Growth Protocol:	The rice plants were grown in a light incubator for 14 days with 12 h light and 12 h dark conditions.
Treatment Protocol:	Spore concentration was adjusted to 5 × 105 spores/mL with 0.02% Tween-20, H2O with 0.02% Tween-20 was used as mock treatment. The fungal-inoculated rice seedlings were kept in a dark chamber at 25 ◦C with 85% humidity for 24 hours, then the plants were maintained in the growth chamber at 26/24 ◦C in a 14 h light/10 h dark cycle with 85% humidity.
Extract Protocol:	Total RNA quality detection was performed with a Nanodrop for determining the RNA concentration; nondenaturing agarose electrophoresis for determining RNA integrity; and an Agilent 2100 Bioanalyser for determining the total RNA.
Library Construction Protocol:	RNA libraries were prepared for sequencing using standard Illumina protocols

Molecule Type:	rRNA- RNA
Library Source:
Library Layout:	SINGLE
Library Strand:	-
Platform:	BGISEQ
Instrument Model:	BGISEQ-500
Strand-Specific:	Unspecific

Data Resource	GEN Sample ID	GEN Dataset ID	Project ID	BioProject ID	Sample ID	Sample Name	BioSample ID	Sample Accession	Experiment Accession	Release Date	Submission Date	Update Date	Species	Race	Ethnicity	Age	Age Unit	Gender	Source Name	Tissue	Cell Type	Cell Subtype	Cell Line	Disease	Disease State	Development Stage	Mutation	Phenotype	Condition Detail	Growth Protocol	Treatment Protocol	Extract Protocol	Library Construction Protocol	Molecule Type	Library Layout	Strand-Specific	Library Strand	Spike-In	Strategy	Platform	Instrument Model	Cell Number	Reads Number	Gbases	AvgSpotLen1	AvgSpotLen2	Uniq Mapping Rate	Multiple Mapping Rate	Coverage Rate