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Dixon, L. E.

Publications and source records attributed to Dixon, L. E..

2 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↗

Speed breeding: a powerful tool to accelerate crop research and breeding

The growing human population and a changing environment have raised significant concern for global food security, with the current improvement rate of several important crops inadequate to meet future demand [1]. This slow improvement rate is attributed partly to the long generation times of crop plants. Here we present a method called speed breeding, which greatly shortens generation time and accelerates breeding and research programs. Speed breeding can be used to achieve up to 6 generations per year for spring wheat (Triticum aestivum), durum wheat (T. durum), barley (Hordeum vulgare), chickpea (Cicer arietinum), and pea (Pisum sativum) and 4 generations for canola (Brassica napus), instead of 2-3 under normal glasshouse conditions. We demonstrate that speed breeding in fully-enclosed controlled-environment growth chambers can accelerate plant development for research purposes, including phenotyping of adult plant traits, mutant studies, and transformation. The use of supplemental lighting in a glasshouse environment allows rapid generation cycling through single seed descent and potential for adaptation to larger-scale crop improvement programs. Cost-saving through LED supplemental lighting is also outlined. We envisage great potential for integrating speed breeding with other modern crop breeding technologies, including high-throughput genotyping, genome editing, and genomic selection, accelerating the rate of crop improvement.

plant biology↗