Abstract

Simple SummaryThis paper reported a novel type of branched spike wheat from a natural mutation event. The branched spike was controlled by a heterozygous genotype. The genetic patterns showed that gametophytic male sterility probably contributed to the heterozygous genotype responsible for the branched spike trait. Expressional levels and Wheat FRIZZY PANICLE (WFZP) sequencing between the mutant with the branched spike and the wild-type with the normal spike showed that WFZP was not the causal gene for the branched spike. Data from transcriptome sequencing indicated that carbohydrate metabolism might be involved in the formation of the branched spike trait.Wheat (Triticum aestivum L.) spike architecture is an important trait associated with spike development and grain yield. Here, we report a naturally occurring wheat mutant with branched spikelets (BSL) from its wild-type YD-16, which has a normal spike trait and confers a moderate level of resistance to wheat Fusarium head blight (FHB). The lateral meristems positioned at the basal parts of the rachis node of the BSL mutant develop into ramified spikelets characterized as multiple spikelets. The BSL mutant shows three to four-day longer growth period but less 1000-grain weight than the wild type, and it becomes highly susceptible to FHB infection, indicating that the locus controlling the BSL trait may have undergone an intensively artificial and/or natural selection in modern breeding process. The self-pollinated descendants of the lines with the BSL trait consistently segregated with an equal ratio of branched and normal spikelets (NSL) wheat, and homozygotes with the BSL trait could not be achieved even after nine cycles of self-pollination. Distinct segregation patterns both from the self-pollinated progenies of the BSL plants and from the reciprocal crosses between the BSL plants with their sister NSL plants suggested that gametophytic male sterility was probably associated with the heterozygosity for the BSL trait. Transcriptome sequencing of the RNA bulks contrasting in the two types of spike trait at the heading stage indicated that the genes on chromosome 2DS may be critical for the BSL trait formation since 329 out of 2540 differentially expressed genes (DEGs) were located on that chromosome, and most of them were down-regulated. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis showed that carbohydrate metabolism may be involved in the BSL trait expression. This work provides valuable clues into understanding development and domestication of wheat spike as well as the association of the BSL trait with FHB susceptibility.

Highlights

  • Wheat (Triticum aestivum L.) is one of the world’s most widely cultivated crops, and it feeds nearly 30% of the world population [1]

  • The results showed that 34 out of 93 markers failed to produce any bands, 15 markers produced two or more fragments of unexpected sizes (Table S2, Figure S1), and 44 markers produced clear target bands, but they were monomorphic between the branched spikelets (BSL) and normal spikelets (NSL) plants, suggesting that most of the SNPs between the BSL and NSL bulks were false positive and the BSL trait was from a natural mutation rather than outcrossing

  • It was interesting that the wild-type YD-16 showed moderate resistance to Fusarium head blight (FHB), whereas the BSL plants became highly susceptible, indicating that the spike architecture change was associated with FHB resistance

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Summary

Introduction

Wheat (Triticum aestivum L.) is one of the world’s most widely cultivated crops, and it feeds nearly 30% of the world population [1]. The spike architecture of wheat, known as the compound inflorescence, is normally composed of sessile spikelets arranged in two opposite rows along the main axis (the rachis), with each spikelet producing three to five florets [2]. Grain yield depends mainly on number of spikes per unit crop area, number of grains per spike, and grain weight. Of these factors, grain number per spike is influenced by inflorescence architecture and floral development processes [3]. Plant development depends on the activity of various types of meristems that generate organs such as leaves and floral organs throughout the life cycle. Wheat floral organs provide the basis for grain formation such that wheat yield and quality are directly influenced by floral organ development [7]

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