SRX3030475 GSM2716155 SRP113458 SRS2379363 GSM2716155 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716155 GSM2716155 GEO Accession GSM2716155 SRX3030476 GSM2716156 SRP113458 SRS2379364 GSM2716156 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716156 GSM2716156 GEO Accession GSM2716156 SRX3030477 GSM2716157 SRP113458 SRS2379365 GSM2716157 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716157 GSM2716157 GEO Accession GSM2716157 SRX3030478 GSM2716158 SRP113458 SRS2379366 GSM2716158 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716158 GSM2716158 GEO Accession GSM2716158 SRX3030479 GSM2716159 SRP113458 SRS2379390 GSM2716159 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716159 GSM2716159 GEO Accession GSM2716159 SRX3030480 GSM2716160 SRP113458 SRS2379367 GSM2716160 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716160 GSM2716160 GEO Accession GSM2716160 SRX3030481 GSM2716161 SRP113458 SRS2379368 GSM2716161 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716161 GSM2716161 GEO Accession GSM2716161 SRX3030482 GSM2716162 SRP113458 SRS2379370 GSM2716162 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716162 GSM2716162 GEO Accession GSM2716162 SRX3030483 GSM2716163 SRP113458 SRS2379372 GSM2716163 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716163 GSM2716163 GEO Accession GSM2716163 SRX3030484 GSM2716164 SRP113458 SRS2379371 GSM2716164 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716164 GSM2716164 GEO Accession GSM2716164 SRX3030485 GSM2716165 SRP113458 SRS2379389 GSM2716165 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716165 GSM2716165 GEO Accession GSM2716165 SRX3030486 GSM2716166 SRP113458 SRS2379374 GSM2716166 ChIP-Seq GENOMIC ChIP S. pombe (ChIP) :Cells grown in YES medium were harvested at OD595 of ~1.0, followed by fixation with 1% formaldehyde for 15 min. Cell pellets were re-suspended in the lysis buffer (50 mM HEPES, pH 7.6, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.2% SDS and proteinase inhibitors), and were disrupted in a bead beater (Biospec). The cell lysate was sonicated six times (20s on, 180s off) using an ultrasonicator with a microtip at 35% of maximum amplitude. The lysates were immunoprecipitated with antibodies and protein A/G beads over-night. The immunoprecipitated DNA was eluted using SigmaPrep™ spin column and then subjected to protease treatment and cross-linking reversal. Subsequently, the DNA was purified using Qiaquick PCR purification kit (Qiagen). ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716166 GSM2716166 GEO Accession GSM2716166 SRX3030487 GSM2716167 SRP113458 SRS2379373 GSM2716167 RNA-Seq TRANSCRIPTOMIC cDNA S. pombe (RNA isolation): DNase-treated mRNA was purified using NEBNext® Poly(A) mRNA Magnetic Isolation Module (NEB), and subjected to library preparation using NEXTflex™ Rapid Directional mRNA-Seq Kit (BIOO) following the manufacturer’s instructions. ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716167 GSM2716167 GEO Accession GSM2716167 SRX3030488 GSM2716168 SRP113458 SRS2379375 GSM2716168 RNA-Seq TRANSCRIPTOMIC cDNA S. pombe (RNA isolation): DNase-treated mRNA was purified using NEBNext® Poly(A) mRNA Magnetic Isolation Module (NEB), and subjected to library preparation using NEXTflex™ Rapid Directional mRNA-Seq Kit (BIOO) following the manufacturer’s instructions. ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716168 GSM2716168 GEO Accession GSM2716168 SRX3030489 GSM2716169 SRP113458 SRS2379376 GSM2716169 RNA-Seq TRANSCRIPTOMIC cDNA S. pombe (RNA isolation): DNase-treated mRNA was purified using NEBNext® Poly(A) mRNA Magnetic Isolation Module (NEB), and subjected to library preparation using NEXTflex™ Rapid Directional mRNA-Seq Kit (BIOO) following the manufacturer’s instructions. ChIP-seq libraries for genome-wide sequencing were prepared using 10 ng of input DNA or 1 to 10 ng of eluted ChIP DNA using NEXTflex ChIP-Seq kit, Bioo Scientific (cat.5143). mRNA-seq libraries were made using NEXTflexTM Rapid RNA-Seq kit (cat. 5138) from isolated mRNA. Illumina HiSeq 2500 gds 302716169 GSM2716169 GEO Accession GSM2716169