Considerations for the use of transcriptomics in identifying the ‘genes that matter’ for environmental adaptation

ABSTRACT Transcriptomics has emerged as a powerful approach for exploring physiological responses to the environment. However, like any other experimental approach, transcriptomics has its limitations. Transcriptomics has been criticized as an inappropriate method to identify genes with large impacts on adaptive responses to the environment because: (1) genes with large impacts on fitness are rare; (2) a large change in gene expression does not necessarily equate to a large effect on fitness; and (3) protein activity is most relevant to fitness, and mRNA abundance is an unreliable indicator of protein activity. In this review, these criticisms are re-evaluated in the context of recent systems-level experiments that provide new insight into the relationship between gene expression and fitness during environmental stress. In general, these criticisms remain valid today, and indicate that exclusively using transcriptomics to screen for genes that underlie environmental adaptation will overlook constitutively expressed regulatory genes that play major roles in setting tolerance limits. Standard practices in transcriptomic data analysis pipelines may also be limiting insight by prioritizing highly differentially expressed and conserved genes over those genes that undergo moderate fold-changes and cannot be annotated. While these data certainly do not undermine the continued and widespread use of transcriptomics within environmental physiology, they do highlight the types of research questions for which transcriptomics is best suited and the need for more gene functional analyses. Such information is pertinent at a time when transcriptomics has become increasingly tractable and many researchers may be contemplating integrating transcriptomics into their research programs. Summary: The ability of transcriptomics to identify genes that underlie environmental adaptation is explored in the context of recent systems-level experiments that provide new insights into the relationship between gene expression and fitness.

[1]  T. Oliver,et al.  Genomic basis for coral resilience to climate change , 2013, Proceedings of the National Academy of Sciences.

[2]  T. Ideker,et al.  Integrating phenotypic and expression profiles to map arsenic-response networks , 2004, Genome Biology.

[3]  G. Hofmann,et al.  Constitutive roles for inducible genes: evidence for the alteration in expression of the inducible hsp70 gene in Antarctic notothenioid fishes. , 2004, American journal of physiology. Regulatory, integrative and comparative physiology.

[4]  Anushya Muruganujan,et al.  PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification , 2003, Nucleic Acids Res..

[5]  Francesco Falciani,et al.  Towards a System Level Understanding of Non-Model Organisms Sampled from the Environment: A Network Biology Approach , 2011, PLoS Comput. Biol..

[6]  W. J. Dickinson,et al.  Marginal fitness contributions of nonessential genes in yeast. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[7]  Anders Blomberg,et al.  High-resolution yeast phenomics resolves different physiological features in the saline response , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Wei-Po Lee,et al.  Computational methods for discovering gene networks from expression data , 2009, Briefings Bioinform..

[9]  Corey Nislow,et al.  Multiple Means to the Same End: The Genetic Basis of Acquired Stress Resistance in Yeast , 2011, PLoS genetics.

[10]  E. Carpenter,et al.  Emiliania huxleyi increases calcification but not expression of calcification-related genes in long-term exposure to elevated temperature and pCO2 , 2013, Philosophical Transactions of the Royal Society B: Biological Sciences.

[11]  G. Somero,et al.  Changes in gene expression associated with acclimation to constant temperatures and fluctuating daily temperatures in an annual killifish Austrofundulus limnaeus , 2004, Journal of Experimental Biology.

[12]  D. Manahan,et al.  Gene expression profiling of genetically determined growth variation in bivalve larvae (Crassostrea gigas) , 2010, Journal of Experimental Biology.

[13]  A. Cossins,et al.  Application of microarray technology in environmental and comparative physiology. , 2003, Annual review of physiology.

[14]  G. Hofmann,et al.  Regulation of heat shock genes in isolated hepatocytes from an Antarctic fish, Trematomus bernacchii , 2004, Journal of Experimental Biology.

[15]  C. Vulpe,et al.  Déjà vu in proteomics. A hit parade of repeatedly identified differentially expressed proteins , 2008, Proteomics.

[16]  D. Jenkinson,et al.  COMPARATIVE PHYSIOLOGY OF SWEATING , 1973, The British journal of dermatology.

