Literature DB >> 29082913

Human gene essentiality.

István Bartha1, Julia di Iulio1, J Craig Venter1,2, Amalio Telenti1,2.   

Abstract

A gene can be defined as essential when loss of its function compromises viability of the individual (for example, embryonic lethality) or results in profound loss of fitness. At the population level, identification of essential genes is accomplished by observing intolerance to loss-of-function variants. Several computational methods are available to score gene essentiality, and recent progress has been made in defining essentiality in the non-coding genome. Haploinsufficiency is emerging as a critical aspect of gene essentiality: approximately 3,000 human genes cannot tolerate loss of one of the two alleles. Genes identified as essential in human cell lines or knockout mice may be distinct from those in living humans. Reconciling these discrepancies in how we evaluate gene essentiality has applications in clinical genetics and may offer insights for drug development.

Entities:  

Mesh:

Substances:

Year:  2017        PMID: 29082913     DOI: 10.1038/nrg.2017.75

Source DB:  PubMed          Journal:  Nat Rev Genet        ISSN: 1471-0056            Impact factor:   53.242


  82 in total

1.  Enhancer mutations and phenotype modularity.

Authors:  Christopher T Gordon; Stanislas Lyonnet
Journal:  Nat Genet       Date:  2014-01       Impact factor: 38.330

2.  Mechanisms of haploinsufficiency revealed by genome-wide profiling in yeast.

Authors:  Adam M Deutschbauer; Daniel F Jaramillo; Michael Proctor; Jochen Kumm; Maureen E Hillenmeyer; Ronald W Davis; Corey Nislow; Guri Giaever
Journal:  Genetics       Date:  2005-02-16       Impact factor: 4.562

3.  Too many roads not taken.

Authors:  Aled M Edwards; Ruth Isserlin; Gary D Bader; Stephen V Frye; Timothy M Willson; Frank H Yu
Journal:  Nature       Date:  2011-02-10       Impact factor: 49.962

4.  Genetic variants regulating expression levels and isoform diversity during embryogenesis.

Authors:  Enrico Cannavò; Nils Koelling; Dermot Harnett; David Garfield; Francesco P Casale; Lucia Ciglar; Hilary E Gustafson; Rebecca R Viales; Raquel Marco-Ferreres; Jacob F Degner; Bingqing Zhao; Oliver Stegle; Ewan Birney; Eileen E M Furlong
Journal:  Nature       Date:  2016-12-26       Impact factor: 49.962

5.  LoFtool: a gene intolerance score based on loss-of-function variants in 60 706 individuals.

Authors:  João Fadista; Nikolay Oskolkov; Ola Hansson; Leif Groop
Journal:  Bioinformatics       Date:  2017-02-15       Impact factor: 6.937

6.  A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease.

Authors:  Damian Smedley; Max Schubach; Julius O B Jacobsen; Sebastian Köhler; Tomasz Zemojtel; Malte Spielmann; Marten Jäger; Harry Hochheiser; Nicole L Washington; Julie A McMurry; Melissa A Haendel; Christopher J Mungall; Suzanna E Lewis; Tudor Groza; Giorgio Valentini; Peter N Robinson
Journal:  Am J Hum Genet       Date:  2016-08-25       Impact factor: 11.025

7.  A high-resolution map of human evolutionary constraint using 29 mammals.

Authors:  Kerstin Lindblad-Toh; Manuel Garber; Or Zuk; Michael F Lin; Brian J Parker; Stefan Washietl; Pouya Kheradpour; Jason Ernst; Gregory Jordan; Evan Mauceli; Lucas D Ward; Craig B Lowe; Alisha K Holloway; Michele Clamp; Sante Gnerre; Jessica Alföldi; Kathryn Beal; Jean Chang; Hiram Clawson; James Cuff; Federica Di Palma; Stephen Fitzgerald; Paul Flicek; Mitchell Guttman; Melissa J Hubisz; David B Jaffe; Irwin Jungreis; W James Kent; Dennis Kostka; Marcia Lara; Andre L Martins; Tim Massingham; Ida Moltke; Brian J Raney; Matthew D Rasmussen; Jim Robinson; Alexander Stark; Albert J Vilella; Jiayu Wen; Xiaohui Xie; Michael C Zody; Jen Baldwin; Toby Bloom; Chee Whye Chin; Dave Heiman; Robert Nicol; Chad Nusbaum; Sarah Young; Jane Wilkinson; Kim C Worley; Christie L Kovar; Donna M Muzny; Richard A Gibbs; Andrew Cree; Huyen H Dihn; Gerald Fowler; Shalili Jhangiani; Vandita Joshi; Sandra Lee; Lora R Lewis; Lynne V Nazareth; Geoffrey Okwuonu; Jireh Santibanez; Wesley C Warren; Elaine R Mardis; George M Weinstock; Richard K Wilson; Kim Delehaunty; David Dooling; Catrina Fronik; Lucinda Fulton; Bob Fulton; Tina Graves; Patrick Minx; Erica Sodergren; Ewan Birney; Elliott H Margulies; Javier Herrero; Eric D Green; David Haussler; Adam Siepel; Nick Goldman; Katherine S Pollard; Jakob S Pedersen; Eric S Lander; Manolis Kellis
Journal:  Nature       Date:  2011-10-12       Impact factor: 49.962

