Generation of a multipurpose Prdm16 mouse allele by targeted gene trapping

ABSTRACT Gene trap mutagenesis is a powerful tool to create loss-of-function mutations in mice and other model organisms. Modifications of traditional gene trap cassettes, including addition of conditional features in the form of Flip-excision (FlEx) arrays to enable directional gene trap cassette inversions by Cre and Flpe site-specific recombinases, greatly enhanced their experimental potential. By taking advantage of these conditional gene trap cassettes, we developed a generic strategy for generating conditional mutations and validated this strategy in mice carrying a multipurpose allele of the Prdm16 transcription factor gene. We demonstrate that the gene trap insertion creates a null mutation replicating the Pierre Robin sequence-type cleft palate phenotype of other Prdm16 mutant mice. Consecutive breeding to Flpe and Emx1IREScre deleter mice spatially restricted Prdm16 loss to regions of the forebrain expressing the homeobox gene Emx1, demonstrating the utility of the technology for the analysis of tissue-specific gene functions. Summary: Described is the first targeting of an invertible gene trap to generate a conditional Prdm16 mouse allele and its use to assess phenotypic consequences of Prdm16 loss during craniofacial and brain development.

[1]  Daniel H. Lackner,et al.  A generic strategy for CRISPR-Cas9-mediated gene tagging , 2015, Nature Communications.

[2]  A. Nagy Manipulating the mouse embryo , 2013 .

[3]  P. Farlie,et al.  Developmental and genetic perspectives on Pierre Robin sequence , 2013, American journal of medical genetics. Part C, Seminars in medical genetics.

[4]  R. Jaenisch,et al.  One-Step Generation of Mice Carrying Reporter and Conditional Alleles by CRISPR/Cas-Mediated Genome Engineering , 2013, Cell.

[5]  G. Musso,et al.  Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. , 2013, American journal of human genetics.

[6]  Rudolf Jaenisch,et al.  One-Step Generation of Mice Carrying Mutations in Multiple Genes by CRISPR/Cas-Mediated Genome Engineering , 2013, Cell.

[7]  Steve D. M. Brown,et al.  The mammalian gene function resource: the international knockout mouse consortium , 2012, Mammalian Genome.

[8]  A. Joyner,et al.  MASTR: a technique for mosaic mutant analysis with spatial and temporal control of recombination using conditional floxed alleles in mice. , 2012, Cell reports.

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

[10]  I. Lemischka,et al.  Prdm16 is a physiologic regulator of hematopoietic stem cells. , 2011, Blood.

[11]  L. Pevny,et al.  SOX2 expression levels distinguish between neural progenitor populations of the developing dorsal telencephalon. , 2011, Developmental biology.

[12]  B. Levi,et al.  Prdm16 promotes stem cell maintenance in multiple tissues, partly by regulating oxidative stress , 2010, Nature Cell Biology.

[13]  B. Bjork,et al.  Prdm16 is required for normal palatogenesis in mice. , 2010, Human molecular genetics.

[14]  Daniel J. O'Connell,et al.  Temporomandibular joint formation requires two distinct hedgehog-dependent steps , 2009, Proceedings of the National Academy of Sciences.

[15]  Danielle M. Andrade,et al.  Genetic basis in epilepsies caused by malformations of cortical development and in those with structurally normal brain , 2009, Human Genetics.

[16]  W. Wurst,et al.  Enhanced gene trapping in mouse embryonic stem cells , 2008, Nucleic acids research.

[17]  B. Spiegelman,et al.  PRDM16 controls a brown fat/skeletal muscle switch , 2008, Nature.

[18]  B. Spiegelman,et al.  Regulation of the brown and white fat gene programs through a PRDM16/CtBP transcriptional complex. , 2008, Genes & development.

[19]  B. Spiegelman,et al.  Transcriptional control of brown fat determination by PRDM16. , 2007, Cell metabolism.

