{"title":"纺锤体微管附着对着丝点上CENP-E组织的调节。","authors":"D A Thrower, M A Jordan, L Wilson","doi":"10.1002/(SICI)1097-0169(1996)35:2<121::AID-CM5>3.0.CO;2-D","DOIUrl":null,"url":null,"abstract":"<p><p>CENP-E is a protein of the kinesin superfamily that appears as small paired globules at kinetochores of chromosomes in mammalian cells during prometaphase and metaphase of mitosis [Yen et al., 1992: Nature 359:536-539]. In the present study we found that a significant number of chromosomes during early prometaphase in HeLa cells (approximately 30%) were stained with a CENP-E antibody in the form of large C-shaped \"collars\" that partially encircled the chromosomes. The C-shaped CENP-E collars were present only transiently and were completely replaced by small paired globular forms prior to metaphase. Most chromosomes had persistent CENP-E collars in cells blocked at mitosis with a vinblastine concentration sufficient to prevent all microtubule formation. Attachment of newly formed microtubules to the kinetochores after removal of vinblastine resulted in loss of the collars and replacement with small paired globules. Similarly, a higher proportion of chromosomes isolated from vinblastine-treated cells contained CENP-E collars (73%), and the \"capture\" (i.e., attachment) of microtubules by the chromosomes resulted in conversion of the collars into small paired globules in vitro. Thus, the CENP-E collars form prior to microtubule attachment and disappear after attachment of the chromosomes to the spindle. The CENP-E collars may facilitate capture of microtubules by chromosomes during prometaphase.</p>","PeriodicalId":9675,"journal":{"name":"Cell motility and the cytoskeleton","volume":"35 2","pages":"121-33"},"PeriodicalIF":0.0000,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/(SICI)1097-0169(1996)35:2<121::AID-CM5>3.0.CO;2-D","citationCount":"62","resultStr":"{\"title\":\"Modulation of CENP-E organization at kinetochores by spindle microtubule attachment.\",\"authors\":\"D A Thrower, M A Jordan, L Wilson\",\"doi\":\"10.1002/(SICI)1097-0169(1996)35:2<121::AID-CM5>3.0.CO;2-D\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>CENP-E is a protein of the kinesin superfamily that appears as small paired globules at kinetochores of chromosomes in mammalian cells during prometaphase and metaphase of mitosis [Yen et al., 1992: Nature 359:536-539]. In the present study we found that a significant number of chromosomes during early prometaphase in HeLa cells (approximately 30%) were stained with a CENP-E antibody in the form of large C-shaped \\\"collars\\\" that partially encircled the chromosomes. The C-shaped CENP-E collars were present only transiently and were completely replaced by small paired globular forms prior to metaphase. Most chromosomes had persistent CENP-E collars in cells blocked at mitosis with a vinblastine concentration sufficient to prevent all microtubule formation. Attachment of newly formed microtubules to the kinetochores after removal of vinblastine resulted in loss of the collars and replacement with small paired globules. Similarly, a higher proportion of chromosomes isolated from vinblastine-treated cells contained CENP-E collars (73%), and the \\\"capture\\\" (i.e., attachment) of microtubules by the chromosomes resulted in conversion of the collars into small paired globules in vitro. Thus, the CENP-E collars form prior to microtubule attachment and disappear after attachment of the chromosomes to the spindle. The CENP-E collars may facilitate capture of microtubules by chromosomes during prometaphase.</p>\",\"PeriodicalId\":9675,\"journal\":{\"name\":\"Cell motility and the cytoskeleton\",\"volume\":\"35 2\",\"pages\":\"121-33\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1996-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/(SICI)1097-0169(1996)35:2<121::AID-CM5>3.0.CO;2-D\",\"citationCount\":\"62\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell motility and the cytoskeleton\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/(SICI)1097-0169(1996)35:2<121::AID-CM5>3.0.CO;2-D\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell motility and the cytoskeleton","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/(SICI)1097-0169(1996)35:2<121::AID-CM5>3.0.CO;2-D","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 62
摘要
CENP-E是一种激酶蛋白超家族蛋白,在哺乳动物细胞有丝分裂前期和中期以小的成对小球的形式出现在染色体的着丝点上[Yen et al., 1992: Nature 359:536-539]。在本研究中,我们发现HeLa细胞早期中期的大量染色体(约30%)被CENP-E抗体以部分环绕染色体的大c形“项圈”的形式染色。c形的CENP-E项圈仅短暂存在,在中期之前完全被成对的小球体形式所取代。大多数染色体在细胞有丝分裂时具有持续的CENP-E环,长春碱浓度足以阻止所有微管的形成。去除长春花碱后,新形成的微管附着在着丝点上,导致项圈丢失,取而代之的是成对的小球体。同样,从长春花碱处理的细胞中分离出的较高比例的染色体含有CENP-E项圈(73%),并且染色体对微管的“捕获”(即附着)导致项圈在体外转化为成对的小球体。因此,CENP-E项圈在微管附着之前形成,在染色体附着到纺锤体后消失。CENP-E项圈可能有助于染色体在前期捕获微管。
Modulation of CENP-E organization at kinetochores by spindle microtubule attachment.
CENP-E is a protein of the kinesin superfamily that appears as small paired globules at kinetochores of chromosomes in mammalian cells during prometaphase and metaphase of mitosis [Yen et al., 1992: Nature 359:536-539]. In the present study we found that a significant number of chromosomes during early prometaphase in HeLa cells (approximately 30%) were stained with a CENP-E antibody in the form of large C-shaped "collars" that partially encircled the chromosomes. The C-shaped CENP-E collars were present only transiently and were completely replaced by small paired globular forms prior to metaphase. Most chromosomes had persistent CENP-E collars in cells blocked at mitosis with a vinblastine concentration sufficient to prevent all microtubule formation. Attachment of newly formed microtubules to the kinetochores after removal of vinblastine resulted in loss of the collars and replacement with small paired globules. Similarly, a higher proportion of chromosomes isolated from vinblastine-treated cells contained CENP-E collars (73%), and the "capture" (i.e., attachment) of microtubules by the chromosomes resulted in conversion of the collars into small paired globules in vitro. Thus, the CENP-E collars form prior to microtubule attachment and disappear after attachment of the chromosomes to the spindle. The CENP-E collars may facilitate capture of microtubules by chromosomes during prometaphase.