TY - JOUR
T1 - Coordinated Pulses of mRNA and of Protein Translation or Degradation Produce EGF-Induced Protein Bursts
AU - Golan-Lavi, Roni
AU - Giacomelli, Chiara
AU - Fuks, Garold
AU - Zeisel, Amit
AU - Sonntag, Johanna
AU - Sinha, Sanchari
AU - Kostler, Wolfgang
AU - Wiemann, Stefan
AU - Korf, Ulrike
AU - Yarden, Yosef
AU - Domany, Eytan
AU - Köstler, Wolfgang
N1 - Publisher Copyright: © 2017 The Author(s)
PY - 2017/3/28
Y1 - 2017/3/28
N2 - Protein responses to extracellular cues are governed by gene transcription, mRNA degradation and translation, and protein degradation. In order to understand how these time-dependent processes cooperate to generate dynamic responses, we analyzed the response of human mammary cells to the epidermal growth factor (EGF). Integrating time-dependent transcript and protein data into a mathematical model, we inferred for several proteins their pre- and post-stimulus translation and degradation coefficients and found that they exhibit complex, time-dependent variation. Specifically, we identified strategies of protein production and degradation acting in concert to generate rapid, transient protein bursts in response to EGF. Remarkably, for some proteins, for which the response necessitates rapidly decreased abundance, cells exhibit a transient increase in the corresponding degradation coefficient. Our model and analysis allow inference of the kinetics of mRNA translation and protein degradation, without perturbing cells, and open a way to understanding the fundamental processes governing time-dependent protein abundance profiles.
AB - Protein responses to extracellular cues are governed by gene transcription, mRNA degradation and translation, and protein degradation. In order to understand how these time-dependent processes cooperate to generate dynamic responses, we analyzed the response of human mammary cells to the epidermal growth factor (EGF). Integrating time-dependent transcript and protein data into a mathematical model, we inferred for several proteins their pre- and post-stimulus translation and degradation coefficients and found that they exhibit complex, time-dependent variation. Specifically, we identified strategies of protein production and degradation acting in concert to generate rapid, transient protein bursts in response to EGF. Remarkably, for some proteins, for which the response necessitates rapidly decreased abundance, cells exhibit a transient increase in the corresponding degradation coefficient. Our model and analysis allow inference of the kinetics of mRNA translation and protein degradation, without perturbing cells, and open a way to understanding the fundamental processes governing time-dependent protein abundance profiles.
KW - dynamic protein response
KW - post-transcriptional processes
KW - pulsed protein degradation
UR - http://www.scopus.com/inward/record.url?scp=85016260772&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.celrep.2017.03.014
DO - https://doi.org/10.1016/j.celrep.2017.03.014
M3 - مقالة
SN - 2211-1247
VL - 18
SP - 3129
EP - 3142
JO - Cell Reports
JF - Cell Reports
IS - 13
ER -