Literature DB >> 24954581

Exposing synonymous mutations.

Ryan C Hunt1, Vijaya L Simhadri2, Matthew Iandoli2, Zuben E Sauna3, Chava Kimchi-Sarfaty4.   

Abstract

Synonymous codon changes, which do not alter protein sequence, were previously thought to have no functional consequence. Although this concept has been overturned in recent years, there is no unique mechanism by which these changes exert biological effects. A large repertoire of both experimental and bioinformatic methods has been developed to understand the effects of synonymous variants. Results from this body of work have provided global insights into how biological systems exploit the degeneracy of the genetic code to control gene expression, protein folding efficiency, and the coordinated expression of functionally related gene families. Although it is now clear that synonymous variants are important in a variety of contexts, from human disease to the safety and efficacy of therapeutic proteins, there is no clear consensus on the approaches to identify and validate these changes. Here, we review the diverse methods to understand the effects of synonymous mutations. Published by Elsevier Ltd.

Entities:  

Keywords:  codon usage; mRNA structure; synonymous mutation; synonymous single nucleotide polymorphism; translation speed

Mesh:

Substances:

Year:  2014        PMID: 24954581     DOI: 10.1016/j.tig.2014.04.006

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  116 in total

Review 1.  The Code of Silence: Widespread Associations Between Synonymous Codon Biases and Gene Function.

Authors:  Fran Supek
Journal:  J Mol Evol       Date:  2015-11-04       Impact factor: 2.395

2.  Genetic Variants in the Activation of the Brown-Like Adipocyte Pathway and the Risk for Severe Obesity.

Authors:  Ana Carolina Proença da Fonseca; Guilherme Proença da Fonseca; Bruna Marchesini; Danielle Dutra Voigt; Mario Campos Junior; Verônica Marques Zembrzuski; João Regis Ivar Carneiro; José Firmino Nogueira Neto; Pedro Hernan Cabello; Giselda Maria Kalil Cabello
Journal:  Obes Facts       Date:  2020-04-23       Impact factor: 3.942

3.  Leveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants among exon-captured variants of uncertain significance.

Authors:  Zachry T Soens; Justin Branch; Shijing Wu; Zhisheng Yuan; Yumei Li; Hui Li; Keqing Wang; Mingchu Xu; Lavan Rajan; Fabiana L Motta; Renata T Simões; Irma Lopez-Solache; Radwan Ajlan; David G Birch; Peiquan Zhao; Fernanda B Porto; Juliana Sallum; Robert K Koenekoop; Ruifang Sui; Rui Chen
Journal:  Hum Mutat       Date:  2017-08-18       Impact factor: 4.878

Review 4.  Human gene essentiality.

Authors:  István Bartha; Julia di Iulio; J Craig Venter; Amalio Telenti
Journal:  Nat Rev Genet       Date:  2017-10-30       Impact factor: 53.242

5.  Increased fire frequency promotes stronger spatial genetic structure and natural selection at regional and local scales in Pinus halepensis Mill.

Authors:  Katharina B Budde; Santiago C González-Martínez; Miguel Navascués; Concetta Burgarella; Elena Mosca; Zaida Lorenzo; Mario Zabal-Aguirre; Giovanni G Vendramin; Miguel Verdú; Juli G Pausas; Myriam Heuertz
Journal:  Ann Bot       Date:  2017-04-01       Impact factor: 4.357

Review 6.  The stop-and-go traffic regulating protein biogenesis: How translation kinetics controls proteostasis.

Authors:  Kevin C Stein; Judith Frydman
Journal:  J Biol Chem       Date:  2018-11-30       Impact factor: 5.157

7.  Synonymous variants that disrupt messenger RNA structure are significantly constrained in the human population.

Authors:  Jeffrey B S Gaither; Grant E Lammi; James L Li; David M Gordon; Harkness C Kuck; Benjamin J Kelly; James R Fitch; Peter White
Journal:  Gigascience       Date:  2021-04-05       Impact factor: 6.524

Review 8.  Settling the score: variant prioritization and Mendelian disease.

Authors:  Karen Eilbeck; Aaron Quinlan; Mark Yandell
Journal:  Nat Rev Genet       Date:  2017-08-14       Impact factor: 53.242

9.  Functional analysis of rare variants in mismatch repair proteins augments results from computation-based predictive methods.

Authors:  Sanjeevani Arora; Peter J Huwe; Rahmat Sikder; Manali Shah; Amanda J Browne; Randy Lesh; Emmanuelle Nicolas; Sanat Deshpande; Michael J Hall; Roland L Dunbrack; Erica A Golemis
Journal:  Cancer Biol Ther       Date:  2017-05-11       Impact factor: 4.742

10.  Codon bias among synonymous rare variants is associated with Alzheimer's disease imaging biomarker.

Authors:  Jason E Miller; Manu K Shivakumar; Shannon L Risacher; Andrew J Saykin; Seunggeun Lee; Kwangsik Nho; Dokyoon Kim
Journal:  Pac Symp Biocomput       Date:  2018
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