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转基因浓度、侧翼基质附着区域和RecA包被对胞质内精子注射介导的小鼠转基因效率的影响。

Effect of transgene concentration, flanking matrix attachment regions, and RecA-coating on the efficiency of mouse transgenesis mediated by intracytoplasmic sperm injection.

作者信息

Moreira Pedro Nuno, Pérez-Crespo Miriam, Ramírez Miguel Angel, Pozueta Julio, Montoliu Lluís, Gutiérrez-Adán Alfonso

机构信息

Departamento de Reproducción Animal y Conservación de Recursos Zoogenéticos, Instituto National de Investigación y Technología Agranria, 28040 Madrid, Spain.

出版信息

Biol Reprod. 2007 Feb;76(2):336-43. doi: 10.1095/biolreprod.106.056952. Epub 2006 Oct 11.

Abstract

Intracytoplasmic sperm injection (ICSI) of DNA-loaded sperm cells has been shown to be a valuable tool for the production of transgenic animals, especially when DNA constructs with submegabase magnitude are used. In order to optimize and to understand the mechanism of the ICSI-mediated transgenesis, we have evaluated the impact of transgene DNA concentration, transgene flanking with nuclear matrix attachment regions (MARs), and the use of recombinase A (RecA)-coated DNA on the efficiency of mouse transgenesis production by ICSI. Presented data include assays with three DNA constructs; an enhanced green fluorescent protein (EGFP) plasmid of 5.4 kb, this plasmid flanked with two MAR elements (2.3 Kb of the human beta-interferon domain boundaries), and a yeast artificial chromosome (YAC) construct of approximately 510 kb (the largest transgenic construct introduced by ICSI that we have seen reported). ICSI-mediated transgenesis was done in the B6D2 mouse strain using different concentrations for each construct. Analysis of generated data indicated that ICSI allows the use of higher DNA concentrations than the ones used for pronuclear microinjection, however, when a certain threshold is exceeded, embryo/fetal viability decrease dramatically. In addition, independently of the transgene concentration tested, transgene flanking with MAR sequences did not have a significant impact on the efficiency of this transgenesis method. Finally, we observed that although the overall efficiency of ICSI-mediated transgenesis with fresh spermatozoa and RecA-complexed DNA was similar to the one obtained with the common ICSI-mediated transgenesis approach with frozen-thawed spermatozoa and RecA free DNA, this method was not as efficient in maintaining a low frequency of founder animal mosaicism, suggesting that different mechanisms of transgene integration might result from each procedure.

摘要

将携带DNA的精子细胞进行胞浆内精子注射(ICSI)已被证明是生产转基因动物的一种有价值的工具,特别是当使用具有亚兆碱基大小的DNA构建体时。为了优化并理解ICSI介导的转基因机制,我们评估了转基因DNA浓度、与核基质附着区(MARs)侧翼的转基因以及使用重组酶A(RecA)包被的DNA对通过ICSI生产小鼠转基因的效率的影响。呈现的数据包括对三种DNA构建体的检测;一个5.4 kb的增强型绿色荧光蛋白(EGFP)质粒,该质粒侧翼有两个MAR元件(人β-干扰素结构域边界的2.3 Kb),以及一个约510 kb的酵母人工染色体(YAC)构建体(我们所见到报道的由ICSI引入的最大转基因构建体)。使用每种构建体的不同浓度,在B6D2小鼠品系中进行ICSI介导的转基因操作。对所生成数据的分析表明,ICSI允许使用比原核显微注射更高的DNA浓度,然而,当超过某个阈值时,胚胎/胎儿活力会急剧下降。此外,与所测试的转基因浓度无关,侧翼有MAR序列的转基因对这种转基因方法的效率没有显著影响。最后,我们观察到,尽管用新鲜精子和RecA复合DNA进行ICSI介导的转基因的总体效率与用冻融精子和无RecA DNA的常见ICSI介导的转基因方法所获得的效率相似,但这种方法在维持低频率的奠基动物嵌合方面效率不高,这表明每种程序可能导致不同的转基因整合机制。

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