Production of quail ( Coturnix japonica) germline chimeras by transfer of gonadal primordial germ cells into recipient embryos
The possibility of producing quail germline chimeras by the transfer of gonadal primordial germ cells (gPGCs) into recipient embryos was investigated. Japanese quail of the black (D: homozygous for the autosomal incomplete dominant gene D) and wild-type plumage (WP: d + / d + ) strains were used as...
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Veröffentlicht in: | Theriogenology 2005-02, Vol.63 (3), p.774-782 |
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creator | Kim, Mi A. Park, Tae Sub Kim, Jin Nam Park, Hyun Jeong Lee, Young Mok Ono, Tamao Lim, Jeong Mook Han, Jae Yong |
description | The possibility of producing quail germline chimeras by the transfer of gonadal primordial germ cells (gPGCs) into recipient embryos was investigated. Japanese quail of the black (D: homozygous for the autosomal incomplete dominant gene
D) and wild-type plumage (WP:
d
+
/
d
+
) strains were used as donors and recipients, respectively. Gonadal cells were retrieved from the gonads of 5-day-old D embryos, and gPGCs were enriched by magnetism-activated cell sorting. Fresh (noncultured) gPGCs or those isolated after culture for 3 days with gonadal stromal cells present in the mixed cell population were introduced into the dorsal aorta of 2-day-old recipient WP embryos. Hatchability of the recipient embryos was 23.7% (31/131) and 34.4% (31/90) for those transfused with cultured or noncultured gPGCs, respectively. Of the hatched quail, 28 acquired sexual maturity; among these animals, 7.1% (1/14) and 21.4% (3/14) of those that received cultured or noncultured gPGCs, respectively, were proved to be germline chimeras. The percentage of germline transmission to the donor-derived gametes in the chimeras that received cultured and noncultured gPGCs were 1.9 and 2.2–4.7%, respectively. In conclusion, quail gPGCs retrieved from 5-day-old embryos were thus transmitted in the germline after their transfer to quail embryos of a different strain. This property of the gPGCs was not adversely affected by culture for up to 3 days. |
doi_str_mv | 10.1016/j.theriogenology.2004.04.014 |
format | Article |
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D) and wild-type plumage (WP:
d
+
/
d
+
) strains were used as donors and recipients, respectively. Gonadal cells were retrieved from the gonads of 5-day-old D embryos, and gPGCs were enriched by magnetism-activated cell sorting. Fresh (noncultured) gPGCs or those isolated after culture for 3 days with gonadal stromal cells present in the mixed cell population were introduced into the dorsal aorta of 2-day-old recipient WP embryos. Hatchability of the recipient embryos was 23.7% (31/131) and 34.4% (31/90) for those transfused with cultured or noncultured gPGCs, respectively. Of the hatched quail, 28 acquired sexual maturity; among these animals, 7.1% (1/14) and 21.4% (3/14) of those that received cultured or noncultured gPGCs, respectively, were proved to be germline chimeras. The percentage of germline transmission to the donor-derived gametes in the chimeras that received cultured and noncultured gPGCs were 1.9 and 2.2–4.7%, respectively. In conclusion, quail gPGCs retrieved from 5-day-old embryos were thus transmitted in the germline after their transfer to quail embryos of a different strain. This property of the gPGCs was not adversely affected by culture for up to 3 days.</description><identifier>ISSN: 0093-691X</identifier><identifier>EISSN: 1879-3231</identifier><identifier>DOI: 10.1016/j.theriogenology.2004.04.014</identifier><identifier>PMID: 15629796</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Aorta - embryology ; Cells, Cultured ; Chimera ; chimerism ; Coturnix - embryology ; embryo (animal) ; genetically modified organisms ; Germ Cells - cytology ; Germ Cells - transplantation ; Germline chimera ; Germline transmission ; Gonads - cytology ; Gonads - embryology ; Microinjections ; Primordial germ cell ; Quail ; Time Factors</subject><ispartof>Theriogenology, 2005-02, Vol.63 (3), p.774-782</ispartof><rights>2004 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-263fc8294adc1ebfa6c3d2e6c42a08e978b01bb5d1be9ab16486f39a219dcac13</citedby><cites>FETCH-LOGICAL-c408t-263fc8294adc1ebfa6c3d2e6c42a08e978b01bb5d1be9ab16486f39a219dcac13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.theriogenology.2004.04.014$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15629796$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Mi A.