Transcriptional Profiling of Biofilm Regulators Identified by an Overexpression Screen in Saccharomyces cerevisiae.
Gareth A CromieZhihao TanMichelle HaysAmy SirrEric W JefferyAimeé M DudleyPublished in: G3 (Bethesda, Md.) (2017)
Biofilm formation by microorganisms is a major cause of recurring infections and removal of biofilms has proven to be extremely difficult given their inherent drug resistance . Understanding the biological processes that underlie biofilm formation is thus extremely important and could lead to the development of more effective drug therapies, resulting in better infection outcomes. Using the yeast Saccharomyces cerevisiae as a biofilm model, overexpression screens identified DIG1, SFL1, HEK2, TOS8, SAN1, and ROF1/YHR177W as regulators of biofilm formation. Subsequent RNA-seq analysis of biofilm and nonbiofilm-forming strains revealed that all of the overexpression strains, other than DIG1 and TOS8, were adopting a single differential expression profile, although induced to varying degrees. TOS8 adopted a separate profile, while the expression profile of DIG1 reflected the common pattern seen in most of the strains, plus substantial DIG1-specific expression changes. We interpret the existence of the common transcriptional pattern seen across multiple, unrelated overexpression strains as reflecting a transcriptional state, that the yeast cell can access through regulatory signaling mechanisms, allowing an adaptive morphological change between biofilm-forming and nonbiofilm states.
Keyphrases
- biofilm formation
- saccharomyces cerevisiae
- transcription factor
- escherichia coli
- single cell
- candida albicans
- rna seq
- pseudomonas aeruginosa
- staphylococcus aureus
- high throughput
- cell proliferation
- poor prognosis
- gene expression
- cystic fibrosis
- type diabetes
- stem cells
- genome wide
- diabetic rats
- cell therapy
- oxidative stress
- weight loss
- heat stress
- binding protein
- endothelial cells