FP7Reintegration grant2014–2018

THE NASCENT CODE · Unravelling the Nascent Code: Signals sensed and transmitted by the nascent chain to acquire its functional state or reprogram gene expression

FP7 — People (Marie Curie Actions)

Duration
2014-07-14 → 2018-07-13
EU contribution
€100,000
Participants
1
Scheme
MC-CIG

Lines connect the coordinator with its partners.

Results in brief

Unravelling the Nascent Code: Signals sensed and transmitted by the nascent chain to acquire its functional state or reprogram gene expression

Emerging biochemical and biophysical data strongly suggest that the transformation of the potential set of proteins, encrypted in the genome of the cell, into its actual vital functional set, is a function not just of the genetic code but of an additional layer of information encoded within the newly synthesised polypeptide nascent chain (NC). Depending on the cellular status and starting on the very first steps of synthesis, a variety of signals are indeed formed within the ribosome and the evolving NC. These signals, by acting directly on the ribosome or by recruiting additional cellular machines, have the ability to pause or even abrogate the synthesis itself of the NC or to guide it towards the acquisition of its final functional state and cellular location. As a result, the translational step, becomes a new strategic pivotal point to sense the specific cellular status and accordingly complete, abrogate or re-program gene expression. Due to its distinct nature, I prefer to refer to this ensemble of signals as “the nascent code”. Despite our knowledge on the importance and existence of the nascent code, we know very little about its mechanism of action. The ultimate goal of this research line is to unravel the molecular determinants of the nascent code elucidating at the structural level its role during gene expression and regulation. Capitalising on the gathered expertise within our group and our collaboration partners, as well as the ideal environment offered by our Host Institute, CIC bioGUNE, we have settled on using a multidisciplinary approach based on x-ray crystallography, NMR and CryoEM to investigate from a macroscopic to atomic level the dynamics, structure and interactions of some the key players involved in the vital process of protein synthesis. The results obtained on the mechanism of action of chaperones and small molecules, among which new anti-infective agents, pave the way for the development of a new set of tools to control and modulate the essential ability of the cell to regulate gene expression at the translational level.

Data: CORDIS, © European Union

Project objective

Emerging biochemical and biophysical data strongly suggest that the transformation of the potential set of proteins, encrypted in the genome, into its actual vital functional set, is a manifestation not just of the genetic code, but of an additional layer of information encoded within the newly synthesized polypeptide nascent chain. To date, we know that immediately upon the first steps of protein synthesis, a variety of signals are formed within the evolving nascent chain (NC). These signals, by acting directly on the ribosome or by recruiting additional cellular machines, have the ability to direct new steps in the transformation of the NC and guide it towards the acquisition of its final functional state and cellular location. Due to its distinct nature, I will refer this ensemble of signals as THE NASCENT CODE. Despite our knowledge of its existence, we know very little about its mechanism of action. The goal of this research is to unravel the molecular determinants of the nascent code and to decipher how the signals, embedded in the primary sequence of the NC, orchestrate the concerted action of the ribosome and its ancillary factors (i,e, SecA, TF). The approach entails the reconstructing of the process describing the birth of a protein and following its progress over time. The techniques used in the analysis of this process, namely fluorescence spectroscopy, Cryo electron microscopy, solid state NMR-DNP, solution state NMR and X-ray crystallography, will illuminate macroscopic to atomic level details of the dynamics, structure and interactions of the key players involved. The realization of this research project will allow us to understand an essential process in the cell, for which very little structural information is currently available, and provide the structural foundation to intervene and control this process for biotechnological or therapeutic reasons.""

Original text from CORDIS.

Participants

  • ASOCIACION CENTRO DE INVESTIGACION COOPERATIVA EN BIOCIENCIAS · DERIO VIZCAYACoordinatorSpain

Links

Data: CORDIS, © European Union