Evidence map›Paper›PMID 32552824›Full record

ArticleBMC biology2020

Tandem gene duplications drive divergent evolution of caffeine and crocin biosynthetic pathways in plants.

Zhichao Xu, Xiangdong Pu, Ranran Gao, Olivia Costantina Demurtas, Steven J Fleck, Michaela Richter, Chunnian He, Aijia Ji, Wei Sun, Jianqiang Kong and 12 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
8.0field-weighted citation impact, top 2% of its field
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

83 citing papers in PubMed, 155 citations in OpenAlex.

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  12. Evolutionary adaptation of CCD4 enzymes inFrontiers in plant science · 2026
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23 more citing papers are in PubMed but not listed here.

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

22 authors at 7 institutions in 6 countries.

Zhichao XuKey Lab of Chinese Medicine Resources Conservation, State Administration of Traditional Chinese Medicine of the People's Republic of China, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China.
Xiangdong PuKey Lab of Chinese Medicine Resources Conservation, State Administration of Traditional Chinese Medicine of the People's Republic of China, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China.
Ranran GaoKey Lab of Chinese Medicine Resources Conservation, State Administration of Traditional Chinese Medicine of the People's Republic of China, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China.
Olivia Costantina DemurtasItalian National Agency for New Technologies, Energy and Sustainable Economic Development (ENEA), Casaccia Res. Ctr, 00123, Rome, Italy.
Steven J FleckDepartment of Biological Sciences, University at Buffalo, Buffalo, NY, 14260, USA.
Michaela RichterDepartment of Biological Sciences, University at Buffalo, Buffalo, NY, 14260, USA.
Chunnian HeKey Lab of Chinese Medicine Resources Conservation, State Administration of Traditional Chinese Medicine of the People's Republic of China, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China.
Aijia JiKey Lab of Chinese Medicine Resources Conservation, State Administration of Traditional Chinese Medicine of the People's Republic of China, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China.
Wei SunInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, 100700, China.
Jianqiang KongInstitute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, China.
Kaizhi HuChongqing Institute of Medicinal Plant Cultivation, Chongqing, 408435, China.
Fengming RenKey Lab of Chinese Medicine Resources Conservation, State Administration of Traditional Chinese Medicine of the People's Republic of China, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China.
Jiejie SongCollege of Life Sciences, Qingdao Agricultural University, Qingdao, 266109, China.
Zhe WangInstitute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, China.
Ting GaoCollege of Life Sciences, Qingdao Agricultural University, Qingdao, 266109, China.
Chao XiongInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, 100700, China.
Haoying YuKey Lab of Chinese Medicine Resources Conservation, State Administration of Traditional Chinese Medicine of the People's Republic of China, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China.
Tianyi XinKey Lab of Chinese Medicine Resources Conservation, State Administration of Traditional Chinese Medicine of the People's Republic of China, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China.
Victor A AlbertDepartment of Biological Sciences, University at Buffalo, Buffalo, NY, 14260, USA.
Giovanni GiulianoItalian National Agency for New Technologies, Energy and Sustainable Economic Development (ENEA), Casaccia Res. Ctr, 00123, Rome, Italy. giovanni.giuliano@enea.it.
Shilin ChenEngineering Research Center of Chinese Medicine Resource, Ministry of Education, Beijing, 100193, China. slchen@icmm.ac.cn.
Jingyuan SongKey Lab of Chinese Medicine Resources Conservation, State Administration of Traditional Chinese Medicine of the People's Republic of China, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China. jysong@implad.ac.cn.ORCID 0000-0003-2733-0416
Chinese Academy of Medical Sciences & Peking Union Medical College · CNQingdao Agricultural University · CNMinistry of Education of the People's Republic of China · CNNational Agency for New Technologies, Energy and Sustainable Economic Development · ITUniversity at Buffalo, State University of New York · USInstitute of Medicinal Plant Development · CNNanyang Technological University · SG

Funding

CAMS Innovation Fund for Medical Sciences 2016-I2M-3-016EU grant DISCO 613513National Natural Science Foundation of China 81973424National Science Foundation 1442190
6 · The paper itself

Abstract

backgroundPlants have evolved a panoply of specialized metabolites that increase their environmental fitness. Two examples are caffeine, a purine psychotropic alkaloid, and crocins, a group of glycosylated apocarotenoid pigments. Both classes of compounds are found in a handful of distantly related plant genera (Coffea, Camellia, Paullinia, and Ilex for caffeine; Crocus, Buddleja, and Gardenia for crocins) wherein they presumably evolved through convergent evolution. The closely related Coffea and Gardenia genera belong to the Rubiaceae family and synthesize, respectively, caffeine and crocins in their fruits.

resultsHere, we report a chromosomal-level genome assembly of Gardenia jasminoides, a crocin-producing species, obtained using Oxford Nanopore sequencing and Hi-C technology. Through genomic and functional assays, we completely deciphered for the first time in any plant the dedicated pathway of crocin biosynthesis. Through comparative analyses with Coffea canephora and other eudicot genomes, we show that Coffea caffeine synthases and the first dedicated gene in the Gardenia crocin pathway, GjCCD4a, evolved through recent tandem gene duplications in the two different genera, respectively. In contrast, genes encoding later steps of the Gardenia crocin pathway, ALDH and UGT, evolved through more ancient gene duplications and were presumably recruited into the crocin biosynthetic pathway only after the evolution of the GjCCD4a gene.

conclusionsThis study shows duplication-based divergent evolution within the coffee family (Rubiaceae) of two characteristic secondary metabolic pathways, caffeine and crocin biosynthesis, from a common ancestor that possessed neither complete pathway. These findings provide significant insights on the role of tandem duplications in the evolution of plant specialized metabolism.

Indexed as

Evolution, MolecularGene DuplicationBiosynthetic PathwaysCaffeineCarotenoidsGardeniaGenome, PlantCaffeineCarotenoidscrocinAldehyde dehydrogenasesCaffeine biosynthesisCarotenoid cleavage dioxygenasesCoffea canephoraCrocin biosynthesisGardenia jasminoidesGenomicsN-MethyltransferasesUDP-glucosyltransferases

Identifiers

PMID32552824
PMCPMC7302004
OpenAlexW3036938386

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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 OpenQuestion graph.