[20]  M. Pisano,et al.  PRDM16/MEL1: a novel Smad binding protein expressed in murine embryonic orofacial tissue. , 2007, Biochimica et biophysica acta.

[21]  S. Mcconnell,et al.  Gene targeting using a promoterless gene trap vector ("targeted trapping") is an efficient method to mutate a large fraction of genes. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[22]  Claudia Seisenberger,et al.  Genomewide production of multipurpose alleles for the functional analysis of the mouse genome. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[23]  J. Rogers,et al.  Mutagenic Insertion and Chromosome Engineering Resource (MICER) , 2004, Nature Genetics.

[24]  M. Trigg Hematopoietic stem cells. , 2004, Pediatrics.

[25]  Peter Vogel,et al.  Wnk1 kinase deficiency lowers blood pressure in mice: A gene-trap screen to identify potential targets for therapeutic intervention , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[26]  Luis Puelles,et al.  Cortical Excitatory Neurons and Glia, But Not GABAergic Neurons, Are Produced in the Emx1-Expressing Lineage , 2002, The Journal of Neuroscience.

[27]  Philippe Soriano,et al.  Widespread recombinase expression using FLPeR (Flipper) mice , 2000, Genesis.

[28]  Jerilyn A. Walker,et al.  Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT). , 2000, BioTechniques.

[29]  M. Komada,et al.  E-MAP-115, encoding a microtubule-associated protein, is a retinoic acid-inducible gene required for spermatogenesis. , 2000, Genes & development.

[30]  P. Hoodless,et al.  Smad2 and Smad3 positively and negatively regulate TGF beta-dependent transcription through the forkhead DNA-binding protein FAST2. , 1998, Molecular cell.

[31]  Christophe Person,et al.  Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells , 1998, Nature.

[32]  Minoru Watanabe,et al.  Smad4 and FAST-1 in the assembly of activin-responsive factor , 1997, Nature.

[33]  R. Behringer,et al.  Goosecoid is not an essential component of the mouse gastrula organizer but is required for craniofacial and rib development. , 1995, Development.

[34]  P. Gruss,et al.  Targeted mutation of the murine goosecoid gene results in craniofacial defects and neonatal death. , 1995, Development.

[35]  Philippe Soriano,et al.  Promoter traps in embryonic stem cells: a genetic screen to identify and mutate developmental genes in mice. , 1991, Genes & development.

[36]  R. Bronson,et al.  Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene , 1991, Cell.

[37]  S. Robertson,et al.  Neuropsychiatric disease in patients with periventricular heterotopia. , 2013, The Journal of neuropsychiatry and clinical neurosciences.

[38]  I. Lemischka,et al.  Prdm 16 is a physiologic regulator of hematopoietic stem cells , 2011 .

[39]  Philippe Soriano,et al.  Gene trap mutagenesis in the mouse. , 2010, Methods in enzymology.

[40]  D. Beier,et al.  Using ENU mutagenesis for phenotype-driven analysis of the mouse. , 2010, Methods in enzymology.

[41]  David Bouchez,et al.  Manipulating the Mouse Embryo , 2007 .

[42]  H. Kiyonari,et al.  Gene disruption/knock-in analysis of mONT3: vector construction by employing both in vivo and in vitro recombinations. , 2005, The International journal of developmental biology.

[43]  C. Branda,et al.  Talking about a revolution: The impact of site-specific recombinases on genetic analyses in mice. , 2004, Developmental cell.

[44]  J. Yokota,et al.  A novel gene, MEL1, mapped to 1p36.3 is highly homologous to the MDS1/EVI1 gene and is transcriptionally activated in t(1;3)(p36;q21)-positive leukemia cells. , 2000, Blood.

[45]  T. Takeuchi,et al.  Mouse gene trap approach: identification of novel genes and characterization of their biological functions. , 1998, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[46]  G. Martin,et al.  Analysis of Fgf8 gene function in vertebrate development. , 1997, Cold Spring Harbor symposia on quantitative biology.