ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/038/SRR23362838/SRR23362838_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/036/SRR23362836/SRR23362836_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/040/SRR23362840/SRR23362840_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/042/SRR23362842/SRR23362842_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/038/SRR23362838/SRR23362838_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/039/SRR23362839/SRR23362839_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/036/SRR23362836/SRR23362836_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/035/SRR23362835/SRR23362835_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/042/SRR23362842/SRR23362842_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/037/SRR23362837/SRR23362837_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/039/SRR23362839/SRR23362839_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/041/SRR23362841/SRR23362841_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/037/SRR23362837/SRR23362837_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/035/SRR23362835/SRR23362835_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/041/SRR23362841/SRR23362841_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR233/040/SRR23362840/SRR23362840_1.fastq.gzprimaryOK200Genomicsthe Key Laboratory of Developmental Genes and Human Disease, Institute of Life Sciences, Southeast Universityhttps://www.ebi.ac.uk/ena/browser/view/PRJNA932346Homo sapiensxref:PubMed:37528066The P-TEFb-containing super elongation complex (SEC) plays the essential role in transcriptional elongation control. The AF4/FMR2 family members AFF1 and AFF4 are the central scaffold proteins of SEC, associated with different human diseases. However, their specific roles in transcriptional control remain unclear. Here, we report that AFF1 and AFF4 show distinct genomic distribution patterns around TSS. AFF1 binds upstream of TSS, while AFF4 is enriched downstream of TSS. Pol II occupancies are reduced genome-widely after depletion of AFF1, but not AFF4. Interestingly, in a subset of active genes with broad AFF4 binding signature, AFF4 disruption causes slow elongation and early termination, while AFF1 deletion mirrors the transcriptional defects observed in the fast Pol II mutant. Furthermore, AFF4 knockdown leads to increased AFF1 levels at chromatin, and vice versa. In summary, our data demonstrate that AFF1 and AFF4 function, to some extent, antagonistically to ensure proper Pol II transcription. Overall design: Expression profiling by high throughput sequencing. RNA-seq was performed in WT ，AFF1 KO and AFF4 KO serum-induced HCT116 cells for two replicates.ENAfalseDistinct roles of the two SEC scaffold proteins, AFF1 and AFF4, in regulating RNA Pol II transcription elongation [RNA-seq 2]Distinct roles of the two SEC scaffold proteins, AFF1 and AFF4, in regulating RNA Pol II transcription elongation [RNA-seq 2]2025-09-242023-07-03PRJNA932346GSE224754960637528066