度方面的作用。
Dev Biol. 2005 Jun 1;282(1):84-94. doi: 10.1016/j.ydbio.2005.02.028.
7
Deletion of the ecdysis-triggering hormone gene leads to lethal ecdysis deficiency.蜕皮触发激素基因的缺失导致致命的蜕皮缺陷。
Development. 2002 Jan;129(2):493-503. doi: 10.1242/dev.129.2.493.

从幼虫全身样本中定量测定蜕皮激素

Ecdysone Quantification from Whole Body Samples of Larvae.

作者信息

Koyama Takashi, Mirth Christen K

机构信息

Instituto Gulbenkian de Ciência, Rua da Quinta Grande, 6, Oeiras 2780-156, Portugal.

出版信息

Bio Protoc. 2021 Feb 5;11(3):e3915. doi: 10.21769/BioProtoc.3915.

DOI:10.21769/BioProtoc.3915
PMID:33732802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7952929/
Abstract

Steroid hormones strictly control the timing of sexual maturation and final body size both in vertebrates and invertebrates. In insects, the steroid hormone ecdysone controls the timing of the molts between larval instars as well as the transition to metamorphosis. Growth during the final instar accounts for over 80% of the increase in final mass in insects, and the duration of this growth period is driven by a sequence of small ecdysone pulses that ultimately induce metamorphosis. Historically the biologically active form of ecdysone, 20-hydroxyecdysone (20E), was quantified using radio-immunoassays, bioassays, or chromatography assays. However, these assays are methodologically complicated and often time consuming. Furthermore, collecting samples for precise measurements of ecdysone concentrations using these assays is limited in small insects like Here, we describe an accurate and sensitive method to collect carefully-staged third instar larvae suitable for preparing samples for ecdysone quantification using a commercially-available 20E enzyme immunoassay (EIA). Because we resynchronize larval development at the molt to the final instar, collect large samples, and weigh each sample, we are able to detect a small ecdysone peak early in the final instar known as the critical weight ecdysone peak. This method detects peaks as low as 6 pg 20E/mg larval sample, allowing us to quantify other small ecdysone peaks in flies - the necessary prerequisite for eventually determining their regulation and function.

摘要

类固醇激素严格控制着脊椎动物和无脊椎动物性成熟的时间以及最终的体型大小。在昆虫中,类固醇激素蜕皮激素控制着幼虫龄期之间蜕皮的时间以及向变态发育的转变。末龄幼虫阶段的生长占昆虫最终体重增加的80%以上,而这个生长阶段的持续时间由一系列小的蜕皮激素脉冲驱动,这些脉冲最终诱导变态发育。从历史上看,蜕皮激素的生物活性形式20-羟基蜕皮激素(20E)是通过放射免疫测定、生物测定或色谱测定来定量的。然而,这些测定方法在方法上很复杂,而且通常很耗时。此外,使用这些测定方法收集用于精确测量蜕皮激素浓度的样本,对于像这样的小昆虫来说是有限的。在这里,我们描述了一种准确且灵敏的方法,用于收集精心安排的三龄幼虫,这些幼虫适合使用市售的20E酶免疫测定(EIA)来制备用于蜕皮激素定量的样本。因为我们在蜕皮到末龄幼虫时使幼虫发育重新同步,收集大量样本并对每个样本称重,所以我们能够在末龄幼虫早期检测到一个小的蜕皮激素峰值,即临界体重蜕皮激素峰值。这种方法能够检测低至6 pg 20E/毫克幼虫样本的峰值,使我们能够定量果蝇中其他小的蜕皮激素峰值——这是最终确定其调节和功能的必要前提条件。