The goal of the Transgenic Mouse Core is to provide the investigators of each project with assistance in the design and production of genetically modified mice. To achieve this goal, the core will perform the following functions:
Specific Aim 1. Design and construct transgenes and develop genotyping assays. Core personnel will consult with the project leaders regarding the goal for each proposed transgenic model. Appropriate DNA constructs will then be designed using optimal promoter and coding sequences. The required genomic or cDNA clones for the gene of interest will be acquired and cloned downstream from the desired promoter. Transgene DNA will be purified for microinjection, and genotyping assays will be designed and tested.
Specific Aim 2. Generate transgenic founders via microinjection of transgene DNA. Fertilized eggs from the C57BL/6 strain of mice will be used for pro-nuclear injection of transgene construct DNA. Potentially transgenic offspring will be identified using genotyping assays developed in Specific Aim 1. Founder mice will be characterized for the ability to transmit the transgene to offspring. The number of independent chromosomal integration sites in each founder will be determined. Germline-competent mice, each with a transgene integrated at a single genomic locus, will be delivered to project leaders.
Specific Aim 3. Assist in the characterization of transgenic mice. Quantitative reverse-transcriptase polymerase chain reaction (RT-PCR) assays will be designed to specifically detect transgene mRNAs and then used to determine the tissue distribution of transgene mRNA expression. If transgene expression is low, core personnel will assist the Project Leader in identifying reasons for low expression and optimizing transgene design to overcome the problem. Transgenic mice are increasingly used to address questions in aging and skeletal research. Experiments in transgenic mice allow investigators to determine whether phenomena observed in cell lines and primary cell cultures also occur in vivo. In addition, transgenic mice can be used to test hypotheses that cannot be convincingly addressed in any in vitro system. Thus timely and efficient production of transgenic mice is essential to the overall goal of the Program which is to improve the understanding of the pathophysiology of the bone fragility syndrome of osteoporosis and thereby rationalize and optimize its treatment.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG013918-15
Application #
8073010
Study Section
Special Emphasis Panel (ZAG1)
Project Start
Project End
2012-04-30
Budget Start
2010-06-01
Budget End
2012-04-30
Support Year
15
Fiscal Year
2010
Total Cost
$182,850
Indirect Cost
Name
University of Arkansas for Medical Sciences
Department
Type
DUNS #
122452563
City
Little Rock
State
AR
Country
United States
Zip Code
72205
Farr, Joshua N; Almeida, Maria (2018) The Spectrum of Fundamental Basic Science Discoveries Contributing to Organismal Aging. J Bone Miner Res 33:1568-1584
Piemontese, Marilina; Almeida, Maria; Robling, Alexander G et al. (2017) Old age causes de novo intracortical bone remodeling and porosity in mice. JCI Insight 2:
Weinstein, Robert S; Hogan, Erin A; Borrelli, Michael J et al. (2017) The Pathophysiological Sequence of Glucocorticoid-Induced Osteonecrosis of the Femoral Head in Male Mice. Endocrinology 158:3817-3831
Kim, Ha-Neui; Chang, Jianhui; Shao, Lijian et al. (2017) DNA damage and senescence in osteoprogenitors expressing Osx1 may cause their decrease with age. Aging Cell 16:693-703
Ucer, Serra; Iyer, Srividhya; Kim, Ha-Neui et al. (2017) The Effects of Aging and Sex Steroid Deficiency on the Murine Skeleton Are Independent and Mechanistically Distinct. J Bone Miner Res 32:560-574
Iyer, Srividhya; Han, Li; Ambrogini, Elena et al. (2017) Deletion of FoxO1, 3, and 4 in Osteoblast Progenitors Attenuates the Loss of Cancellous Bone Mass in a Mouse Model of Type 1 Diabetes. J Bone Miner Res 32:60-69
Almeida, Maria; Laurent, Michaƫl R; Dubois, Vanessa et al. (2017) Estrogens and Androgens in Skeletal Physiology and Pathophysiology. Physiol Rev 97:135-187
Piemontese, Marilina; Xiong, Jinhu; Fujiwara, Yuko et al. (2016) Cortical bone loss caused by glucocorticoid excess requires RANKL production by osteocytes and is associated with reduced OPG expression in mice. Am J Physiol Endocrinol Metab 311:E587-93
Fujiwara, Toshifumi; Ye, Shiqiao; Castro-Gomes, Thiago et al. (2016) PLEKHM1/DEF8/RAB7 complex regulates lysosome positioning and bone homeostasis. JCI Insight 1:e86330
Fujiwara, T; Zhou, J; Ye, S et al. (2016) RNA-binding protein Musashi2 induced by RANKL is critical for osteoclast survival. Cell Death Dis 7:e2300

Showing the most recent 10 out of 162 publications