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Gauley, A.

Publications and source records attributed to Gauley, A..

3 recordsLinked to original sources

VERNALIZATION2 (VRN2) alters early tiller development in a facultative spring hexaploid bread wheat (Triticum aestivum)

Plants coordinate growth and development with environmental signals. Specifically, temperature and photoperiod are important regulators to time the transition from vegetative to floral growth. Through utilising these environmental signals potential reproductive success is optimised, which is critical for the production of high crop yields. For cereals, some require a winter before undergoing reproductive development. This extended period of cold exposure enables the process of vernalization and is also important for the synchronised timing of the floral transition. The cereal-specific floral repressor VERNALIZATION2 (VRN2) has an integral role in this pathway, yet this locus remains poorly characterised in hexaploid wheat. Our research in a facultative wheat suggests that the tandemly duplicated genes comprising the VRN2 locus, ZCCT1 and ZCCT2, respond to multiple environmental factors and have differences in gene expression patterns at a gene and sub-genome level. These genes also show co-regulation, forming a regulatory loop between ZCCT-D1 and ZCCT-D2. The function of these genes beyond the classic vernalization response is explored in a facultative wheat with VRN-D2 identified to regulate early tiller development, with an accelerated rate of secondary tiller emergence and presence of coleoptile tillers. This phenotype increases ground coverage more rapidly, which provides agronomic benefits including improved competition with biological stressors. The findings identify that the VRN2 loci in bread wheat is formed of multiple genes which have overlapping but also unique regulation and function. Selecting these genes individually may offer a route to alter wheat plant architecture without directly impacting vernalization requirement. Highlight

plant biology↗

Harnessing Landrace Diversity Empowers Wheat Breeding for Climate Resilience

Breeding crops resilient to climate change is urgently needed to help ensure food security. A key challenge is to harness genetic diversity to optimise adaptation, yield, stress resilience and nutrition. We examined the genetic and phenotypic diversity of the A.E. Watkins landrace collection of bread wheat (Triticum aestivum), a major global cereal, through whole-genome re-sequencing (827 Watkins landraces and 208 modern cultivars) and in-depth field evaluation spanning a decade. We discovered that modern cultivars are derived from just two of the seven ancestral groups of wheat, leaving five groups as previously untapped sources for breeding. This provides access to landrace-specific functional variations using structured germplasm, genotyping and informatics resources. Employing complementary genetic populations and approaches, we identified thousands of high-resolution quantitative trait loci (QTL) and significant marker-trait associations for major traits, revealing many Watkins-unique loci that can confer superior traits in modern wheat. Furthermore, we identified and functionally verified causative genes for climate-change adaptation, nutritional enhancement and resistance to wheat blast. Finally, we assessed the phenotypic effects of 44,338 Watkins-unique haplotypes, introgressed from 143 prioritised QTL in the context of modern cultivars, bridging the gap between landrace diversity and current breeding. This study establishes a framework for systematically utilising genetic diversity in crop improvement to achieve sustainable food security.

plant biology↗

Step-wise increases in FT1 expression regulate seasonal progression of flowering in wheat (Triticum aestivum L.)

ABSTRACTFlowering is regulated by genes that respond to changing daylengths and temperature, which have been well-studied using controlled conditions; however, the molecular processes underpinning flowering in nature remain poorly understood. Here, we investigate the genetic pathways that coordinate flowering and inflorescence development of wheat as daylengths extend naturally in the field, using lines that contain variant alleles for the key photoperiod gene, Photoperiod-1 (Ppd-1). We found flowering involves a step-wise increase in the expression of FLOWERING LOCUS T1 (FT1), which initiates under day-neutral conditions of early spring. The incremental rise in FT1 expression is overridden in plants that contain a photoperiod-insensitive allele of Ppd-1, which hastens the completion of spikelet development and accelerates flowering time. The accelerated inflorescence development of photoperiod-insensitive lines is promoted by advanced seasonal expression of floral meristem identity genes. The completion of spikelet formation is promoted by FLOWERING LOCUS T2, which regulates spikelet number and is activated by Ppd-1. In wheat, flowering under natural photoperiods is regulated by step-wise increases in the expression of FT1, which responds dynamically to extending daylengths to promote early inflorescence development. This research provides a strong foundation to improve yield potential by fine-tuning the photoperiod-dependent control of inflorescence development.Competing Interest StatementThe authors have declared no competing interest.View Full Text

plant biology↗