MeGT2.6 increases cellulose synthesis and active gibberellin content to promote cell enlargement in cassava

Author:

Bao Ruxue1ORCID,Zeng Changying1,Li Ke1,Li Mengtao1,Li Yajun23,Zhou Xincheng1234,Wang Haiyan23,Wang Yajie234,Huang Dongyi1,Wang Wenquan1,Chen Xin1234

Affiliation:

1. Sanya Institute of Breeding and Multiplication Hainan University/National Key Laboratory for Tropical Crop Breeding Sanya 572025 Hainan China

2. Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences Haikou 571101 Hainan China

3. Key Laboratory for Biology and Genetic Resources of Tropical Crops of Hainan Province, Hainan Institute for Tropical Agricultural Resources Haikou 571101 Hainan China

4. Sanya Research Institute, Chinese Academy of Tropical Agricultural Sciences Sanya 572025 Hainan China

Abstract

SUMMARYCassava, a pivotal tropical crop, exhibits rapid growth and possesses a substantial biomass. Its stem is rich in cellulose and serves as a crucial carbohydrate storage organ. The height and strength of stems restrict the mechanised operation and propagation of cassava. In this study, the triple helix transcription factor MeGT2.6 was identified through yeast one‐hybrid assay using MeCesA1pro as bait, which is critical for cellulose synthesis. Over‐expression and loss‐of‐function lines were generated, and results revealed that MeGT2.6 could promote a significant increase in the plant height, stem diameter, cell size and thickness of SCW of cassava plant. Specifically, MeGT2.6 upregulated the transcription activity of MeGA20ox1 and downregulated the expression level of MeGA2ox1, thereby enhancing the content of active GA3, resulting in a large cell size, high plant height and long stem diameter in cassava. Moreover, MeGT2.6 upregulated the transcription activity of MeCesA1, which promoted the synthesis of cellulose and hemicellulose and produced a thick secondary cell wall. Finally, MeGT2.6 could help supply additional substrates for the synthesis of cellulose and hemicellulose by upregulating the invertase genes (MeNINV1/6). Thus, MeGT2.6 was found to be a multiple regulator; it was involved in GA metabolism and sucrose decomposition and the synthesis of cellulose and hemicellulose.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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