A highly contiguous genome assembly of red perilla (Perilla frutescens) domesticated in Japan

Author:

Tamura Keita12ORCID,Sakamoto Mika3ORCID,Tanizawa Yasuhiro3ORCID,Mochizuki Takako3,Matsushita Shuji4,Kato Yoshihiro5,Ishikawa Takeshi5,Okuhara Keisuke16,Nakamura Yasukazu3ORCID,Bono Hidemasa12ORCID

Affiliation:

1. Laboratory of Genome Informatics, Graduate School of Integrated Sciences for Life, Hiroshima University , Higashi-Hiroshima, Hiroshima 739-0046 , Japan

2. Laboratory of BioDX, Genome Editing Innovation Center, Hiroshima University , Higashi-Hiroshima, Hiroshima 739-0046 , Japan

3. Genome Informatics Laboratory, Department of Informatics, National Institute of Genetics , Mishima, Shizuoka 411-8540 , Japan

4. Agricultural Technology Research Center, Hiroshima Prefectural Technology Research Institute , Higashi-Hiroshima, Hiroshima 739-0151 , Japan

5. Mishima Foods Co., Ltd. , Hiroshima City, Hiroshima 733-0036 , Japan

6. PtBio Inc. , Higashi-Hiroshima, Hiroshima 739-0046 , Japan

Abstract

Abstract Perilla frutescens (Lamiaceae) is an important herbal plant with hundreds of bioactive chemicals, among which perillaldehyde and rosmarinic acid are the two major bioactive compounds in the plant. The leaves of red perilla are used as traditional Kampo medicine or food ingredients. However, the medicinal and nutritional uses of this plant could be improved by enhancing the production of valuable metabolites through the manipulation of key enzymes or regulatory genes using genome editing technology. Here, we generated a high-quality genome assembly of red perilla domesticated in Japan. A near-complete chromosome-level assembly of P. frutescens was generated contigs with N50 of 41.5 Mb from PacBio HiFi reads. 99.2% of the assembly was anchored into 20 pseudochromosomes, among which seven pseudochromosomes consisted of one contig, while the rest consisted of less than six contigs. Gene annotation and prediction of the sequences successfully predicted 86,258 gene models, including 76,825 protein-coding genes. Further analysis showed that potential targets of genome editing for the engineering of anthocyanin pathways in P. frutescens are located on the late-stage pathways. Overall, our genome assembly could serve as a valuable reference for selecting target genes for genome editing of P. frutescens.

Funder

Hiroshima Prefectural Government

JSPS

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,General Medicine

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