• 中文
    • English
  • English 
    • 中文
    • English
  • Login
View Item 
  •   DSpace Home
  • 生命科学学院
  • 生命科学-已发表论文
  • View Item
  •   DSpace Home
  • 生命科学学院
  • 生命科学-已发表论文
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

The Roles of Multiple Importins for Nuclear Import of Murine Aristaless-related Homeobox Protein

Thumbnail
Full Text
The Roles of Multiple Importins for Nuclear Import of Murine Aristaless-related Homeobox Protein.htm (392bytes)
Date
2009
Author
Tao, Tao
陶涛
Yu, Yinhua
Golden, Jeffrey A.
Tartakoff, Alan M.
Collections
  • 生命科学-已发表论文 [5901]
Show full item record
Abstract
Nuclear import of proteins with nuclear localization signals (NLSs) is mediated by shuttling carriers, the importins. Some cargoes display more than a single NLS, and among these are homeodomain proteins such as Arx, which is critical for development of multiple tissues. Arx has two functional NLSs. The present studies show that several pathways can import Arx via its NLS2, which is within its DNA binding homeodomain. Using an in vitro nuclear import assay, we show that import of Arx via NLS2 can be mediated by importin beta 1, importin 9, or importin 13, with binding being strongest to importin beta 1. All binding is sensitive to RanGTP. Experiments based on precise domain deletions indicate that NLS2 binds imp beta 1, imp9, and imp13 and includes both an importin binding subdomain and a regulatory subdomain with arginine residues being important for function. Moreover, Arx can be co-precipitated with these importins when NLS2 is present. Although nuclear import of Arx can be mediated by these three importin beta s, importin beta 1 seems to play the major role judging from in vivo small interfering RNA ablations and the in vitro import assay. This is the first evidence to show the role of importin beta 1 in nuclear import of paired-type homeodomain proteins. We propose a novel and possibly quite general mechanism for nuclear import of paired-type homeodomain proteins which is critical for development.
Citation
The Journal of Biological Chemistry, 284, 20428-20439. July 24, 2009
URI
http://dx.doi.org/doi:10.1074/jbc.M109.004242
https://dspace.xmu.edu.cn/handle/2288/10446

copyright © 2002-2016  Duraspace  Theme by @mire  厦门大学图书馆  
About | Policies
 

 

Browse

All of DSpaceCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsThis CollectionBy Issue DateAuthorsTitlesSubjects

My Account

LoginRegister

copyright © 2002-2016  Duraspace  Theme by @mire  厦门大学图书馆  
About | Policies