Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening

Identifying genes that are important for embryo development is a crucial first step towards understanding their many functions in driving the ordered growth, differentiation and organogenesis of embryos. It can also shed light on the origins of developmental disease and congenital abnormalities. Current international efforts to examine gene function in the mouse provide a unique opportunity to pinpoint genes that are involved in embryogenesis, owing to the emergence of embryonic lethal knockout mutants. Through internationally coordinated efforts, the International Knockout Mouse Consortium (IKMC) has generated a public resource of mouse knockout strains and, in April 2012, the International Mouse Phenotyping Consortium (IMPC), supported by the EU InfraCoMP programme, convened a workshop to discuss developing a phenotyping pipeline for the investigation of embryonic lethal knockout lines. This workshop brought together over 100 scientists, from 13 countries, who are working in the academic and commercial research sectors, including experts and opinion leaders in the fields of embryology, animal imaging, data capture, quality control and annotation, high-throughput mouse production, phenotyping, and reporter gene analysis. This article summarises the outcome of the workshop, including (1) the vital scientific importance of phenotyping embryonic lethal mouse strains for basic and translational research; (2) a common framework to harmonise international efforts within this context; (3) the types of phenotyping that are likely to be most appropriate for systematic use, with a focus on 3D embryo imaging; (4) the importance of centralising data in a standardised form to facilitate data mining; and (5) the development of online tools to allow open access to and dissemination of the phenotyping data.

[1]  J. Rossant,et al.  Phenotypic annotation of the mouse X chromosome. , 2010, Genome research.

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

[3]  R. Henkelman,et al.  Comparative SNR for high‐throughput mouse embryo MR microscopy , 2010, Magnetic resonance in medicine.

[4]  Bill Hill,et al.  The Edinburgh Mouse Atlas: Basic Structure and Informatics , 2002 .

[5]  Richard Baldock,et al.  Deciphering the Mechanisms of Developmental Disorders (DMDD): a new programme for phenotyping embryonic lethal mice , 2013, Disease Models & Mechanisms.

[6]  Judith A. Blake,et al.  The Mouse Genome Database (MGD): comprehensive resource for genetics and genomics of the laboratory mouse , 2011, Nucleic Acids Res..

[7]  S. Neubauer,et al.  Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique , 2004, BMC Developmental Biology.

[8]  K. Garber Targeting vessel abnormalization in cancer. , 2007, Journal of the National Cancer Institute.

[9]  R. M. Henkelman,et al.  Mouse embryonic phenotyping by morphometric analysis of MR images , 2010, Physiological genomics.

[10]  D. Norris,et al.  Mouse models of ciliopathies: the state of the art , 2012, Disease Models & Mechanisms.

[11]  Lindsay S. Cahill,et al.  Multiple-mouse Neuroanatomical Magnetic Resonance Imaging , 2011, Journal of visualized experiments : JoVE.

[12]  Mark W. Moore,et al.  Towards an encyclopaedia of mammalian gene function: the International Mouse Phenotyping Consortium , 2012, Disease Models & Mechanisms.

[13]  J. Hecksher-Sørensen,et al.  Optical Projection Tomography as a Tool for 3D Microscopy and Gene Expression Studies , 2002, Science.

[14]  A. Reymond,et al.  A High-Resolution Anatomical Atlas of the Transcriptome in the Mouse Embryo , 2011, PLoS biology.

[15]  J. Lary,et al.  Sex differences in the prevalence of human birth defects: a population-based study. , 2001, Teratology.

[16]  A. Copp,et al.  Death before birth: clues from gene knockouts and mutations. , 1995, Trends in genetics : TIG.

[17]  Kirill V Larin,et al.  Optical Coherence Tomography for live imaging of mammalian development. , 2011, Current opinion in genetics & development.

[18]  Diego Rasskin-Gutman,et al.  High-resolution episcopic microscopy: a rapid technique for high detailed 3D analysis of gene activity in the context of tissue architecture and morphology , 2006, Anatomy and Embryology.

[19]  J. Seidman,et al.  Congenital heart disease caused by mutations in the transcription factor NKX2-5. , 1998, Science.

[20]  M. J. Harris,et al.  An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure. , 2010, Birth defects research. Part A, Clinical and molecular teratology.

[21]  B. Metscher MicroCT for comparative morphology: simple staining methods allow high-contrast 3D imaging of diverse non-mineralized animal tissues , 2009, BMC Physiology.

[22]  R. Mark Henkelman,et al.  A novel 3D mouse embryo atlas based on micro-CT , 2012, Development.

[23]  R. Machiraju,et al.  Atypical E2F repressors and activators coordinate placental development. , 2012, Developmental cell.

[24]  Marc Modat,et al.  Magnetic resonance virtual histology for embryos: 3D atlases for automated high-throughput phenotyping , 2011, NeuroImage.

[25]  R. Mark Henkelman,et al.  High resolution three-dimensional brain atlas using an average magnetic resonance image of 40 adult C57Bl/6J mice , 2008, NeuroImage.

[26]  F. Foster,et al.  Comprehensive transthoracic cardiac imaging in mice using ultrasound biomicroscopy with anatomical confirmation by magnetic resonance imaging. , 2004, Physiological genomics.

[27]  J. Rossant,et al.  Placental development: Lessons from mouse mutants , 2001, Nature Reviews Genetics.

[28]  M. Loane,et al.  The prevalence of congenital anomalies in Europe. , 2010, Advances in experimental medicine and biology.

[29]  N. Greene,et al.  Inositol prevents folate-resistant neural tube defects in the mouse , 1997, Nature Medicine.

[30]  Kathryn E. Hentges,et al.  Discovery of Candidate Disease Genes in ENU–Induced Mouse Mutants by Large-Scale Sequencing, Including a Splice-Site Mutation in Nucleoredoxin , 2009, PLoS genetics.