INVESTIGATING THE ROLE OF THE 3’ UNTRANSLATED REGION (3’UTR) OF PHO84 IN GENE REGULATION IN BUDDING YEAST
Gene expression is a complex process by which genetic information flow from genes to proteins. Factors regulating gene expression are diverse ranging from sequence elements on DNA, to various types of RNA, to proteins. These factors are categorized into two main categories, cis-acting elements and trans-acting elements. PHO84 is a budding yeast gene that was previously reported to be regulated by its cognate antisense transcripts both in cis and in trans. The antisense transcripts of PHO84 are a group of long non-coding RNAs (lncRNAs). In my project, I performed RNA-seq and TT-seq analysis to investigate the global correlation of sense/antisense pairs, which showed that the model of sense/antisense negative correlation is not always true for PHO84 locus as well as others. I conducted a series of gene expression analysis experiments to decipher the mechanisms regulating PHO84 gene, which showed that the 3’ untranslated region (3’UTR) of PHO84 plays a regulatory role in the sense expression, an activity not linked to the antisense transcript levels. I also performed a genetic screen to identify trans-acting protein factors that promote the 3’UTR-dependent regulation at PHO84 locus.
Taken together, I provided insights on both cis- and trans-acting elements controlling the expression of the model gene PHO84. Such information can be taken further and be applied to other higher organisms, with possible implication in the identification of key players in human diseases arising from gene expression dysregulation.
Funding
NIH R01
History
Degree Type
- Doctor of Philosophy
Department
- Biochemistry
Campus location
- West Lafayette