The rice PLATZ protein SHORT GRAIN6 determines grain size by
发布时间:2024-06-08 01:56
Grain size is a major determinant of cereal grain yields; however, the relevant regulatory mechanisms controlling this trait have not been fully elucidated. The rice(Oryza sativa) mutant short grain6(sg6) was identified based on its reduced grain length and weight. Here, we functionally characterized the role of SG6 in determining grain size through the regulation of spikelet hull cell division. SG6 encodes a previously uncharacterized plant ATrich sequence and zinc-binding(PLATZ) protein that i...
【文章页数】:18 页
【文章目录】:
INTRODUCTION
RESULTS
sg6 produces shorter grains
SG6 encodes a novel PLATZ protein,and its overexpression significantly enlarges seed size and weight
SG6 regulates the cell division of the spikelet hulls
SG6 is preferentially expressed in the panicles
SG6 promotes the expression of cell‐cycle‐related genes
SG6 interacts with putative cell proliferation‐related regulators
DISCUSSION
SG6 is a novel and important regulator of grain size
SG6 regulates the cell cycle
PLATZ family proteins are functionally diverse
MATERIALS AND METHODS
Plant materials and growth conditions
Constructs and phenotype analysis
RNA extraction and real‐time PCR analysis
Promoter‐GUS fusion study
Subcellular localization study
Yeast two hybrid analysis
Histological analysis
RNA‐seq analysis
Flow cytometric analysis
Accession numbers
AUTHOR CONTRIBUTIONS
SUPPORTING INFORMATION
本文编号:3991277
【文章页数】:18 页
【文章目录】:
INTRODUCTION
RESULTS
sg6 produces shorter grains
SG6 encodes a novel PLATZ protein,and its overexpression significantly enlarges seed size and weight
SG6 regulates the cell division of the spikelet hulls
SG6 is preferentially expressed in the panicles
SG6 promotes the expression of cell‐cycle‐related genes
SG6 interacts with putative cell proliferation‐related regulators
DISCUSSION
SG6 is a novel and important regulator of grain size
SG6 regulates the cell cycle
PLATZ family proteins are functionally diverse
MATERIALS AND METHODS
Plant materials and growth conditions
Constructs and phenotype analysis
RNA extraction and real‐time PCR analysis
Promoter‐GUS fusion study
Subcellular localization study
Yeast two hybrid analysis
Histological analysis
RNA‐seq analysis
Flow cytometric analysis
Accession numbers
AUTHOR CONTRIBUTIONS
SUPPORTING INFORMATION
本文编号:3991277
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