[17]  Y. Ba,et al.  RNA-Seq technology and its application in fish transcriptomics. , 2014, Omics : a journal of integrative biology.

[18]  R. Morimoto,et al.  A Genetic Screening Strategy Identifies Novel Regulators of the Proteostasis Network , 2011, PLoS genetics.

[19]  A. Cashikar,et al.  Ssd1 Is Required for Thermotolerance and Hsp104-Mediated Protein Disaggregation in Saccharomyces cerevisiae , 2008, Molecular and Cellular Biology.

[20]  G. Hofmann,et al.  Comparison of Hsc70 orthologs from polar and temperate notothenioid fishes: differences in prevention of aggregation and refolding of denatured proteins. , 2005, American journal of physiology. Regulatory, integrative and comparative physiology.

[21]  G. Somero,et al.  A microarray-based transcriptomic time-course of hyper- and hypo-osmotic stress signaling events in the euryhaline fish Gillichthys mirabilis: osmosensors to effectors , 2008, Journal of Experimental Biology.

[22]  Zhong-Hui Duan,et al.  Fold change and p-value cutoffs significantly alter microarray interpretations , 2012, BMC Bioinformatics.

[23]  K. Golic,et al.  Loss of Hsp70 in Drosophila Is Pleiotropic, With Effects on Thermotolerance, Recovery From Heat Shock and Neurodegeneration , 2006, Genetics.

[24]  L. MacNeil,et al.  Gene regulatory networks and the role of robustness and stochasticity in the control of gene expression. , 2011, Genome research.

[25]  V. Jain,et al.  Insights into the regulation of bacteriophage endolysin: multiple means to the same end. , 2015, Microbiology.

[26]  Luis Serrano,et al.  Correlation of mRNA and protein in complex biological samples , 2009, FEBS letters.

[27]  Gilles Celeux,et al.  Data-based filtering for replicated high-throughput transcriptome sequencing experiments , 2013, Bioinform..

[28]  G. Warr,et al.  A transcriptomic analysis of land‐use impacts on the oyster, Crassostrea virginica, in the South Atlantic bight , 2009, Molecular ecology.

[29]  B. Reading,et al.  Ovary Transcriptome Profiling via Artificial Intelligence Reveals a Transcriptomic Fingerprint Predicting Egg Quality in Striped Bass, Morone saxatilis , 2014, PloS one.

[30]  2DE-proteomics meta-data indicate the existence of distinct cellular stress-responsive mechanisms , 2009, Expert review of proteomics.

[31]  Hannah Jaris,et al.  The simple fool's guide to population genomics via RNA‐Seq: an introduction to high‐throughput sequencing data analysis , 2012, Molecular ecology resources.

[32]  B. O’Hara,et al.  Changes in gene expression , 2021, Reference Module in Neuroscience and Biobehavioral Psychology.

[33]  G. Somero,et al.  Transcriptomic responses to heat stress in invasive and native blue mussels (genus Mytilus): molecular correlates of invasive success , 2010, Journal of Experimental Biology.

[34]  Ann M. Hess,et al.  which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Filtering for increased power for microarray data analysis , 2008 .

[35]  Todd H. Oakley,et al.  The Ecoresponsive Genome of Daphnia pulex , 2011, Science.

[36]  David Botstein,et al.  Yeast metabolic and signaling genes are required for heat-shock survival and have little overlap with the heat-induced genes , 2013, Proceedings of the National Academy of Sciences.

[37]  L. Tomanek Variation in the heat shock response and its implication for predicting the effect of global climate change on species' biogeographical distribution ranges and metabolic costs , 2010, Journal of Experimental Biology.

[38]  E. Osborne,et al.  Heat shock response of killifish (Fundulus heteroclitus): candidate gene and heterologous microarray approaches. , 2010, Physiological genomics.

[39]  J. Curtis,et al.  Transcriptomics of environmental acclimatization and survival in wild adult Pacific sockeye salmon (Oncorhynchus nerka) during spawning migration , 2011, Molecular ecology.

[40]  J. Bähler,et al.  Tuning gene expression to changing environments: from rapid responses to evolutionary adaptation , 2008, Nature Reviews Genetics.

