A computational study of nucleosomal binding and alternative isoforms of human transcription factors

Abstract

Eukaryotic transcription factors (TFs) are proteins that bind short DNA motifs and regulate gene transcription. Because genomic DNA is organised into nucleosomes via binding histone octamers, TFs compete with histones for binding DNA. Also, the functions of a TF are mainly defined by its domains; therefore, a TF gene can vary the characteristics of its protein product through the expression of alternative isoforms with different domains. However, the mechanisms of TF-nucleosome interactions and the functional importance of alternative TF isoforms are not fully understood. Here, I address these two problems computationally via the integrative analysis of publicly available in vivo human sequencing data. First, I evaluated a novel, gyre-spanning, mode of TF-nucleosome binding proposed recently by another lab based on in vitro evidence. Analysing the nucleosome occupancy and TF binding in the human genome, I found no evidence of such binding and concluded that it must be extremely rare, if at all present. Secondly, I studied the alternative isoforms of human TFs genome-wide. I found that independently of the gene length and the number of exons, TF genes more efficiently sample the set of possible alternative isoforms than non-TF genes, suggesting the particular importance of alternative isoforms for TFs. Also, I found that TF isoforms without a DNA-binding domain (DBD) are produced by almost a third of all human TFs, tend to be tissue-specific and likely reverse the transcription regulation effect of DBD-containing isoforms. Moreover, I demonstrated that the switches of the highest-expressed TF isoforms across human adult tissues may represent a widespread functional mechanism. Finally, I collected a compendium of human TFs with experimentally characterised alternative isoforms which will hopefully serve as a resource for future studies. In summary, my analysis further developed the fundamental knowledge about the TF-nucleosome interactions and the alternative isoforms of TFs in humans.