Epistasis between promoter activity and coding mutations shapes gene evolvability

Author:

Cisneros Angel F.1234ORCID,Gagnon-Arsenault Isabelle12345ORCID,Dubé Alexandre K.12345ORCID,Després Philippe C.1234ORCID,Kumar Pradum16ORCID,Lafontaine Kiana37,Pelletier Joelle N.378ORCID,Landry Christian R.12345ORCID

Affiliation:

1. Département de biochimie, de microbiologie et de bio-informatique, Faculté des sciences et de génie, Université Laval, G1V 0A6, Québec, Canada.

2. Institut de biologie intégrative et des systèmes, Université Laval, G1V 0A6, Québec, Canada.

3. PROTEO, Le regroupement québécois de recherche sur la fonction, l’ingénierie et les applications des protéines, Université Laval, G1V 0A6, Québec, Canada.

4. Centre de recherche sur les données massives, Université Laval, G1V 0A6, Québec, Canada.

5. Département de biologie, Faculté des sciences et de génie, Université Laval, G1V 0A6, Québec, Canada.

6. Department of Biosciences and Bioengineering, Indian Institute of Technology Roorkee, Roorkee, 247667, India.

7. Département de biochimie et de médecine moléculaire, Faculté de médecine, Université de Montréal, H3C 3J7, Montréal, Canada.

8. Département de chimie, Faculté des arts et des sciences, Université de Montréal, H3C 3J7, Montréal, Canada.

Abstract

The evolution of protein-coding genes proceeds as mutations act on two main dimensions: regulation of transcription level and the coding sequence. The extent and impact of the connection between these two dimensions are largely unknown because they have generally been studied independently. By measuring the fitness effects of all possible mutations on a protein complex at various levels of promoter activity, we show that promoter activity at the optimal level for the wild-type protein masks the effects of both deleterious and beneficial coding mutations. Mutations that are deleterious at low activity but masked at optimal activity are slightly destabilizing for individual subunits and binding interfaces. Coding mutations that increase protein abundance are beneficial at low expression but could potentially incur a cost at high promoter activity. We thereby demonstrate that promoter activity in interaction with protein properties can dictate which coding mutations are beneficial, neutral, or deleterious.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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