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Nuclear targeting signal recognistion: a key control point in nuclear transport?

dc.contributor.authorJans, David A
dc.contributor.authorXiao, Chong-Yun
dc.contributor.authorLam, Mark H C
dc.date.accessioned2015-12-13T23:15:46Z
dc.date.issued2000
dc.date.updated2015-12-12T08:45:05Z
dc.description.abstractRecent progress indicates that there are multiple pathways of nucleocytoplasmic transport which involve specific targeting sequences, such as nuclear localization sequences (NLSs), and cytosolic receptor molecules of the importin/karyopherin superfamily which recognise and dock the NLS-containing proteins at the nuclear pore. This first step of nuclear import/export is of central importance, with the affinity of the importin-targeting sequence interaction a critical parameter in determining transport efficiency. Different importins possess distinct NLS-binding specificities, which allows the system to be modulated through differential expression of the importins themselves, as well as through competition between different importins for the same protein, and between different proteins for the same importin. The targeting sequence-importin interaction can also be influenced directly by phosphorylation increasing the affinity of the interaction with importins or by targeting sequence masking through phosphorylation or specific protein binding. Targeting sequence recognition thus appears to represent a key control point in the regulation of nuclear transport. (C) 2000 John Wiley and Sons, Inc.
dc.identifier.issn0265-9247
dc.identifier.urihttp://hdl.handle.net/1885/89048
dc.publisherThe Company of Biologists Ltd
dc.sourceBioessays
dc.subjectKeywords: differential display; importin; karyopherin; nuclear localization sequence; nucleocytoplasmic transport; protein binding; protein phosphorylation; protein targeting; Amino Acid Sequence; Animals; Binding, Competitive; Biological Transport, Active; Cell Nu
dc.titleNuclear targeting signal recognistion: a key control point in nuclear transport?
dc.typeJournal article
local.bibliographicCitation.lastpage402
local.bibliographicCitation.startpage395
local.contributor.affiliationJans, David A, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationXiao, Chong-Yun, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationLam, Mark H C, College of Medicine, Biology and Environment, ANU
local.contributor.authoruidJans, David A, u9306667
local.contributor.authoruidXiao, Chong-Yun, u4016996
local.contributor.authoruidLam, Mark H C, u9900453
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor060111 - Signal Transduction
local.identifier.ariespublicationMigratedxPub18952
local.identifier.citationvolume22
local.identifier.doi10.1002/(SICI)1521-1878(200006)22:6<532::AID-BIES6>3.0.CO;2-O
local.identifier.scopusID2-s2.0-0034041537
local.type.statusPublished Version

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