[41]  A. Gracey Interpreting physiological responses to environmental change through gene expression profiling , 2007, Journal of Experimental Biology.

[42]  L. Hurst,et al.  Evolution of chromosome organization driven by selection for reduced gene expression noise , 2007, Nature Genetics.

[43]  A. Cossins,et al.  Post-genomic approaches to understanding the mechanisms of environmentally induced phenotypic plasticity , 2006, Journal of Experimental Biology.

[44]  B. Bettencourt,et al.  Inducible and constitutive heat shock gene expression responds to modification of Hsp70 copy number in Drosophila melanogaster but does not compensate for loss of thermotolerance in Hsp70 null flies , 2008, BMC Biology.

[45]  G. Somero,et al.  Transcriptional responses to thermal acclimation in the eurythermal fish Gillichthys mirabilis (Cooper 1864). , 2010, American journal of physiology. Regulatory, integrative and comparative physiology.

[46]  V. Thorsson,et al.  Integrated Genomic and Proteomic Analyses of Gene Expression in Mammalian Cells*S , 2004, Molecular & Cellular Proteomics.

[47]  Luke A. Gilbert,et al.  Repurposing CRISPR as an RNA-Guided Platform for Sequence-Specific Control of Gene Expression , 2013, Cell.

[48]  G. Somero Comparative physiology: a "crystal ball" for predicting consequences of global change. , 2011, American journal of physiology. Regulatory, integrative and comparative physiology.

[49]  R. Durbin,et al.  The Genome Sequence of Caenorhabditis briggsae: A Platform for Comparative Genomics , 2003, PLoS biology.

[50]  M. Feder,et al.  The biological limitations of transcriptomics in elucidating stress and stress responses , 2005, Journal of evolutionary biology.

[51]  Gary D Bader,et al.  The Genetic Landscape of a Cell , 2010, Science.

[52]  Ping Wang,et al.  Generally detected proteins in comparative proteomics – A matter of cellular stress response? , 2009, Proteomics.

[53]  Corey Nislow,et al.  The Yeast Deletion Collection: A Decade of Functional Genomics , 2014, Genetics.

[54]  C Sander,et al.  Bioinformatics and the discovery of gene function. , 1996, Trends in genetics : TIG.

[55]  Jung-Hsien Chiang,et al.  Molecular mechanisms of system responses to novel stimuli are predictable from public data , 2013, Nucleic acids research.

[56]  Luke A. Gilbert,et al.  CRISPR interference (CRISPRi) for sequence-specific control of gene expression , 2013, Nature Protocols.

[57]  Ben-Yang Liao,et al.  Mouse duplicate genes are as essential as singletons. , 2007, Trends in genetics : TIG.

[58]  Steven A. Harvey,et al.  A systematic genome-wide analysis of zebrafish protein-coding gene function , 2013, Nature.

[59]  A. Whitehead Comparative genomics in ecological physiology: toward a more nuanced understanding of acclimation and adaptation , 2012, Journal of Experimental Biology.

[60]  Brendan J. Frey,et al.  Challenges in estimating percent inclusion of alternatively spliced junctions from RNA-seq data , 2012, BMC Bioinformatics.

[61]  S Airaksinen,et al.  Heat-shock protein expression is absent in the antarctic fish Trematomus bernacchii (family Nototheniidae). , 2000, The Journal of experimental biology.

[62]  G. Somero,et al.  cDNA microarray analysis reveals the capacity of the cold-adapted Antarctic fish Trematomus bernacchii to alter gene expression in response to heat stress , 2009, Polar Biology.

[63]  W. Miller,et al.  Polar Bears Exhibit Genome-Wide Signatures of Bioenergetic Adaptation to Life in the Arctic Environment , 2014, Genome biology and evolution.

[64]  John D. Storey,et al.  Statistical significance for genomewide studies , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[65]  Melanie A. Huntley,et al.  Evolution of genes and genomes on the Drosophila phylogeny , 2007, Nature.

[66]  A. Abzhanov,et al.  The calmodulin pathway and evolution of elongated beak morphology in Darwin's finches , 2006, Nature.

[67]  D. Kültz,et al.  Evolution of the cellular stress proteome: from monophyletic origin to ubiquitous function , 2003, Journal of Experimental Biology.

