The OsNAC23-Tre6P-SnRK1a feed-forward loop regulates sugar homeostasis and grain yield in rice

Tre6P (trehalose-6-phosphate) mediates sensing of carbon availability to maintain sugar homeostasis in plants, which underpins crop yield and resilience. However, how Tre6P responds to fluctuations in sugar levels and regulates the utilization of sugars for growth remains to be addressed. Here, we r...

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Veröffentlicht in:Molecular plant 2022-04, Vol.15 (4), p.706-722
Hauptverfasser: Li, Zhiyong, Wei, Xiangjin, Tong, Xiaohong, Zhao, Juan, Liu, Xixi, Wang, Huimei, Tang, Liqun, Shu, Yazhou, Li, Guanghao, Wang, Yifeng, Ying, Jiezheng, Jiao, Guiai, Hu, Honghong, Hu, Peisong, Zhang, Jian
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container_end_page 722
container_issue 4
container_start_page 706
container_title Molecular plant
container_volume 15
creator Li, Zhiyong
Wei, Xiangjin
Tong, Xiaohong
Zhao, Juan
Liu, Xixi
Wang, Huimei
Tang, Liqun
Shu, Yazhou
Li, Guanghao
Wang, Yifeng
Ying, Jiezheng
Jiao, Guiai
Hu, Honghong
Hu, Peisong
Zhang, Jian
description Tre6P (trehalose-6-phosphate) mediates sensing of carbon availability to maintain sugar homeostasis in plants, which underpins crop yield and resilience. However, how Tre6P responds to fluctuations in sugar levels and regulates the utilization of sugars for growth remains to be addressed. Here, we report that the sugar-inducible rice NAC transcription factor OsNAC23 directly represses the transcription of the Tre6P phosphatase gene TPP1 to simultaneously elevate Tre6P and repress trehalose levels, thus facilitating carbon partitioning from source to sink organs. Meanwhile, OsNAC23 and Tre6P suppress the transcription and enzyme activity of SnRK1a, a low-carbon sensor and antagonist of OsNAC23, to prevent the SnRK1a-mediated phosphorylation and degradation of OsNAC23. Thus, OsNAC23, Tre6P, and SnRK1a form a feed-forward loop to sense sugar and maintain sugar homeostasis by transporting sugars to sink organs. Importantly, plants over-expressing OsNAC23 exhibited an elevated photosynthetic rate, sugar transport, and sink organ size, which consistently increased rice yields by 13%–17% in three elite-variety backgrounds and two locations, suggesting that manipulation of OsNAC23 expression has great potential for rice improvement. Collectively, these findings enhance our understanding of Tre6P-mediated sugar signaling and homeostasis, and provide a new strategy for genetic improvement of rice and possibly also other crops. Sugar-inducible rice NAC transcription factor OsNAC23 directly represses TPP1 to elevate Tre6P levels. OsNAC23, Tre6P and SnRK1a form a feed-forward loop to sense sugar and maintain sugar homeostasis by transporting sugars to sink organs. Over-expressing OsNAC23 consistently increased rice yields, showing great potential for rice improvement.
