Genome Regulation in Fission Yeast
Jurg Bahler, Professor, University College London
Data on absolute molecule
numbers will empower the modeling, understanding, and comparison of cellular
functions and biological systems. We quantified transcriptomes and proteomes in
fission yeast during cellular proliferation and quiescence. For the transcriptome
quantification we calibrated RNA-seq data with absolute data from nCounter
analyses. This rich resource provides the first comprehensive reference for all
RNA and most protein concentrations in a eukaryote under two key
physiological conditions. The integrated data set supports quantitative biology
and affords unique insights into cell regulation. Although mRNAs are typically
expressed in a narrow range above 1 copy/cell, most long, noncoding RNAs,
except for a distinct subset, are tightly repressed below 1 copy/cell.
Cell-cycle-regulated transcription tunes mRNA numbers to phase-specific
requirements but can also bring about more switch-like expression. Proteins
greatly exceed mRNAs in abundance and dynamic range, and concentrations are
regulated to functional demands. Upon transition to quiescence, the proteome
changes substantially, but, in stark contrast to mRNAs, proteins do not
uniformly decrease but scale with cell volume. I will also briefly talk about
our analyses of non-coding RNAs, alternative splicing and intronic
lariats/branch points based on RNA-seq data sampled in different physiological
conditions and mutant backgrounds.
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