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采用整合遗传-基因组-分析化学方法鉴定草莓风味基因候选物。

Identification of a strawberry flavor gene candidate using an integrated genetic-genomic-analytical chemistry approach.

机构信息

Horticultural Sciences Department, University of Florida, Gainesville, FL, USA.

出版信息

BMC Genomics. 2014 Apr 17;15:217. doi: 10.1186/1471-2164-15-217.

Abstract

BACKGROUND

There is interest in improving the flavor of commercial strawberry (Fragaria × ananassa) varieties. Fruit flavor is shaped by combinations of sugars, acids and volatile compounds. Many efforts seek to use genomics-based strategies to identify genes controlling flavor, and then designing durable molecular markers to follow these genes in breeding populations. In this report, fruit from two cultivars, varying for presence-absence of volatile compounds, along with segregating progeny, were analyzed using GC/MS and RNAseq. Expression data were bulked in silico according to presence/absence of a given volatile compound, in this case γ-decalactone, a compound conferring a peach flavor note to fruits.

RESULTS

Computationally sorting reads in segregating progeny based on γ-decalactone presence eliminated transcripts not directly relevant to the volatile, revealing transcripts possibly imparting quantitative contributions. One candidate encodes an omega-6 fatty acid desaturase, an enzyme known to participate in lactone production in fungi, noted here as FaFAD1. This candidate was induced by ripening, was detected in certain harvests, and correlated with γ-decalactone presence. The FaFAD1 gene is present in every genotype where γ-decalactone has been detected, and it was invariably missing in non-producers. A functional, PCR-based molecular marker was developed that cosegregates with the phenotype in F1 and BC1 populations, as well as in many other cultivars and wild Fragaria accessions.

CONCLUSIONS

Genetic, genomic and analytical chemistry techniques were combined to identify FaFAD1, a gene likely controlling a key flavor volatile in strawberry. The same data may now be re-sorted based on presence/absence of any other volatile to identify other flavor-affecting candidates, leading to rapid generation of gene-specific markers.

摘要

背景

人们对改善商业草莓(Fragaria ×ananassa)品种的风味很感兴趣。水果的风味是由糖、酸和挥发性化合物的组合形成的。许多人试图利用基于基因组学的策略来识别控制风味的基因,然后设计持久的分子标记来跟踪这些基因在育种群中的存在。在本报告中,对两个品种的果实进行了分析,这两个品种的果实存在或不存在挥发性化合物,同时还有分离的后代,使用 GC/MS 和 RNAseq 进行了分析。根据是否存在特定挥发性化合物(在这种情况下为γ-癸内酯,一种赋予果实桃味的化合物),对后代的表达数据进行了计算机批量处理。

结果

根据γ-癸内酯的存在与否对分离后代的reads 进行计算排序,排除了与挥发性物质不直接相关的转录本,揭示了可能赋予定量贡献的转录本。一个候选基因编码一种ω-6 脂肪酸去饱和酶,该酶已知参与真菌中内酯的产生,在这里被称为 FaFAD1。该候选基因受成熟诱导,在某些收获期被检测到,并与γ-癸内酯的存在相关。FaFAD1 基因存在于所有检测到γ-癸内酯的基因型中,而在非产生者中则始终缺失。开发了一种基于 PCR 的功能分子标记,该标记与 F1 和 BC1 群体中的表型共分离,也与许多其他品种和野生 Fragaria 材料共分离。

结论

遗传、基因组和分析化学技术相结合,鉴定出 FaFAD1,这是一个可能控制草莓中关键风味挥发性物质的基因。现在可以根据任何其他挥发性物质的存在与否重新对数据进行排序,以鉴定其他影响风味的候选基因,从而快速生成基因特异性标记。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19a7/4023330/3f98d71294b6/1471-2164-15-217-1.jpg

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