Transcriptome analysis reveals an Atoh1b-dependent gene set downstream of Dlx3b/4b during early inner ear development in zebrafish

ABSTRACT The vertebrate inner ear is the sensory organ mediating hearing and balance. The entire organ develops from the otic placode, which itself originates from the otic-epibranchial progenitor domain (OEPD). Multiple studies in various species have shown the importance of the forkhead-box and distal-less homeodomain transcription factor families for OEPD and subsequent otic placode formation. However, the transcriptional networks downstream of these factors are only beginning to be understood. Using transcriptome analysis, we here reveal numerous genes regulated by the distal-less homeodomain transcription factors Dlx3b and Dlx4b (Dlx3b/4b). We identify known and novel transcripts displaying widespread OEPD expression in a Dlx3b/4b-dependent manner. Some genes, with a known OEPD expression in other vertebrate species, might be members of a presumptive vertebrate core module required for proper otic development. Moreover, we identify genes controlling early-born sensory hair cell formation as well as regulating biomineral tissue development, both consistent with defective sensory hair cell and otolith formation observed in dlx3b/4b mutants. Finally, we show that ectopic Atoh1b expression can rescue early sensorigenesis even in the absence of Dlx3b/4b. Taken together, our data will help to unravel the gene regulatory network underlying early inner ear development and provide insights into the molecular control of vertebrate inner ear formation to restore hearing loss in humans ultimately.

[1]  A. Streit,et al.  Enhancer activation by FGF signalling during otic induction , 2020, Developmental biology.

[2]  Peter Aleström,et al.  Zebrafish: Housing and husbandry recommendations , 2019, Laboratory animals.

[3]  J. Vilo,et al.  g:Profiler: a web server for functional enrichment analysis and conversions of gene lists (2019 update) , 2019, Nucleic Acids Res..

[4]  Blaine R. Roberts,et al.  The inner ear proteome of fish , 2018, The FEBS journal.

[5]  A. Streit,et al.  Lsd1 interacts with cMyb to demethylate repressive histone marks and maintain inner ear progenitor identity , 2018, Development.

[6]  M. Brand,et al.  Dlx3b/4b is required for early-born but not later-forming sensory hair cells during zebrafish inner ear development , 2017, Biology Open.

[7]  A. Streit,et al.  A gene network regulated by FGF signalling during ear development , 2017, Scientific Reports.

[8]  R. Ladher Changing shape and shaping change: Inducing the inner ear. , 2017, Seminars in cell & developmental biology.

[9]  A. Streit,et al.  A systems-level approach reveals new gene regulatory modules in the developing ear , 2017, Development.

[10]  K. Kaestner,et al.  Fox transcription factors: from development to disease , 2016, Development.

[11]  M. Wolman,et al.  Novel roles for the radial spoke head protein 9 in neural and neurosensory cilia , 2016, Scientific Reports.

[12]  Rosa A. Uribe,et al.  Histone demethylase KDM4B regulates otic vesicle invagination via epigenetic control of Dlx3 expression , 2015, The Journal of cell biology.

[13]  C. Moens,et al.  Rapid reverse genetic screening using CRISPR in zebrafish , 2015, Nature Methods.

[14]  S. Baxendale,et al.  Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin , 2015, Development.

[15]  K. L. Kramer,et al.  Mechanisms of otoconia and otolith development , 2015, Developmental dynamics : an official publication of the American Association of Anatomists.

[16]  R. Ladher,et al.  Early steps in inner ear development: induction and morphogenesis of the otic placode , 2015, Front. Pharmacol..

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

[18]  M. Radosevic,et al.  The Role of her4 in Inner Ear Development and Its Relationship with Proneural Genes and Notch Signalling , 2014, PloS one.

[19]  A. Groves,et al.  Foxi3 is necessary for the induction of the chick otic placode in response to FGF signaling. , 2014, Developmental biology.

[20]  S. Baxendale,et al.  Semicircular canal morphogenesis in the zebrafish inner ear requires the function of gpr126 (lauscher), an adhesion class G protein-coupled receptor gene , 2013, Development.

