SRX7114900 GSM4153720 SRP229082 SRS5625745 GSM4153720 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the TRIzol® method following the manufacturer's protocol. Bulk cells or filamentous fungus are grounded to a powder using liquid nitrogen, and the powder was transferred into the 2ml tube contains 1.5ml Trizol reagent. The mix was shaked for 3min, and kept for 5min at room temperature, then was Centrifuged at 10,000×g for 5min at 4°C. The supernatant was added 200μL of chloroform/isoamyl alcohol (24:1) with 1ml lysis reagents. After centrifuged at 10,000×g for 10min at 4°C, the supernatant was transferred into another new tube with equal volume of isopropanol and put in the refrigerator at -20°C for 1h. After centrifuged at 13600×g for 20min at 4°C, the supernatant was precipitated by 1 mL of 75% ethanol and let dry for 3-5min. The RNA pellet was dissolved with 30-100μL of DEPC water or RNase-free water. The concentration of the extracted RNA samples was determined using a Nanodrop system (NanoDrop, Madison, USA), and the integrity of the RNA was examined by the RNA integrity number (RIN) using an Agilent 2100 bioanalyzer (Agilent, Santa Clara, USA). Oligo(dT)-attached magnetic beads were used to purified mRNA. Purified mRNA was fragmented into small pieces with fragment buffer at appropriate temperature. Then First-strand cDNA was generated using random hexamer-primed reverse transcription, followed by a second-strand cDNA synthesis. afterwards, A-Tailing Mix and RNA Index Adapters were added by incubating to end repair. The cDNA fragments obtained from previous step were amplified by PCR, and products were purified by Ampure XP Beads, then dissolved in EB solution. The product was validated on the Agilent Technologies 2100 bioanalyzer for quality control. The double stranded PCR products from previous step were heated denatured and circularized by the splint oligo sequence to get the final library. The single strand circle DNA (ssCir DNA) was formatted as the final library. The final library was amplified with phi29 to make DNA nanoball (DNB) which had more than 300 copies of one molecular, DNBs were loaded into the patterned nanoarray and single end 50 bases reads were generated on BGIseq500 platform (BGI-Shenzhen, China). BGISEQ-500 gds 304153720 GSM4153720 GEO Accession GSM4153720 SRX7114901 GSM4153721 SRP229082 SRS5625746 GSM4153721 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the TRIzol® method following the manufacturer's protocol. Bulk cells or filamentous fungus are grounded to a powder using liquid nitrogen, and the powder was transferred into the 2ml tube contains 1.5ml Trizol reagent. The mix was shaked for 3min, and kept for 5min at room temperature, then was Centrifuged at 10,000×g for 5min at 4°C. The supernatant was added 200μL of chloroform/isoamyl alcohol (24:1) with 1ml lysis reagents. After centrifuged at 10,000×g for 10min at 4°C, the supernatant was transferred into another new tube with equal volume of isopropanol and put in the refrigerator at -20°C for 1h. After centrifuged at 13600×g for 20min at 4°C, the supernatant was precipitated by 1 mL of 75% ethanol and let dry for 3-5min. The RNA pellet was dissolved with 30-100μL of DEPC water or RNase-free water. The concentration of the extracted RNA samples was determined using a Nanodrop system (NanoDrop, Madison, USA), and the integrity of the RNA was examined by the RNA integrity number (RIN) using an Agilent 2100 bioanalyzer (Agilent, Santa Clara, USA). Oligo(dT)-attached magnetic beads were used to purified mRNA. Purified mRNA was fragmented into small pieces with fragment buffer at appropriate temperature. Then First-strand cDNA was generated using random hexamer-primed reverse transcription, followed by a second-strand cDNA synthesis. afterwards, A-Tailing Mix and RNA Index Adapters were added by incubating to end repair. The cDNA fragments obtained from previous step were amplified by PCR, and products were purified by Ampure XP Beads, then dissolved in EB solution. The product was validated on the Agilent Technologies 2100 bioanalyzer for quality control. The double stranded PCR products from previous step were heated denatured and circularized by the splint oligo sequence to get the final library. The single strand circle DNA (ssCir DNA) was formatted as the final library. The final library was amplified with phi29 to make DNA nanoball (DNB) which had more than 300 copies of one molecular, DNBs were loaded into the patterned nanoarray and single end 50 bases reads were generated on BGIseq500 platform (BGI-Shenzhen, China). BGISEQ-500 gds 304153721 GSM4153721 GEO Accession GSM4153721 