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Genome-wide identification of loci modifying spike-branching in tetraploid wheat

KEY MESSAGE: Genetic modification of spike architecture is essential for improving wheat yield. Newly identified loci for the ‘Miracle wheat’ phenotype on chromosomes 1AS and 2BS have significant effects on spike traits. ABSTRACT: The wheat (Triticum ssp.) inflorescence, also known as a spike, forms...

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Detalles Bibliográficos
Autores principales: Wolde, Gizaw M., Schreiber, Mona, Trautewig, Corinna, Himmelbach, Axel, Sakuma, Shun, Mascher, Martin, Schnurbusch, Thorsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263435/
https://www.ncbi.nlm.nih.gov/pubmed/33961064
http://dx.doi.org/10.1007/s00122-020-03743-5
Descripción
Sumario:KEY MESSAGE: Genetic modification of spike architecture is essential for improving wheat yield. Newly identified loci for the ‘Miracle wheat’ phenotype on chromosomes 1AS and 2BS have significant effects on spike traits. ABSTRACT: The wheat (Triticum ssp.) inflorescence, also known as a spike, forms an unbranched inflorescence in which the inflorescence meristem generates axillary spikelet meristems (SMs) destined to become sessile spikelets. Previously, we identified the putatively causative mutation in the branched head(t) (bh(t)) gene (TtBH-A1) of tetraploid wheat (T. turgidum convar. compositum (L.f.) Filat.) responsible for the loss of SM identity, converting the non-branching spike to a branched wheat spike. In the current study, we performed whole-genome quantitative trait loci (QTL) analysis using 146 recombinant inbred lines (RILs) derived from a cross between spike-branching wheat (‘Miracle wheat’) and an elite durum wheat cultivar showing broad phenotypic variation for spike architecture. Besides the previously found gene at the bh(t)-A1 locus on the short arm of chromosome 2A, we also mapped two new modifier QTL for spike-branching on the short arm of chromosome 1A, termed bh(t)-A2, and 2BS. Using biparental mapping population and GWAS in 302 diverse accessions, the 2BS locus was highly associated with coding sequence variation found at the homoeo-allele of TtBH-B1 (bh(t)-B1). Thus, RILs that combined both bh(t)-A1 and bh(t)-B1 alleles showed additive genetic effects leading to increased penetrance and expressivity of the supernumerary spikelet and/or mini-spike formation. SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s00122-020-03743-5) contains supplementary material, which is available to authorized users.