[21]  Åsa K. Björklund,et al.  Smart-seq2 for sensitive full-length transcriptome profiling in single cells , 2013, Nature Methods.

[22]  Susan R. Wente,et al.  Efficient multiplex biallelic zebrafish genome editing using a CRISPR nuclease system , 2013, Proceedings of the National Academy of Sciences.

[23]  Wei Shi,et al.  featureCounts: an efficient general purpose program for assigning sequence reads to genomic features , 2013, Bioinform..

[24]  M. Brand,et al.  Zebrafish Foxi1 provides a neuronal ground state during inner ear induction preceding the Dlx3b/4b-regulated sensory lineage , 2013, Development.

[25]  A. Streit,et al.  Induction of the inner ear: Stepwise specification of otic fate from multipotent progenitors , 2013, Hearing Research.

[26]  V. Vassilev,et al.  Analysis of FGF-Dependent and FGF-Independent Pathways in Otic Placode Induction , 2013, PloS one.

[27]  Zachary R. Lewis,et al.  Graded levels of Pax2a and Pax8 regulate cell differentiation during sensory placode formation , 2012, Development.

[28]  W. Driever,et al.  Fluorescence-activated cell sorting (FACS) of fluorescently tagged cells from zebrafish larvae for RNA isolation. , 2012, Cold Spring Harbor protocols.

[29]  A. Schier,et al.  The role of hair cells, cilia and ciliary motility in otolith formation in the zebrafish otic vesicle , 2012, Development.

[30]  J. Jontes,et al.  Differential expression, alternative splicing, and adhesive properties of the zebrafish δ1-protocadherins , 2011, Neuroscience.

[31]  B. Riley,et al.  Sox2 and Fgf interact with Atoh1 to promote sensory competence throughout the zebrafish inner ear. , 2011, Developmental biology.

[32]  K. Kawakami,et al.  Formation of the spinal network in zebrafish determined by domain‐specific pax genes , 2011, The Journal of comparative neurology.

[33]  Y. Oda,et al.  Origin of Inner Ear Hair Cells: Morphological and Functional Differentiation from Ciliary Cells into Hair Cells in Zebrafish Inner Ear , 2011, The Journal of Neuroscience.

[34]  Sudipto Roy,et al.  Cilia-driven fluid flow as an epigenetic cue for otolith biomineralization on sensory hair cells of the inner ear , 2011, Development.

[35]  J. Kaslin,et al.  Generation of a non‐leaky heat shock–inducible Cre line for conditional Cre/lox strategies in zebrafish , 2011, Developmental dynamics : an official publication of the American Association of Anatomists.

[36]  S. Heller,et al.  Mechanosensitive Hair Cell-like Cells from Embryonic and Induced Pluripotent Stem Cells , 2010, Cell.

[37]  Serban Nacu,et al.  Fast and SNP-tolerant detection of complex variants and splicing in short reads , 2010, Bioinform..

[38]  Israel Steinfeld,et al.  BMC Bioinformatics BioMed Central , 2008 .

[39]  S. Rinkwitz,et al.  Progressive restriction of otic fate: the role of FGF and Wnt in resolving inner ear potential , 2008, Development.

[40]  A. Streit The preplacodal region: an ectodermal domain with multipotential progenitors that contribute to sense organs and cranial sensory ganglia. , 2007, The International journal of developmental biology.

[41]  Sheng-Ping L. Hwang,et al.  Characterization of the agr2 gene, a homologue of X. laevis anterior gradient 2, from the zebrafish, Danio rerio. , 2007, Gene expression patterns : GEP.

[42]  B. Riley,et al.  Zebrafish atoh1 genes: classic proneural activity in the inner ear and regulation by Fgf and Notch , 2007, Development.

[43]  Lisha Xu,et al.  The Forkhead Transcription Factor FoxI1 Remains Bound to Condensed Mitotic Chromosomes and Stably Remodels Chromatin Structure , 2006, Molecular and Cellular Biology.

