Polymerase chain reaction-based assays facilitate the breeding and study of mouse models of Klinefelter syndrome
Haixia ZhangiD, Wenyan Xu, Yulin ZhouiD, Xiao-Lu CheniD, Jiayang JiangiD, Xiaoman ZhouiD, Zengge WangiD, Rongqin KeiD, Qiwei GuoiD
Abstract
Klinefelter syndrome (KS) is one of the most frequent genetic abnormalities and the leading genetic cause of non-obstructive azoospermia. The breeding of mouse models of KS and their study are essential to advance our knowledge of the pathologic mechanism. Karyotyping and fluorescence in situ hybridization are reliable methods for identifying chromosomal contents. However, technical issues associated with these methods can decrease the efficiency of breeding KS mouse models and limit studies that require rapid identification of target mice. To overcome these limitations, we developed three polymerase chain reaction-based assays to measure the specific genetic information, including the presence or absence of Sry, copy number of Amelx, and Xist RNA transcript levels. Through a combined analysis of the assay results, we can infer the karyotype of target mice. We confirmed the utility of our assays with the successful generation of KS mouse models. Our assays are rapid, inexpensive, high capacity, easy to perform, and require small amounts of sample. Therefore, they facilitate the breeding and study of KS mouse models and help advance our knowledge of the pathologic mechanism underlying KS.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- FWCI
- 0.00
- Field percentile
- 7th percentile
- Organism
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Reversal learning performance in the XY* mouse model of Klinefelter and Turner Syndromes
S. M. Aarde, H. Hrncir, … J. D. Jentsch·bioRxiv·Jun 14, 2019
- Testicular mosaicism in non-mosaic postpubertal Klinefelter patients with focal spermatogenesis and in non-mosaic prepubertal Klinefelter boys
Semir Gül, Veerle Vloeberghs, … Ellen Goossens·Human ReproductionPeer-reviewed·Aug 9, 2024
- Low XIST expression in Sertoli cells of Klinefelter syndrome patients caused the high susceptibility of these cells to an extra X chromosome
Liangyu Zhao, Peng Li, … Zheng Li·bioRxiv·Aug 26, 2020
- Generation of clonal male and female mice through CRISPR/Cas9-mediated Y chromosome deletion in embryonic stem cells
Yiren Qin, Bokey Wong, … Duancheng Wen·The CRISPR JournalPeer-reviewed·Feb 1, 2021
- X-chromosome loss rescues Sertoli cell maturation and spermatogenesis in Klinefelter syndrome
Sofia Boeg Winge, Niels Erik Skakkebæk, … Kristian Almstrup·Cell Death and DiseasePeer-reviewed·Jun 5, 2024
- Stepwise approach to oocyte depletion in Sry mutated XY female mice
Akihiko Sakashita, Takuya Wakai, … Tomohiro Kono·bioRxiv·Jun 6, 2017