Manipulating the Xenopus genome with transposable elements

被引:0
|
作者
Yergeau D.A. [1 ]
Mead P.E. [1 ]
机构
[1] Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN 38105, North Lauderdale Street
来源
Genome Biology | / 8卷 / Suppl 1期
关键词
Sleep Beauty; Enhancer Trap; phiC31 Integrase; Transposase Enzyme; Insertional Mutagenesis Screen;
D O I
10.1186/gb-2007-8-s1-s11
中图分类号
学科分类号
摘要
The study of amphibian embryogenesis has provided important insight into the mechanisms of vertebrate development. The frog Xenopus laevis has been an important model of vertebrate cell biology and development for many decades. Genetic studies in this organism are not practical because of the tetraploid nature of the genome and the long generation time of this species. Recently, a closely related frog, namely Xenopus tropicalis, has been proposed as an alternative system; it shares all of the physical characteristics that make X. laevis a useful model but has the advantage of a diploid genome and short generation time. The rapid accumulation of genetic resources for this animal and the success of pilot mutagenesis screens have helped propel this model system forward. Transposable elements will provide invaluable tools for manipulating the frog genome. These integration systems are ideally suited to transgenesis and insertional mutagenesis strategies in the frog. The high fecundity of the frog combined with the ability to remobilize transposon transgenes integrated into frog genome will allow large-scale insertional mutagenesis screens to be performed in laboratories with modest husbandry capacities. © 2007 BioMed Central Ltd.
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