Transcriptional Regulatory Features associated with Coccidioides immitis phase transition

Coccidioidomycosis (Valley Fever) is an emerging endemic fungal infection with a rising incidence and an expanding geographic range. It is caused by Coccidiodes, which are thermally dimorphic fungi that grow as mycelia in soil but transition in the lung to form pathogenic spherules. The regulatory mechanisms underlying this transition are not understood. Exploiting capped small (cs)RNA-seq, which identifies actively initiated stable and unstable transcripts and thereby detects acute changes in gene regulation with remarkable sensitivity, here we report the changes in architectural organization and key sequence features underlying phase transition of this highly pathogenic fungus. Spherule transition was accompanied by large-scale transcriptional reprogramming, functional changes in transcript isoforms, and a massive increase in promoter-distal transcription of ncRNAs. Analysis of spherule-activated regulatory elements revealed a motif predicted to recruit a WOPR family transcription factor, which are known regulators of virulence in other fungi. We identify CIMG_02671 as a C. immitis WOPR homologue and show that it activates transcription in a WOPR motif-dependent manner, suggesting it is an important regulator of pathogenic phase transition. Collectively, this also highlights csRNA-seq as a powerful means to identify transcriptional mechanisms that control pathogenesis.

[1]  J. Stajich,et al.  Transcriptional Analysis of Coccidioides immitis Mycelia and Spherules by RNA Sequencing , 2021, Journal of fungi.

[2]  M. Sarofim,et al.  Economic Valuation of Coccidioidomycosis (Valley Fever) Projections in the United States in Response to Climate Change. , 2021, Weather, climate, and society.

[3]  Danielle Hagee,et al.  Genomic clustering within functionally related gene families in Ascomycota fungi , 2020, Computational and structural biotechnology journal.

[4]  B. Barker,et al.  Defining Critical Genes During Spherule Remodeling and Endospore Development in the Fungal Pathogen, Coccidioides posadasii , 2020, Frontiers in Genetics.

[5]  Zhenguo Lin,et al.  The origin and evolution of a distinct mechanism of transcription initiation in yeasts , 2020, bioRxiv.

[6]  C. Benner,et al.  Identification and dynamic quantification of regulatory elements using total RNA , 2019, Genome Research.

[7]  Torsten Schwede,et al.  SWISS-MODEL: homology modelling of protein structures and complexes , 2019 .

[8]  Geo Pertea,et al.  Transcriptome assembly from long-read RNA-seq alignments with StringTie2 , 2019, Genome Biology.

[9]  D. Engelthaler,et al.  Update on the Epidemiology of coccidioidomycosis in the United States. , 2019, Medical mycology.

[10]  J. Fierer,et al.  Coccidioides immitis and posadasii; A review of their biology, genomics, pathogenesis, and host immunity , 2018, Virulence.

[11]  C. Glass,et al.  Analysis of Genetically Diverse Macrophages Reveals Local and Domain-wide Mechanisms that Control Transcription Factor Binding and Function , 2018, Cell.

[12]  Torsten Schwede,et al.  SWISS-MODEL: homology modelling of protein structures and complexes , 2018, Nucleic Acids Res..

[13]  J. Stajich,et al.  Analysis of Transposable Elements in Coccidioides Species , 2018, Journal of fungi.

[14]  T. Ideker,et al.  The Dfm1 Derlin Is Required for ERAD Retrotranslocation of Integral Membrane Proteins. , 2018, Molecular cell.

[15]  Long Vo Ngoc,et al.  The human initiator is a distinct and abundant element that is precisely positioned in focused core promoters , 2017, Genes & development.

[16]  C. Benner,et al.  Nascent RNA sequencing reveals distinct features in plant transcription , 2016, Proceedings of the National Academy of Sciences.

[17]  Sarah A. Gilmore,et al.  Genome-Wide Reprogramming of Transcript Architecture by Temperature Specifies the Developmental States of the Human Pathogen Histoplasma , 2015, PLoS genetics.

[18]  D. Corcoran,et al.  Human promoters are intrinsically directional. , 2015, Molecular cell.

[19]  Martina Rath,et al.  Enhancer–core-promoter specificity separates developmental and housekeeping gene regulation , 2014, Nature.

[20]  W. Huber,et al.  Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2 , 2014, Genome Biology.

[21]  Jianping Ding,et al.  Crystal structure of the WOPR-DNA complex and implications for Wor1 function in white-opaque switching of Candida albicans , 2014, Cell Research.

[22]  R. Stroud,et al.  Structure of a new DNA-binding domain which regulates pathogenesis in a wide variety of fungi , 2014, Proceedings of the National Academy of Sciences.

[23]  S. Beyhan,et al.  A Temperature-Responsive Network Links Cell Shape and Virulence Traits in a Primary Fungal Pathogen , 2013, PLoS biology.

[24]  J. Goldberg,et al.  Gene expression in human fungal pathogen Coccidioides immitis changes as arthroconidia differentiate into spherules and mature , 2013, BMC Microbiology.

