Background <p>The genus <i>Isatis</i> contains medicinally important but taxonomically controversial species in China. Reliable genomic resources are urgently needed for accurate species identification and phylogenetic clarification.</p> Results <p>We assembled and characterized the complete chloroplast genomes of seven <i>Isatis</i> species. The genomes (153,260–153,872&#xa0;bp) exhibited the typical quadripartite structure. Sequence variation was heterogeneous: the small single-copy (SSC) region was the most polymorphic (12.3 single-nucleotide polymorphisms (SNPs)/kb), followed by the large single-copy (LSC, 8.9 SNPs/kb) and inverted repeat (IR, 1.7 SNPs/kb) regions. Noncoding sequences showed 3.2-fold greater polymorphism than coding sequences. The <i>rpl32–trn</i>L intergenic spacer was identified as a promising molecular marker due to its high nucleotide diversity (<i>π</i> = 0.0582). While most protein-coding genes were under strong purifying selection, <i>ycf1</i> and <i>ycf2</i> exhibited elevated substitution rates. Phylogenomic analyses strongly supported the monophyly of the tribe Isatideae and the genus <i>Isatis</i> (100% bootstrap support (BS)), validating the recent inclusion of <i>I. gymnocarpa</i> and <i>I. multicaulis</i>. We detected significant misidentification in public databases for key taxa (<i>I. costata</i>, <i>I. tinctoria</i>, <i>I. indigotica</i>). The <i>rpl32–trn</i>L spacer effectively distinguished most species but revealed the non-monophyly of <i>I. costata</i>, with one lineage being indistinguishable from <i>I. tinctoria</i>. The phylogenetic separation of the morphologically similar <i>I. minima</i> and <i>I. violascens</i> suggests potential convergent evolution.</p> Conclusion <p>Our study provides essential chloroplast genomic resources for <i>Isatis</i>. The findings not only clarify long-standing taxonomic controversies and validate recent reclassifications but also highlight the utility of the <i>rpl32–trn</i>L spacer as a powerful marker for species discrimination and evolutionary studies within this genus.</p>

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Insights into the chloroplast genome diversity of the genus Isatis in China

  • Min Wei,
  • Chengxiang Wang,
  • Yong Su,
  • Hongzhuan Shi,
  • Liangju Ma,
  • Tao Bao,
  • Qiaosheng Guo

摘要

Background

The genus Isatis contains medicinally important but taxonomically controversial species in China. Reliable genomic resources are urgently needed for accurate species identification and phylogenetic clarification.

Results

We assembled and characterized the complete chloroplast genomes of seven Isatis species. The genomes (153,260–153,872 bp) exhibited the typical quadripartite structure. Sequence variation was heterogeneous: the small single-copy (SSC) region was the most polymorphic (12.3 single-nucleotide polymorphisms (SNPs)/kb), followed by the large single-copy (LSC, 8.9 SNPs/kb) and inverted repeat (IR, 1.7 SNPs/kb) regions. Noncoding sequences showed 3.2-fold greater polymorphism than coding sequences. The rpl32–trnL intergenic spacer was identified as a promising molecular marker due to its high nucleotide diversity (π = 0.0582). While most protein-coding genes were under strong purifying selection, ycf1 and ycf2 exhibited elevated substitution rates. Phylogenomic analyses strongly supported the monophyly of the tribe Isatideae and the genus Isatis (100% bootstrap support (BS)), validating the recent inclusion of I. gymnocarpa and I. multicaulis. We detected significant misidentification in public databases for key taxa (I. costata, I. tinctoria, I. indigotica). The rpl32–trnL spacer effectively distinguished most species but revealed the non-monophyly of I. costata, with one lineage being indistinguishable from I. tinctoria. The phylogenetic separation of the morphologically similar I. minima and I. violascens suggests potential convergent evolution.

Conclusion

Our study provides essential chloroplast genomic resources for Isatis. The findings not only clarify long-standing taxonomic controversies and validate recent reclassifications but also highlight the utility of the rpl32–trnL spacer as a powerful marker for species discrimination and evolutionary studies within this genus.