Literature DB >> 23333204

Understanding the immunological impact of the human mutation explosion.

T D Andrews1, G Sjollema, C C Goodnow.   

Abstract

The recent development of human exome sequencing technology has revealed that our immune system is riddled with more genetic defects than anyone imagined. As a legacy of the recent human population explosion, we each inherit hundreds of rare mutations that alter the sequence of proteins. This mutation load is ten times higher than that induced by experimental treatment of mice by ethylnitrosourea; a high fraction of which has substantial effects on immune function. This mutation burden is likely to be a major factor in the incidence of many human immune disorders, but understanding this at the level of individual patients will require new bioinformatics and experimental strategies to assess the impact of individual and combined mutations on immune response pathways.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23333204     DOI: 10.1016/j.it.2012.12.001

Source DB:  PubMed          Journal:  Trends Immunol        ISSN: 1471-4906            Impact factor:   16.687


  8 in total

1.  Quantitative reduction of the TCR adapter protein SLP-76 unbalances immunity and immune regulation.

Authors:  Owen M Siggs; Lisa A Miosge; Stephen R Daley; Kelly Asquith; Paul S Foster; Adrian Liston; Christopher C Goodnow
Journal:  J Immunol       Date:  2015-02-06       Impact factor: 5.422

2.  Autism-associated missense genetic variants impact locomotion and neurodevelopment in Caenorhabditis elegans.

Authors:  Wan-Rong Wong; Katherine I Brugman; Shayda Maher; Jun Young Oh; Kevin Howe; Mihoko Kato; Paul W Sternberg
Journal:  Hum Mol Genet       Date:  2019-07-01       Impact factor: 6.150

3.  A ZAP-70 kinase domain variant prevents thymocyte-positive selection despite signalling CD69 induction.

Authors:  Owen M Siggs; Adèle L Yates; Susan Schlenner; Adrian Liston; Sylvie Lesage; Christopher C Goodnow
Journal:  Immunology       Date:  2014-04       Impact factor: 7.397

4.  Comparison of predicted and actual consequences of missense mutations.

Authors:  Lisa A Miosge; Matthew A Field; Yovina Sontani; Vicky Cho; Simon Johnson; Anna Palkova; Bhavani Balakishnan; Rong Liang; Yafei Zhang; Stephen Lyon; Bruce Beutler; Belinda Whittle; Edward M Bertram; Anselm Enders; Christopher C Goodnow; T Daniel Andrews
Journal:  Proc Natl Acad Sci U S A       Date:  2015-08-12       Impact factor: 11.205

5.  A novel Zap70 mutation with reduced protein stability demonstrates the rate-limiting threshold for Zap70 in T-cell receptor signalling.

Authors:  Bénédicte Cauwe; Lei Tian; Dean Franckaert; Wim Pierson; Kim A Staats; Susan M Schlenner; Adrian Liston
Journal:  Immunology       Date:  2014-03       Impact factor: 7.397

6.  Guidelines for genetic studies in single patients: lessons from primary immunodeficiencies.

Authors:  Jean-Laurent Casanova; Mary Ellen Conley; Stephen J Seligman; Laurent Abel; Luigi D Notarangelo
Journal:  J Exp Med       Date:  2014-10-13       Impact factor: 14.307

7.  Protein structure aids predicting functional perturbation of missense variants in SCN5A and KCNQ1.

Authors:  Brett M Kroncke; Jeffrey Mendenhall; Derek K Smith; Charles R Sanders; John A Capra; Alfred L George; Jeffrey D Blume; Jens Meiler; Dan M Roden
Journal:  Comput Struct Biotechnol J       Date:  2019-02-01       Impact factor: 7.271

8.  Rare missense variants in the human cytosolic antibody receptor preserve antiviral function.

Authors:  Jingwei Zeng; Greg Slodkowicz; Leo C James
Journal:  Elife       Date:  2019-10-15       Impact factor: 8.140

  8 in total

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