[44]  R. Dildrop,et al.  Expression of the zebrafish Iroquois genes during early nervous system formation and patterning , 2005, The Journal of comparative neurology.

[45]  Dean Y. Li,et al.  roundabout4 is essential for angiogenesis in vivo. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[46]  A. Moon,et al.  FGF8 initiates inner ear induction in chick and mouse. , 2005, Genes & development.

[47]  A. Groves,et al.  Dlx gene expression during chick inner ear development , 2005, The Journal of comparative neurology.

[48]  B. Adolf,et al.  atoh1.2 and beta3.1 are two new bHLH-encoding genes expressed in selective precursor cells of the zebrafish anterior hindbrain. , 2004, Gene expression patterns : GEP.

[49]  M. Westerfield,et al.  Pax8 and Pax2a function synergistically in otic specification, downstream of the Foxi1 and Dlx3b transcription factors , 2004, Development.

[50]  D. Riethmacher,et al.  Requirements for FGF3 and FGF10 during inner ear formation , 2003, Development.

[51]  Tracy J. Wright,et al.  Fgf3 and Fgf10 are required for mouse otic placode induction , 2003, Development.

[52]  A. Amsterdam,et al.  Zebrafish foxi one modulates cellular responses to Fgf signaling required for the integrity of ear and jaw patterning , 2003, Development.

[53]  A. Fritz,et al.  Zebrafish foxi1 mediates otic placode formation and jaw development , 2003, Development.

[54]  H. Zoghbi,et al.  The zinc finger transcription factor Gfi1, implicated in lymphomagenesis, is required for inner ear hair cell differentiation and survival , 2003, Development.

[55]  M. Brand,et al.  Fgf8 and Fgf3 are required for zebrafish ear placode induction, maintenance and inner ear patterning , 2002, Mechanisms of Development.

[56]  A. Fritz,et al.  Concerted action of two dlx paralogs in sensory placode formation. , 2002, Development.

[57]  R. Mahmood,et al.  Fgf3 and Fgf8 are required together for formation of the otic placode and vesicle. , 2002, Development.

[58]  K. Bolding,et al.  Zebrafish fgf3 and fgf8 encode redundant functions required for otic placode induction. , 2001, Developmental biology.

[59]  M. Itoh,et al.  Expression of proneural and neurogenic genes in the zebrafish lateral line primordium correlates with selection of hair cell fate in neuromasts , 2001, Mechanisms of Development.

[60]  Y. Yan,et al.  Two sox9 genes on duplicated zebrafish chromosomes: expression of similar transcription activators in distinct sites. , 2001, Developmental biology.

[61]  R. Geisler,et al.  Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness. , 2000, Human molecular genetics.

[62]  G. Robinson,et al.  Placental failure in mice lacking the homeobox gene Dlx3. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[63]  C. Janetopoulos,et al.  A critical period of ear development controlled by distinct populations of ciliated cells in the zebrafish. , 1997, Developmental biology.

[64]  J. Lewis,et al.  Early ear development in the embryo of the Zebrafish, Danio rerio , 1996, The Journal of comparative neurology.

[65]  C. Kimmel,et al.  Stages of embryonic development of the zebrafish , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.

[66]  A. Groves,et al.  The mouse Foxi3 transcription factor is necessary for the development of posterior placodes. , 2016, Developmental biology.

[67]  Koichi Kawakami,et al.  Tol2-mediated transgenesis, gene trapping, enhancer trapping, and the Gal4-UAS system. , 2011, Methods in cell biology.

[68]  U. Strähle,et al.  Parapineal specific expression of gfi1 in the zebrafish epithalamus. , 2004, Gene expression patterns : GEP.

[69]  Michael Brand,et al.  Keeping and raising zebrafish , 2002 .

[70]  Bernd Fritzsch,et al.  Auditory system development: primary auditory neurons and their targets. , 2002, Annual review of neuroscience.

[71]  Y. Benjamini,et al.  Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .