Evidence map›Paper›PMID 24391508›Full record

ArticlePLoS genetics2014

ADP1 affects plant architecture by regulating local auxin biosynthesis.

Ruixi Li, Jieru Li, Shibai Li, Genji Qin, Ondřej Novák, Aleš Pěnčík, Karin Ljung, Takashi Aoyama, Jingjing Liu, Angus Murphy and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
7.0field-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

27 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
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  9. Frontiers in plant science · 2022
    Article
  10. Article
  11. qTGW12a, a naturally varying QTL, regulates grain weight in rice.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2021
    Article
  12. Article
  13. Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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  16. Review
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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

13 authors at 7 institutions in 5 countries.

Ruixi LiState Key Laboratory of Protein and Plant Gene Research, Peking-Yale Joint Research Center for Plant Molecular Genetics and AgroBiotechnology, Peking-Tsinghua Center for Life Sciences, College of Life Sciences, Peking University, Beijing, People's Republic of China.
Jieru LiState Key Laboratory of Protein and Plant Gene Research, Peking-Yale Joint Research Center for Plant Molecular Genetics and AgroBiotechnology, Peking-Tsinghua Center for Life Sciences, College of Life Sciences, Peking University, Beijing, People's Republic of China.
Shibai LiState Key Laboratory of Protein and Plant Gene Research, Peking-Yale Joint Research Center for Plant Molecular Genetics and AgroBiotechnology, Peking-Tsinghua Center for Life Sciences, College of Life Sciences, Peking University, Beijing, People's Republic of China.
Genji QinState Key Laboratory of Protein and Plant Gene Research, Peking-Yale Joint Research Center for Plant Molecular Genetics and AgroBiotechnology, Peking-Tsinghua Center for Life Sciences, College of Life Sciences, Peking University, Beijing, People's Republic of China.
Ondřej NovákDepartment of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden ; Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Šlechtitelů 21, Olomouc, Czech Republic.
Aleš PěnčíkDepartment of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
Karin LjungDepartment of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
Takashi AoyamaInstitute for Chemical Research, Kyoto University, Gokasho Uji, Kyoto, Japan.
Jingjing LiuState Key Laboratory of Protein and Plant Gene Research, Peking-Yale Joint Research Center for Plant Molecular Genetics and AgroBiotechnology, Peking-Tsinghua Center for Life Sciences, College of Life Sciences, Peking University, Beijing, People's Republic of China.
Angus MurphyDepartment of Horticulture and Landscape Architecture, Purdue University, West Lafayette, Indiana, United States of America.
Hongya GuState Key Laboratory of Protein and Plant Gene Research, Peking-Yale Joint Research Center for Plant Molecular Genetics and AgroBiotechnology, Peking-Tsinghua Center for Life Sciences, College of Life Sciences, Peking University, Beijing, People's Republic of China ; National Plant Gene Research Center (Beijing), Beijing, People's Republic of China.
Tomohiko TsugeInstitute for Chemical Research, Kyoto University, Gokasho Uji, Kyoto, Japan.
Li-Jia QuState Key Laboratory of Protein and Plant Gene Research, Peking-Yale Joint Research Center for Plant Molecular Genetics and AgroBiotechnology, Peking-Tsinghua Center for Life Sciences, College of Life Sciences, Peking University, Beijing, People's Republic of China ; National Plant Gene Research Center (Beijing), Beijing, People's Republic of China.
Center for Life Sciences · CNPeking University · CNUmeå Plant Science Centre · SEKyoto University · JPKyoto University Institute for Chemical ResearchPurdue University West Lafayette · USSwedish University of Agricultural Sciences · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant architecture is one of the key factors that affect plant survival and productivity. Plant body structure is established through the iterative initiation and outgrowth of lateral organs, which are derived from the shoot apical meristem and root apical meristem, after embryogenesis. Here we report that ADP1, a putative MATE (multidrug and toxic compound extrusion) transporter, plays an essential role in regulating lateral organ outgrowth, and thus in maintaining normal architecture of Arabidopsis. Elevated expression levels of ADP1 resulted in accelerated plant growth rate, and increased the numbers of axillary branches and flowers. Our molecular and genetic evidence demonstrated that the phenotypes of plants over-expressing ADP1 were caused by reduction of local auxin levels in the meristematic regions. We further discovered that this reduction was probably due to decreased levels of auxin biosynthesis in the local meristematic regions based on the measured reduction in IAA levels and the gene expression data. Simultaneous inactivation of ADP1 and its three closest homologs led to growth retardation, relative reduction of lateral organ number and slightly elevated auxin level. Our results indicated that ADP1-mediated regulation of the local auxin level in meristematic regions is an essential determinant for plant architecture maintenance by restraining the outgrowth of lateral organs.

Indexed as

ArabidopsisArabidopsis ProteinsFlowersGene Expression Regulation, PlantIndoleacetic AcidsMeristemOrganic Cation Transport ProteinsPlant RootsPlant ShootsArabidopsis ProteinsAt4g29140 protein, ArabidopsisIndoleacetic AcidsOrganic Cation Transport Proteins

Identifiers

PMID24391508
PMCPMC3879159
OpenAlexW2055071483

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.