SRX7114902 GSM4153722 SRP229082 SRS5625747 GSM4153722 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the TRIzol® method following the manufacturer's protocol. Bulk cells or filamentous fungus are grounded to a powder using liquid nitrogen, and the powder was transferred into the 2ml tube contains 1.5ml Trizol reagent. The mix was shaked for 3min, and kept for 5min at room temperature, then was Centrifuged at 10,000×g for 5min at 4°C. The supernatant was added 200μL of chloroform/isoamyl alcohol (24:1) with 1ml lysis reagents. After centrifuged at 10,000×g for 10min at 4°C, the supernatant was transferred into another new tube with equal volume of isopropanol and put in the refrigerator at -20°C for 1h. After centrifuged at 13600×g for 20min at 4°C, the supernatant was precipitated by 1 mL of 75% ethanol and let dry for 3-5min. The RNA pellet was dissolved with 30-100μL of DEPC water or RNase-free water. The concentration of the extracted RNA samples was determined using a Nanodrop system (NanoDrop, Madison, USA), and the integrity of the RNA was examined by the RNA integrity number (RIN) using an Agilent 2100 bioanalyzer (Agilent, Santa Clara, USA). Oligo(dT)-attached magnetic beads were used to purified mRNA. Purified mRNA was fragmented into small pieces with fragment buffer at appropriate temperature. Then First-strand cDNA was generated using random hexamer-primed reverse transcription, followed by a second-strand cDNA synthesis. afterwards, A-Tailing Mix and RNA Index Adapters were added by incubating to end repair. The cDNA fragments obtained from previous step were amplified by PCR, and products were purified by Ampure XP Beads, then dissolved in EB solution. The product was validated on the Agilent Technologies 2100 bioanalyzer for quality control. The double stranded PCR products from previous step were heated denatured and circularized by the splint oligo sequence to get the final library. The single strand circle DNA (ssCir DNA) was formatted as the final library. The final library was amplified with phi29 to make DNA nanoball (DNB) which had more than 300 copies of one molecular, DNBs were loaded into the patterned nanoarray and single end 50 bases reads were generated on BGIseq500 platform (BGI-Shenzhen, China). BGISEQ-500 gds 304153722 GSM4153722 GEO Accession GSM4153722 SRX7114903 GSM4153723 SRP229082 SRS5625748 GSM4153723 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the TRIzol® method following the manufacturer's protocol. Bulk cells or filamentous fungus are grounded to a powder using liquid nitrogen, and the powder was transferred into the 2ml tube contains 1.5ml Trizol reagent. The mix was shaked for 3min, and kept for 5min at room temperature, then was Centrifuged at 10,000×g for 5min at 4°C. The supernatant was added 200μL of chloroform/isoamyl alcohol (24:1) with 1ml lysis reagents. After centrifuged at 10,000×g for 10min at 4°C, the supernatant was transferred into another new tube with equal volume of isopropanol and put in the refrigerator at -20°C for 1h. After centrifuged at 13600×g for 20min at 4°C, the supernatant was precipitated by 1 mL of 75% ethanol and let dry for 3-5min. The RNA pellet was dissolved with 30-100μL of DEPC water or RNase-free water. The concentration of the extracted RNA samples was determined using a Nanodrop system (NanoDrop, Madison, USA), and the integrity of the RNA was examined by the RNA integrity number (RIN) using an Agilent 2100 bioanalyzer (Agilent, Santa Clara, USA). Oligo(dT)-attached magnetic beads were used to purified mRNA. Purified mRNA was fragmented into small pieces with fragment buffer at appropriate temperature. Then First-strand cDNA was generated using random hexamer-primed reverse transcription, followed by a second-strand cDNA synthesis. afterwards, A-Tailing Mix and RNA Index Adapters were added by incubating to end repair. The cDNA fragments obtained from previous step were amplified by PCR, and products were purified by Ampure XP Beads, then dissolved in EB solution. The product was validated on the Agilent Technologies 2100 bioanalyzer for quality control. The double stranded PCR products from previous step were heated denatured and circularized by the splint oligo sequence to get the final library. The single strand circle DNA (ssCir DNA) was formatted as the final library. The final library was amplified with phi29 to make DNA nanoball (DNB) which had more than 300 copies of one molecular, DNBs were loaded into the patterned nanoarray and single end 50 bases reads were generated on BGIseq500 platform (BGI-Shenzhen, China). BGISEQ-500 gds 304153723 GSM4153723 GEO Accession GSM4153723