Aurora kinase B, epigenetic state of centromeric heterochromatin and chiasma resolution in oocytes
Abstract Aurora kinases comprise a family of phosphoproteins performing multiple functions in mitosis and meiosis. Because Aurora kinase B (AURKB) expression is altered in aged oocytes and there is only limited information on its function in meiosis, it was decided to study the spatial distribution...
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description | Abstract Aurora kinases comprise a family of phosphoproteins performing multiple functions in mitosis and meiosis. Because Aurora kinase B (AURKB) expression is altered in aged oocytes and there is only limited information on its function in meiosis, it was decided to study the spatial distribution and co-localization of AURKB with other regulatory proteins at centromeres during mouse oocyte maturation. AURKB associates with chromosomes after germinal vesicle breakdown, is enriched at centromeres from prometaphase I and transits to the spindle midzone at late anaphase I. Preferential inhibition of AURKB by low concentrations of ZM 447439 inhibitor prevents polar body formation and affects spindle formation and chromosome congression at meiosis I, associated with expression of BubR1 checkpoint protein at kinetochores. Release of cohesion between sister chromatids appears inhibited resulting in failure of chiasma resolution in oocytes progressing to anaphase I. Concomitantly, the inhibitor reduces histone H3 lysine 9 trimethylation at centromeric heterochromatin and affects chromosome condensation. The cytokinesis arrest protects young, healthy oocytes from errors in chromosome segregation although increasing polyploidy. This study shows that changes in activity of AURKB may increase risks for chromosome non-disjunction and aneuploidy in mammalian oocytes, irrespective of age. |
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Because Aurora kinase B (AURKB) expression is altered in aged oocytes and there is only limited information on its function in meiosis, it was decided to study the spatial distribution and co-localization of AURKB with other regulatory proteins at centromeres during mouse oocyte maturation. AURKB associates with chromosomes after germinal vesicle breakdown, is enriched at centromeres from prometaphase I and transits to the spindle midzone at late anaphase I. Preferential inhibition of AURKB by low concentrations of ZM 447439 inhibitor prevents polar body formation and affects spindle formation and chromosome congression at meiosis I, associated with expression of BubR1 checkpoint protein at kinetochores. Release of cohesion between sister chromatids appears inhibited resulting in failure of chiasma resolution in oocytes progressing to anaphase I. Concomitantly, the inhibitor reduces histone H3 lysine 9 trimethylation at centromeric heterochromatin and affects chromosome condensation. The cytokinesis arrest protects young, healthy oocytes from errors in chromosome segregation although increasing polyploidy. This study shows that changes in activity of AURKB may increase risks for chromosome non-disjunction and aneuploidy in mammalian oocytes, irrespective of age.</description><identifier>ISSN: 1472-6483</identifier><identifier>EISSN: 1472-6491</identifier><identifier>DOI: 10.1016/S1472-6483(10)60169-1</identifier><identifier>PMID: 19778480</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Aneuploidy ; Animals ; Aurora kinase ; Aurora Kinase B ; Aurora Kinases ; Benzamides - pharmacology ; Centromere - drug effects ; Centromere - genetics ; Centromere - metabolism ; chromosome cohesion ; Chromosome Segregation - drug effects ; Chromosome Segregation - genetics ; Epigenesis, Genetic - physiology ; Female ; heterochromatin ; Heterochromatin - drug effects ; Heterochromatin - genetics ; Heterochromatin - metabolism ; Histones - antagonists & inhibitors ; Histones - metabolism ; Meiosis - drug effects ; Meiosis - genetics ; Mice ; Nondisjunction, Genetic - genetics ; Obstetrics and Gynecology ; oocyte ; Oocytes - drug effects ; Oocytes - metabolism ; Oogenesis - drug effects ; Oogenesis - genetics ; Protein Kinase Inhibitors - pharmacology ; Protein-Serine-Threonine Kinases - antagonists & inhibitors ; Protein-Serine-Threonine Kinases - genetics ; Protein-Serine-Threonine Kinases - metabolism ; Quinazolines - pharmacology ; spindle ; Spindle Apparatus - drug effects ; Spindle Apparatus - metabolism</subject><ispartof>Reproductive biomedicine online, 2009, Vol.19 (3), p.352-368</ispartof><rights>Reproductive Healthcare Ltd, Duck End Farm, Dry Drayton, Cambridge CB23 8DB, UK</rights><rights>2009 Reproductive Healthcare Ltd, Duck End Farm, Dry Drayton, Cambridge CB23 