Analysis of chromosome behavior in intact mammalian oocytes: monitoring the segregation of a univalent chromosome during female meiosis
To monitor the behavior of specific chromosomes at various stages of mammalian female meiosis, we have combined immunofluorescence staining and fluorescence in situ hybridization (FISH) on intact oocytes. We have utilized this technique to evaluate the behavior of the single X chromosome in oocytes...
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Veröffentlicht in: | Human molecular genetics 1995-11, Vol.4 (11), p.2007-2012 |
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creator | Hunt, Patricia LeMaire, Renée Embury, Paula Sheean, Leon Mroz, Karen |
description | To monitor the behavior of specific chromosomes at various stages of mammalian female meiosis, we have combined immunofluorescence staining and fluorescence in situ hybridization (FISH) on intact oocytes. We have utilized this technique to evaluate the behavior of the single X chromosome in oocytes from XO female mice, providing the first observations on segregation of an achiasmate chromosome during mammalian female meiosis and its effect on the meiotic process. As has been described in other species, we found that the univalent chromosome could either segregate as an intact chromosome to one pole or divide equationally at the first meiotic division. Our results also indicate that the presence of a univalent chromosome causes severe meiotic disruption during mammalian meiosis, affecting the alignment and segregation of other chromosomes in the complement. Despite these meiotic abnormalities, the vast majority of oocytes from XO females were able to resume and successfully complete the first meiotic division. This is in contrast to previous studies of male mice with sex chromosome abnormalities where the presence of a univalent acts to arrest meiosis at metaphase of the first meiotic division. This sex-specific difference in the ability of a cell with a univalent chromosome to initiate anaphase suggests that cell cycle control differs between male and female meiosis and that monitoring of meiotic chromosome behavior is less efficient in the female. The combined use of immunofluorescence staining and FISH on intact oocytes has obvious application to the study of meiotic chromosome non-disjunction in the human female. Simultaneous study of the meiotic cell cycle, protein components of the meiotic apparatus, and chromosome-specific behaviors during mammalian female meiosis provides a new approach to defining age-related changes in the meiotic process that result in increased chromosome maisegregation. |
doi_str_mv | 10.1093/hmg/4.11.2007 |
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We have utilized this technique to evaluate the behavior of the single X chromosome in oocytes from XO female mice, providing the first observations on segregation of an achiasmate chromosome during mammalian female meiosis and its effect on the meiotic process. As has been described in other species, we found that the univalent chromosome could either segregate as an intact chromosome to one pole or divide equationally at the first meiotic division. Our results also indicate that the presence of a univalent chromosome causes severe meiotic disruption during mammalian meiosis, affecting the alignment and segregation of other chromosomes in the complement. Despite these meiotic abnormalities, the vast majority of oocytes from XO females were able to resume and successfully complete the first meiotic division. This is in contrast to previous studies of male mice with sex chromosome abnormalities where the presence of a univalent acts to arrest meiosis at metaphase of the first meiotic division. This sex-specific difference in the ability of a cell with a univalent chromosome to initiate anaphase suggests that cell cycle control differs between male and female meiosis and that monitoring of meiotic chromosome behavior is less efficient in the female. The combined use of immunofluorescence staining and FISH on intact oocytes has obvious application to the study of meiotic chromosome non-disjunction in the human female. Simultaneous study of the meiotic cell cycle, protein components of the meiotic apparatus, and chromosome-specific behaviors during mammalian female meiosis provides a new approach to defining age-related changes in the meiotic process that result in increased chromosome maisegregation.</description><identifier>ISSN: 0964-6906</identifier><identifier>EISSN: 1460-2083</identifier><identifier>DOI: 10.1093/hmg/4.11.2007</identifier><identifier>PMID: 8589675</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Anaphase ; Animals ; Biological and medical sciences ; Cell Cycle ; Cytogenetics ; Female ; Fluorescent Antibody Technique ; Fundamental and applied biological sciences. Psychology ; Genetics of eukaryotes. 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We have utilized this technique to evaluate the behavior of the single X chromosome in oocytes from XO female mice, providing the first observations on segregation of an achiasmate chromosome during mammalian female meiosis and its effect on the meiotic process. As has been described in other species, we found that the univalent chromosome could either segregate as an intact chromosome to one pole or divide equationally at the first meiotic division. Our results also indicate that the presence of a univalent chromosome causes severe meiotic disruption during mammalian meiosis, affecting the alignment and segregation of other chromosomes in the complement. Despite these meiotic abnormalities, the vast majority of oocytes from XO females were able to resume and successfully complete the first meiotic division. This is in contrast to previous studies of male mice with sex chromosome abnormalities where the presence of a univalent acts to arrest meiosis at metaphase of the first meiotic division. This sex-specific difference in the ability of a cell with a univalent chromosome to initiate anaphase suggests that cell cycle control differs between male and female meiosis and that monitoring of meiotic chromosome behavior is less efficient in the female. The combined use of immunofluorescence staining and FISH on intact oocytes has obvious application to the study of meiotic chromosome non-disjunction in the human female. Simultaneous study of the meiotic cell cycle, protein components of the meiotic apparatus, and chromosome-specific behaviors during mammalian female meiosis provides a new approach to defining age-related changes in the meiotic process that result in increased chromosome maisegregation.