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精子染色体筛查后后代的生产:使用小鼠模型的实验。

Production of offspring after sperm chromosome screening: an experiment using the mouse model.

机构信息

Department of Biological Sciences, Asahikawa Medical University, Asahikawa 078-8510, Japan.

出版信息

Hum Reprod. 2013 Feb;28(2):531-7. doi: 10.1093/humrep/des388. Epub 2012 Nov 7.

Abstract

STUDY QUESTION

Is it possible to produce offspring after sperm chromosome screening?

SUMMARY ANSWER

It is possible to produce zygotes after examining the genome of individual spermatozoa prior to embryo production.

WHAT IS KNOWN ALREADY

Chromosomal aberrations in gametes are a major cause of pregnancy loss in women treated with assisted reproductive technology. However, to our knowledge, there are no reports on the successful genomic screening of spermatozoa, although some attempts have been made using the mouse as a model.

STUDY DESIGN

To prevent the transmission of chromosomal aberrations from fathers to offspring, we performed sperm chromosome screening (SCS) prior to fertilization using the mouse as a model. The production of offspring after SCS consists of (i) replication of the sperm chromosomes, (ii) analysis of one copy of the replicated sperm chromosomes, (iii) construction of a zygote using another set of chromosomes and (iv) production of a transferable embryo.

MATERIALS, SETTING, METHODS: A single spermatozoon of a male mouse, with or without a Robertsonian translocation, was injected into an enucleated oocyte to allow the replication of sperm chromosomes. One of the sister blastomeres of a haploid androgenic 2-cell embryo was used for chromosome analysis. The other blastomere was fused with an unfertilized oocyte, activated and allowed to develop to a blastocyst before transfer to a surrogate mother.

MAIN RESULTS AND ROLE OF CHANCE

With high efficiency, we were able to analyze sperm chromosomes in a blastomere from the androgenic 2-cell embryos and culture zygotes, with and without aberrant chromosomes, to the blastocyst stage before embryo transfer. The karyotypes of the offspring faithfully reflected those of the blastomeres used for SCS.

LIMITATIONS, REASONS FOR CAUTION: This study was conducted using a mouse model; whether or not the method is applicable to humans is not known.

WIDER IMPLICATIONS OF THE FINDINGS

This study has shown that it is possible to produce zygotes without any paternally inherited aberrations by examining the genome of individual spermatozoa prior to embryo production.

摘要

研究问题

在进行胚胎生产之前,通过检查单个精子的基因组,是否有可能产生后代?

总结答案

在进行胚胎生产之前,通过检查单个精子的基因组,可以产生受精卵。

已知信息

配子中的染色体异常是接受辅助生殖技术治疗的女性妊娠丢失的主要原因。然而,据我们所知,虽然已经有人尝试使用小鼠作为模型进行精子的基因组筛查,但尚无成功筛查精子的报道。

研究设计

为了防止父亲的染色体异常遗传给后代,我们使用小鼠作为模型,在受精前进行精子染色体筛查(SCS)。SCS 后产生后代包括(i)精子染色体复制,(ii)分析复制后的精子染色体的一个拷贝,(iii)使用另一组染色体构建受精卵,以及(iv)产生可转移的胚胎。

材料、设置、方法:将有或没有罗伯逊易位的雄性小鼠的单个精子注入去核卵母细胞中,以允许精子染色体复制。雄性 2 细胞胚胎的一个姐妹胚细胞用于染色体分析。另一个胚细胞与未受精的卵母细胞融合,激活并允许其发育至囊胚阶段,然后转移到代孕母亲体内。

主要结果和机会作用

我们能够以高效率分析来自雄性 2 细胞胚胎的胚细胞中的精子染色体,并在胚胎转移前将带有或不带有异常染色体的受精卵培养至囊胚阶段。后代的核型忠实地反映了用于 SCS 的胚细胞的核型。

局限性、谨慎的原因:本研究使用小鼠模型进行;该方法是否适用于人类尚不清楚。

研究结果的意义

本研究表明,通过在胚胎生产之前检查单个精子的基因组,可以在不遗传父系异常的情况下产生受精卵。

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