Evidence map›Paper›PMID 36723676›Full record

ArticlePlant cell reports2023

Comparative transcriptomics and co-expression networks reveal cultivar-specific molecular signatures associated with reproductive-stage cold stress in rice.

Yuan Niu, Song Fan, Baoshan Cheng, Henan Li, Jiang Wu, Hongliang Zhao, Zhiwei Huang, Feiyu Yan, Bo Qi, Linqing Zhang and 1 more

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Article in Plant cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Yuan Niu *School of Life Science and Food Engineering, Huaiyin Institute of Technology, Huai'an, 223003, China.
Song Fan *School of Life Science and Food Engineering, Huaiyin Institute of Technology, Huai'an, 223003, China.
Baoshan ChengHuaiyin Institute of Agricultural Science in Xuhuai Region of Jiangsu Province, Huai'an, 223001, China. bs_cheng1981@163.com.
Henan LiShanghai Bioelectronica Limited Liability Company, Shanghai, 200131, China.
Jiang WuSchool of Life Science and Food Engineering, Huaiyin Institute of Technology, Huai'an, 223003, China.
Hongliang ZhaoSchool of Life Science and Food Engineering, Huaiyin Institute of Technology, Huai'an, 223003, China.
Zhiwei HuangSchool of Life Science and Food Engineering, Huaiyin Institute of Technology, Huai'an, 223003, China.
Feiyu YanSchool of Life Science and Food Engineering, Huaiyin Institute of Technology, Huai'an, 223003, China.
Bo QiSchool of Life Science and Food Engineering, Huaiyin Institute of Technology, Huai'an, 223003, China.
Linqing ZhangSchool of Life Science and Food Engineering, Huaiyin Institute of Technology, Huai'an, 223003, China.
Guoliang ZhangSchool of Life Science and Food Engineering, Huaiyin Institute of Technology, Huai'an, 223003, China. hgzgl@sina.com.ORCID http://orcid.org/0000-0002-3294-2356

Funding

Département Caractérisation et Élaboration des Produits Issus de lta'Agriculture, Institut National de la Recherche Agronomique Grant No. 2021-ZYXT-02-1Doctoral Start-up Fund of Huaiyin Institute of Technology Grant No. Z301B16523Industry-university-research Cooperation Project of Jiangsu Province Grant No. BY2021382Jiangsu Overseas Visiting Scholar Program for University Prominent Young and Middle-aged Teachers Grant No. 2017Key Laboratory for Palygorskite Science and Applied Technology of Jiangsu Province Grant No. 134Key Projects of Key research and Development Programs of Jiangsu Province Grant No. BE2021323National Natural Science Foundation of China 31271639National Natural Science Foundation of China 31771736Rural Revitalization Project of Huai'an Grant No. HAN202112State Key Laboratory of Soil and Sustainable Agriculture Grant No. Y052010016the Natural Science Foundation of Jiangsu Province Grant No. BK20201068
6 · The paper itself

Abstract

key messageThe resistance of Huaidao5 results from the high constitutive expression of tolerance genes, while that of Huaidao9 is due to the cold-induced resistance in flag leaves and panicles. The regulation mechanism of rice seedlings' cold tolerance is relatively clear, and knowledge of its underlying mechanisms at the reproductive stage is limited. We performed differential expression and co-expression network analyses to transcriptomes from panicle and flag leaf tissues of a cold-tolerant cultivar (Huaidao5), and a sensitive cultivar (Huaidao9), under reproductive-stage cold stress. The results revealed that the expression levels of genes in stress-related pathways such as MAPK signaling pathway, diterpenoid biosynthesis, glutathione metabolism, plant-pathogen interaction and plant hormone signal transduction were constitutively highly expressed in Huaidao5, especially in panicles. Moreover, the Hudaidao5's panicle sample-specific (under cold) module contained some genes related to rice yield, such as GW5L, GGC2, SG1 and CTPS1. However, the resistance of Huaidao9 was derived from the induced resistance to cold in flag leaves and panicles. In the flag leaves, the responses included a series of stress response and signal transduction, while in the panicles nitrogen metabolism was severely affected, especially 66 endosperm-specific genes. Through integrating differential expression with co-expression networks, we predicted 161 candidate genes (79 cold-responsive genes common to both cultivars and 82 cold-tolerance genes associated with differences in cold tolerance between cultivars) potentially affecting cold response/tolerance, among which 85 (52.80%) were known to be cold-related genes. Moreover, 52 (65.82%) cold-responsive genes (e.g., TIFY11C, LSK1 and LPA) could be confirmed by previous transcriptome studies and 72 (87.80%) cold-tolerance genes (e.g., APX5, OsFbox17 and OsSTA109) were located within QTLs associated with cold tolerance. This study provides an efficient strategy for further discovery of mechanisms of cold tolerance in rice.

Indexed as

Cold-Shock ResponseOryzaCold TemperatureGene Expression ProfilingGene Expression Regulation, PlantGenotypeTranscriptomeCo-expression networkCold toleranceReproductive stageRiceTranscriptome

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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.