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利用源自鼻上皮刷取样本的犬嗅觉受体基因表达谱分析。

Dog olfactory receptor gene expression profiling using samples derived from nasal epithelium brushing.

作者信息

Azzouzi Naoual, Guillory Anne-Sophie, Chaudieu Gilles, Galibert Francis

机构信息

UMR6290 IGDR (Institut de Génétique Et Développement de Rennes), Université de Rennes 1, CNRS, 35000, Rennes, France.

Clinique Vétérinaire Pole Santé Chanturgue, 63100, Clermont-Ferrand, France.

出版信息

Canine Med Genet. 2022 May 20;9(1):7. doi: 10.1186/s40575-022-00116-7.

Abstract

Dogs have an exquisite sense of olfaction. In many instances this ability has been utilized by humans for a wide range of important situations including detecting explosives and illegal drugs. It is accepted that some breeds have better senses of smell than others. Dogs can detect many volatile compounds at extremely low concentrations in air. To achieve such high levels of detection, the canine olfactory system is both complex and highly developed requiring a high density of olfactory receptors capable of detecting volatiles. Consequently the dog genome encodes a large number of olfactory receptor (OR) genes. However, it remains unclear as to what extent are all of these OR genes expressed on the cell surface. To facilitate such studies, a nasal brushing method was developed to recover dog nasal epithelial cell samples from which total RNA could be extracted and used to prepare high quality cDNA libraries. After capture by hybridization with an extensive set of oligonucleotides, the level of expression of each transcript was measured following next generation sequencing (NGS). The reproducibility of this sampling approach was checked by analyzing replicate samples from the same animal (up to 6 per each naris). The quality of the hybridization capture was also checked by analyzing two DNA libraries; this offered an advantage over RNA libraries by having an equal presence for each gene. Finally, we compared this brushing method performed on living dogs to a nasal epithelium biopsy approach applied to two euthanized terminally ill dogs, following consent from their owners.Comparison the expression levels of each transcript indicate that the ratios of expression between the highest and the least expressed OR in each sample are greater than 10,000 (paralog variation). Furthermore, it was clear that a number of OR genes are not expressed.The method developed and described here will allow researchers to further address whether variations observed in the OR transcriptome relate to dog 'life experiences' and whether any differences observed between samples are dog-specific or breed-specific.

摘要

狗具有敏锐的嗅觉。在许多情况下,人类利用这种能力处理各种重要事务,包括探测爆炸物和非法毒品。人们公认某些犬种的嗅觉比其他犬种更灵敏。狗能够检测空气中极低浓度的多种挥发性化合物。为实现如此高的检测水平,犬类嗅觉系统既复杂又高度发达,需要高密度的能够检测挥发性物质的嗅觉受体。因此,狗的基因组编码了大量嗅觉受体(OR)基因。然而,目前尚不清楚所有这些OR基因在细胞表面的表达程度如何。为便于开展此类研究,开发了一种鼻刷法来获取狗的鼻上皮细胞样本,从中可提取总RNA并用于制备高质量的cDNA文库。与大量寡核苷酸杂交捕获后,通过下一代测序(NGS)测量每个转录本的表达水平。通过分析来自同一动物的重复样本(每个鼻孔最多6个)来检查这种采样方法的可重复性。还通过分析两个DNA文库来检查杂交捕获的质量;与RNA文库相比,这具有每个基因等量存在的优势。最后,在获得狗主人同意后,我们将对活狗进行的这种刷鼻法与应用于两只安乐死的晚期病犬的鼻上皮活检方法进行了比较。比较每个转录本的表达水平表明,每个样本中表达最高和最低的OR之间的表达比率大于10000(旁系同源变异)。此外,很明显有一些OR基因不表达。本文开发和描述的方法将使研究人员能够进一步探讨在OR转录组中观察到的变异是否与狗的“生活经历”有关,以及样本之间观察到的任何差异是特定于某只狗还是特定于某个犬种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f2/9121576/ac3c86b4e02f/40575_2022_116_Fig1_HTML.jpg

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