Literature DB >> 33438800

The GENDULF algorithm: mining transcriptomics to uncover modifier genes for monogenic diseases.

Noam Auslander1,2, Daniel M Ramos3, Ivette Zelaya4, Hiren Karathia5, Thomas O Crawford6,7, Alejandro A Schäffer1, Charlotte J Sumner3,7, Eytan Ruppin1.   

Abstract

Modifier genes are believed to account for the clinical variability observed in many Mendelian disorders, but their identification remains challenging due to the limited availability of genomics data from large patient cohorts. Here, we present GENDULF (GENetic moDULators identiFication), one of the first methods to facilitate prediction of disease modifiers using healthy and diseased tissue gene expression data. GENDULF is designed for monogenic diseases in which the mechanism is loss of function leading to reduced expression of the mutated gene. When applied to cystic fibrosis, GENDULF successfully identifies multiple, previously established disease modifiers, including EHF, SLC6A14, and CLCA1. It is then utilized in spinal muscular atrophy (SMA) and predicts U2AF1 as a modifier whose low expression correlates with higher SMN2 pre-mRNA exon 7 retention. Indeed, knockdown of U2AF1 in SMA patient-derived cells leads to increased full-length SMN2 transcript and SMN protein expression. Taking advantage of the increasing availability of transcriptomic data, GENDULF is a novel addition to existing strategies for prediction of genetic disease modifiers, providing insights into disease pathogenesis and uncovering novel therapeutic targets.
© 2020 The Authors. Published under the terms of the CC BY 4.0 license.

Entities:  

Keywords:  cystic fibrosis; digenic inheritance; gene expression; modifier gene; spinal muscular atrophy

Year:  2020        PMID: 33438800      PMCID: PMC7754056          DOI: 10.15252/msb.20209701

Source DB:  PubMed          Journal:  Mol Syst Biol        ISSN: 1744-4292            Impact factor:   11.429


  83 in total

1.  Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.

Authors:  J Zielenski; M Corey; R Rozmahel; D Markiewicz; I Aznarez; T Casals; S Larriba; B Mercier; G R Cutting; A Krebsova; M Macek; E Langfelder-Schwind; B C Marshall; J DeCelie-Germana; M Claustres; A Palacio; J Bal; A Nowakowska; C Ferec; X Estivill; P Durie; L C Tsui
Journal:  Nat Genet       Date:  1999-06       Impact factor: 38.330

Review 2.  Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamics.

Authors:  K M Dipple; E R McCabe
Journal:  Am J Hum Genet       Date:  2000-05-01       Impact factor: 11.025

3.  Modifier variant of METTL13 suppresses human GAB1-associated profound deafness.

Authors:  Rizwan Yousaf; Zubair M Ahmed; Arnaud Pj Giese; Robert J Morell; Ayala Lagziel; Alain Dabdoub; Edward R Wilcox; Sheikh Riazuddin; Thomas B Friedman; Saima Riazuddin
Journal:  J Clin Invest       Date:  2018-03-12       Impact factor: 14.808

4.  Genetic modifiers of lung disease in cystic fibrosis.

Authors:  Mitchell L Drumm; Michael W Konstan; Mark D Schluchter; Allison Handler; Rhonda Pace; Fei Zou; Maimoona Zariwala; David Fargo; Airong Xu; John M Dunn; Rebecca J Darrah; Ruslan Dorfman; Andrew J Sandford; Mary Corey; Julian Zielenski; Peter Durie; Katrina Goddard; James R Yankaskas; Fred A Wright; Michael R Knowles
Journal:  N Engl J Med       Date:  2005-10-06       Impact factor: 91.245

5.  SMN2 exon 7 splicing is inhibited by binding of hnRNP A1 to a common ESS motif that spans the 3' splice site.

Authors:  Thomas Koed Doktor; Lisbeth Dahl Schroeder; Anne Vested; Johan Palmfeldt; Henriette Skovgaard Andersen; Niels Gregersen; Brage Storstein Andresen
Journal:  Hum Mutat       Date:  2011-01-25       Impact factor: 4.878

6.  Gene modifiers of cystic fibrosis lung disease: A systematic review.

Authors:  Shivanthan Shanthikumar; Melanie N Neeland; Richard Saffery; Sarath Ranganathan
Journal:  Pediatr Pulmonol       Date:  2019-05-29

7.  Integrative approaches for large-scale transcriptome-wide association studies.

Authors:  Alexander Gusev; Arthur Ko; Huwenbo Shi; Gaurav Bhatia; Wonil Chung; Brenda W J H Penninx; Rick Jansen; Eco J C de Geus; Dorret I Boomsma; Fred A Wright; Patrick F Sullivan; Elina Nikkola; Marcus Alvarez; Mete Civelek; Aldons J Lusis; Terho Lehtimäki; Emma Raitoharju; Mika Kähönen; Ilkka Seppälä; Olli T Raitakari; Johanna Kuusisto; Markku Laakso; Alkes L Price; Päivi Pajukanta; Bogdan Pasaniuc
Journal:  Nat Genet       Date:  2016-02-08       Impact factor: 38.330

8.  A-44G transition in SMN2 intron 6 protects patients with spinal muscular atrophy.

Authors:  Xingxing Wu; Shu-Huei Wang; Junjie Sun; Adrian R Krainer; Yimin Hua; Thomas W Prior
Journal:  Hum Mol Genet       Date:  2017-07-15       Impact factor: 6.150

9.  Interaction between a novel TGFB1 haplotype and CFTR genotype is associated with improved lung function in cystic fibrosis.

Authors:  Lindsay A Bremer; Scott M Blackman; Lori L Vanscoy; Kathryn E McDougal; Amanda Bowers; Kathleen M Naughton; David J Cutler; Garry R Cutting
Journal:  Hum Mol Genet       Date:  2008-04-17       Impact factor: 6.150

10.  HTSeq--a Python framework to work with high-throughput sequencing data.

Authors:  Simon Anders; Paul Theodor Pyl; Wolfgang Huber
Journal:  Bioinformatics       Date:  2014-09-25       Impact factor: 6.937

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  2 in total

Review 1.  Spinal muscular atrophy.

Authors:  Eugenio Mercuri; Charlotte J Sumner; Francesco Muntoni; Basil T Darras; Richard S Finkel
Journal:  Nat Rev Dis Primers       Date:  2022-08-04       Impact factor: 65.038

2.  A high-throughput genome-wide RNAi screen identifies modifiers of survival motor neuron protein.

Authors:  Nikki M McCormack; Mahlet B Abera; Eveline S Arnold; Rebecca M Gibbs; Scott E Martin; Eugen Buehler; Yu-Chi Chen; Lu Chen; Kenneth H Fischbeck; Barrington G Burnett
Journal:  Cell Rep       Date:  2021-05-11       Impact factor: 9.423

  2 in total

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