Evidence map›Paper›PMID 36588161›Full record

ArticleBMC plant biology2023

Maize cytolines as models to study the impact of different cytoplasms on gene expression under heat stress conditions.

Ioana V Ardelean, Loredana Bălăcescu, Oana Sicora, Ovidiu Bălăcescu, Lia Mladin, Voichița Haș, Mihai Miclăuș

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Article in BMC plant biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Ioana V ArdeleanBiological Research Center, "Babeș-Bolyai" University, Jibou, Romania.
Loredana BălăcescuThe Oncology Institute "Prof Dr Ion Chiricuta", Cluj-Napoca, Romania.
Oana SicoraBiological Research Center, "Babeș-Bolyai" University, Jibou, Romania.
Ovidiu BălăcescuThe Oncology Institute "Prof Dr Ion Chiricuta", Cluj-Napoca, Romania.
Lia MladinBiological Research Center, "Babeș-Bolyai" University, Jibou, Romania.
Voichița HașAgricultural Research and Development Station, Turda, Romania.
Mihai MiclăușNIRDBS, Institute of Biological Research, Cluj-Napoca, Romania. mihai.miclaus@icbcluj.ro.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCrops are under constant pressure due to global warming, which unfolds at a much faster pace than their ability to adapt through evolution. Agronomic traits are linked to cytoplasmic-nuclear genome interactions. It thus becomes important to understand the influence exerted by the organelles on gene expression under heat stress conditions and profit from the available genetic diversity. Maize (Zea mays) cytolines allow us to investigate how the gene expression changes under heat stress conditions in three different cytoplasmic environments, but each having the same nucleus. Analyzing retrograde signaling in such an experimental set-up has never been done before. Here, we quantified the response of three cytolines to heat stress as differentially expressed genes (DEGs), and studied gene expression patterns in the context of existing polymorphism in their organellar genomes.

resultsOur study unveils a plethora of new genes and GO terms that are differentially expressed or enriched, respectively, in response to heat stress. We report 19,600 DEGs as responding to heat stress (out of 30,331 analyzed), which significantly enrich 164 GO biological processes, 30 GO molecular functions, and 83 GO cell components. Our approach allowed for the discovery of a significant number of DEGs and GO terms that are not common in the three cytolines and could therefore be linked to retrograde signaling. Filtering for DEGs with a fold regulation > 2 (absolute values) that are exclusive to just one of the cytolines, we find a total of 391 up- and down-DEGs. Similarly, there are 19 GO terms with a fold enrichment > 2 that are cytoline-specific. Using GBS data we report contrasting differences in the number of DEGs and GO terms in each cytoline, which correlate with the genetic distances between the mitochondrial genomes (but not chloroplast) and the original nuclei of the cytolines, respectively.

conclusionsThe experimental design used here adds a new facet to the paradigm used to explain how gene expression changes in response to heat stress, capturing the influence exerted by different organelles upon one nucleus rather than investigating the response of several nuclei in their innate cytoplasmic environments.

Indexed as

Heat-Shock ResponseZea maysCytoplasmGene ExpressionGene Expression ProfilingGene Expression Regulation, PlantPhenotypeGene expression profilingHeat-shock responseOrganellesRetrograde signalingZea mays

Identifiers

PMID36588161
PMCPMC9806912

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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.