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Evaluation of DNase activity in seminal plasma and uptake of exogenous DNA by spermatozoa of the Brazilian flounder Paralichthys orbignyanus

机译:巴西比目鱼Paralichthys orbignyanus精子对精浆中DNase活性和外源DNA吸收的评估

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摘要

Sperm mediated gene transfer (SMGT) has been successfully used in mammals, amphibians, birds, and some invertebrates. In fish, this methodology has failed or had poor efficiency for the production of transgenic specimens, presumably because the processes regulating the interaction between spermatozoa and exogenous DNA are not well understood. Therefore, the objective was to develop a SMGT protocol for the Brazilian flounder Paralichthys orbignyanus, with an emphasis on the role of seminal plasma DNase on exogenous DNA uptake by fish spermatozoa. In this study, there was strong DNase activity in the seminal plasma of P. orbignyanus; however, this DNase activity was decreased or eliminated by washing the spermatozoa with solutions containing EDTA (DNase activity was completely inhibited by 40 mM EDTA). Three washing solutions were tested, all of which maintained sperm quality. Moreover, it was determined that the no more than 50 ng of exogenous DNA/10(6) cells should be used for SMGT in fish. Finally, it was demonstrated that fish spermatozoa were capable of spontaneous uptake of exogenous DNA after elimination of DNase activity; this was confirmed by exogenous DNA amplification (PCR using sperm genomic DNA as a template) after DNase I treatment.We concluded that whereas DNase activity was an important obstacle for exogenous DNA uptake by fish spermatozoa; controlling this activity improved the efficiency of SMGT in fish.
机译:精子介导的基因转移(SMGT)已成功用于哺乳动物,两栖动物,鸟类和一些无脊椎动物。在鱼类中,这种方法对于生产转基因标本失败或效率低下,这可能是因为调节精子与外源DNA之间相互作用的过程尚未得到很好的理解。因此,目的是为巴西比目鱼Paralichthys orbignyanus开发一种SMGT方案,重点在于精浆DNase对鱼精子摄取外源DNA的作用。在这项研究中,P。orbignyanus的精浆中有很强的DNase活性。但是,通过用含EDTA的溶液洗涤精子可降低或消除这种DNase活性(DNase活性被40 mM EDTA完全抑制)。测试了三种洗涤溶液,所有溶液均保持精子质量。此外,已确定鱼类中SMGT的外源DNA / 10(6)细胞不得超过50 ng。最后,证明了鱼类的精子在消除DNase活性后能够自发摄取外源DNA。 DNase I处理后,通过外源DNA扩增(以精子基因组DNA为模板进行PCR)证实了这一点。我们的结论是,DNase活性是鱼类精子摄取外源DNA的重要障碍。控制此活动可提高鱼中SMGT的效率。

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