Structure and function of kinetochores in budding yeast.
about
The genome sequence of Schizosaccharomyces pombeCENP-V is required for centromere organization, chromosome alignment and cytokinesis.Lesions in many different spindle components activate the spindle checkpoint in the budding yeast Saccharomyces cerevisiaeHec1p, an evolutionarily conserved coiled-coil protein, modulates chromosome segregation through interaction with SMC proteinsMore surprises from KinetoplastidaRegulation of Saccharomyces cerevisiae kinetochores by the type 1 phosphatase Glc7p.Chromatin assembly factor I and Hir proteins contribute to building functional kinetochores in S. cerevisiae.Budding yeast centromere composition and assembly as revealed by in vivo cross-linking.The yeast RSC chromatin-remodeling complex is required for kinetochore function in chromosome segregation.Chl4p and iml3p are two new members of the budding yeast outer kinetochore.The conserved protein kinase Ipl1 regulates microtubule binding to kinetochores in budding yeastPolyploids require Bik1 for kinetochore-microtubule attachment.A putative protein complex consisting of Ctf19, Mcm21, and Okp1 represents a missing link in the budding yeast kinetochore.Ctf7p is essential for sister chromatid cohesion and links mitotic chromosome structure to the DNA replication machinery.Misregulation of Scm3p/HJURP causes chromosome instability in Saccharomyces cerevisiae and human cells.Bipolar localization of a chromosome partition protein in Bacillus subtilisHistone-histone interactions and centromere function.Cell cycle arrest in cdc20 mutants of Saccharomyces cerevisiae is independent of Ndc10p and kinetochore function but requires a subset of spindle checkpoint genes.Differential requirements for DNA replication in the activation of mitotic checkpoints in Saccharomyces cerevisiae.Yeast kinetochore microtubule dynamics analyzed by high-resolution three-dimensional microscopy.Yeast kinetochores do not stabilize Stu2p-dependent spindle microtubule dynamicsCloning of a centromere binding factor 3d (CBF3D) gene from Candida glabrata.Centromere identity from the DNA point of view.Determining centromere identity: cyclical stories and forking paths.Phosphorylation by casein kinase 2 facilitates Psh1 protein-assisted degradation of Cse4 proteinA region of the Sir1 protein dedicated to recognition of a silencer and required for interaction with the Orc1 protein in saccharomyces cerevisiae.The activation of a neocentromere in Drosophila requires proximity to an endogenous centromere.Comparative autoregressive moving average analysis of kinetochore microtubule dynamics in yeast.Repetitive elements in genomes of parasitic protozoaRetention of the BUB3 checkpoint protein on lagging chromosomes.Resinless section electron microscopy reveals the yeast cytoskeleton.Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag.Probing the architecture of a simple kinetochore using DNA-protein crosslinking.Altered dosage and mislocalization of histone H3 and Cse4p lead to chromosome loss in Saccharomyces cerevisiae.Histone H2A is required for normal centromere function in Saccharomyces cerevisiaeMapping of a human centromere onto the DNA by topoisomerase II cleavageThe Saccharomyces cerevisiae kinetochore.The SWI/SNF complex acts to constrain distribution of the centromeric histone variant Cse4.Discovery of an unconventional centromere in budding yeast redefines evolution of point centromeres.Cohesin ensures bipolar attachment of microtubules to sister centromeres and resists their precocious separation.
P2860
Q21972841-5FAC331C-1409-43B3-945E-4535499F1854Q24310616-6EB5CE0A-D4F9-4281-9EED-3AF5E25FC42CQ24548054-4B80A1E9-AAB6-441E-B49F-4BC1CB196B31Q24554466-14F6D730-FF8C-4007-BEA7-BB22625E0A71Q24620538-6E8F500D-4A27-4265-9D3A-525BCBB34C1FQ27931654-AF01018F-7280-405E-843F-B4962D2109B6Q27932579-F139D409-226C-425A-93F1-A1E1BAC1A99DQ27933562-A91A7320-3303-47AD-96F8-C2D47B71C991Q27936620-86FF2EB8-ED8F-41C4-AA5C-2A811FCAE12EQ27937271-A106EE19-B8C7-4D31-9ECC-3F0B9317DDD8Q27937537-78B19A2B-D2A8-4931-9E24-29D774944856Q27937672-CC58B26A-E87E-4C44-94D9-F2D7337622E1Q27938830-54385425-0F73-4809-B201-C69042EF6DEEQ27939220-E411148A-93C4-415B-AABD-105C42687E7BQ28477293-4030F4C4-4278-4C9C-9AB9-02110D50006CQ28488948-687544B1-E1D5-4C0C-98A4-F44DAFE7E52CQ30305835-9151F031-9F2D-4B19-BE9B-A62A650CEA87Q30446001-FFECB3E3-54A8-4EED-B6E5-2C8CCC6A125EQ30452670-9E095566-2535-4861-A7BF-E096AED317B2Q30476783-A9ED4A6A-430A-4B20-A27B-85630B6F16E1Q30480609-3DC57241-1FD7-493E-AE9E-E02261B457B3Q30730663-EC9B4D5D-91FE-471D-867B-CF9FE4A33901Q33935413-8BA9BD7D-B9AB-4602-A89B-4FFFC6F6356CQ34325316-CDE184F7-C5E8-41D5-8923-5026CB9ECED8Q34355799-31F42C60-9CCC-4402-AB64-DE80755AA7E6Q34606092-F0D3FBD3-9836-480F-B3D2-AE3ADEEF0EDFQ34613070-306DE320-0337-4C8D-9664-032A6950AFB4Q35012265-2289B9C3-9D7F-4C20-B788-BE6737F5F645Q35215945-C8A5291C-3A22-47B6-90F2-EBD33E3A461DQ35552257-1DE44596-A443-4234-87E3-B1189BB165CCQ36104942-02452C97-5A52-46F8-9F5E-3C2CCDCA4514Q36138989-DD6017B2-1221-47CE-AEF9-47137B037698Q36254959-D34D4483-972C-41F0-9457-8C8DE437E339Q36665818-48473B28-1662-4B69-B904-37FE4102FC93Q40410847-CB95E7DD-ADF7-4761-9139-27C9EEFEA759Q40819118-14385A70-715F-4D18-A0B7-5F9B01913C42Q41017137-45BBBBFD-6497-4A9E-B1C9-CC0001628A8AQ42051038-30EE36F0-15D2-44DB-960A-37ED847B13D8Q42436460-B37AE0B3-D285-4A8B-B13A-E190FE4C494DQ54041268-2A1EA3B5-0C23-4A03-97AD-A2D7FE1DC321
P2860
Structure and function of kinetochores in budding yeast.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Structure and function of kinetochores in budding yeast.
@en
type
label
Structure and function of kinetochores in budding yeast.
@en
prefLabel
Structure and function of kinetochores in budding yeast.
@en
P1476
Structure and function of kinetochores in budding yeast.
@en
P2093
P304
P356
10.1146/ANNUREV.CB.11.110195.002351
P577
1995-01-01T00:00:00Z