8DB, UK</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c532t-c86b942b3db86855493aad15b4400e5337c16ec64dcc3556935f2c73d22337743</citedby><cites>FETCH-LOGICAL-c532t-c86b942b3db86855493aad15b4400e5337c16ec64dcc3556935f2c73d22337743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S1472-6483(10)60169-1$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19778480$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vogt, E</creatorcontrib><creatorcontrib>Kipp, A</creatorcontrib><creatorcontrib>Eichenlaub-Ritter, U</creatorcontrib><title>Aurora kinase B, epigenetic state of centromeric heterochromatin and chiasma resolution in oocytes</title><title>Reproductive biomedicine online</title><addtitle>Reprod Biomed Online</addtitle><description>Abstract Aurora kinases comprise a family of phosphoproteins performing multiple functions in mitosis and meiosis. Because Aurora kinase B (AURKB) expression is altered in aged oocytes and there is only limited information on its function in meiosis, it was decided to study the spatial distribution and co-localization of AURKB with other regulatory proteins at centromeres during mouse oocyte maturation. AURKB associates with chromosomes after germinal vesicle breakdown, is enriched at centromeres from prometaphase I and transits to the spindle midzone at late anaphase I. Preferential inhibition of AURKB by low concentrations of ZM 447439 inhibitor prevents polar body formation and affects spindle formation and chromosome congression at meiosis I, associated with expression of BubR1 checkpoint protein at kinetochores. Release of cohesion between sister chromatids appears inhibited resulting in failure of chiasma resolution in oocytes progressing to anaphase I. Concomitantly, the inhibitor reduces histone H3 lysine 9 trimethylation at centromeric heterochromatin and affects chromosome condensation. The cytokinesis arrest protects young, healthy oocytes from errors in chromosome segregation although increasing polyploidy. This study shows that changes in activity of AURKB may increase risks for chromosome non-disjunction and aneuploidy in mammalian oocytes, irrespective of age.</description><subject>Aneuploidy</subject><subject>Animals</subject><subject>Aurora kinase</subject><subject>Aurora Kinase B</subject><subject>Aurora Kinases</subject><subject>Benzamides - pharmacology</subject><subject>Centromere - drug effects</subject><subject>Centromere - genetics</subject><subject>Centromere - metabolism</subject><subject>chromosome cohesion</subject><subject>Chromosome Segregation - drug effects</subject><subject>Chromosome Segregation - genetics</subject><subject>Epigenesis, Genetic - physiology</subject><subject>Female</subject><subject>heterochromatin</subject><subject>Heterochromatin - drug effects</subject><subject>Heterochromatin - genetics</subject><subject>Heterochromatin - metabolism</subject><subject>Histones - antagonists & inhibitors</subject><subject>Histones - metabolism</subject><subject>Meiosis - drug effects</subject><subject>Meiosis - genetics</subject><subject>Mice</subject><subject>Nondisjunction, Genetic - genetics</subject><subject>Obstetrics and Gynecology</subject><subject>oocyte</subject><subject>Oocytes - drug effects</subject><subject>Oocytes - metabolism</subject><subject>Oogenesis - drug effects</subject><subject>Oogenesis - genetics</subject><subject>Protein Kinase Inhibitors - pharmacology</subject><subject>Protein-Serine-Threonine Kinases - antagonists & inhibitors</subject><subject>Protein-Serine-Threonine Kinases - genetics</subject><subject>Protein-Serine-Threonine Kinases - metabolism</subject><subject>Quinazolines - pharmacology</subject><subject>spindle</subject><subject>Spindle Apparatus - drug effects</subject><subject>Spindle Apparatus - metabolism</subject><issn>1472-6483</issn><issn>1472-6491</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtv1TAQhS1ERUvhJ4C8AyQCdvyIswGVCgpSJRbA2nImc7luE_vWdpDuv8f3ISp1w2o8Z86ckT9CXnD2jjOu3__gsmsbLY14zdkbXaW-4Y_I2VHu-eN_byNOydOcbxjjhhnxhJzyvuuMNOyMDBdLisnRWx9cRvrpLcWN_40BiweaiytI44oChpLijKmKayyYIqxr74oP1IWRwtq7PDuaMMdpKT4GWicxwrZgfkZOVm7K-PxYz8mvL59_Xn5trr9ffbu8uG5AibY0YPTQy3YQ42C0UUr2wrmRq0FKxlAJ0QHXCFqOAEIp3Qu1aqETY9vWWSfFOXl1yN2keLdgLnb2GXCaXMC4ZNsJoQ03WlenOjghxZwTruwm-dmlreXM7ujaPV27Q7eT9nQtr3svjxeWYcbxfuuIsxo-HgxY__nHY7IZPAbA0SeEYsfo_3viw4MEmHzw4KZb3GK-iUsKFaLlNreWHUJ2GZztE7j4C_adnp0</recordid><startdate>2009</startdate><enddate>2009</enddate><creator>Vogt, E</creator><creator>Kipp, A</creator><creator>Eichenlaub-Ritter, U</creator><general>Elsevier Ltd</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></search><sort><creationdate>2009</creationdate><title>Aurora kinase B, epigenetic state of centromeric heterochromatin and chiasma resolution in oocytes</title><author>Vogt, E ; Kipp, A ; Eichenlaub-Ritter, U</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c532t-c86b942b3db86855493aad15b4400e5337c16ec64dcc3556935f2c73d22337743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aneuploidy</topic><topic>Animals</topic><topic>Aurora