Aug 2026· Biochemical Society Transactions· Vol 54, pp. 1065 - 1077· 0 citations· 99 references
Medicine
TL;DR
The hierarchical transitions between phosphorylation states are explored, highlighting how combinatorial marks rather than isolated modifications shape transcriptional progression and prevent cryptic initiation through cross-talk with the histone code.
Abstract
Abstract The C-terminal domain (CTD) of the largest subunit of RNA polymerase II serves as a dynamic platform coordinating transcription and RNA processing. Recent advances in mass spectrometry, structural biology, and sequencing approaches have revealed a far more complex, combinatorial CTD code than previously appreciated. The present review examines the CTD as an integrative signaling hub that translates diverse environmental signals into genomic outputs. We explore the hierarchical transitions between phosphorylation states, highlighting how combinatorial marks rather than isolated modifications shape transcriptional progression and prevent cryptic initiation through cross-talk with the histone code. Special focus is given to the roles of ‘enigmatic’ marks such as pTyr1 and pThr4, whose functional significance has been complicated by biochemical masking effects and species-specific regulatory nodes. We also discuss emerging evidence that CTD remodeling contributes to stress-responsive transcription, including oxidative stress, heat shock, and DNA damage. Together, these observations support a dynamic model of the CTD in which combinatorial phosphorylation states coordinate transcriptional progression, genome stability, and stress-responsive gene regulation.
This work establishes that multisite phosphorylation of the SPT5 CTR1 domain modulates a heterogeneous interaction landscape shaped by sequence context, and emphasizes the nontrivial difference between serine and threonine phosphorylation as a mechanism to regulate disordered protein structure–function relationships.
Rong Hu, E. Usher, Olivia A Fraser et al.· Journal of Physical Chemistr...· 0 citations
Phosphorylation plays a central role in coordinating transcription with pre-mRNA maturation, yet the mechanistic understanding of how transcription is regulated by phosphorylation remains limited. The PP1 phosphatase removes Cdk9-dependent phosphorylation of Pol II and Spt5, triggering transcription termination. Here...
Alex Au, Abigail Southers, Krzysztof Kuś et al.· Nature Communications· 1 citation
This Review focuses on transcription by RNA polymerase II (Pol II) and discusses the integrated roles of the universal promoter scaffold factor TFIID, the transcription co-activator Mediator and the epigenetic status of the +1 nucleosome.
This review highlights the key differences between PAR and nucleic acids, emphasizing why PAR could be an especially effective scaffold, and compares PAR structures with nucleic acids, and examines the physicochemical factors that influence PAR structure and its condensate formation.
Lipika Baidya, Hung T. Nguyen· Frontiers in Biophysics· 0 citations
The central dogma of molecular biology, which delineates the flow of genetic information from DNA to RNA to proteins, is fundamental to cellular identity and functionality. This process involves intricate steps of transcription, mRNA processing, translation, and protein processing, each of which has been studied extens...
Bo-Kai Zhu· Advances in Experimental Med...· 0 citations
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