Title | Spatial organization of bacterial transcription and translation. |
Publication Type | Journal Article |
Year of Publication | 2016 |
Authors | Castellana, M, Li, SHsin-Jung, Wingreen, NS |
Journal | Proc Natl Acad Sci U S A |
Volume | 113 |
Issue | 33 |
Pagination | 9286-91 |
Date Published | 2016 Aug 16 |
ISSN | 1091-6490 |
Keywords | Cell Cycle, Diffusion, Escherichia coli, Protein Biosynthesis, Ribosomes, RNA, Messenger, Transcription, Genetic |
Abstract | <p>In bacteria such as Escherichia coli, DNA is compacted into a nucleoid near the cell center, whereas ribosomes-molecular complexes that translate mRNAs into proteins-are mainly localized to the poles. We study the impact of this spatial organization using a minimal reaction-diffusion model for the cellular transcriptional-translational machinery. Although genome-wide mRNA-nucleoid segregation still lacks experimental validation, our model predicts that [Formula: see text] of mRNAs are segregated to the poles. In addition, our analysis reveals a "circulation" of ribosomes driven by the flux of mRNAs, from synthesis in the nucleoid to degradation at the poles. We show that our results are robust with respect to multiple, biologically relevant factors, such as mRNA degradation by RNase enzymes, different phases of the cell division cycle and growth rates, and the existence of nonspecific, transient interactions between ribosomes and mRNAs. Finally, we confirm that the observed nucleoid size stems from a balance between the forces that the chromosome and mRNAs exert on each other. This suggests a potential global feedback circuit in which gene expression feeds back on itself via nucleoid compaction.</p> |
DOI | 10.1073/pnas.1604995113 |
Alternate Journal | Proc Natl Acad Sci U S A |
PubMed ID | 27486246 |
PubMed Central ID | PMC4995950 |
Grant List | DP1 DA026192 / DA / NIDA NIH HHS / United States R21 AI102187 / AI / NIAID NIH HHS / United States |