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热带爪蟾中Tol2转座子的重新激活

Remobilization of Tol2 transposons in Xenopus tropicalis.

作者信息

Yergeau Donald A, Kelley Clair M, Kuliyev Emin, Zhu Haiqing, Sater Amy K, Wells Dan E, Mead Paul E

机构信息

Department of Pathology, St, Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105, USA.

出版信息

BMC Dev Biol. 2010 Jan 22;10:11. doi: 10.1186/1471-213X-10-11.

Abstract

BACKGROUND

The Class II DNA transposons are mobile genetic elements that move DNA sequence from one position in the genome to another. We have previously demonstrated that the naturally occurring Tol2 element from Oryzias latipes efficiently integrates its corresponding non-autonomous transposable element into the genome of the diploid frog, Xenopus tropicalis. Tol2 transposons are stable in the frog genome and are transmitted to the offspring at the expected Mendelian frequency.

RESULTS

To test whether Tol2 transposons integrated in the Xenopus tropicalis genome are substrates for remobilization, we injected in vitro transcribed Tol2 mRNA into one-cell embryos harbouring a single copy of a Tol2 transposon. Integration site analysis of injected embryos from two founder lines showed at least one somatic remobilization event per embryo. We also demonstrate that the remobilized transposons are transmitted through the germline and re-integration can result in the generation of novel GFP expression patterns in the developing tadpole. Although the parental line contained a single Tol2 transposon, the resulting remobilized tadpoles frequently inherit multiple copies of the transposon. This is likely to be due to the Tol2 transposase acting in discrete blastomeres of the developing injected embryo during the cell cycle after DNA synthesis but prior to mitosis.

CONCLUSIONS

In this study, we demonstrate that single copy Tol2 transposons integrated into the Xenopus tropicalis genome are effective substrates for excision and random re-integration and that the remobilized transposons are transmitted through the germline. This is an important step in the development of 'transposon hopping' strategies for insertional mutagenesis, gene trap and enhancer trap screens in this highly tractable developmental model organism.

摘要

背景

II类DNA转座子是可移动的遗传元件,可将DNA序列从基因组中的一个位置移动到另一个位置。我们之前已经证明,来自青鳉的天然存在的Tol2元件可将其相应的非自主转座元件有效地整合到二倍体青蛙热带爪蟾的基因组中。Tol2转座子在青蛙基因组中是稳定的,并以预期的孟德尔频率传递给后代。

结果

为了测试整合到热带爪蟾基因组中的Tol2转座子是否是重新移动的底物,我们将体外转录的Tol2 mRNA注射到含有单个Tol2转座子拷贝的单细胞胚胎中。对来自两个奠基系的注射胚胎的整合位点分析表明,每个胚胎至少有一次体细胞重新移动事件。我们还证明,重新移动的转座子通过种系传递,重新整合可导致发育中的蝌蚪产生新的绿色荧光蛋白(GFP)表达模式。虽然亲本品系含有单个Tol2转座子,但产生的重新移动的蝌蚪经常继承多个转座子拷贝。这可能是由于Tol2转座酶在DNA合成后但在有丝分裂前的细胞周期中作用于发育中的注射胚胎的离散卵裂球。

结论

在本研究中,我们证明整合到热带爪蟾基因组中的单拷贝Tol2转座子是切除和随机重新整合的有效底物,并且重新移动的转座子通过种系传递。这是在这种高度易处理的发育模型生物中开发用于插入诱变、基因捕获和增强子捕获筛选的“转座子跳跃”策略的重要一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d7/2848417/94059dc0924e/1471-213X-10-11-1.jpg

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