Literature DB >> 23136143

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

H Watanabe1, H Kusakabe, H Mori, R Yanagimachi, H Tateno.   

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.

Entities:  

Mesh:

Year:  2012        PMID: 23136143     DOI: 10.1093/humrep/des388

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  5 in total

1.  Sperm proteins ODF2 and PAWP as markers of fertility in breeding bulls.

Authors:  Abdullah Kaya; Sule Dogan; Peter Vargovic; Naseer Ahmad Kutchy; Pablo Ross; Einko Topper; Richard Oko; Frans van der Hoorn; Peter Sutovsky; Erdogan Memili
Journal:  Cell Tissue Res       Date:  2021-11-11       Impact factor: 5.249

2.  Risk of chromosomal aberration in spermatozoa during intracytoplasmic sperm injection.

Authors:  Hiroyuki Watanabe
Journal:  J Reprod Dev       Date:  2018-07-07       Impact factor: 2.214

Review 3.  Mysteries and unsolved problems of mammalian fertilization and related topics.

Authors:  Ryuzo Yanagimachi
Journal:  Biol Reprod       Date:  2022-04-26       Impact factor: 4.161

4.  Experimental approach to prezygotic chromosome screening using only a single pair of gametes in mice.

Authors:  Hiroyuki Watanabe; Atsushi Kohda; Hiroyuki Tateno
Journal:  J Reprod Dev       Date:  2015-08-03       Impact factor: 2.214

5.  Transient exposure to calcium ionophore enables in vitro fertilization in sterile mouse models.

Authors:  Felipe A Navarrete; Antonio Alvau; Hoi Chang Lee; Lonny R Levin; Jochen Buck; Patricia Martin-De Leon; Celia M Santi; Dario Krapf; Jesse Mager; Rafael A Fissore; Ana M Salicioni; Alberto Darszon; Pablo E Visconti
Journal:  Sci Rep       Date:  2016-09-15       Impact factor: 4.379

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.