Elaine Sia

Elaine Sia


  • Professor
  • Associate Dean of Academic Affairs


Not Research Active

Office Location
334A Hutchison
(585) 275-9275

Office Hours: By appointment

Research Overview

Our lab is interested in replication, repair, and maintenance of mitochondrial DNA (mtDNA). We utilize a variety of genetic and molecular techniques to identify proteins that function in these pathways, in order to better understand the unique requirements of this subcellular genome.

Figure 1

Mitochondria are important eukaryotic organelles. They are usually pictured as static, bean-like shapes floating within the cytoplasm, but they are in fact marvelously dynamic structures that fuse and divide in response to cellular demands. Moreover, their involvement in cellular processes and architecture is almost certainly more extensive than previously imagined. Mitochondria are familiar to most people as the powerhouses of the cell, as they are responsible for the conversion of metabolic intermediates into cellular energy in the form of ATP. As a byproduct of this process, mitochondria are also the major source of intracellular reactive oxygen species, or free radicals. Additionally, however, mitochondria also serve as agents of calcium homeostasis and regulators of apoptosis, both of which are central to cellular integrity. Failure to maintain mitochondrial function, therefore, results in cellular dysfunction, which in multicellular organisms can mean disease.

Mitochondria contain their own genomes, encoding proteins essential for respiration and oxidative phosphorylation. Maintaining error-free mtDNA is necessary for proper mitochondrial function. Not until the mid-1980s were the first mitochondrial diseases identified, but since that time the field of mitochondrial medicine has grown considerably. Relative to the nuclear genome, however, knowledge of the genes involved in mtDNA stability and the molecular actions of their encoded proteins is sparse.

Figure 2

Stained mitochondria in wild-type yeast (left) and the mutant msh1-G776D, defective in mtDNA stability. Maintenance of mtDNA is linked to structural stability of the organelle. Top panels show mitochondrial structures, bottom panels show mtDNA.

The budding yeast Saccharomyces cerevisiae is an ideal model system for studying mitochondria. It is a facultative anaerobe, able to survive without respiration when given a fermentable carbon source. For this reason, although mitochondria are still required for viability, their function is dispensable. Yeast are also one of the few systems in which the mitochondrial genome can be directly manipulated to generate recombinant mtDNA. These qualities are useful for studying many aspects of mitochondria, such as respiration, mitochondrial protein import, and transcription and translation of mitochondrial genes

The goal of our lab is to understand the processes that govern mitochondrial DNA. Many of these are likely to be similar to those that occur in nuclear DNA. However, mtDNA is unique in several aspects. It is extremely AT-rich, highly repetitive, and multi-copy. Additionally, in higher eukaryotes it is almost exclusively maternally derived, and is therefore subject to different evolutionary forces as well. Our work focuses primarily on genetic analysis of genes known to function in mtDNA metabolism, including the mitochondrial polymerase Mip1p (Pol gamma), the mismatch repair homolog Msh1p, and the maintenance protein Mgm101p. For much of this work we utilize DNA reporter constructs that allow us to measure rates of mtDNA alterations both by mutation and recombination. We are also conducting screens to identify pathway partners of these known genes and in this way contribute to what is known about the yeast mitochondrial proteome.

Research Interests

  • Molecular biology and genetics
  • Mutagenesis and repair of the mitochondrial genome of Saccharomyces cerevisiae

Selected Publications