Literature DB >> 18775913

Rapid whole-genome mutational profiling using next-generation sequencing technologies.

Douglas R Smith1, Aaron R Quinlan, Heather E Peckham, Kathryn Makowsky, Wei Tao, Betty Woolf, Lei Shen, William F Donahue, Nadeem Tusneem, Michael P Stromberg, Donald A Stewart, Lu Zhang, Swati S Ranade, Jason B Warner, Clarence C Lee, Brittney E Coleman, Zheng Zhang, Stephen F McLaughlin, Joel A Malek, Jon M Sorenson, Alan P Blanchard, Jarrod Chapman, David Hillman, Feng Chen, Daniel S Rokhsar, Kevin J McKernan, Thomas W Jeffries, Gabor T Marth, Paul M Richardson.   

Abstract

Forward genetic mutational studies, adaptive evolution, and phenotypic screening are powerful tools for creating new variant organisms with desirable traits. However, mutations generated in the process cannot be easily identified with traditional genetic tools. We show that new high-throughput, massively parallel sequencing technologies can completely and accurately characterize a mutant genome relative to a previously sequenced parental (reference) strain. We studied a mutant strain of Pichia stipitis, a yeast capable of converting xylose to ethanol. This unusually efficient mutant strain was developed through repeated rounds of chemical mutagenesis, strain selection, transformation, and genetic manipulation over a period of seven years. We resequenced this strain on three different sequencing platforms. Surprisingly, we found fewer than a dozen mutations in open reading frames. All three sequencing technologies were able to identify each single nucleotide mutation given at least 10-15-fold nominal sequence coverage. Our results show that detecting mutations in evolved and engineered organisms is rapid and cost-effective at the whole-genome level using new sequencing technologies. Identification of specific mutations in strains with altered phenotypes will add insight into specific gene functions and guide further metabolic engineering efforts.

Entities:  

Mesh:

Year:  2008        PMID: 18775913      PMCID: PMC2556265          DOI: 10.1101/gr.077776.108

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  10 in total

1.  A general approach to single-nucleotide polymorphism discovery.

Authors:  G T Marth; I Korf; M D Yandell; R T Yeh; Z Gu; H Zakeri; N O Stitziel; L Hillier; P Y Kwok; W R Gish
Journal:  Nat Genet       Date:  1999-12       Impact factor: 38.330

2.  Wood ingestion by passalid beetles in the presence of xylose-fermenting gut yeasts.

Authors:  Sung-Oui Suh; Christopher J Marshall; Joseph V McHugh; Meredith Blackwell
Journal:  Mol Ecol       Date:  2003-11       Impact factor: 6.185

3.  NUMTs in sequenced eukaryotic genomes.

Authors:  Erik Richly; Dario Leister
Journal:  Mol Biol Evol       Date:  2004-03-10       Impact factor: 16.240

4.  Automating sequence-based detection and genotyping of SNPs from diploid samples.

Authors:  Matthew Stephens; James S Sloan; P D Robertson; Paul Scheet; Deborah A Nickerson
Journal:  Nat Genet       Date:  2006-02-19       Impact factor: 38.330

5.  Pyrobayes: an improved base caller for SNP discovery in pyrosequences.

Authors:  Aaron R Quinlan; Donald A Stewart; Michael P Strömberg; Gábor T Marth
Journal:  Nat Methods       Date:  2008-01-13       Impact factor: 28.547

Review 6.  Next-generation sequencing transforms today's biology.

