The TCP transcription factor HvTB2 heterodimerizes with VRS5 and controls spike architecture in barley

生物 调节器 普通大麦 转录因子 大麦 遗传学 计算生物学 基因 植物 禾本科
作者
Tatiana de Souza Moraes,Sam W. van Es,Inmaculada Hernández‐Pinzón,Gwendolyn K. Kirschner,Froukje van der Wal,Sylvia Rodrigues da Silveira,Jacqueline Busscher‐Lange,Gerco C. Angenent,Matthew Moscou,Richard G. H. Immink,G. Wilma van Esse
出处
期刊:Plant reproduction [Springer Science+Business Media]
卷期号:35 (3): 205-220 被引量:16
标识
DOI:10.1007/s00497-022-00441-8
摘要

KEY MESSAGE: Understanding the molecular network, including protein-protein interactions, of VRS5 provide new routes towards the identification of other key regulators of plant architecture in barley. The TCP transcriptional regulator TEOSINTE BRANCHED 1 (TB1) is a key regulator of plant architecture. In barley, an important cereal crop, HvTB1 (also referred to as VULGARE SIX-ROWED spike (VRS) 5), inhibits the outgrowth of side shoots, or tillers, and grains. Despite its key role in barley development, there is limited knowledge on the molecular network that is utilized by VRS5. In this work, we performed protein-protein interaction studies of VRS5. Our analysis shows that VRS5 potentially interacts with a diverse set of proteins, including other class II TCP's, NF-Y TF, but also chromatin remodelers. Zooming in on the interaction capacity of VRS5 with other TCP TFs shows that VRS5 preferably interacts with other class II TCP TFs in the TB1 clade. Induced mutagenesis through CRISPR-Cas of one of the putative VRS5 interactors, HvTB2 (also referred to as COMPOSITUM 1 and BRANCHED AND INDETERMINATE SPIKELET 1), resulted in plants that have lost their characteristic unbranched spike architecture. More specifically, hvtb2 mutants exhibited branches arising at the main spike, suggesting that HvTB2 acts as inhibitor of branching. Our protein-protein interaction studies of VRS5 resulted in the identification of HvTB2 as putative interactor of VRS5, another key regulator of spike architecture in barley. The study presented here provides a first step to underpin the protein-protein interactome of VRS5 and to identify other, yet unknown, key regulators of barley plant architecture.
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