</creatorcontrib><creatorcontrib>Park, Tae Sub</creatorcontrib><creatorcontrib>Kim, Jin Nam</creatorcontrib><creatorcontrib>Park, Hyun Jeong</creatorcontrib><creatorcontrib>Lee, Young Mok</creatorcontrib><creatorcontrib>Ono, Tamao</creatorcontrib><creatorcontrib>Lim, Jeong Mook</creatorcontrib><creatorcontrib>Han, Jae Yong</creatorcontrib><title>Production of quail ( Coturnix japonica) germline chimeras by transfer of gonadal primordial germ cells into recipient embryos</title><title>Theriogenology</title><addtitle>Theriogenology</addtitle><description>The possibility of producing quail germline chimeras by the transfer of gonadal primordial germ cells (gPGCs) into recipient embryos was investigated. Japanese quail of the black (D: homozygous for the autosomal incomplete dominant gene
D) and wild-type plumage (WP:
d
+
/
d
+
) strains were used as donors and recipients, respectively. Gonadal cells were retrieved from the gonads of 5-day-old D embryos, and gPGCs were enriched by magnetism-activated cell sorting. Fresh (noncultured) gPGCs or those isolated after culture for 3 days with gonadal stromal cells present in the mixed cell population were introduced into the dorsal aorta of 2-day-old recipient WP embryos. Hatchability of the recipient embryos was 23.7% (31/131) and 34.4% (31/90) for those transfused with cultured or noncultured gPGCs, respectively. Of the hatched quail, 28 acquired sexual maturity; among these animals, 7.1% (1/14) and 21.4% (3/14) of those that received cultured or noncultured gPGCs, respectively, were proved to be germline chimeras. The percentage of germline transmission to the donor-derived gametes in the chimeras that received cultured and noncultured gPGCs were 1.9 and 2.2–4.7%, respectively. In conclusion, quail gPGCs retrieved from 5-day-old embryos were thus transmitted in the germline after their transfer to quail embryos of a different strain. This property of the gPGCs was not adversely affected by culture for up to 3 days.</description><subject>Animals</subject><subject>Aorta - embryology</subject><subject>Cells, Cultured</subject><subject>Chimera</subject><subject>chimerism</subject><subject>Coturnix - embryology</subject><subject>embryo (animal)</subject><subject>genetically modified organisms</subject><subject>Germ Cells - cytology</subject><subject>Germ Cells - transplantation</subject><subject>Germline chimera</subject><subject>Germline transmission</subject><subject>Gonads - cytology</subject><subject>Gonads - embryology</subject><subject>Microinjections</subject><subject>Primordial germ cell</subject><subject>Quail</subject><subject>Time Factors</subject><issn>0093-691X</issn><issn>1879-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU2LFDEQhoMo7rj6FzQHET30mI_edAe8yOCqsKCgC95CPqp7M3Qns0m3OBd_uwkzIN6EgtThfaveeoLQS0q2lFDxdr9d7iD5OEKIUxyPW0ZIu61F2wdoQ_tONpxx-hBtCJG8EZL-uEBPct4TQrgQ9DG6oFeCyU6KDfr9NUW32sXHgOOA71ftJ_wa7-KypuB_4b0-xOCtfoNHSPPkA2B752dIOmNzxEvSIQ-QqneMQTs94UPyc0zOl7Z6sIVpytiHJeIE1h88hAXDbNIx5qfo0aCnDM_O7yW6vf7wffepufny8fPu_U1jW9IvDRN8sD2TrXaWghm0sNwxELZlmvQgu94QasyVowakNlS0vRi41IxKZ7Wl_BK9Os09pHi_Ql7U7HMNpgPENSvR8bYs6Yrw3UloU8w5waDqOTodFSWq8ld79S9_VfmrWrQt9ufnPauZwf01n4EXwYuTYNBR6TH5rG6_MUJ5-atOiLYmuD4poPD46SGpbAsyC84XfIty0f9flj9Uf6ys</recordid><startdate>20050201</startdate><enddate>20050201</enddate><creator>Kim, Mi A.