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四倍体甜罗勒(Ocimum basilicum L.)基因组序列为高级基因组编辑和分子育种提供了工具。

The genome sequence of tetraploid sweet basil, Ocimum basilicum L., provides tools for advanced genome editing and molecular breeding.

机构信息

Unit of Aromatic and Medicinal Plants, Newe Ya'ar Research Center, Agricultural Research Organization, Ramat Yishay, Israel.

NRGene Ltd, Park HaMada, Ness Ziona, Israel.

出版信息

DNA Res. 2020 Dec 3;27(5). doi: 10.1093/dnares/dsaa027.

DOI:10.1093/dnares/dsaa027
PMID:33340318
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7758295/
Abstract

Sweet basil, Ocimum basilicum L., is a well-known culinary herb grown worldwide, but its uses go beyond the kitchen to traditional medicine, cosmetics and gardening. To date, the lack of an available reference genome has limited the utilization of advanced molecular breeding methods. We present a draft version of the sweet basil genome of the cultivar 'Perrie', a fresh-cut Genovese-type basil. Genome sequencing showed basil to be a tetraploid organism with a genome size of 2.13 Gbp, assembled in 12,212 scaffolds, with > 90% of the assembly being composed of 107 scaffolds. About 76% of the genome is composed of repetitive elements, with the majority being long-terminal repeats. We constructed and annotated 62,067 protein-coding genes and determined their expression in different plant tissues. We analysed the currently known phenylpropanoid volatiles biosynthesis genes. We demonstrated the necessity of the reference genome for a comprehensive understanding of this important pathway in the context of tetraploidy and gene redundancy. A complete reference genome is essential to overcome this redundancy and to avoid off-targeting when designing a CRISPR: Cas9-based genome editing research. This work bears promise for developing fast and accurate breeding tools to provide better cultivars for farmers and improved products for consumers.

摘要

甜罗勒(Ocimum basilicum L.)是一种广受欢迎的烹饪香草,在世界各地种植,但它的用途不仅限于厨房,还涉及传统医学、化妆品和园艺。迄今为止,由于缺乏可用的参考基因组,限制了先进的分子育种方法的利用。我们呈现了一个栽培品种“Perrie”甜罗勒的基因组草案版本,这是一种新鲜的 Genovese 型罗勒。基因组测序表明,罗勒是一种四倍体生物,基因组大小为 2.13 Gbp,组装成 12,212 个支架,>90%的组装由 107 个支架组成。大约 76%的基因组由重复元件组成,其中大部分是长末端重复。我们构建并注释了 62,067 个蛋白质编码基因,并确定了它们在不同植物组织中的表达情况。我们分析了目前已知的苯丙烷类挥发性生物合成基因。我们证明了参考基因组对于全面了解四倍体和基因冗余背景下这一重要途径的必要性。完整的参考基因组对于克服这种冗余和避免在设计基于 CRISPR:Cas9 的基因组编辑研究时的脱靶至关重要。这项工作有望开发快速准确的育种工具,为农民提供更好的品种,并为消费者提供改进的产品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90da/7758295/3d4f64d0dd61/dsaa027f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90da/7758295/62672d025b6b/dsaa027f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90da/7758295/9f2487186873/dsaa027f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90da/7758295/dc4eaea2da19/dsaa027f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90da/7758295/3d4f64d0dd61/dsaa027f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90da/7758295/62672d025b6b/dsaa027f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90da/7758295/9f2487186873/dsaa027f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90da/7758295/dc4eaea2da19/dsaa027f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90da/7758295/3d4f64d0dd61/dsaa027f4.jpg

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