These reference assemblies place the P. frutescens mitogenome in a close-relative context and document structural differences among the sampled representatives to provide a comparative organellar resource for future validation in broader accession panels.
Abstract
Perilla frutescens
(L.) Britton is an economically important aromatic industrial crop in East Asia and an increasingly important target for genomic resource development and germplasm improvement. Research has focused largely on metabolomics, nuclear genomes, and plastomes, and the published
P. frutescens
mitogenome has not been compared systematically with those of close relatives.
We assembled, annotated, and compared mitogenomes from five sampled representatives:
P. frutescens
,
Keiskea sinensis
Diels,
Mosla soochouensis
Matsuda,
M. chinensis
Maxim., and the
M. chinensis
cultivar ‘Jiangxiangru’. The analysis used PacBio HiFi reads for
P. frutescens
and
K. sinensis
, together with publicly available PacBio reads for the three sampled
Mosla
representatives. The assembled mitochondrial genomes ranged in size from 299,551 to 347,981 bp, whereas GC content varied narrowly (44.8–45.2%). Gene content was broadly similar among the sampled representatives, whereas structural features were more variable. Dispersed repeats occupied 6.65–17.77% of the mitogenomes. In pairwise comparisons with the other four sampled mitogenomes, collinear blocks covered 39–68% of the sampled
P. frutescens
mitogenome. Candidate mitochondrial plastid DNA sequences (MTPTs) were detected in all five mitogenomes but differed in number, length, and sequence identity to the corresponding plastome. We predicted 282–374 candidate RNA-editing sites per sampled mitogenome, most involving C-to-U changes. Plastid and mitochondrial trees agreed for the focal representatives but differed at broader taxonomic levels.
These reference assemblies place the
P. frutescens
mitogenome in a close-relative context and document structural differences among the sampled representatives. They provide a comparative organellar resource for future validation in broader accession panels.
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