doi_str_mv 10.1016/j.molp.2022.01.016
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However, how Tre6P responds to fluctuations in sugar levels and regulates the utilization of sugars for growth remains to be addressed. Here, we report that the sugar-inducible rice NAC transcription factor OsNAC23 directly represses the transcription of the Tre6P phosphatase gene TPP1 to simultaneously elevate Tre6P and repress trehalose levels, thus facilitating carbon partitioning from source to sink organs. Meanwhile, OsNAC23 and Tre6P suppress the transcription and enzyme activity of SnRK1a, a low-carbon sensor and antagonist of OsNAC23, to prevent the SnRK1a-mediated phosphorylation and degradation of OsNAC23. Thus, OsNAC23, Tre6P, and SnRK1a form a feed-forward loop to sense sugar and maintain sugar homeostasis by transporting sugars to sink organs. Importantly, plants over-expressing OsNAC23 exhibited an elevated photosynthetic rate, sugar transport, and sink organ size, which consistently increased rice yields by 13%–17% in three elite-variety backgrounds and two locations, suggesting that manipulation of OsNAC23 expression has great potential for rice improvement. Collectively, these findings enhance our understanding of Tre6P-mediated sugar signaling and homeostasis, and provide a new strategy for genetic improvement of rice and possibly also other crops. Sugar-inducible rice NAC transcription factor OsNAC23 directly represses TPP1 to elevate Tre6P levels. OsNAC23, Tre6P and SnRK1a form a feed-forward loop to sense sugar and maintain sugar homeostasis by transporting sugars to sink organs. Over-expressing OsNAC23 consistently increased rice yields, showing great potential for rice improvement.</description><identifier>ISSN: 1674-2052</identifier><identifier>EISSN: 1752-9867</identifier><identifier>DOI: 10.1016/j.molp.2022.01.016</identifier><identifier>PMID: 35093592</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>antagonists ; carbon ; carbon partitioning ; enzyme activity ; genes ; genetic improvement ; grain yield ; Homeostasis ; NAC transcription factor ; Oryza - genetics ; Oryza - metabolism ; phosphorylation ; Photosynthesis ; Plants - metabolism ; rice ; Sucrose - metabolism ; sugar homeostasis ; Sugar Phosphates - metabolism ; transcription factors ; Tre6P ; trehalose</subject><ispartof>Molecular plant, 2022-04, Vol.15 (4), p.706-722</ispartof><rights>2022 The Author</rights><rights>Copyright © 2022 The Author. Published by Elsevier Inc. 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Importantly, plants over-expressing OsNAC23 exhibited an elevated photosynthetic rate, sugar transport, and sink organ size, which consistently increased rice yields by 13%–17% in three elite-variety backgrounds and two locations, suggesting that manipulation of OsNAC23 expression has great potential for rice improvement. Collectively, these findings enhance our understanding of Tre6P-mediated sugar signaling and homeostasis, and provide a new strategy for genetic improvement of rice and possibly also other crops. Sugar-inducible rice NAC transcription factor OsNAC23 directly represses TPP1 to elevate Tre6P levels. OsNAC23, Tre6P and SnRK1a form a feed-forward loop to sense sugar and maintain sugar homeostasis by transporting sugars to sink organs. 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However, how Tre6P responds to fluctuations in sugar levels and regulates the utilization of sugars for growth remains to be addressed. Here, we report that the sugar-inducible rice NAC transcription factor OsNAC23 directly represses the transcription of the Tre6P phosphatase gene TPP1 to simultaneously elevate Tre6P and repress trehalose levels, thus facilitating carbon partitioning from source to sink organs. Meanwhile, OsNAC23 and Tre6P suppress the transcription and enzyme activity of SnRK1a, a low-carbon sensor and antagonist of OsNAC23, to prevent the SnRK1a-mediated phosphorylation and degradation of OsNAC23. Thus, OsNAC23, Tre6P, and SnRK1a form a feed-forward loop to sense sugar and maintain sugar homeostasis by transporting sugars to sink organs. Importantly, plants over-expressing OsNAC23 exhibited an elevated photosynthetic rate, sugar transport, and sink organ size, which consistently increased rice yields by 13%–17% in three elite-variety backgrounds and two locations, suggesting that manipulation of OsNAC23 expression has great potential for rice improvement. Collectively, these findings enhance our understanding of Tre6P-mediated sugar signaling and homeostasis, and provide a new strategy for genetic improvement of rice and possibly also other crops. Sugar-inducible rice NAC transcription factor OsNAC23 directly represses TPP1 to elevate Tre6P levels. OsNAC23, Tre6P and SnRK1a form a feed-forward loop to sense sugar and maintain sugar homeostasis by transporting sugars to sink organs. Over-expressing OsNAC23 consistently increased rice yields, showing great potential for rice improvement.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>35093592</pmid><doi>10.1016/j.molp.2022.01.016</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0003-2804-0162</orcidid><oa>free_for_read</oa></addata></record>
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subjects antagonists
carbon
carbon partitioning
enzyme activity
genes
genetic improvement
grain yield
Homeostasis
NAC transcription factor
Oryza - genetics
Oryza - metabolism
phosphorylation
Photosynthesis
Plants - metabolism
rice
Sucrose - metabolism
sugar homeostasis
Sugar Phosphates - metabolism
transcription factors
Tre6P
trehalose
title The OsNAC23-Tre6P-SnRK1a feed-forward loop regulates sugar homeostasis and grain yield in rice
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