Gα Solicits OsNYC4 and GW2-WG1-OsbZIP47 Modules to Regulate Grain Size in Rice (Oryza sativa L.)

Author:

Ma Shiwei1ORCID,Sun Yiqiong2,Chen Xuan2,Guo Jiayi2,Wu Shuhong2,Wu Guofeng2,Huang Guanpeng2,Kabore Manegdebwaoga Arthur Fabrice2,Woldegiorgis Samuel Tareke2,Ai Yufang2,Zhang Lina2,Liu Wei2ORCID,He Huaqin2

Affiliation:

1. College of Environmental and Biological Engineering, Putian University, Putian 351100, China

2. College of Life Sciences, Fujian Agriculture and Forestry University, Fuzhou 350002, China

Abstract

Grain size is one of the critical factors determining rice yield. Previous studies have found the grain-size-regulating function of Gα in rice. However, the regulatory mechanism underlying the development of rice grain mediated by Gα is still unclear. To reveal the functional mechanism of Gα in grain size regulation, a mutant of Gα (Gα-Cas9) was firstly constructed through a CRISPR/Cas9 strategy and was then grown in a greenhouse and field. The results showed that the seed length, plant height, 1000-grain weight, and spike length were significantly decreased in Gα-Cas9 compared to wild-type (WT) Pi-4b. During the grain filling stage, the increase in the grain dry weight of Pi-4b occurred earlier than that of Gα-Cas9. The total starch content and amylose content of matured grains of Pi-4b were higher than those of Gα-Cas9. Secondly, transcriptome sequencing analysis of Gα-Cas9 and Pi-4b during grain filling was performed to elucidate the functional pathways regulated by Gα. In total, 2867 and 4534 differentially expressed genes (DEGs) were discovered at 5 DAF and 10 DAF, and the starch and sucrose metabolism pathway enriched by DEGs was involved in grain size regulation mediated by Gα. Gα regulated the expression of starch-synthesis-related genes during grain filling, and the Gα protein interacted with OsNYC4 to trigger the sugar signaling pathway to promote starch accumulation in grain. Additionally, the GW2-WG1-OsbZIP47 pathway was switched off by Gα to relieve the inhibition of rice grain development. In this study, the results should provide new insights into the G protein signal transduction pathway.

Funder

Natural Science Foundation of China

Natural Science Foundation of Fujian

Key Science Project of Fujian

Startup Fund for Advanced Talents of Putian University

Publisher

MDPI AG

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