Evidence map›Paper›PMID 39388604›Full record

ArticleGigaScience2024

High-quality assembly of the T2T genome for Isodon rubescens f. lushanensis reveals genomic structure variations between 2 typical forms of Isodon rubescens.

Hao Yang, Conglong Lian, Jinlu Liu, Hongwei Yu, Le Zhao, Ni He, Xiuyu Liu, Shujuan Xue, Xiaoya Sun, Liping Zhang and 7 more

Abstract read
In one paragraph

Article in GigaScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. A Near-Telomere-to-Telomere Genome Assembly of the Spotted Seal (International journal of molecular sciences · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Hao YangCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.ORCID 0009-0006-0997-3994
Conglong LianCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.ORCID 0000-0002-8454-5264
Jinlu LiuCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.
Hongwei YuInstitute of Bioengineering, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, PR China.
Le ZhaoCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.ORCID 0000-0002-1213-1126
Ni HeInstitute of Bioengineering, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, PR China.
Xiuyu LiuCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.
Shujuan XueCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.
Xiaoya SunCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.
Liping ZhangCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.
Lili WangCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.
Jingfan YangCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.
Yu FuCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.
Rui MaCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.ORCID 0009-0006-7869-0947
Bao ZhangCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.
Lidan YeInstitute of Bioengineering, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, PR China.ORCID 0000-0002-6248-8457
Suiqing ChenCollege of Pharmacy, Henan Key Laboratory of Chinese Medicine Resources and Chemistry, Henan University of Chinese Medicine, Zhengzhou 450046, PR China.ORCID 0000-0003-0449-168X

Funding

National Natural Science Foundation of China 81173486
6 · The paper itself

Abstract

backgroundRabdosiae rubescentis herba (Isodon rubescens) is widely used as a folk medicine to treat esophageal cancer and sore throat in China. Its germplasm resources are abundant in China, with I. rubescens (Hemsl.) Hara and I. rubescens f. lushanensis as 2 typical forms. I. rubescens (Hemsl.) Hara is featured by biosynthesis of the diterpenoid oridonin with strong anticancer activity, while I. rubescens f. lushanensis produces another diterpenoid with anticancer activity, lushanrubescensin. However, the biosynthetic pathways of both still need to be fully understood. In particular, little is known about the genetic background of I. rubescens f. lushanensis.

findingsWe used Pacific Biosciences (PacBio) single-molecule real-time and Nanopore Ultra-long sequencing platforms, respectively, and obtained 139.07 Gb of high-quality data, with a sequencing depth of about 328×. We also obtained a high-quality reference genome for I. rubescens f. lushanensis, with a genome size of 349 Mb and a contig N50 of 28.8 Mb. The heterozygosity of the genome is 1.7% and the repeatability is 83.43%. In total, 34,865 protein-coding genes were predicted. Moreover, we found that most of the variant or unique genes in the diterpenoid synthesis pathways of I. rubescens f. lushanensis and I. rubescens (Hemsl.) Hara were enriched in diterpene synthases.

conclusionsWe provide the first genome sequence and gene annotation for the I. rubescens f. lushanensis, which provides molecular evidence for understanding the chemotypic differences of I. rubescens.

Indexed as

Genome, PlantIsodonDiterpenesGenomicsHigh-Throughput Nucleotide SequencingMolecular Sequence AnnotationDiterpenesditerpene synthaseevolutionI. rubescens f. lushanensisplant diterpenoid biosynthesistelomere-to-telomere genome sequencing

Identifiers

PMID39388604
PMCPMC11466039

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