Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pgen.1003610
DC FieldValue
dc.titleMonopolin Subunit Csm1 Associates with MIND Complex to Establish Monopolar Attachment of Sister Kinetochores at Meiosis I
dc.contributor.authorSarkar S.
dc.contributor.authorShenoy R.T.
dc.contributor.authorDalgaard J.Z.
dc.contributor.authorNewnham L.
dc.contributor.authorHoffmann E.
dc.contributor.authorMillar J.B.A.
dc.contributor.authorArumugam P.
dc.date.accessioned2019-11-06T09:26:16Z
dc.date.available2019-11-06T09:26:16Z
dc.date.issued2013
dc.identifier.citationSarkar S., Shenoy R.T., Dalgaard J.Z., Newnham L., Hoffmann E., Millar J.B.A., Arumugam P. (2013). Monopolin Subunit Csm1 Associates with MIND Complex to Establish Monopolar Attachment of Sister Kinetochores at Meiosis I. PLoS Genetics 9 (7) : e1003610. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pgen.1003610
dc.identifier.issn15537390
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161620
dc.description.abstractSexually reproducing organisms halve their cellular ploidy during gametogenesis by undergoing a specialized form of cell division known as meiosis. During meiosis, a single round of DNA replication is followed by two rounds of nuclear divisions (referred to as meiosis I and II). While sister kinetochores bind to microtubules emanating from opposite spindle poles during mitosis, they bind to microtubules originating from the same spindle pole during meiosis I. This phenomenon is referred to as mono-orientation and is essential for setting up the reductional mode of chromosome segregation during meiosis I. In budding yeast, mono-orientation depends on a four component protein complex referred to as monopolin which consists of two nucleolar proteins Csm1 and Lrs4, meiosis-specific protein Mam1 of unknown function and casein kinase Hrr25. Monopolin complex binds to kinetochores during meiosis I and prevents bipolar attachments. Although monopolin associates with kinetochores during meiosis I, its binding site(s) on the kinetochore is not known and its mechanism of action has not been established. By carrying out an imaging-based screen we have found that the MIND complex, a component of the central kinetochore, is required for monopolin association with kinetochores during meiosis. Furthermore, we demonstrate that interaction of monopolin subunit Csm1 with the N-terminal domain of MIND complex subunit Dsn1, is essential for both the association of monopolin with kinetochores and for monopolar attachment of sister kinetochores during meiosis I. As such this provides the first functional evidence for a monopolin-binding site at the kinetochore. © 2013 Sarkar et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectbinding protein
dc.subjectCsm1 protein
dc.subjectMIND complex
dc.subjectmonopolin
dc.subjectnuclear protein
dc.subjectunclassified drug
dc.subjectamino terminal sequence
dc.subjectarticle
dc.subjectbinding site
dc.subjectcentromere
dc.subjectcontrolled study
dc.subjectmeiosis
dc.subjectmicrotubule assembly
dc.subjectmitosis
dc.subjectmitosis spindle
dc.subjectnonhuman
dc.subjectprotein binding
dc.subjectprotein interaction
dc.subjectyeast
dc.subjectCasein Kinase I
dc.subjectCell Cycle Proteins
dc.subjectChromosomal Proteins, Non-Histone
dc.subjectDNA Replication
dc.subjectKinetochores
dc.subjectMeiosis
dc.subjectMicrotubules
dc.subjectMultiprotein Complexes
dc.subjectNuclear Proteins
dc.subjectSaccharomyces cerevisiae
dc.subjectSaccharomyces cerevisiae Proteins
dc.subjectSister Chromatid Exchange
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1371/journal.pgen.1003610
dc.description.sourcetitlePLoS Genetics
dc.description.volume9
dc.description.issue7
dc.description.pagee1003610
Appears in Collections:Elements
Staff Publications

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1371_journal_pgen_1003610.pdf2.12 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons