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豌豆蚜 Acyrthosiphon pisum 全胚胎荧光原位杂交(FISH)的可靠方案:全面调查与分析。

Reliable protocols for whole-mount fluorescent in situ hybridization (FISH) in the pea aphid Acyrthosiphon pisum: a comprehensive survey and analysis.

机构信息

Laboratory for Genetics and Development, Department of Entomology/Institute of Biotechnology, College of Bioresources and Agriculture, National Taiwan University, Taipei, Taiwan.

出版信息

Insect Sci. 2014 Jun;21(3):265-77. doi: 10.1111/1744-7917.12086. Epub 2014 Jan 15.

Abstract

RNA in situ hybridization (ISH), including chromogenic ISH (CISH) and fluorescent ISH (FISH), has become a powerful tool for revealing the spatial distribution of gene transcripts in model organisms. Previously, we developed a robust protocol for whole-mount RNA CISH in the pea aphid Acyrthosiphon pisum, an emerging insect genomic model. In order to improve the resolving capacity of gene detection, we comprehensively surveyed current protocols of whole-mount RNA-FISH and developed protocols that allow, using confocal microscopy, clearer visualization of target messenger RNAs (mRNAs) - including those subcellularly localized and those with spatially overlapping expression. We find that Fast dye-based substrate fluorescence (SF), tyramide signal amplification (TSA), and TSA Plus all enable identifying gene expression thanks to multiplex amplification of fluorescent signals. By contrast, methods of direct fluorescence (DF) do not allow visualizing signals. Detection of a single gene target was achieved with SF and TSA Plus for most mRNAs, whereas TSA only allowed visualization of abundant transcripts such as Apvas1 and Appiwi2 in the germ cells. For detection of multiple gene targets using double FISH, we recommend: (i) TSA/TSA, rather than TSA Plus/TSA Plus for colocalized mRNAs abundantly expressed in germ cells, as proteinase K treatment can be omitted; and (ii) SF/TSA Plus for other gene targets such as Apen1 and Apen2 as inactivation of enzyme conjugates is not required. SF/SF is not ideal for double FISH experiments due to signal blurring. Based on these new conditions for RNA-FISH, we have obtained a better understanding of germline specification and embryonic segmentation in the pea aphid. We anticipate that the RNA-FISH protocols for the pea aphid may also be used for other aphids and possibly other insect species, thus expanding the range of species from which useful insights into development and evolution may be obtained.

摘要

RNA 原位杂交(ISH),包括显色原位杂交(CISH)和荧光原位杂交(FISH),已成为揭示基因转录本在模式生物中空间分布的有力工具。此前,我们开发了一种用于豌豆蚜 Acyrthosiphon pisum 整体 RNA CISH 的稳健方案,这是一种新兴的昆虫基因组模式。为了提高基因检测的分辨率,我们全面调查了目前的整体 RNA-FISH 方案,并开发了允许使用共聚焦显微镜更清晰地可视化靶信使 RNA(mRNA)的方案,包括那些亚细胞定位的和那些表达空间重叠的。我们发现,基于 Fast 染料的底物荧光(SF)、酪胺信号放大(TSA)和 TSA Plus 都可以通过荧光信号的多重扩增来识别基因表达。相比之下,直接荧光(DF)方法无法观察到信号。对于大多数 mRNA,SF 和 TSA Plus 可用于检测单个基因靶标,而 TSA 仅允许在生殖细胞中可视化 Apvas1 和 Appiwi2 等丰度较高的转录本。对于使用双 FISH 检测多个基因靶标,我们建议:(i)对于在生殖细胞中丰度表达的共定位 mRNA,使用 TSA/TSA,而不是 TSA Plus/TSA Plus,因为可以省略蛋白酶 K 处理;(ii)对于 Apen1 和 Apen2 等其他基因靶标,使用 SF/TSA Plus,因为不需要失活酶偶联物。SF/SF 不适合双 FISH 实验,因为信号模糊。基于这些新的 RNA-FISH 条件,我们对豌豆蚜的生殖系特化和胚胎分段有了更好的理解。我们预计豌豆蚜的 RNA-FISH 方案也可用于其他蚜虫,甚至可能用于其他昆虫物种,从而扩大了可以从中获得有关发育和进化的有用见解的物种范围。

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