Abstract

Genetic novelties are important nucleators of adaptive speciation. Transgressive segregation is a major mechanism that creates genetic novelties with morphological and developmental attributes that confer adaptive advantages in certain environments. This study examined the morpho-developmental and physiological profiles of recombinant inbred lines (RILs) from the salt-sensitive IR29 and salt-tolerant Pokkali rice, representing the total range of salt tolerance including the outliers at both ends of the spectrum. Morpho-developmental and physiological profiles were integrated with a hypothesis-driven interrogation of mRNA and miRNA transcriptomes to uncover the critical genetic networks that have been rewired for novel adaptive architecture. The transgressive super-tolerant FL510 had a characteristic small tiller angle and wider, more erect, sturdier, and darker green leaves. This unique morphology resulted in lower transpiration rate, which also conferred a special ability to retain water more efficiently for osmotic avoidance. The unique ability for water retention conferred by such adaptive morphology appeared to enhance the efficacy of defenses mediated by Na+ exclusion mechanism (SalTol-effects) inherited from Pokkali. The super-tolerant FL510 and super-sensitive FL499 had the smallest proportions of differentially expressed genes with little overlaps. Genes that were steadily upregulated in FL510 comprised a putative cytokinin-regulated genetic network that appeared to maintain robust growth under salt stress through well-orchestrated cell wall biogenesis and cell expansion, likely through major regulatory (OsRR23, OsHK5) and biosynthetic (OsIPT9) genes in the cytokinin signaling pathway. Meanwhile, a constitutively expressed cluster in FL510 prominently featured two transcription factors (OsIBH1, TAC3) that control tiller angle and growth habit through the brassinosteroid signaling pathway. Both the putative cytokinin-mediated and brassinosteroid-mediated clusters appeared to function as highly coordinated network synergies in FL510. In contrast, both networks appeared to be sub-optimal and inferior in the other RILs and parents as they were disjointed and highly fragmented. Transgressively expressed miRNAs (miR169, miR397, miR827) were also identified as prominent signatures of FL510, with functional implications to mechanisms that support robust growth, homeostasis, and osmotic stress avoidance. Results of this study demonstrate how genetic recombination creates novel morphology that complements inducible defenses hence transgressive adaptive phenotypes.

Highlights

  • Adaptation to the dynamic nature of abiotic and biotic factors in the environment is crucial for plant survival and reproduction (Anderson et al, 2011)

  • Transgresssive segregation for salt tolerance was uncovered in a recombinant inbred population (F8-recombinant inbred lines (RILs)) of rice derived from the improved high-yielding Xian/Indica cultivar IR29 and the Indian Aus landrace Pokkali, based on integrative molecular, biochemical, macrophysiological, and real-time growth profiling approach to phenotyping (Pabuayon et al, 2020)

  • Transgressive segregation is observed both in nature and in artificial populations created by plant breeding

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Summary

Introduction

Adaptation to the dynamic nature of abiotic and biotic factors in the environment is crucial for plant survival and reproduction (Anderson et al, 2011). Recent studies supported the role of natural hybridization between genetically distant parents as important mechanism for the creation of rare developmental, morphological, and/or adaptive traits that are outliers from the majority of the population, i.e., genetic novelties. These novelties have been proposed to set foundations for new phylogenetic lineages that adapt to new ecological niches (Wagner and Lynch, 2010). The Green Revolution in the 1960’s was hallmarked by the creation of novel plant architecture that was optimal for managed environments with ideal water and nutrient inputs. Ideotype breeding created an adaptive plant architecture for water-rich and nutrient-rich environments (Vergara, 1988; Khush, 1995a)

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