4.7 Article

SWI2/SNF2 chromatin remodeling ATPases SPLAYED and BRAHMA control embryo development in rice

Journal

PLANT CELL REPORTS
Volume 41, Issue 6, Pages 1389-1401

Publisher

SPRINGER
DOI: 10.1007/s00299-022-02864-z

Keywords

Chromatin remodeling; SPLAYED; BRAHMA; Embryo; Rice

Categories

Funding

  1. National Natural Science Foundation of China [31872855, 31971842]

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This study reveals the important roles of chromatin remodeling ATPases OsSYD and OsBRM in rice embryo development. The expression of OSH genes is affected by OsSYD and OsBRM, leading to defective shoot establishment during embryogenesis. The interaction between OsSYD and RFL suggests the ubiquity of the interaction between LFY homolog and chromatin remodeling ATPases in plants. These findings provide a foundation for understanding the functions of OsSYD and OsBRM in rice embryo development.
Key message Chromatin remodeling ATPases OsSYD and OsBRM are involved in shoot establishment, and both affect OSH gene transcription. OsSYD protein interacts with RFL, but OsBRM does not. In plants, SPLAYED (SYD) and BRAHMA (BRM) encode chromatin remodeling ATPases that use the energy derived from ATP hydrolysis to restructure nucleosomes and render certain genomic regions available to transcription factors. However, the function of SYD and BRM on rice growth and development is unknown. Here, we constructed ossyd and osbrm mutants using CRISPR/Cas9 technology and analyzed the effects of mutations on rice embryo development. We discovered that the ossyd and osbrm mutants exhibited severe defects during embryonic development, whereas endosperm development was normal. These results indicated that the development of the embryo and endosperm is independent of each other. Consequently, the ossyd- and osbrm-null mutants did not germinate due to the abnormal embryos. Furthermore, we observed the embryos of ossyd- and osbrm-null mutants, and they indeed had distinct differentiation defects in shoot establishment, acquired during embryogenesis. To verify the function of OsSYD and OsBRM in embryogenesis, we measured the transcript levels of marker genes at different stages. Compared with wild type, the expression levels of multiple OSH genes were significantly reduced in the mutants, which was consistent with the defective shoot establishment phenotypes. The interaction between SYD and RICE FLORICAULA/LFY (RFL) was revealed using a yeast two-hybrid screening system, suggesting that the interaction between the LFY homolog and chromatin remodeling ATPases is ubiquitous in plants. Collectively, our findings provide the basis for elucidating the function of OsSYD and OsBRM during embryo development in rice.

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