» Articles » PMID: 39446980

Higher-order Epistasis Within Pol II Trigger Loop Haplotypes

Overview
Journal Genetics
Specialty Genetics
Date 2024 Oct 24
PMID 39446980
Authors
Affiliations
Soon will be listed here.
Abstract

RNA polymerase II (Pol II) has a highly conserved domain, the trigger loop (TL), that controls transcription fidelity and speed. We previously probed pairwise genetic interactions between residues within and surrounding the TL for the purpose of understand functional interactions between residues and to understand how individual mutants might alter TL function. We identified widespread incompatibility between TLs of different species when placed in the Saccharomyces cerevisiae Pol II context, indicating species-specific interactions between otherwise highly conserved TLs and its surroundings. These interactions represent epistasis between TL residues and the rest of Pol II. We sought to understand why certain TL sequences are incompatible with S. cerevisiae Pol II and to dissect the nature of genetic interactions within multiply substituted TLs as a window on higher order epistasis in this system. We identified both positive and negative higher-order residue interactions within example TL haplotypes. Intricate higher-order epistasis formed by TL residues was sometimes only apparent from analysis of intermediate genotypes, emphasizing complexity of epistatic interactions. Furthermore, we distinguished TL substitutions with distinct classes of epistatic patterns, suggesting specific TL residues that potentially influence TL evolution. Our examples of complex residue interactions suggest possible pathways for epistasis to facilitate Pol II evolution.

References
1.
Mosaei H, Zenkin N . Two distinct pathways of RNA polymerase backtracking determine the requirement for the Trigger Loop during RNA hydrolysis. Nucleic Acids Res. 2021; 49(15):8777-8784. PMC: 8421135. DOI: 10.1093/nar/gkab675. View

2.
Starr T, Thornton J . Epistasis in protein evolution. Protein Sci. 2016; 25(7):1204-18. PMC: 4918427. DOI: 10.1002/pro.2897. View

3.
Wang D, Bushnell D, Huang X, Westover K, Levitt M, Kornberg R . Structural basis of transcription: backtracked RNA polymerase II at 3.4 angstrom resolution. Science. 2009; 324(5931):1203-6. PMC: 2718261. DOI: 10.1126/science.1168729. View

4.
Barnes C, Calero M, Malik I, Graham B, Spahr H, Lin G . Crystal Structure of a Transcribing RNA Polymerase II Complex Reveals a Complete Transcription Bubble. Mol Cell. 2015; 59(2):258-69. PMC: 4643057. DOI: 10.1016/j.molcel.2015.06.034. View

5.
Reddy G, Desai M . Global epistasis emerges from a generic model of a complex trait. Elife. 2021; 10. PMC: 8057814. DOI: 10.7554/eLife.64740. View