8.  Genic intolerance to functional variation and the interpretation of personal genomes.

Authors:  Slavé Petrovski; Quanli Wang; Erin L Heinzen; Andrew S Allen; David B Goldstein
Journal:  PLoS Genet       Date:  2013-08-22       Impact factor: 5.917

9.  An expanded sequence context model broadly explains variability in polymorphism levels across the human genome.

Authors:  Varun Aggarwala; Benjamin F Voight
Journal:  Nat Genet       Date:  2016-02-15       Impact factor: 38.330

10.  Analysis of stop-gain and frameshift variants in human innate immunity genes.

Authors:  Antonio Rausell; Pejman Mohammadi; Paul J McLaren; Istvan Bartha; Ioannis Xenarios; Jacques Fellay; Amalio Telenti
Journal:  PLoS Comput Biol       Date:  2014-07-24       Impact factor: 4.475

View more
  66 in total

Review 1.  Measuring intolerance to mutation in human genetics.

Authors:  Zachary L Fuller; Jeremy J Berg; Hakhamanesh Mostafavi; Guy Sella; Molly Przeworski
Journal:  Nat Genet       Date:  2019-04-08       Impact factor: 38.330

Review 2.  Genetic-Driven Druggable Target Identification and Validation.

Authors:  Matteo Floris; Stefania Olla; David Schlessinger; Francesco Cucca
Journal:  Trends Genet       Date:  2018-05-23       Impact factor: 11.639

Review 3.  Biophysical and Mechanistic Models for Disease-Causing Protein Variants.

Authors:  Amelie Stein; Douglas M Fowler; Rasmus Hartmann-Petersen; Kresten Lindorff-Larsen
Journal:  Trends Biochem Sci       Date:  2019-01-31       Impact factor: 13.807

Review 4.  Genetic interaction networks in cancer cells.

Authors:  Barbara Mair; Jason Moffat; Charles Boone; Brenda J Andrews
Journal:  Curr Opin Genet Dev       Date:  2019-04-08       Impact factor: 5.578

5.  The human noncoding genome defined by genetic diversity.

Authors:  Julia di Iulio; Istvan Bartha; Emily H M Wong; Hung-Chun Yu; Victor Lavrenko; Dongchan Yang; Inkyung Jung; Michael A Hicks; Naisha Shah; Ewen F Kirkness; Martin M Fabani; William H Biggs; Bing Ren; J Craig Venter; Amalio Telenti
Journal:  Nat Genet       Date:  2018-02-26       Impact factor: 38.330

Review 6.  Regulatory genome variants in human susceptibility to infection.

Authors:  Amalio Telenti; Julia di Iulio
Journal:  Hum Genet       Date:  2019-12-05       Impact factor: 4.132

7.  Genetic diagnosis in first or second trimester pregnancy loss using exome sequencing: a systematic review of human essential genes.

Authors:  Sarah M Robbins; Matthew A Thimm; David Valle; Angie C Jelin
Journal:  J Assist Reprod Genet       Date:  2019-07-04       Impact factor: 3.412

Review 8.  Disease-Associated Genetic Variation in Human Mitochondrial Protein Import.

Authors:  Emmanuelle Nicolas; Rossella Tricarico; Michelle Savage; Erica A Golemis; Michael J Hall
Journal:  Am J Hum Genet       Date:  2019-05-02       Impact factor: 11.025

9.  Improved Pathogenic Variant Localization via a Hierarchical Model of Sub-regional Intolerance.

Authors:  Tristan J Hayeck; Nicholas Stong; Charles J Wolock; Brett Copeland; Sitharthan Kamalakaran; David B Goldstein; Andrew S Allen
Journal:  Am J Hum Genet       Date:  2019-01-24       Impact factor: 11.025

10.  Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes.

Authors:  Antonio Rausell; Yufei Luo; Marie Lopez; Yoann Seeleuthner; Franck Rapaport; Antoine Favier; Peter D Stenson; David N Cooper; Etienne Patin; Jean-Laurent Casanova; Lluis Quintana-Murci; Laurent Abel
Journal:  Proc Natl Acad Sci U S A       Date:  2020-06-02       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.