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Higher-order epistasis within Pol II trigger loop haplotypes.
Duan, Bingbing; Qiu, Chenxi; Lockless, Steve W; Sze, Sing-Hoi; Kaplan, Craig D.
Afiliação
  • Duan B; Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA 15260.
  • Qiu C; Department of Genetics, Harvard Medical School, Boston, MA 02215.
  • Lockless SW; Department of Biology, Texas A&M University, College Station, TX 77843.
  • Sze SH; Department of Computer Science & Engineering, Texas A&M University, College Station, TX 77843.
  • Kaplan CD; Department of Biochemistry & Biophysics, Texas A&M University, College Station, TX 77843.
bioRxiv ; 2024 Sep 25.
Article em En | MEDLINE | ID: mdl-38293233
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article