Evidence map›Paper›PMID 38053331›Full record

ArticlePlant communications2024

The APETALA2-MYBL2 module represses proanthocyanidin biosynthesis by affecting formation of the MBW complex in seeds of Arabidopsis thaliana.

Wenbo Jiang, Qinggang Yin, Jinyue Liu, Xiaojia Su, Xiaoyan Han, Qian Li, Jin Zhang, Yongzhen Pang

Open access · goldAbstract read
In one paragraph

Article in Plant communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  14. Genome-wide identification ofFrontiers in plant science · 2025
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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

8 authors at 2 institutions in 1 country.

Wenbo JiangInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China. Electronic address: jiangwenbo@caas.cn.
Qinggang YinKey Laboratory of Plant Resources and Beijing Botanical Garden, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China.
Jinyue LiuKey Laboratory of Plant Resources and Beijing Botanical Garden, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China.
Xiaojia SuKey Laboratory of Plant Resources and Beijing Botanical Garden, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China.
Xiaoyan HanKey Laboratory of Plant Resources and Beijing Botanical Garden, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China.
Qian LiInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Jin ZhangInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Yongzhen PangInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China. Electronic address: pangyongzhen@caas.cn.
Chinese Academy of Agricultural Sciences · CNChinese Academy of Sciences · CN

Funding

Non-US Government Research Support type
6 · The paper itself

Abstract

Proanthocyanidins (PAs) are the second most abundant plant phenolic natural products. PA biosynthesis is regulated by the well-documented MYB/bHLH/WD40 (MBW) complex, but how this complex itself is regulated remains ill defined. Here, in situ hybridization and β-glucuronidase staining show that APETALA2 (AP2), a well-defined regulator of flower and seed development, is strongly expressed in the seed coat endothelium, where PAs accumulate. AP2 negatively regulates PA content and expression levels of key PA pathway genes. AP2 activates MYBL2 transcription and interacts with MYBL2, a key suppressor of the PA pathway. AP2 exerts its function by directly binding to the AT-rich motifs near the promoter region of MYBL2. Molecular and biochemical analyses revealed that AP2 forms AP2-MYBL2-TT8/EGL3 complexes, disrupting the MBW complex and thereby repressing expression of ANR, TT12, TT19, and AHA10. Genetic analyses revealed that AP2 functions upstream of MYBL2, TT2, and TT8 in PA regulation. Our work reveals a new role of AP2 as a key regulator of PA biosynthesis in Arabidopsis. Overall, this study sheds new light on the comprehensive regulation network of PA biosynthesis as well as the dual regulatory roles of AP2 in seed development and accumulation of major secondary metabolites in Arabidopsis.

Indexed as

ArabidopsisArabidopsis ProteinsProanthocyanidinsBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsHomeodomain ProteinsSeedsTranscription FactorsAPETALA2 protein, ArabidopsisArabidopsis ProteinsAtmybL2 protein, ArabidopsisBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsHomeodomain ProteinsProanthocyanidinsTranscription Factors

Identifiers

PMID38053331
PMCPMC10943577
OpenAlexW4389340652

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.