[68]  R. Martienssen,et al.  Transposon Mutagenesis in the Study of Plant Development , 2003 .

[69]  J. Stillman,et al.  Seasonal and latitudinal acclimatization of cardiac transcriptome responses to thermal stress in porcelain crabs, Petrolisthes cinctipes , 2009, Molecular ecology.

[70]  Model of gene expression in extreme cold - reference transcriptome for the high-Antarctic cryopelagic notothenioid fish Pagothenia borchgrevinki , 2013, BMC Genomics.

[71]  G. Ammerer,et al.  Controlling gene expression in response to stress , 2011, Nature Reviews Genetics.

[72]  G. Somero,et al.  Transcriptomic responses to salinity stress in invasive and native blue mussels (genus Mytilus) , 2011, Molecular ecology.

[73]  Pablo Tamayo,et al.  Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[74]  H. Bohnert,et al.  Life at the extreme: lessons from the genome , 2012, Genome Biology.

[75]  A. Coulson,et al.  Genomics in C. elegans: so many genes, such a little worm. , 2005, Genome research.

[76]  Anne E Carpenter,et al.  Systematic genome-wide screens of gene function , 2004, Nature Reviews Genetics.

[77]  Ben Lehner Selection to minimise noise in living systems and its implications for the evolution of gene expression , 2008, Molecular systems biology.

[78]  M. Gerstein,et al.  RNA-Seq: a revolutionary tool for transcriptomics , 2009, Nature Reviews Genetics.

[79]  L. Aravind,et al.  Interplay between gene expression noise and regulatory network architecture. , 2012, Trends in genetics : TIG.

[80]  S. Palumbi,et al.  Mechanisms of reef coral resistance to future climate change , 2014, Science.

[81]  R. H. Gross,et al.  Natural Selection Canalizes Expression Variation of Environmentally Induced Plasticity-Enabling Genes , 2014, Molecular biology and evolution.

[82]  P. Finn,et al.  Hubs in biological interaction networks exhibit low changes in expression in experimental asthma , 2007, Molecular systems biology.

[83]  D. Field,et al.  Orphans as taxonomically restricted and ecologically important genes. , 2005, Microbiology.

[84]  R. Li,et al.  Sequencing‐based gene network analysis provides a core set of gene resource for understanding thermal adaptation in Zhikong scallop Chlamys farreri , 2014, Molecular ecology resources.

[85]  T. Fan,et al.  Hypoxia-induced mobilization of stored triglycerides in the euryoxic goby Gillichthys mirabilis , 2011, Journal of Experimental Biology.

[86]  T. Bosch,et al.  More than just orphans: are taxonomically-restricted genes important in evolution? , 2009, Trends in genetics : TIG.

[87]  Lan V. Zhang,et al.  Evidence for dynamically organized modularity in the yeast protein–protein interaction network , 2004, Nature.

[88]  Ronald W. Davis,et al.  Functional profiling of the Saccharomyces cerevisiae genome , 2002, Nature.

[89]  R. Morimoto,et al.  Identification of a Tissue-Selective Heat Shock Response Regulatory Network , 2013, PLoS genetics.

[90]  Fatih Ozsolak,et al.  RNA sequencing: advances, challenges and opportunities , 2011, Nature Reviews Genetics.

[91]  G. Hofmann,et al.  Defining the limits of physiological plasticity: how gene expression can assess and predict the consequences of ocean change , 2012, Philosophical Transactions of the Royal Society B: Biological Sciences.

[92]  M. Selbach,et al.  Global quantification of mammalian gene expression control , 2011, Nature.

[93]  A. Whitehead,et al.  Genomic mechanisms of evolved physiological plasticity in killifish distributed along an environmental salinity gradient , 2011, Proceedings of the National Academy of Sciences.

[94]  Brad T. Sherman,et al.  Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources , 2008, Nature Protocols.

[95]  J. Plotkin Transcriptional regulation is only half the story , 2010, Molecular systems biology.

[96]  Mike Tyers,et al.  Evolutionary and Physiological Importance of Hub Proteins , 2006, PLoS Comput. Biol..