</description><subject>Anaphase</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Cycle</subject><subject>Cytogenetics</subject><subject>Female</subject><subject>Fluorescent Antibody Technique</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Male</subject><subject>Mammals</subject><subject>Meiosis - genetics</subject><subject>Metaphase</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Oocytes - cytology</subject><subject>Telophase</subject><subject>Vertebrata</subject><subject>X Chromosome</subject><issn>0964-6906</issn><issn>1460-2083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1rVDEUhi-i1LG6dClkIe7uNF83H-5KsY4w4KagdBNyc8-did4kNcmUzi_o3_aOHUZ3woGzeJ88h_A2zVuClwRrdrENmwu-JGRJMZbPmgXhArcUK_a8WWAteCs0Fi-bV6X8wJgIzuRZc6Y6pYXsFs3jZbTTvviC0ojcNqeQSgqAetjae58y8nGeal1FwYZgJ28jSsntK5SPKKToa8o-blDdAiqwybCx1ad40Fm0i_7eThDrv-ph9-fBCLMNUACf5vOvmxejnQq8Oe7z5ub6083Vql1__fzl6nLdOt7R2vag9QgSRmnFYAnFhBHSAaMdGUZKJGdYCUcoZb1T_eGzQirF-TCCJhzYefPhSXuX068dlGqCLw6myUZIu2KkVFjyWfM_kAitCRZ0Btsn0OVUSobR3GUfbN4bgs2hIDMXZLghxBwKmvl3R_GuDzCc6GMjc_7-mNvi7DRmG50vJ4wqjamUf8_6UuHhFNv80wjJZGdW32-N-sZu1yvBzIr9BsrtqkM</recordid><startdate>19951101</startdate><enddate>19951101</enddate><creator>Hunt, Patricia</creator><creator>LeMaire, Renée</creator><creator>Embury, Paula</creator><creator>Sheean, Leon</creator><creator>Mroz, Karen</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19951101</creationdate><title>Analysis of chromosome behavior in intact mammalian oocytes: monitoring the segregation of a univalent chromosome during female meiosis</title><author>Hunt, Patricia ; LeMaire, Renée ; Embury, Paula ; Sheean, Leon ; Mroz, Karen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c452t-be99fe7ef7a6da12013115e3251df21743086c1223bc8b6437678844dfe914e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Anaphase</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Cycle</topic><topic>Cytogenetics</topic><topic>Female</topic><topic>Fluorescent Antibody Technique</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Male</topic><topic>Mammals</topic><topic>Meiosis - genetics</topic><topic>Metaphase</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Oocytes - cytology</topic><topic>Telophase</topic><topic>Vertebrata</topic><topic>X Chromosome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hunt, Patricia</creatorcontrib><creatorcontrib>LeMaire, Renée</creatorcontrib><creatorcontrib>Embury, Paula</creatorcontrib><creatorcontrib>Sheean, Leon</creatorcontrib><creatorcontrib>Mroz, Karen</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Human molecular genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hunt, Patricia</au><au>LeMaire, Renée</au><au>Embury, Paula</au><au>Sheean, Leon</au><au>Mroz, Karen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of chromosome behavior in intact mammalian oocytes: monitoring the segregation of a univalent chromosome during female meiosis</atitle><jtitle>Human molecular genetics</jtitle><addtitle>Hum Mol Genet</addtitle><date>1995-11-01</date><risdate>1995</risdate><volume>4</volume><issue>11</issue><spage>2007</spage><epage>2012</epage><pages>2007-2012</pages><issn>0964-6906</issn><eissn>1460-2083</eissn><abstract>To monitor the behavior of specific chromosomes at various stages of mammalian female meiosis, we have combined immunofluorescence staining and fluorescence in situ hybridization (FISH) on intact oocytes. We have utilized this technique to evaluate the behavior of the single X chromosome in oocytes from XO female mice, providing the first observations on segregation of an achiasmate chromosome during mammalian female meiosis and its effect on the meiotic process. As has been described in other species, we found that the univalent chromosome could either segregate as an intact chromosome to one pole or divide equationally at the first meiotic division. Our results also indicate that the presence of a univalent chromosome causes severe meiotic disruption during mammalian meiosis, affecting the alignment and segregation of other chromosomes in the complement. Despite these meiotic abnormalities, the vast majority of oocytes from XO females were able to resume and successfully complete the first meiotic division. This is in contrast to previous studies of male mice with sex chromosome abnormalities where the presence of a univalent acts to arrest meiosis at metaphase of the first meiotic division. This sex-specific difference in the ability of a cell with a univalent chromosome to initiate anaphase suggests that cell cycle control differs between male and female meiosis and that monitoring of meiotic chromosome behavior is less efficient in the female. The combined use of immunofluorescence staining and FISH on intact oocytes has obvious application to the study of meiotic chromosome non-disjunction in the human female. Simultaneous study of the meiotic cell cycle, protein components of the meiotic apparatus, and chromosome-specific behaviors during mammalian female meiosis provides a new approach to defining age-related changes in the meiotic process that result in increased chromosome maisegregation.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>8589675</pmid><doi>10.1093/hmg/4.11.2007</doi><tpages>6</tpages></addata></record> |
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subjects | Anaphase Animals Biological and medical sciences Cell Cycle Cytogenetics Female Fluorescent Antibody Technique Fundamental and applied biological sciences. Psychology Genetics of eukaryotes. Biological and molecular evolution Humans In Situ Hybridization, Fluorescence Male Mammals Meiosis - genetics Metaphase Mice Mice, Inbred C57BL Oocytes - cytology Telophase Vertebrata X Chromosome |
title | Analysis of chromosome behavior in intact mammalian oocytes: monitoring the segregation of a univalent chromosome during female meiosis |
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