Abstract

Cells must adjust their gene expression in order to compete in a constantly changing environment. Two alternative strategies could in principle ensure optimal coordination of gene expression with physiological requirements. First, characters of the internal physiological state, such as growth rate, metabolite levels, or energy availability, could be feedback to tune gene expression. Second, internal needs could be inferred from the external environment, using evolutionary-tuned signaling pathways. Coordination of ribosomal biogenesis with the requirement for protein synthesis is of particular importance, since cells devote a large fraction of their biosynthetic capacity for ribosomal biogenesis. To define the relative contribution of internal vs. external sensing to the regulation of ribosomal biogenesis gene expression in yeast, we subjected S. cerevisiae cells to conditions which decoupled the actual vs. environmentally-expected growth rate. Gene expression followed the environmental signal according to the expected, but not the actual, growth rate. Simultaneous monitoring of gene expression and growth rate in continuous cultures further confirmed that ribosome biogenesis genes responded rapidly to changes in the environments but were oblivious to longer-term changes in growth rate. Our results suggest that the capacity to anticipate and prepare for environmentally-mediated changes in cell growth presented a major selection force during yeast evolution.

Highlights

  • Cellular functionality is tightly coupled to the external environment

  • Our results suggest that the capacity to anticipate and prepare for environmentally-mediated changes in growth rate, before such changes occur, presented a major selection force during yeast evolution

  • Histidine limited chemostat medium consisted of bacto-yeast nitrogen base without amino acids and with ammonium sulfate (0.67%), glucose (2%) and a drop-out mix (0.2%) of the following combination: L-Histidine (1.3 mg), Adenine sulfate (20 mg), Uracil (20 mg), L-Tryptophan (20 mg), L-Leucine (100 mg), L-Arginine (20 mg), L-Methionine (20 mg), L-Tyrosine (30 mg), L-Isoleucine (30 mg), L-Lysine (30 mg), L-Phenylalanine (50 mg), L-Glutamic acid (100 mg), L-Aspartic acid (100 mg), L-Valine (150 mg), L-Threonine (200 mg), L-Serine (400 mg)

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Summary

Introduction

Cellular functionality is tightly coupled to the external environment. The type of nutrients available defines the internal metabolic flow, while their abundance often limits the rate of biomass production and energy available for growth. An abundance of toxins impede upon various aspects of cellular machinery, including metabolic capacity, protein stability or DNA integrity. Cells may encounter virtually endless environmental states at widely different frequencies. Maintaining optimal functionality in the presence of such external variability is a central evolutionary constraint. Gene expression plays a central role in the adaptation to changing conditions. Studies in the budding yeast S. cerevisiae, for example, have shown that cellular transcription program is dramatically modified by changes in nutrient availability, growth conditions, temperature, and a variety of other environmental condition tested

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