研究报告

外源基因对精子的影响及其在山羊早期胚胎中的表达

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  • 1. 军事医学科学院实验动物中心, 北京 100071;
    2. 北京市农林科学院畜牧兽医研究所, 北京 100097;
    3. 首都医科大学实验动物部, 北京 100069

收稿日期: 2008-02-29

  修回日期: 2008-06-10

  网络出版日期: 2008-11-10

Exogenous DNA influencing fertilization of goat sperm cells and ex-pression in early embryos

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  • 1. Laboratory Animal Center, Academy of Military Medical Sciences, Beijing 100071, China;
    2. Institute of Husbandry and Veterinary Science, Beijing Academy of Agriculture and Forestry, Beijing 100097, China;
    3. Laboratory Animal Center, Capital University of Medical Sciences, Beijing 100069, China

Received date: 2008-02-29

  Revised date: 2008-06-10

  Online published: 2008-11-10

摘要

摘要: 在前期实验中发现, 山羊精子可自发结合外源DNA, 但结合能力在不同动物个体之间差异显著。挑选结合能力明显不同的3只公羊, 进一步探讨了外源DNA对精子的影响及其在早期胚胎中的表达, 结果发现: 外源基因与精子共同孵育后, 精子的活率、顶体反应发生率和受精能力均呈下降态势, 其降幅与精子的结合能力密切相关。利用与DNA共育后的精子进行体外受精, 外源基因可被导入卵母细胞并在早期胚胎中获得表达, 但胚胎阳性率因精子供体不同而差异显著(P<0.05); 其中来源于高、中结合能力供体生产的胚胎, 分别有16.2%(25/154)和5.3%(4/76)可检测到外源基因存在, 但表达仅见于高结合能力供体生产的早期胚胎, 表达率为6.5%(10/154); 低结合能力供体生产的胚胎无外源基因。研究表明, 在以精子载体方法生产转基因动物的实验过程中, 筛选对DNA结合能力较强的精子供体是提高转基因效率的前提, 但需要考虑外源DNA对精子受精能力的影响。

本文引用格式

叶华虎,董罡,袁菊芳,隋丽华,胡娟峰,李瑞生,刘彦,马啸,陈振文,曾林 . 外源基因对精子的影响及其在山羊早期胚胎中的表达[J]. 遗传, 2008 , 30(11) : 1421 -1426 . DOI: 10.3724/SP.J.1005.2008.01421

Abstract

Abstract: Our early study found that goat spermatozoa could spontaneously take up foreign DNA and vary in capabilities of spermatozoa from different donors to bind and internalize exogenous DNA. In this study, three goats with considerable differences of capability were used to investigate the effect of exogenous DNA on goat spermatozoa, and feasibility and efficiency of transgenic embryo production by sperm-mediated gene transfer method. The viability, acrosomal reaction fre-quencies and cleavages were decreased in the groups co-cultured with exogenous DNA, compared with the control groups, and the range of decrease was correlated with the capability of sperm cells up-take foreign DNA. After fertilizing with co-cultured spermatozoa, GFP gene was introduced into oocytes and expressed in early embryos. However, different effi-ciencies of transgenic embryos appeared in sperm donors (P<0.05). GFP gene was detected in 16.2% (25/154), 5.3% (4/76), and 0% (0/36) embryos, respectively, when high, middle and low capability of sperm donors were used. But only 6.5% (10/154) embryos from high capability sperm donor expressed GFP. Our results demonstrate that selecting high capability of sperm donor is a key step for improving efficiency of sperm mediated-gene transfer method. However, the adverse influ-ence of foreign DNA on spermatozoa needs to be further studied.
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