</creator><creator>Park, Tae Sub</creator><creator>Kim, Jin Nam</creator><creator>Park, Hyun Jeong</creator><creator>Lee, Young Mok</creator><creator>Ono, Tamao</creator><creator>Lim, Jeong Mook</creator><creator>Han, Jae Yong</creator><general>Elsevier Inc</general><scope>FBQ</scope><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></search><sort><creationdate>20050201</creationdate><title>Production of quail ( Coturnix japonica) germline chimeras by transfer of gonadal primordial germ cells into recipient embryos</title><author>Kim, Mi A. ; Park, Tae Sub ; Kim, Jin Nam ; Park, Hyun Jeong ; Lee, Young Mok ; Ono, Tamao ; Lim, Jeong Mook ; Han, Jae Yong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-263fc8294adc1ebfa6c3d2e6c42a08e978b01bb5d1be9ab16486f39a219dcac13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Aorta - embryology</topic><topic>Cells, Cultured</topic><topic>Chimera</topic><topic>chimerism</topic><topic>Coturnix - embryology</topic><topic>embryo (animal)</topic><topic>genetically modified organisms</topic><topic>Germ Cells - cytology</topic><topic>Germ Cells - transplantation</topic><topic>Germline chimera</topic><topic>Germline transmission</topic><topic>Gonads - cytology</topic><topic>Gonads - embryology</topic><topic>Microinjections</topic><topic>Primordial germ cell</topic><topic>Quail</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Mi A.</creatorcontrib><creatorcontrib>Park, Tae Sub</creatorcontrib><creatorcontrib>Kim, Jin Nam</creatorcontrib><creatorcontrib>Park, Hyun Jeong</creatorcontrib><creatorcontrib>Lee, Young Mok</creatorcontrib><creatorcontrib>Ono, Tamao</creatorcontrib><creatorcontrib>Lim, Jeong Mook</creatorcontrib><creatorcontrib>Han, Jae Yong</creatorcontrib><collection>AGRIS</collection><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><jtitle>Theriogenology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Mi A.</au><au>Park, Tae Sub</au><au>Kim, Jin Nam</au><au>Park, Hyun Jeong</au><au>Lee, Young Mok</au><au>Ono, Tamao</au><au>Lim, Jeong Mook</au><au>Han, Jae Yong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Production of quail ( Coturnix japonica) germline chimeras by transfer of gonadal primordial germ cells into recipient embryos</atitle><jtitle>Theriogenology</jtitle><addtitle>Theriogenology</addtitle><date>2005-02-01</date><risdate>2005</risdate><volume>63</volume><issue>3</issue><spage>774</spage><epage>782</epage><pages>774-782</pages><issn>0093-691X</issn><eissn>1879-3231</eissn><abstract>The possibility of producing quail germline chimeras by the transfer of gonadal primordial germ cells (gPGCs) into recipient embryos was investigated. Japanese quail of the black (D: homozygous for the autosomal incomplete dominant gene
D) and wild-type plumage (WP:
d
+
/
d
+
) strains were used as donors and recipients, respectively. Gonadal cells were retrieved from the gonads of 5-day-old D embryos, and gPGCs were enriched by magnetism-activated cell sorting. Fresh (noncultured) gPGCs or those isolated after culture for 3 days with gonadal stromal cells present in the mixed cell population were introduced into the dorsal aorta of 2-day-old recipient WP embryos. Hatchability of the recipient embryos was 23.7% (31/131) and 34.4% (31/90) for those transfused with cultured or noncultured gPGCs, respectively. Of the hatched quail, 28 acquired sexual maturity; among these animals, 7.1% (1/14) and 21.4% (3/14) of those that received cultured or noncultured gPGCs, respectively, were proved to be germline chimeras. The percentage of germline transmission to the donor-derived gametes in the chimeras that received cultured and noncultured gPGCs were 1.9 and 2.2–4.7%, respectively. In conclusion, quail gPGCs retrieved from 5-day-old embryos were thus transmitted in the germline after their transfer to quail embryos of a different strain. This property of the gPGCs was not adversely affected by culture for up to 3 days.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15629796</pmid><doi>10.1016/j.theriogenology.2004.04.014</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Aorta - embryology Cells, Cultured Chimera chimerism Coturnix - embryology embryo (animal) genetically modified organisms Germ Cells - cytology Germ Cells - transplantation Germline chimera Germline transmission Gonads - cytology Gonads - embryology Microinjections Primordial germ cell Quail Time Factors |
title | Production of quail ( Coturnix japonica) germline chimeras by transfer of gonadal primordial germ cells into recipient embryos |
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