A CYC/TB1-type TCP transcription factor controls spikelet meristem identity in barley

Author:

Shang Yi12,Yuan Lu3,Di Zhaocan3,Jia Yong4,Zhang Zhenlan1,Li Sujuan5,Xing Liping3,Qi Zengjun3,Wang Xiaoyun6,Zhu Jinghuan2,Hua Wei2,Wu Xiaojian2,Zhu Minqiu3,Li Gang78,Li Chengdao49ORCID

Affiliation:

1. Hybrid Rapeseed Research Center of Shaanxi Province, Yangling, China

2. Institute of Crop and Nuclear Technology Utilization, Zhejiang Academy of Agricultural Science, Hangzhou, China

3. National Key Laboratory of Crop Genetics and Germplasm Enhancement, Cytogenetics Institute, Nanjing Agricultural University/ JCIC-MCP, Nanjing, Jiangsu, China

4. Western Barley Genetics Alliance, Murdoch University, Murdoch WA, Australia

5. Central Laboratory of Zhejiang Academy of Agricultural Science, Hangzhou, China

6. Jiangxi University of Traditional Chinese Medicine, Nanchang, China

7. Wheat Research Institute, School of Life Sciences and Engineering, Southwest University of Science and Technology, Mianyang, Sichuan, China

8. School of Agriculture, Food, and Wine, University of Adelaide, Waite campus, Urrbrae, South Australia, Australia

9. Hubei Collaborative Innovation Centre for Grain Industry, Yangtze University, Jingzhou, Hubei, China

Abstract

Abstract Barley possesses a branchless, spike-shaped inflorescence where determinate spikelets attach directly to the main axis, but the developmental mechanism of spikelet identity remains largely unknown. Here we report the functional analysis of the barley gene BRANCHED AND INDETERMINATE SPIKELET 1 (BDI1), which encodes a TCP transcription factor and plays a crucial role in determining barley inflorescence architecture and spikelet development. The bdi1 mutant exhibited indeterminate spikelet meristems that continued to grow and differentiate after producing a floret meristem; some spikelet meristems at the base of the spike formed two fully developed seeds or converted to branched spikelets, producing a branched inflorescence. Map-based cloning analysis showed that this mutant has a deletion of ~600 kb on chromosome 5H containing three putative genes. Expression analysis and virus-induced gene silencing confirmed that the causative gene, BDI1, encodes a CYC/TB1-type TCP transcription factor and is highly conserved in both wild and cultivated barley. Transcriptome and regulatory network analysis demonstrated that BDI1 may integrate regulation of gene transcription cell wall modification and known trehalose-6-phosphate homeostasis to control spikelet development. Together, our findings reveal that BDI1 represents a key regulator of inflorescence architecture and meristem determinacy in cereal crop plants.

Funder

Natural Science Foundation of Zhejiang Province

Nanjing Agricultural University

Key Research Foundation of Science and Technology Department

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Physiology

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