Cytonuclear interactions modulate the plasticity of photosynthetic rhythmicity and growth in wild barley

Author:

Tiwari Lalit Dev1,Bdolach Eyal12,Prusty Manas Ranjan1,Bodenheimer Schewach13,Be'ery Avital1,Faigenboim‐Doron Adi1,Yamamoto Eiji4,Panzarová Klára5,Kashkush Khalil2,Shental Noam6,Fridman Eyal1ORCID

Affiliation:

1. Plant Sciences Institute, Volcani Agricultural Research Organization (ARO) Bet Dagan Israel

2. Department of Life Sciences Ben‐Gurion University Beer‐Sheva Israel

3. The Robert H. Smith Institute of Plant Sciences and Genetics in Agriculture The Hebrew University of Jerusalem Rehovot Israel

4. Graduate School of Agriculture Meiji University Kawasaki Kanagawa Japan

5. PSI (Photon Systems Instruments), Ltd. Czech Republic

6. Department of Mathematics and Computer Science The Open University of Israel Raanana Israel

Abstract

AbstractIn plants, the contribution of the plasmotype (mitochondria and chloroplast) in controlling the circadian clock plasticity and possible consequences on cytonuclear genetic makeup have yet to be fully elucidated. A genome‐wide association study in the wild barley (Hordeum vulgare ssp. spontaneum) B1K collection identified overlap with our previously mapped DRIVERS OF CLOCKS (DOCs) loci in wild‐cultivated interspecific population. Moreover, we identified non‐random segregation and epistatic interactions between nuclear DOCs loci and the chloroplastic RpoC1 gene, indicating an adaptive value for specific cytonuclear gene combinations. Furthermore, we show that DOC1.1, which harbours the candidate SIGMA FACTOR‐B (SIG‐B) gene, is linked with the differential expression of SIG‐B and CCA1 genes and contributes to the circadian gating response to heat. High‐resolution temporal growth and photosynthesis measurements of B1K also link the DOCs loci to differential growth, Chl content and quantum yield. To validate the involvement of the Plastid encoded polymerase (PEP) complex, we over‐expressed the two barley chloroplastic RpoC1 alleles in Arabidopsis and identified significant differential plasticity under elevated temperatures. Finally, enhanced clock plasticity of de novo ENU (N‐Ethyl‐N‐nitrosourea) ‐induced barley rpoB1 mutant further implicates the PEP complex as a key player in regulating the circadian clock output. Overall, this study highlights the contribution of specific cytonuclear interaction between rpoC1 (PEP gene) and SIG‐B with distinct circadian timing regulation under heat, and their pleiotropic effects on growth implicate an adaptive value.

Funder

Israel Science Foundation

Horizon 2020 Framework Programme

Publisher

Wiley

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