The Key Laboratory of Developmental Genes and Human Disease, School of Life Science and Technology, Southeast University, Nanjing 210096, China.
Co-innovation Center of Neuroregeneration, Nantong University, Nantong 226001, China.
J Mol Cell Biol. 2024 Jan 17;15(8). doi: 10.1093/jmcb/mjad049.
The super elongation complex (SEC) containing positive transcription elongation factor b plays a critical role in regulating transcription elongation. AFF1 and AFF4, two members of the AF4/FMR2 family, act as central scaffold proteins of SEC and are associated with various human diseases. However, their precise roles in transcriptional control remain unclear. Here, we investigate differences in the genomic distribution patterns of AFF1 and AFF4 around transcription start sites (TSSs). AFF1 mainly binds upstream of the TSS, while AFF4 is enriched downstream of the TSS. Notably, disruption of AFF4 results in slow elongation and early termination in a subset of AFF4-bound active genes, whereas AFF1 deletion leads to fast elongation and transcriptional readthrough in the same subset of genes. Additionally, AFF1 knockdown increases AFF4 levels at chromatin, and vice versa. In summary, these findings demonstrate that AFF1 and AFF4 function antagonistically to regulate RNA polymerase II transcription.
超级延伸复合物(SEC)包含正转录延伸因子 b,在调节转录延伸中发挥着关键作用。AFF1 和 AFF4 是 AF4/FMR2 家族的两个成员,作为 SEC 的中心支架蛋白,与多种人类疾病相关。然而,它们在转录控制中的精确作用仍不清楚。在这里,我们研究了 AFF1 和 AFF4 在转录起始位点(TSS)周围的基因组分布模式的差异。AFF1 主要结合在 TSS 的上游,而 AFF4 在 TSS 的下游富集。值得注意的是,AFF4 的破坏导致一小部分 AFF4 结合的活性基因的延伸缓慢和早期终止,而 AFF1 的缺失导致同一组基因的快速延伸和转录通读。此外,AFF1 的敲低会增加染色质上的 AFF4 水平,反之亦然。总之,这些发现表明 AFF1 和 AFF4 以拮抗的方式发挥作用,调节 RNA 聚合酶 II 转录。