Good planning and serendipity: exploiting the Cre/Lox system in the testis
- PMID: 21084571
- DOI: 10.1530/REP-10-0404
Good planning and serendipity: exploiting the Cre/Lox system in the testis
Abstract
Over the past 20 years, genetic manipulation has revolutionised our understanding of male reproductive development and function. The advent of transgenic mouse lines has permitted elegant dissection of previously intractable issues. The development of the Cre/Lox system, which has permitted spatial and temporal localisation of genetic manipulation, has expanded upon this, and now makes up one of the primary approaches underpinning our increasing understanding of testis development and function. The success of conditional gene targeting is largely reliant upon the choice of Cre recombinase expressing mouse line, which is required to specifically target the correct cell type at the correct time. Presupposition that Cre lines will behave as expected has been one of the main oversights in the design of Cre/Lox experiments, as in practice, many Cre lines are prone to ectopic expression (both temporal and spatial), transgene silencing or genetic background effects. Empirical validation of the spatiotemporal profile of Cre expression prior to undertaking conditional gene targeting studies is essential and can be achieved through a combination of molecular and immunohistochemical approaches, along with in vivo examination of reporter gene expression in targeted tissues. This paper details the key considerations associated with exploitation of the Cre/Lox system and highlights a variety of validated Cre lines that have utility for conditional gene targeting within the testis.
Similar articles
-
Metabolic pitfalls of CNS Cre-based technology.Cell Metab. 2013 Jul 2;18(1):21-8. doi: 10.1016/j.cmet.2013.05.019. Cell Metab. 2013. PMID: 23823475
-
Incomplete cre-mediated excision leads to phenotypic differences between Stra8-iCre; Mov10l1(lox/lox) and Stra8-iCre; Mov10l1(lox/Δ) mice.Genesis. 2013 Jul;51(7):481-90. doi: 10.1002/dvg.22389. Epub 2013 Mar 30. Genesis. 2013. PMID: 23554062 Free PMC article.
-
Temporal and tight hepatitis C virus gene activation in cultured human hepatoma cells mediated by a cell-permeable Cre recombinase.Acta Biochim Biophys Sin (Shanghai). 2004 Oct;36(10):687-94. doi: 10.1093/abbs/36.10.687. Acta Biochim Biophys Sin (Shanghai). 2004. PMID: 15483749
-
Pancreas-specific Cre driver lines and considerations for their prudent use.Cell Metab. 2013 Jul 2;18(1):9-20. doi: 10.1016/j.cmet.2013.06.011. Cell Metab. 2013. PMID: 23823474 Free PMC article. Review.
-
[Issues and solutions of conditional gene targeting].Yi Chuan. 2011 May;33(5):469-84. doi: 10.3724/sp.j.1005.2011.00469. Yi Chuan. 2011. PMID: 21586394 Review. Chinese.
Cited by
-
Reserve Stem Cells in Intestinal Homeostasis and Injury.Gastroenterology. 2018 Nov;155(5):1348-1361. doi: 10.1053/j.gastro.2018.08.016. Epub 2018 Aug 15. Gastroenterology. 2018. PMID: 30118745 Free PMC article. Review.
-
Epigenetic regulation of the histone-to-protamine transition during spermiogenesis.Reproduction. 2016 May;151(5):R55-70. doi: 10.1530/REP-15-0562. Epub 2016 Feb 5. Reproduction. 2016. PMID: 26850883 Free PMC article. Review.
-
Unlocking Genetic Mysteries during the Epic Sperm Journey toward Fertilization: Further Expanding Cre Mouse Lines.Biomolecules. 2024 Apr 28;14(5):529. doi: 10.3390/biom14050529. Biomolecules. 2024. PMID: 38785936 Free PMC article. Review.
-
An inducible knockout mouse to model the cell-autonomous role of PTEN in initiating endometrial, prostate and thyroid neoplasias.Dis Model Mech. 2013 May;6(3):710-20. doi: 10.1242/dmm.011445. Epub 2013 Feb 8. Dis Model Mech. 2013. PMID: 23471917 Free PMC article.
-
Craniofacial skeletal response to encephalization: How do we know what we think we know?Am J Phys Anthropol. 2019 Jan;168 Suppl 67(Suppl 67):27-46. doi: 10.1002/ajpa.23766. Am J Phys Anthropol. 2019. PMID: 30680710 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous
