MOUSE GENE MANIPULATION CORE (CORE E) ABSTRACT The primary objective of the Mouse Gene Manipulation Core is to provide all our IDDRC investigators with a centralized, affordable and quality-controlled service, using state-of-the art genome editing technology, for the rapid and efficient generation of genetically altered mouse lines. Our goal is aid our PIs in their work on identifying the role of particular genes in the development of the nervous system and in modelling intellectual disability and neurodevelopmental disorders, with a view in particular of identifying preclinically, novel biomarkers of these disorders and for evaluating the efficacy of new therapeutic approaches. Although manipulation of the mouse genome has been well established for several decades using homologous combination in embryonic stem cells for gene targeting and random insertion of DNA in zygotes for making transgenic mice, and this Core has very effectively used these approaches to generate many mouse models of neurodevelopmental disorders, during the course of the present grant cycle transformative advances have been made in our capacity for genome editing. This core has enthusiastically embraced and mastered the new CRISPR/Cas9 technology for disrupting gene expression by base insertion/deletion (INDELS), and using homology directed repair (HDR) for introducing mutations, inserting reporters, Cre or Flp drivers and indeed making many kinds of changes to the genome ? in a manner that is both efficient and fast. We will continue to offer our standard technology since there are users and uses that favor this but anticipate that CRISPR/Cas9 and its evolution will largely take over. The technology has caused immense excitement in the IDDRC community and the demand for our services are set to increase substantially, so that the IDDRC can provide parallel preclinical and clinical phenotyping and efficacy studies. To aid in the uptake of genome editing the core will offer consultation services on the best approach for PIs to use for particular projects, advice on selection of guide RNAs, genotyping and colony management, as well as a new cryopreservation service. Collectively the new services will offer the IDDRC mouse models faster and cheaper with the capacity to preserve these for alter use or sharing.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54HD090255-04
Application #
9748884
Study Section
Special Emphasis Panel (ZHD1)
Project Start
Project End
Budget Start
2019-06-01
Budget End
2020-05-31
Support Year
4
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Boston Children's Hospital
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02115
Yuskaitis, Christopher J; Jones, Brandon M; Wolfson, Rachel L et al. (2018) A mouse model of DEPDC5-related epilepsy: Neuronal loss of Depdc5 causes dysplastic and ectopic neurons, increased mTOR signaling, and seizure susceptibility. Neurobiol Dis 111:91-101
Smith, Lois E H; Hellström, Ann; Stahl, Andreas et al. (2018) Development of a Retinopathy of Prematurity Activity Scale and Clinical Outcome Measures for Use in Clinical Trials. JAMA Ophthalmol :
Gao, Xue; Tao, Yong; Lamas, Veronica et al. (2018) Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agents. Nature 553:217-221
Fu, Zhongjie; Löfqvist, Chatarina A; Liegl, Raffael et al. (2018) Photoreceptor glucose metabolism determines normal retinal vascular growth. EMBO Mol Med 10:76-90
Latremoliere, Alban; Cheng, Long; DeLisle, Michelle et al. (2018) Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon Regeneration. Cell Rep 24:1865-1879.e9
Lodato, Michael A; Rodin, Rachel E; Bohrson, Craig L et al. (2018) Aging and neurodegeneration are associated with increased mutations in single human neurons. Science 359:555-559
Beggs, Alan H; Byrne, Barry J; De Chastonay, Sabine et al. (2018) A multicenter, retrospective medical record review of X-linked myotubular myopathy: The recensus study. Muscle Nerve 57:550-560
Asai, Yukako; Pan, Bifeng; Nist-Lund, Carl et al. (2018) Transgenic Tmc2 expression preserves inner ear hair cells and vestibular function in mice lacking Tmc1. Sci Rep 8:12124
Modi, Meera E; Sahin, Mustafa (2018) A unified circuit for social behavior. Neurobiol Learn Mem :
Hrvatin, Sinisa; Hochbaum, Daniel R; Nagy, M Aurel et al. (2018) Single-cell analysis of experience-dependent transcriptomic states in the mouse visual cortex. Nat Neurosci 21:120-129

Showing the most recent 10 out of 498 publications