kinase</topic><topic>Aurora Kinase B</topic><topic>Aurora Kinases</topic><topic>Benzamides - pharmacology</topic><topic>Centromere - drug effects</topic><topic>Centromere - genetics</topic><topic>Centromere - metabolism</topic><topic>chromosome cohesion</topic><topic>Chromosome Segregation - drug effects</topic><topic>Chromosome Segregation - genetics</topic><topic>Epigenesis, Genetic - physiology</topic><topic>Female</topic><topic>heterochromatin</topic><topic>Heterochromatin - drug effects</topic><topic>Heterochromatin - genetics</topic><topic>Heterochromatin - metabolism</topic><topic>Histones - antagonists & inhibitors</topic><topic>Histones - metabolism</topic><topic>Meiosis - drug effects</topic><topic>Meiosis - genetics</topic><topic>Mice</topic><topic>Nondisjunction, Genetic - genetics</topic><topic>Obstetrics and Gynecology</topic><topic>oocyte</topic><topic>Oocytes - drug effects</topic><topic>Oocytes - metabolism</topic><topic>Oogenesis - drug effects</topic><topic>Oogenesis - genetics</topic><topic>Protein Kinase Inhibitors - pharmacology</topic><topic>Protein-Serine-Threonine Kinases - antagonists & inhibitors</topic><topic>Protein-Serine-Threonine Kinases - genetics</topic><topic>Protein-Serine-Threonine Kinases - metabolism</topic><topic>Quinazolines - pharmacology</topic><topic>spindle</topic><topic>Spindle Apparatus - drug effects</topic><topic>Spindle Apparatus - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vogt, E</creatorcontrib><creatorcontrib>Kipp, A</creatorcontrib><creatorcontrib>Eichenlaub-Ritter, U</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><jtitle>Reproductive biomedicine online</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vogt, E</au><au>Kipp, A</au><au>Eichenlaub-Ritter, U</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aurora kinase B, epigenetic state of centromeric heterochromatin and chiasma resolution in oocytes</atitle><jtitle>Reproductive biomedicine online</jtitle><addtitle>Reprod Biomed Online</addtitle><date>2009</date><risdate>2009</risdate><volume>19</volume><issue>3</issue><spage>352</spage><epage>368</epage><pages>352-368</pages><issn>1472-6483</issn><eissn>1472-6491</eissn><abstract>Abstract Aurora kinases comprise a family of phosphoproteins performing multiple functions in mitosis and meiosis. Because Aurora kinase B (AURKB) expression is altered in aged oocytes and there is only limited information on its function in meiosis, it was decided to study the spatial distribution and co-localization of AURKB with other regulatory proteins at centromeres during mouse oocyte maturation. AURKB associates with chromosomes after germinal vesicle breakdown, is enriched at centromeres from prometaphase I and transits to the spindle midzone at late anaphase I. Preferential inhibition of AURKB by low concentrations of ZM 447439 inhibitor prevents polar body formation and affects spindle formation and chromosome congression at meiosis I, associated with expression of BubR1 checkpoint protein at kinetochores. Release of cohesion between sister chromatids appears inhibited resulting in failure of chiasma resolution in oocytes progressing to anaphase I. Concomitantly, the inhibitor reduces histone H3 lysine 9 trimethylation at centromeric heterochromatin and affects chromosome condensation. The cytokinesis arrest protects young, healthy oocytes from errors in chromosome segregation although increasing polyploidy. This study shows that changes in activity of AURKB may increase risks for chromosome non-disjunction and aneuploidy in mammalian oocytes, irrespective of age.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>19778480</pmid><doi>10.1016/S1472-6483(10)60169-1</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aneuploidy Animals Aurora kinase Aurora Kinase B Aurora Kinases Benzamides - pharmacology Centromere - drug effects Centromere - genetics Centromere - metabolism chromosome cohesion Chromosome Segregation - drug effects Chromosome Segregation - genetics Epigenesis, Genetic - physiology Female heterochromatin Heterochromatin - drug effects Heterochromatin - genetics Heterochromatin - metabolism Histones - antagonists & inhibitors Histones - metabolism Meiosis - drug effects Meiosis - genetics Mice Nondisjunction, Genetic - genetics Obstetrics and Gynecology oocyte Oocytes - drug effects Oocytes - metabolism Oogenesis - drug effects Oogenesis - genetics Protein Kinase Inhibitors - pharmacology Protein-Serine-Threonine Kinases - antagonists & inhibitors Protein-Serine-Threonine Kinases - genetics Protein-Serine-Threonine Kinases - metabolism Quinazolines - pharmacology spindle Spindle Apparatus - drug effects Spindle Apparatus - metabolism |
title | Aurora kinase B, epigenetic state of centromeric heterochromatin and chiasma resolution in oocytes |
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