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性别预选:通过对DNA进行分选再分析,对流式分选的X精子和Y精子的精子性别比例进行实验室验证。

Sex preselection: laboratory validation of the sperm sex ratio of flow sorted X- and Y-sperm by sort reanalysis for DNA.

作者信息

Welch G R, Johnson L A

机构信息

Germplasm & Gamete Physiology Laboratory, U.S. Department of Agriculture, Beltsville, MD 20705, USA.

出版信息

Theriogenology. 1999 Dec;52(8):1343-52. doi: 10.1016/s0093-691x(99)00221-6.

Abstract

Laboratory validation is essential in developing an effective method for separating X and Y sperm to preselect sex. Utilizing sexed sperm from a particular experiment to test fertility and achieve the subsequent phenotypic sex without knowing the likely outcome at conception is too costly for most applications. Further, research advances need to be built on an ongoing assessment with respect to the collection of data to continue progress towards achieving a successful outcome. The Beltsville Sperm Sexing Technology, which is based on the sorting of X- and Y-bearing sperm through the process of flow-cytometric sperm sorting, is also well suited for validation in the laboratory by "sort reanalysis" of the sperm X- and Y-bearing fractions for DNA content. Since the sexing technology is based on the use of Hoechst 33342, a permeant nuclear DNA stain for sorting X- and Y-bearing sperm, it also can be the marker for determining the proportions of X and Y populations by sort reanalysis. The process consists of using an aliquot of the sorted sperm and sonicating to obtain sperm nuclei. The uniformity of the nuclear staining is re-established through the addition of more Hoechst 33342. Separate analysis of each aliquot produces a histogram that is fitted to a double gaussian curve to determine proportions of X and Y populations. The relative breadths of the distributions of DNA of X- and Y-bearing sperm within a species affects interpretations of the histogram. Sort reanalysis is consistently repeatable with differences in X/Y DNA equal to or greater than 3.0%. This information on sex ratio of the sperm then provides the precise tool by which one can predict the outcome in terms of sex, from a particular sample of semen. Simple analysis of unsorted sperm to determine the proportions of X- and Y-bearing sperm based on DNA content is also an effective tool for validating sperm-sex ratio, whether it is in a sample assumed to be 50:50 or predicted to be something other than 50:50. This simple analysis provides for a check on the potential sex ratio of any sample of semen.

摘要

实验室验证对于开发一种有效的分离X和Y精子以进行性别预选的方法至关重要。对于大多数应用来说,利用来自特定实验的经性别分选的精子来测试生育力并在不知道受孕时可能结果的情况下实现随后的表型性别,成本太高。此外,研究进展需要建立在对数据收集的持续评估基础上,以继续朝着实现成功结果取得进展。贝尔茨维尔精子性别分选技术基于通过流式细胞术精子分选过程对携带X和Y的精子进行分选,也非常适合通过对携带X和Y的精子部分进行DNA含量的“分选再分析”在实验室中进行验证。由于性别分选技术基于使用Hoechst 33342(一种用于分选携带X和Y的精子的渗透性核DNA染料),它也可以作为通过分选再分析确定X和Y群体比例的标记。该过程包括使用一部分分选后的精子并进行超声处理以获得精子细胞核。通过添加更多的Hoechst 33342来重新建立核染色的均匀性。对每个部分进行单独分析会产生一个拟合双高斯曲线的直方图,以确定X和Y群体的比例。一个物种内携带X和Y的精子的DNA分布的相对宽度会影响对直方图的解释。分选再分析在X/Y DNA差异等于或大于3.0%时具有一致的可重复性。然后,关于精子性别比例的这些信息提供了一种精确的工具,通过它可以从特定的精液样本中预测性别结果。基于DNA含量对未分选精子进行简单分析以确定携带X和Y的精子的比例,也是验证精子性别比例的有效工具,无论该样本被假定为50:50还是预计为其他比例。这种简单分析可以检查任何精液样本的潜在性别比例。

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