Evidence map›Paper›PMID 26936896›Full record

ArticlePlant physiology2016

Heat stress yields a unique MADS box transcription factor in determining seed size and thermal sensitivity.

Chen Chen, Kevin Begcy, Kan Liu, Jing J Folsom, Zhen Wang, Chi Zhang, Harkamal Walia

Abstract read
In one paragraph

Article in Plant physiology, 2016. 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
–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

83 citing papers in PubMed.

  1. Article
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  9. A Novel OsMPK6-OsMADS47-PPKL1/3 Module Controls Grain Shape and Yield in Rice.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  10. Article
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  14. Review
  15. Characterization analyses ofFrontiers in plant science · 2025
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

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

7 authors.

Chen ChenDepartment of Agronomy and Horticulture (C.C., K.B., J.J.F., Z.W., H.W.) and School of Biological Sciences (K.L., C.Z.), University of Nebraska, Lincoln, Nebraska 68583; andKey Laboratory of Crop Genetics and Physiology of Jiangsu Province and Key Laboratory of Plant Functional Genomics of the Ministry of Education, College of Agriculture, Yangzhou University, Yangzhou 225009, China (C.C.).ORCID 0000-0002-9748-3111
Kevin BegcyDepartment of Agronomy and Horticulture (C.C., K.B., J.J.F., Z.W., H.W.) and School of Biological Sciences (K.L., C.Z.), University of Nebraska, Lincoln, Nebraska 68583; andKey Laboratory of Crop Genetics and Physiology of Jiangsu Province and Key Laboratory of Plant Functional Genomics of the Ministry of Education, College of Agriculture, Yangzhou University, Yangzhou 225009, China (C.C.).
Kan LiuDepartment of Agronomy and Horticulture (C.C., K.B., J.J.F., Z.W., H.W.) and School of Biological Sciences (K.L., C.Z.), University of Nebraska, Lincoln, Nebraska 68583; andKey Laboratory of Crop Genetics and Physiology of Jiangsu Province and Key Laboratory of Plant Functional Genomics of the Ministry of Education, College of Agriculture, Yangzhou University, Yangzhou 225009, China (C.C.).
Jing J FolsomDepartment of Agronomy and Horticulture (C.C., K.B., J.J.F., Z.W., H.W.) and School of Biological Sciences (K.L., C.Z.), University of Nebraska, Lincoln, Nebraska 68583; andKey Laboratory of Crop Genetics and Physiology of Jiangsu Province and Key Laboratory of Plant Functional Genomics of the Ministry of Education, College of Agriculture, Yangzhou University, Yangzhou 225009, China (C.C.).ORCID 0000-0002-5420-7387
Zhen WangDepartment of Agronomy and Horticulture (C.C., K.B., J.J.F., Z.W., H.W.) and School of Biological Sciences (K.L., C.Z.), University of Nebraska, Lincoln, Nebraska 68583; andKey Laboratory of Crop Genetics and Physiology of Jiangsu Province and Key Laboratory of Plant Functional Genomics of the Ministry of Education, College of Agriculture, Yangzhou University, Yangzhou 225009, China (C.C.).
Chi ZhangDepartment of Agronomy and Horticulture (C.C., K.B., J.J.F., Z.W., H.W.) and School of Biological Sciences (K.L., C.Z.), University of Nebraska, Lincoln, Nebraska 68583; andKey Laboratory of Crop Genetics and Physiology of Jiangsu Province and Key Laboratory of Plant Functional Genomics of the Ministry of Education, College of Agriculture, Yangzhou University, Yangzhou 225009, China (C.C.).
Harkamal WaliaDepartment of Agronomy and Horticulture (C.C., K.B., J.J.F., Z.W., H.W.) and School of Biological Sciences (K.L., C.Z.), University of Nebraska, Lincoln, Nebraska 68583; andKey Laboratory of Crop Genetics and Physiology of Jiangsu Province and Key Laboratory of Plant Functional Genomics of the Ministry of Education, College of Agriculture, Yangzhou University, Yangzhou 225009, China (C.C.) hwalia2@unl.edu.ORCID 0000-0002-9712-5824

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early seed development events are highly sensitive to increased temperature. This high sensitivity to a short-duration temperature spike reduces seed viability and seed size at maturity. The molecular basis of heat stress sensitivity during early seed development is not known. We selected rice (Oryza sativa), a highly heat-sensitive species, to explore this phenomenon. Here, we elucidate the molecular pathways that contribute to the heat sensitivity of a critical developmental window during which the endosperm transitions from syncytium to the cellularization stage in young seeds. A transcriptomic comparison of seeds exposed to moderate (35°C) and severe (39°C) heat stress with control (28°C) seeds identified a set of putative imprinted genes, which were down-regulated under severe heat stress. Several type I MADS box genes specifically expressed during the syncytial stage were differentially regulated under moderate and severe heat stress. The suppression and overaccumulation of these genes are associated with precocious and delayed cellularization under moderate and severe stress, respectively. We show that modulating the expression of OsMADS87, one of the heat-sensitive, imprinted genes associated with syncytial stage endosperm, regulates rice seed size. Transgenic seeds deficient in OsMADS87 exhibit accelerated endosperm cellularization. These seeds also have lower sensitivity to a moderate heat stress in terms of seed size reduction compared with seeds from wild-type plants and plants overexpressing OsMADS87 Our findings suggest that OsMADS87 and several other genes identified in this study could be potential targets for improving the thermal resilience of rice during reproductive development.

Indexed as

Cell CycleDNA Transposable ElementsEndospermGene Expression Regulation, PlantGenomic ImprintingHeat-Shock ResponseMADS Domain ProteinsOryzaPlant CellsPlant ProteinsPlants, Genetically ModifiedSeedsDNA Transposable ElementsMADS Domain ProteinsPlant Proteins

Identifiers

PMID26936896
PMCPMC4854699

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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.