4.7 Article

Efficient expression and function of a receptor-like kinase in wheat powdery mildew defence require an intron-located MYB binding site

期刊

PLANT BIOTECHNOLOGY JOURNAL
卷 19, 期 5, 页码 897-909

出版社

WILEY
DOI: 10.1111/pbi.13512

关键词

intron; MYB binding site; powdery mildew; receptor‐ like kinase; TtdLRK10L‐ 1; wheat

资金

  1. key research and development programme of the Ministry of Science and Technology of China [2016YFD0101004, 2017YFD0100600]

向作者/读者索取更多资源

LRK10-like receptor kinases (LRK10L-RLKs) are widely present in higher plants, but the understanding of their expression and function is still limited. Through transgenic wheat research, it was found that TtdLRK10L-1 is regulated in its expression by powdery mildew pathogens and exhibits resistance.
The LRK10-like receptor kinases (LRK10L-RLKs) are ubiquitously present in higher plants, but knowledge of their expression and function is still limited. Here, we report expression and functional analysis of TtdLRK10L-1, a typical LRK10L-RLK in durum wheat (Triticum turgidum L. ssp. durum). The introns of TtdLRK10L-1 contained multiple kinds of predicted cis-elements. To investigate the potential effect of these cis-elements on TtdLRK10L-1 expression and function, two types of transgenic wheat lines were prepared, which expressed a GFP-tagged TtdLRK10L-1 protein (TtdLRK10L-1:GFP) from the cDNA or genomic DNA (gDNA) sequence of TtdLRK10L-1 under the native promoter. TtdLRK10L-1:GFP expression was up-regulated by the powdery mildew pathogen Blumeria graminis f. sp. tritici (Bgt) in both types of transgenic plants, with the scale of the elevation being much stronger in the gDNA lines. Both types of transgenic plants exhibited enhanced resistance to Bgt infection relative to wild type control. Notably, the Bgt defence activated in the gDNA lines was significantly stronger than that in the cDNA lines. Further analysis revealed that a putative MYB transcription factor binding site (MYB-BS, CAGTTA) located in TtdLRK10L-1 intron I was critical for the efficient expression and function of TtdLRK10L-1 in Bgt defence. This MYB-BS could also increase the activity of a superpromoter widely used in ectopic gene expression studies in plants. Together, our results deepen the understanding of the expression and functional characteristics of LRK10L-RLKs. TtdLRK10L-1 is likely useful for further dissecting the molecular processes underlying wheat defence against Bgt and for developing Bgt resistant wheat crops.

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