[25]  Leighton J. Core,et al.  Precise Maps of RNA Polymerase Reveal How Promoters Direct Initiation and Pausing , 2013, Science.

[26]  W. Gilbert,et al.  Alternative transcription start site selection leads to large differences in translation activity in yeast. , 2012, RNA.

[27]  T. Sharpton,et al.  Comparative Transcriptomics of the Saprobic and Parasitic Growth Phases in Coccidioides spp , 2012, PloS one.

[28]  M. Ritchie,et al.  Faculty Opinions recommendation of Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks. , 2012 .

[29]  David R. Kelley,et al.  Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks , 2012, Nature Protocols.

[30]  Alexander D. Johnson,et al.  A Conserved Transcriptional Regulator Governs Fungal Morphology in Widely Diverged Species , 2012, Genetics.

[31]  S. Hahn,et al.  Architecture of the Yeast RNA Polymerase II Open Complex and Regulation of Activity by TFIIF , 2011, Molecular and Cellular Biology.

[32]  Leighton J. Core,et al.  A Rapid, Extensive, and Transient Transcriptional Response to Estrogen Signaling in Breast Cancer Cells , 2011, Cell.

[33]  C. Glass,et al.  Reprogramming Transcription via Distinct Classes of Enhancers Functionally Defined by eRNA , 2011, Nature.

[34]  Helga Thorvaldsdóttir,et al.  Integrative Genomics Viewer , 2011, Nature Biotechnology.

[35]  F. M. De La Vega,et al.  The Transcriptomes of Two Heritable Cell Types Illuminate the Circuit Governing Their Differentiation , 2010, PLoS genetics.

[36]  M. Lohse,et al.  Distinct class of DNA-binding domains is exemplified by a master regulator of phenotypic switching in Candida albicans , 2010, Proceedings of the National Academy of Sciences.

[37]  C. Glass,et al.  Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identities. , 2010, Molecular cell.

[38]  G. Kreiman,et al.  Widespread transcription at neuronal activity-regulated enhancers , 2010, Nature.

[39]  Alexander D. Johnson,et al.  White-opaque switching in Candida albicans. , 2009, Current opinion in microbiology.

[40]  B. Valentine,et al.  Coccidioidomycosis in dogs and cats: a review. , 2008, Journal of the American Animal Hospital Association.

[41]  K. Wannemuehler,et al.  Testing for Coccidioidomycosis among Patients with Community-Acquired Pneumonia , 2008, Emerging infectious diseases.

[42]  A. Sil,et al.  Temperature-induced switch to the pathogenic yeast form of Histoplasma capsulatum requires Ryp1, a conserved transcriptional regulator , 2008, Proceedings of the National Academy of Sciences.

[43]  B. Dunn Computational Analysis , 2007 .

[44]  R. Zordan,et al.  Epigenetic properties of white–opaque switching in Candida albicans are based on a self-sustaining transcriptional feedback loop , 2006, Proceedings of the National Academy of Sciences.

[45]  D. Brow,et al.  Quantitative Analysis of in Vivo Initiator Selection by Yeast RNA Polymerase II Supports a Scanning Model* , 2006, Journal of Biological Chemistry.

[46]  R. Laniado-Laborín,et al.  Coccidioidomycosis—A Fungal Disease of the Americas , 2005, PLoS medicine.

[47]  B. Pugh,et al.  Identification and Distinct Regulation of Yeast TATA Box-Containing Genes , 2004, Cell.

[48]  Xavier Robert,et al.  ESPript/ENDscript: extracting and rendering sequence and 3D information from atomic structures of proteins , 2003, Nucleic Acids Res..

[49]  S. Forsburg,et al.  The Schizosaccharomyces pombe aurora-related kinase Ark1 interacts with the inner centromere protein Pic1 and mediates chromosome segregation and cytokinesis. , 2002, Molecular biology of the cell.

[50]  G. Church,et al.  A computational analysis of whole-genome expression data reveals chromosomal domains of gene expression , 2000, Nature Genetics.

[51]  P Cramer,et al.  Functional association between promoter structure and transcript alternative splicing. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[52]  D. Dorris,et al.  Yeast Vectors and Assays for Expression of Cloned Genes , 1997, Current protocols in molecular biology.

[53]  R. Müller,et al.  Yeast vectors for the controlled expression of heterologous proteins in different genetic backgrounds. , 1995, Gene.

[54]  S. Rabindran,et al.  Molecular cloning and expression of a human heat shock factor, HSF1. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[55]  A. Miller Update in Epidemiology , 1986 .

[56]  T. Ideker,et al.  The Dfm1 Derlin Is Required for ERAD Retrotranslocation of Integral Membrane Proteins. , 2018, Molecules and Cells.

[57]  M. Schmoll,et al.  Gene Expression Systems in Fungi: Advancements and Applications , 2016, Fungal Biology.

[58]  Thomas R. Gingeras,et al.  STAR: ultrafast universal RNA-seq aligner , 2013, Bioinform..

[59]  G. Cole,et al.  The parasitic cell wall of Coccidioides immitis. , 2001, Medical mycology.