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

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 pregnan...

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Veröffentlicht in:Human reproduction (Oxford) 2013-02, Vol.28 (2), p.531-537
Hauptverfasser: Watanabe, H., Kusakabe, H., Mori, H., Yanagimachi, R., Tateno, H.
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container_end_page 537
container_issue 2
container_start_page 531
container_title Human reproduction (Oxford)
container_volume 28
creator Watanabe, H.
Kusakabe, H.
Mori, H.
Yanagimachi, R.
Tateno, H.
description 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. STUDY FUNDING/COMPETING INTERESTS This study was supported by a Grants-in-Aid for Scientific Research (22·8495 and 23890013 to H.W.) from the Japan Society for the Promotion of Science (JSPS). There are no conflicts of interest to be declared.
doi_str_mv 10.1093/humrep/des388
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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. STUDY FUNDING/COMPETING INTERESTS This study was supported by a Grants-in-Aid for Scientific Research (22·8495 and 23890013 to H.W.) from the Japan Society for the Promotion of Science (JSPS). 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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. STUDY FUNDING/COMPETING INTERESTS This study was supported by a Grants-in-Aid for Scientific Research (22·8495 and 23890013 to H.W.) from the Japan Society for the Promotion of Science (JSPS). There are no conflicts of interest to be declared.</description><subject>Abortion</subject><subject>Animal models</subject><subject>Animals</subject><subject>blastocysts</subject><subject>Blastomeres</subject><subject>Blastomeres - cytology</subject><subject>Chromosome Aberrations</subject><subject>chromosome II</subject><subject>chromosome III</subject><subject>Chromosomes</subject><subject>Cytogenetic Analysis</subject><subject>Disease transmission</subject><subject>Embryo transfer</subject><subject>Gametes</subject><subject>Genomes</subject><subject>genomics</subject><subject>Karyotypes</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred ICR</subject><subject>Oocytes</subject><subject>Replication</subject><subject>Reproduction</subject><subject>Semen Analysis</subject><subject>Sperm</subject><subject>Spermatozoa - physiology</subject><subject>Translocation, Genetic</subject><subject>Zygotes</subject><issn>0268-1161</issn><issn>1460-2350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLxDAURoMozji6dCtZuqmTRx-pOxl8wYAudCmlTW5spWlq0oL-e1M66nIgJIGc--Xeg9A5JVeU5Hxdj8ZBv1bguRAHaEnjlESMJ-QQLQlLRURpShfoxPsPQsJVpMdowTjlKY35Er09O6tGOTS2w1aHpX3vmu4dl3oAh30PzmBZO2ustwawlw6gC8A1LjsMX-G9MdANePRT1VADNnb0066gPUVHumw9nO3OFXq9u33ZPETbp_vHzc02kgkRQxRXGRVK5iyPE8VZxSXNpdJCVUxlOZMJlESGuQhVmikOoLJEM5BU8FiTUvMVupxze2c_R_BDYRovoW3LDkI3BeWMCyJEKNiLsownIs7IhEYzKp313oEughpTuu-CkmKSX8zyi1l-4C920WNlQP3Rv7b__7ZjvyfrBzwDkX4</recordid><startdate>20130201</startdate><enddate>20130201</enddate><creator>Watanabe, H.</creator><creator>Kusakabe, H.</creator><creator>Mori, H.</creator><creator>Yanagimachi, R.</creator><creator>Tateno, H.</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20130201</creationdate><title>Production of offspring after sperm chromosome screening: an experiment using the mouse model</title><author>Watanabe, H. ; Kusakabe, H. ; Mori, H. ; Yanagimachi, R. ; Tateno, H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-4b718dc92945d32b3c19cdf8db2d792c5ea0c46001df2d3eed75f2ec1834f0af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Abortion</topic><topic>Animal models</topic><topic>Animals</topic><topic>blastocysts</topic><topic>Blastomeres</topic><topic>Blastomeres - cytology</topic><topic>Chromosome Aberrations</topic><topic>chromosome II</topic><topic>chromosome III</topic><topic>Chromosomes</topic><topic>Cytogenetic Analysis</topic><topic>Disease transmission</topic><topic>Embryo transfer</topic><topic>Gametes</topic><topic>Genomes</topic><topic>genomics</topic><topic>Karyotypes</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred ICR</topic><topic>Oocytes</topic><topic>Replication</topic><topic>Reproduction</topic><topic>Semen Analysis</topic><topic>Sperm</topic><topic>Spermatozoa - physiology</topic><topic>Translocation, Genetic</topic><topic>Zygotes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Watanabe, H.</creatorcontrib><creatorcontrib>Kusakabe, H.</creatorcontrib><creatorcontrib>Mori, H.</creatorcontrib><creatorcontrib>Yanagimachi, R.</creatorcontrib><creatorcontrib>Tateno, H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Watanabe, H.</au><au>Kusakabe, H.</au><au>Mori, H.</au><au>Yanagimachi, R.</au><au>Tateno, H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Production of offspring after sperm chromosome screening: an experiment using the mouse model</atitle><jtitle>Human reproduction (Oxford)</jtitle><addtitle>Hum Reprod</addtitle><date>2013-02-01</date><risdate>2013</risdate><volume>28</volume><issue>2</issue><spage>531</spage><epage>537</epage><pages>531-537</pages><issn>0268-1161</issn><eissn>1460-2350</eissn><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. STUDY FUNDING/COMPETING INTERESTS This study was supported by a Grants-in-Aid for Scientific Research (22·8495 and 23890013 to H.W.) from the Japan Society for the Promotion of Science (JSPS). There are no conflicts of interest to be declared.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>23136143</pmid><doi>10.1093/humrep/des388</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Abortion
Animal models
Animals
blastocysts
Blastomeres
Blastomeres - cytology
Chromosome Aberrations
chromosome II
chromosome III
Chromosomes
Cytogenetic Analysis
Disease transmission
Embryo transfer
Gametes
Genomes
genomics
Karyotypes
Male
Mice
Mice, Inbred C57BL
Mice, Inbred ICR
Oocytes
Replication
Reproduction
Semen Analysis
Sperm
Spermatozoa - physiology
Translocation, Genetic
Zygotes
title Production of offspring after sperm chromosome screening: an experiment using the mouse model
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