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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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1323808818</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/humrep/des388</oup_id><sourcerecordid>1323808818</sourcerecordid><originalsourceid>FETCH-LOGICAL-c508t-4b718dc92945d32b3c19cdf8db2d792c5ea0c46001df2d3eed75f2ec1834f0af3</originalsourceid><addsrcrecordid>eNqFkEtLxDAURoMozji6dCtZuqmTRx-pOxl8wYAudCmlTW5spWlq0oL-e1M66nIgJIGc--Xeg9A5JVeU5Hxdj8ZBv1bguRAHaEnjlESMJ-QQLQlLRURpShfoxPsPQsJVpMdowTjlKY35Er09O6tGOTS2w1aHpX3vmu4dl3oAh30PzmBZO2ustwawlw6gC8A1LjsMX-G9MdANePRT1VADNnb0066gPUVHumw9nO3OFXq9u33ZPETbp_vHzc02kgkRQxRXGRVK5iyPE8VZxSXNpdJCVUxlOZMJlESGuQhVmikOoLJEM5BU8FiTUvMVupxze2c_R_BDYRovoW3LDkI3BeWMCyJEKNiLsownIs7IhEYzKp313oEughpTuu-CkmKSX8zyi1l-4C920WNlQP3Rv7b__7ZjvyfrBzwDkX4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1273584708</pqid></control><display><type>article</type><title>Production of offspring after sperm chromosome screening: an experiment using the mouse model</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Watanabe, H. ; Kusakabe, H. ; Mori, H. ; Yanagimachi, R. ; Tateno, H.</creator><creatorcontrib>Watanabe, H. ; Kusakabe, H. ; Mori, H. ; Yanagimachi, R. ; Tateno, H.</creatorcontrib><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.</description><identifier>ISSN: 0268-1161</identifier><identifier>EISSN: 1460-2350</identifier><identifier>DOI: 10.1093/humrep/des388</identifier><identifier>PMID: 23136143</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>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</subject><ispartof>Human reproduction (Oxford), 2013-02, Vol.28 (2), p.531-537</ispartof><rights>The Author 2012. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-4b718dc92945d32b3c19cdf8db2d792c5ea0c46001df2d3eed75f2ec1834f0af3</citedby><cites>FETCH-LOGICAL-c508t-4b718dc92945d32b3c19cdf8db2d792c5ea0c46001df2d3eed75f2ec1834f0af3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23136143$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Watanabe, H.</creatorcontrib><creatorcontrib>Kusakabe, H.</creatorcontrib><creatorcontrib>Mori, H.</creatorcontrib><creatorcontrib>Yanagimachi, R.</creatorcontrib><creatorcontrib>Tateno, H.</creatorcontrib><title>Production of offspring after sperm chromosome screening: an experiment using the mouse model</title><title>Human reproduction (Oxford)</title><addtitle>Hum Reprod</addtitle><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.</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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