Cell-Specific Paired Interrogation of the Mouse Ovarian Epigenome and Transcriptome

被引:0
|
作者
Ocanas, Sarah R. [1 ,2 ,3 ]
Isola, Jose V. V. [1 ,3 ]
Saccon, Tatiana D. [1 ]
Pham, Kevin D. [2 ]
Chucair-Elliott, Ana J. [2 ]
Schneider, Augusto [4 ]
Freeman, Willard M. [2 ,3 ]
Stout, Michael B. [1 ,3 ]
机构
[1] Oklahoma Med Res Fdn, Aging & Metab Res Program, Oklahoma City, OK 73104 USA
[2] Oklahoma Med Res Fdn, Genes & Human Dis Res Program, Oklahoma City, OK USA
[3] Oklahoma City Vet Affairs Med Ctr, Oklahoma City, OK 73104 USA
[4] Univ Fed Pelotas, Nutr Coll, Pelotas, Brazil
来源
基金
美国国家卫生研究院;
关键词
MENOPAUSE; TISSUES; STROMA; AGE;
D O I
10.3791/64765
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Assessing cell-type-specific epigenomic and transcriptomic changes are key to understanding ovarian aging. To this end, the optimization of the translating ribosome affinity purification (TRAP) method and the isolation of nuclei tagged in specific cell types (INTACT) method was performed for the subsequent paired interrogation of the cell-specific ovarian transcriptome and epigenome using a novel transgenic NuTRAP mouse model. The expression of the NuTRAP allele is under the control of a floxed STOP cassette and can be targeted to specific ovarian cell types using promoter-specific Cre lines. Since recent studies have implicated ovarian stromal cells in driving premature aging phenotypes, the NuTRAP expression system was targeted to stromal cells using a Cyp17a1-Cre driver. The induction of the NuTRAP construct was specific to ovarian stromal fibroblasts, and sufficient DNA and RNA for sequencing studies were obtained from a single ovary. The NuTRAP model and methods presented here can be used to study any ovarian cell type with an available Cre line.
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页数:13
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