Protein Moonlighting Revealed by Noncatalytic Phenotypes of Yeast Enzymes. Issue 1 (1st January 2018)

• Record Type: Journal Article
• Authors: Espinosa-Cantú, Adriana; Ascencio, Diana; Herrera-Basurto, Selene; Xu, Jiewei; Roguev, Assen; Krogan, Nevan J; DeLuna, Alexander
• Is Part Of: Genetics. Volume 208:Issue 1(2018)
• Page Start: 419
• Page End: 431
• Publication Date: 2018-01-01
• Subjects: protein moonlighting -- systems genetics -- pleiotropy -- phenotype -- metabolism -- amino acid biosynthesis -- Saccharomyces cerevisiae; Genetics -- Periodicals; 576.5
• DOI: 10.1534/genetics.117.300377
• Languages: English
• ISSNs: 0016-6731

Abstract

Abstract: An increasing number of multifunctional proteins are being identified, but it is still unclear to what extent proteins moonlight beyond their annotated... A single gene can partake in several biological processes, and therefore gene deletions can lead to different—sometimes unexpected—phenotypes. However, it is not always clear whether such pleiotropy reflects the loss of a unique molecular activity involved in different processes or the loss of a multifunctional protein. Here, using Saccharomyces cerevisiae metabolism as a model, we systematically test the null hypothesis that enzyme phenotypes depend on a single annotated molecular function, namely their catalysis. We screened a set of carefully selected genes by quantifying the contribution of catalysis to gene deletion phenotypes under different environmental conditions. While most phenotypes were explained by loss of catalysis, slow growth was readily rescued by a catalytically inactive protein in about one-third of the enzymes tested. Such noncatalytic phenotypes were frequent in the Alt1 and Bat2 transaminases and in the isoleucine/valine biosynthetic enzymes Ilv1 and Ilv2, suggesting novel "moonlighting" activities in these proteins. Furthermore, differential genetic interaction profiles of gene deletion and catalytic mutants indicated that ILV1 is functionally associated with regulatory processes, specifically to chromatin modification. Our systematic study shows that gene loss phenotypes and their genetic interactions are frequently not driven by the loss of an annotated catalytic function, underscoring the moonlighting nature of cellular metabolism.