Evidence map›Paper›PMID 42556408›Full record

ArticlePhysiologia plantarum

Multi-Omics Reveal Haplotype-Specific BGC Divergence and Organ-Specific Iridoid Glycoside Accumulation in Endemic Species Rehmannia chingii.

Wanbo Zhang, Ying Han, Xinjie Jin, Ke Guo, Xiaowen Jia, Haifeng Wang, Fang Bai, Huijun Bai, Pan Li, Wei Du and 3 more

Abstract read
In one paragraph

Article in Physiologia plantarum. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Wanbo ZhangCollege of Life and Environmental Science, Wenzhou University, Wenzhou, China.ORCID https://orcid.org/0000-0003-2995-2606
Ying HanCollege of Life and Environmental Science, Wenzhou University, Wenzhou, China.
Xinjie JinCollege of Life and Environmental Science, Wenzhou University, Wenzhou, China.ORCID https://orcid.org/0000-0003-3733-1957
Ke GuoCollege of Life and Environmental Science, Wenzhou University, Wenzhou, China.
Xiaowen JiaCollege of Life and Environmental Science, Wenzhou University, Wenzhou, China.
Haifeng WangCollege of Life and Environmental Science, Wenzhou University, Wenzhou, China.
Fang BaiCollege of Life and Environmental Science, Wenzhou University, Wenzhou, China.
Huijun BaiCollege of Life and Environmental Science, Wenzhou University, Wenzhou, China.
Pan LiKey Laboratory of Biodiversity and Environment on the Qinghai-Tibetan Plateau, Ministry of Education, School of Ecology and Environment, Tibet University, Lhasa, China.ORCID https://orcid.org/0000-0002-9407-7740
Wei DuCollege of Life Sciences, Wuhan University, Wuhan, Hubei, China.
Yifan JiangCollege of Horticulture, Nanjing Agricultural University, Nanjing, China.ORCID https://orcid.org/0000-0002-9737-2542
Shanshan ZhuSchool of Marine Sciences, Ningbo University, Ningbo, China.ORCID https://orcid.org/0000-0003-1582-1007
Yonghua ZhangCollege of Life and Environmental Science, Wenzhou University, Wenzhou, China.ORCID https://orcid.org/0000-0002-2676-9059

Funding

the National Natural Science Foundation of China 31800309the National Natural Science Foundation of China 32001086Zhejiang Provincial Key R&D Program 2023C03138Zhejiang Provincial Natural Science Foundation of China LY21C030002
6 · The paper itself

Abstract

Iridoid glycosides (IGs) are key bioactive metabolites within the genus Rehmannia. However, the molecular mechanisms underlying geographical and organ-specific divergence in IG accumulation, and the biosynthetic gene clusters (BGCs) between chromosomal haplotypes, remain poorly understood in Rehmannia chingii, an endemic species in eastern China. Here, we performed a series of analyses using a high-quality, haplotype-resolved genome assembly of R. chingii from the Tianmu Mountain. Combined with the known widely targeted metabolomic profiles, seven differentially accumulated IGs were identified. Due to the higher data completeness of the second haplotype (Haplotype II: 1.1696 Gb), it was selected as the reference genome for transcriptomic analysis to ensure a reliable quantification of the expression levels of core synthase genes. Building upon these multi-omics findings, a putative IG biosynthetic gene cluster on Chr 11 in Haplotype II was further identified, which includes TPS-g, G10H, CYP76, CYP704B, and ADH genes. In contrast, the corresponding region on Chr 11 in Haplotype I (1.1573 Gb) was inferred to constitute a putative fatty acid-terpene biosynthetic gene cluster, primarily due to the presence of a BAHD acyltransferase gene at the distal end of the cluster. Collectively, this study provides comprehensive genomic and metabolic resources for investigating IG biosynthesis in R. chingii from two distinct geographical populations. Our results highlight haplotype-specific divergence in BGC architecture on Chr 11 and provide insights into the regulatory mechanisms underlying organ- and geographic population-specific metabolic variation. These findings also establish a foundation for the conservation and rational utilization of R. chingii germplasm resources.

Indexed as

Iridoid GlycosidesRehmanniaGene Expression Regulation, PlantHaplotypesMultigene FamilyMultiomicsOrgan SpecificityIridoid Glycosides

Identifiers

PMID42556408
PMCPMC13441488

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.