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针对椎实螺(Lymnaea stagnalis)的优化全组织原位杂交方案。

An optimised whole mount in situ hybridisation protocol for the mollusc Lymnaea stagnalis.

作者信息

Hohagen Jennifer, Herlitze Ines, Jackson Daniel John

机构信息

Department of Geobiology, Geosciences Centre, Georg-August University of Göttingen, Goldschmidtstrasse 3, 37077, Göttingen, Germany.

出版信息

BMC Dev Biol. 2015 Mar 28;15:19. doi: 10.1186/s12861-015-0068-7.

Abstract

BACKGROUND

The ability to visualise the expression of individual genes in situ is an invaluable tool for developmental and evolutionary biologists; it allows for the characterisation of gene function, gene regulation and through inter-specific comparisons, the evolutionary history of unique morphological features. For well-established model organisms (e.g., flies, worms, sea urchins) this technique has been optimised to an extent where it can be automated for high-throughput analyses. While the overall concept of in situ hybridisation is simple (hybridise a single-stranded, labelled nucleic acid probe complementary to a target of interest, and then detect the label immunologically using colorimetric or fluorescent methods), there are many parameters in the technique that can significantly affect the final result. Furthermore, due to variation in the biochemical and biophysical properties of different cells and tissues, an in situ technique optimised for one species is often not suitable for another, and often varies depending on the ontogenetic stage within a species.

RESULTS

Using a variety of pre-hybridisation treatments we have identified a set of treatments that greatly increases both whole mount in situ hybridisation (WMISH) signal intensity and consistency while maintaining morphological integrity for early larval stages of Lymnaea stagnalis. These treatments function well for a set of genes with presumably significantly different levels of expression (beta tubulin, engrailed and COE) and for colorimetric as well as fluorescent WMISH. We also identify a tissue-specific background stain in the larval shell field of L. stagnalis and a treatment, which eliminates this signal.

CONCLUSIONS

This method that we present here will be of value to investigators employing L. stagnalis as a model for a variety of research themes (e.g. evolutionary biology, developmental biology, neurobiology, ecotoxicology), and brings a valuable tool to a species in a much understudied clade of animals collectively known as the Spiralia.

摘要

背景

原位可视化单个基因的表达,对于发育生物学家和进化生物学家而言是一项极为宝贵的工具;它有助于表征基因功能、基因调控,并通过种间比较,了解独特形态特征的进化历程。对于成熟的模式生物(如苍蝇、蠕虫、海胆),这项技术已得到优化,在一定程度上可实现自动化高通量分析。虽然原位杂交的总体概念很简单(将与目标感兴趣序列互补的单链标记核酸探针进行杂交,然后使用比色法或荧光法通过免疫检测标记),但该技术中有许多参数会显著影响最终结果。此外,由于不同细胞和组织的生化及生物物理特性存在差异,一种为某一物种优化的原位技术通常不适用于另一物种,而且往往因物种内的个体发育阶段而异。

结果

通过多种预杂交处理,我们确定了一组处理方法,这些方法在保持静水椎实螺早期幼虫阶段形态完整性的同时,能显著提高整体原位杂交(WMISH)信号强度和一致性。这些处理方法对一组推测表达水平差异显著(β微管蛋白、engrailed和COE)的基因以及比色法和荧光WMISH均有效。我们还在静水椎实螺幼虫壳区发现了一种组织特异性背景染色,并确定了一种消除该信号的处理方法。

结论

我们在此介绍的这种方法,将对以静水椎实螺为模型开展各种研究主题(如进化生物学、发育生物学、神经生物学、生态毒理学)的研究人员具有重要价值,并为一个被统称为螺旋动物门、研究较少的动物类群中的一个物种带来了一项宝贵工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e5f/4379745/edf0735487ba/12861_2015_68_Fig1_HTML.jpg

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