How Messenger RNA and Nascent Chain Sequences Regulate Translation Elongation

Author:

Choi Junhong12,Grosely Rosslyn1,Prabhakar Arjun13,Lapointe Christopher P.1,Wang Jinfan1,Puglisi Joseph D.1

Affiliation:

1. Department of Structural Biology, Stanford University School of Medicine, Stanford, California 94305–5126, USA;, , , , ,

2. Department of Applied Physics, Stanford University, Stanford, California 94305–4090, USA

3. Program in Biophysics, Stanford University, Stanford, California 94305, USA

Abstract

Translation elongation is a highly coordinated, multistep, multifactor process that ensures accurate and efficient addition of amino acids to a growing nascent-peptide chain encoded in the sequence of translated messenger RNA (mRNA). Although translation elongation is heavily regulated by external factors, there is clear evidence that mRNA and nascent-peptide sequences control elongation dynamics, determining both the sequence and structure of synthesized proteins. Advances in methods have driven experiments that revealed the basic mechanisms of elongation as well as the mechanisms of regulation by mRNA and nascent-peptide sequences. In this review, we highlight how mRNA and nascent-peptide elements manipulate the translation machinery to alter the dynamics and pathway of elongation.

Publisher

Annual Reviews

Subject

Biochemistry

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