[97]  Dongsup Kim,et al.  Analysis of a genome-wide set of gene deletions in the fission yeast Schizosaccharomyces pombe , 2010, Nature Biotechnology.

[98]  B. Menge,et al.  Transcriptomic responses to ocean acidification in larval sea urchins from a naturally variable pH environment , 2013, Molecular ecology.

[99]  Haiyan Xu,et al.  Hepatic knockdown of stearoyl-CoA desaturase 1 via RNA interference in obese mice decreases lipid content and changes fatty acid composition. , 2007, Frontiers in bioscience : a journal and virtual library.

[100]  R. Suarez,et al.  Metabolism in the age of ‘omes’ , 2012, Journal of Experimental Biology.

[101]  N. Socci,et al.  Role for Stearoyl-CoA Desaturase-1 in Leptin-Mediated Weight Loss , 2002, Science.

[102]  Ronald Jones Déja vu. , 2006, Veterinary anaesthesia and analgesia.

[103]  J. Harrow,et al.  A conditional knockout resource for the genome-wide study of mouse gene function , 2011, Nature.

[104]  M. Gerstein,et al.  Comparing protein abundance and mRNA expression levels on a genomic scale , 2003, Genome Biology.

[105]  Marc W Kirschner,et al.  Protein microarrays for genome‐wide posttranslational modification analysis , 2011, Wiley interdisciplinary reviews. Systems biology and medicine.

[106]  E. Marcotte,et al.  Insights into the regulation of protein abundance from proteomic and transcriptomic analyses , 2012, Nature Reviews Genetics.

[107]  B. Barrell,et al.  The genome sequence of Schizosaccharomyces pombe , 2002, Nature.

[108]  D. Kültz,et al.  Molecular and evolutionary basis of the cellular stress response. , 2005, Annual review of physiology.

[109]  Michael Breitenbach,et al.  Saccharomyces cerevisiae Genes Involved in Survival of Heat Shock , 2013, G3: Genes, Genomes, Genetics.

[110]  Peer Bork,et al.  Younger Genes Are Less Likely to Be Essential than Older Genes, and Duplicates Are Less Likely to Be Essential than Singletons of the Same Age , 2012, Molecular biology and evolution.

[111]  C. Logan,et al.  Transcriptomic responses to environmental temperature in eurythermal and stenothermal fishes , 2015, The Journal of Experimental Biology.

[112]  A. Whitehead,et al.  Common functional targets of adaptive micro‐ and macro‐evolutionary divergence in killifish , 2013, Molecular ecology.

[113]  G. Somero The physiology of global change: linking patterns to mechanisms. , 2012, Annual review of marine science.

[114]  G. Warr,et al.  The transcriptomic responses of the eastern oyster, Crassostrea virginica, to environmental conditions , 2011, Molecular ecology.

[115]  Thomas Mitchell-Olds,et al.  Evolutionary and ecological functional genomics , 2003, Nature Reviews Genetics.

[116]  B. Gaylord,et al.  Evolutionary change during experimental ocean acidification , 2013, Proceedings of the National Academy of Sciences.

[117]  E. Marcotte,et al.  Global signatures of protein and mRNA expression levelsw , 2009 .

[118]  Shinichi Sunagawa,et al.  Rapid Evolution of Coral Proteins Responsible for Interaction with the Environment , 2011, PloS one.

[119]  A. Barabasi,et al.  Lethality and centrality in protein networks , 2001, Nature.

[120]  James A. Cuff,et al.  Distinguishing protein-coding and noncoding genes in the human genome , 2007, Proceedings of the National Academy of Sciences.

[121]  Andreas Wagner,et al.  Duplicate genes and robustness to transient gene knock-downs in Caenorhabditis elegans , 2004, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[122]  C. Fuqua,et al.  Why so many unknown genes? Partitioning orphans from a representative transcriptome of the lone star tick Amblyomma americanum , 2013, BMC Genomics.

[123]  Adam P Arkin,et al.  Modularity of stress response evolution , 2008, Proceedings of the National Academy of Sciences.

[124]  N. Perrimon,et al.  Genome-Wide RNAi Analysis of Growth and Viability in Drosophila Cells , 2004, Science.