Distinct roles of the two SEC scaffold proteins, AFF1 and AFF4, in regulating RNA Pol II transcription elongation

Zhuanzhuan Che; Xiaoxu Liu; Qian Dai; Ke Fang; Chenghao Guo; Junjie Yue; Haitong Fang; Peng Xie; Zhuojuan Luo; Chengqi Lin

doi:10.1093/jmcb/mjad049

Distinct roles of the two SEC scaffold proteins, AFF1 and AFF4, in regulating RNA Pol II transcription elongation

J Mol Cell Biol. 2023 Aug 1:mjad049. doi: 10.1093/jmcb/mjad049. Online ahead of print.

Authors

Zhuanzhuan Che¹, Xiaoxu Liu^{1

2}, Qian Dai¹, Ke Fang¹, Chenghao Guo¹, Junjie Yue¹, Haitong Fang¹, Peng Xie³, Zhuojuan Luo^{1

2}, Chengqi Lin^{1

2}

Affiliations

¹ The Key Laboratory of Developmental Genes and Human Disease, School of Life Science and Technology, Southeast University, Nanjing 210096, China.
² Co-innovation Center of Neuroregeneration, Nantong University, Nantong 226001, China.
³ School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, China.

PMID: 37528066
DOI: 10.1093/jmcb/mjad049

Abstract

The super elongation complex (SEC) containing P-TEFb plays a critical role in regulating transcription elongation. AFF1 and AFF4, 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. We here reveal differences in the genomic distribution patterns of AFF1 and AFF4 around transcription start sites (TSSs). AFF1 mainly binds upstream of the TSSs, while AFF4 is enriched downstream of the TSSs. 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 gene subset. Additionally, AFF1 knockdown increases AFF4 levels at chromatin, and vice versa. In summary, these findings demonstrate that AFF1 and AFF4 function antagonistically to regulate Pol II transcription.

Keywords: AFF1; AFF4; early termination; readthrough transcription; super elongation complex; transcription elongation.