Authors:  Stephan C Schuster
Journal:  Nat Methods       Date:  2007-12-19       Impact factor: 28.547

7.  Disruption of the cytochrome c gene in xylose-utilizing yeast Pichia stipitis leads to higher ethanol production.

Authors:  N Q Shi; B Davis; F Sherman; J Cruz; T W Jeffries
Journal:  Yeast       Date:  1999-08       Impact factor: 3.239

8.  Consed: a graphical tool for sequence finishing.

Authors:  D Gordon; C Abajian; P Green
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

9.  Genome sequence of the lignocellulose-bioconverting and xylose-fermenting yeast Pichia stipitis.

Authors:  Thomas W Jeffries; Igor V Grigoriev; Jane Grimwood; José M Laplaza; Andrea Aerts; Asaf Salamov; Jeremy Schmutz; Erika Lindquist; Paramvir Dehal; Harris Shapiro; Yong-Su Jin; Volkmar Passoth; Paul M Richardson
Journal:  Nat Biotechnol       Date:  2007-03-04       Impact factor: 54.908

10.  A high-resolution, nucleosome position map of C. elegans reveals a lack of universal sequence-dictated positioning.

Authors:  Anton Valouev; Jeffrey Ichikawa; Thaisan Tonthat; Jeremy Stuart; Swati Ranade; Heather Peckham; Kathy Zeng; Joel A Malek; Gina Costa; Kevin McKernan; Arend Sidow; Andrew Fire; Steven M Johnson
Journal:  Genome Res       Date:  2008-05-13       Impact factor: 9.043

  10 in total
  118 in total

Review 1.  Clinical implementation of comprehensive strategies to characterize cancer genomes: opportunities and challenges.

Authors:  Laura E MacConaill; Paul Van Hummelen; Matthew Meyerson; William C Hahn
Journal:  Cancer Discov       Date:  2011-09       Impact factor: 39.397

2.  SNP-Ratio Mapping (SRM): identifying lethal alleles and mutations in complex genetic backgrounds by next-generation sequencing.

Authors:  Heike Lindner; Michael T Raissig; Christian Sailer; Hiroko Shimosato-Asano; Rémy Bruggmann; Ueli Grossniklaus
Journal:  Genetics       Date:  2012-05-29       Impact factor: 4.562

3.  What Next? The Next Transit from Biology to Diagnostics: Next Generation Sequencing for Immunogenetics.

Authors:  Christian Gabriel; Stephanie Stabentheiner; Martin Danzer; Johannes Pröll
Journal:  Transfus Med Hemother       Date:  2011-09-25       Impact factor: 3.747

Review 4.  Next generation sequencing for clinical diagnostics-principles and application to targeted resequencing for hypertrophic cardiomyopathy: a paper from the 2009 William Beaumont Hospital Symposium on Molecular Pathology.

Authors:  Karl V Voelkerding; Shale Dames; Jacob D Durtschi
Journal:  J Mol Diagn       Date:  2010-09       Impact factor: 5.568

5.  The 'Whole Genome Age'

Authors:  Peter Bugert
Journal:  Transfus Med Hemother       Date:  2009       Impact factor: 3.747

6.  Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for resequencing of hypertrophic cardiomyopathy-associated genes.

Authors:  Shale Dames; Jacob Durtschi; Katherine Geiersbach; Jack Stephens; Karl V Voelkerding
Journal:  J Biomol Tech       Date:  2010-07

Review 7.  Next-generation sequencing techniques for eukaryotic microorganisms: sequencing-based solutions to biological problems.

Authors:  Minou Nowrousian
Journal:  Eukaryot Cell       Date:  2010-07-02

8.  A strategy for direct mapping and identification of mutations by whole-genome sequencing.

Authors:  Steven Zuryn; Stéphanie Le Gras; Karine Jamet; Sophie Jarriault
Journal:  Genetics       Date:  2010-07-06       Impact factor: 4.562

9.  Dindel: accurate indel calls from short-read data.

Authors:  Cornelis A Albers; Gerton Lunter; Daniel G MacArthur; Gilean McVean; Willem H Ouwehand; Richard Durbin
Journal:  Genome Res       Date:  2010-10-27       Impact factor: 9.043

10.  Illumina-based analysis of bacterial diversity related to halophytes Salicornia europaea and Sueada aralocaspica.

Authors:  Ying-wu Shi; Kai Lou; Chun Li; Lei Wang; Zhen-yong Zhao; Shuai Zhao; Chang-yan Tian
Journal:  J Microbiol       Date:  2015-10-02       Impact factor: 3.422

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.