Evidence map›Paper›PMID 23267064›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition.

Akiko Yoshida, Masafumi Sasao, Naoko Yasuno, Kyoko Takagi, Yasufumi Daimon, Ruihong Chen, Ryo Yamazaki, Hiroki Tokunaga, Yoshinori Kitaguchi, Yutaka Sato and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed
7.2field-weighted citation impact, top 3% 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

117 citing papers in PubMed, 290 citations in OpenAlex.

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  10. Harnessing neo-domestication of wild pigmented rice for enhanced nutrition and sustainable agriculture.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025
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  11. Characterization and Expression Analysis of thePlants (Basel, Switzerland) · 2025
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  13. Genome-wide identification and characterization ofFrontiers in plant science · 2025
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57 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

16 authors at 5 institutions in 1 country.

Akiko YoshidaGraduate School of Agriculture and Life Sciences, The University of Tokyo, Yayoi, Bunkyo, Tokyo 113-8657, Japan.
Masafumi Sasao
Naoko Yasuno
Kyoko Takagi
Yasufumi Daimon
Ruihong Chen
Ryo Yamazaki
Hiroki Tokunaga
Yoshinori Kitaguchi
Yutaka Sato
Yoshiaki Nagamura
Tomokazu Ushijima
Toshihiro Kumamaru
Shigeru Iida
Masahiko Maekawa
Junko Kyozuka
The University of Tokyo · JPInstitute of Agrobiological Sciences · JPNational Institute for Basic Biology · JPKyushu University · JPOkayama University · JP

Funding

UC Davis Clinical and Translational Science CenterUL1TR000002 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BERGLUND, LARS F · 2012 to 2015
$12.2M
NCATS NIH HHS UL1 TR000002
6 · The paper itself

Abstract

Inflorescence structures result from the activities of meristems, which coordinate both the renewal of stem cells in the center and organ formation at the periphery. The fate of a meristem is specified at its initiation and changes as the plant develops. During rice inflorescence development, newly formed meristems acquire a branch meristem (BM) identity, and can generate further meristems or terminate as spikelets. Thus, the form of rice inflorescence is determined by a reiterative pattern of decisions made at the meristems. In the dominant gain-of-function mutant tawawa1-D, the activity of the inflorescence meristem (IM) is extended and spikelet specification is delayed, resulting in prolonged branch formation and increased numbers of spikelets. In contrast, reductions in TAWAWA1 (TAW1) activity cause precocious IM abortion and spikelet formation, resulting in the generation of small inflorescences. TAW1 encodes a nuclear protein of unknown function and shows high levels of expression in the shoot apical meristem, the IM, and the BMs. TAW1 expression disappears from incipient spikelet meristems (SMs). We also demonstrate that members of the SHORT VEGETATIVE PHASE subfamily of MADS-box genes function downstream of TAW1. We thus propose that TAW1 is a unique regulator of meristem activity in rice and regulates inflorescence development through the promotion of IM activity and suppression of the phase change to SM identity.

Indexed as

DNA Transposable ElementsFluorescenceGene Expression ProfilingGene Expression Regulation, PlantInflorescenceIn Situ HybridizationMADS Domain ProteinsMeristemNuclear ProteinsOryzaPlant ProteinsReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionDNA Transposable ElementsMADS Domain ProteinsNuclear ProteinsPlant Proteins

Identifiers

PMID23267064
PMCPMC3545824
OpenAlexW1999459967

What OpenQuestion holds

Textmetadata
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.