Issue 10, 2015

Next-generation analysis of gene expression regulation – comparing the roles of synthesis and degradation

Abstract

Technological advances now enable routine measurement of mRNA and protein abundances, and estimates of their rates of synthesis and degradation that inform on their values and the degree of change in response to stimuli. Importantly, more and more data on time-series experiments are emerging, e.g. of cells responding to stress, enabling first insights into a new dimension of gene expression regulation – its dynamics and how it allows for very different response signals across genes. This review discusses recently published methods and datasets, their impact on what we now know about the relationships between concentrations and synthesis rates of mRNAs and proteins in yeast and mammalian cells, their evolution, and new hypotheses on translation regulatory mechanisms generated by approaches that involve ribosome footprinting.

Graphical abstract: Next-generation analysis of gene expression regulation – comparing the roles of synthesis and degradation

Supplementary files

Article information

Article type
Review Article
Submitted
01 五月 2015
Accepted
29 七月 2015
First published
29 七月 2015

Mol. BioSyst., 2015,11, 2680-2689

Author version available

Next-generation analysis of gene expression regulation – comparing the roles of synthesis and degradation

J. McManus, Z. Cheng and C. Vogel, Mol. BioSyst., 2015, 11, 2680 DOI: 10.1039/C5MB00310E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements