Format:
Online-Ressource
ISSN:
1460-2075
Content:
Replication protein A (RPA) is a eukaryotic single‐stranded (ss) DNA‐binding protein that is essential for general DNA metabolism. RPA consists of three subunits (70, 33 and 14 kDa). We have identified by two‐hybrid screening a novel Xenopus protein called XRIPα that interacts with the ssDNA‐binding domain of the largest subunit of RPA. XRIPα homologues are found in human and in Drosophila but not in yeast. XRIPα is complexed with RPA in Xenopus egg extracts together with another 90 kDa protein that was identified as importin β. We have demonstrated that XRIPα, but not importin α, is required for nuclear import of RPA. Immunodepletion of XRIPα from the egg extracts blocks nuclear import of RPA but not that of nucleoplasmin, a classical import substrate. RPA import can be restored by addition of recombinant XRIPα. Conversely, depletion of importin α blocks import of nucleoplasmin but not that of RPA. GST–XRIPα pull‐down assay shows that XRIPα interacts directly with recombinant importin β as well as with RPA in vitro. Finally, RPA import can be reconstituted from the recombinant proteins. We propose that XRIPα plays the role of importin α in the RPA import scheme: XRIPα serves as an adaptor to link RPA to importin β.
In:
volume:18
In:
number:15
In:
year:1999
In:
pages:4348-4358
In:
extent:11
In:
European Molecular Biology Organization, The EMBO journal, Heidelberg : EMBO Press, 1982-, 18, Heft 15 (1999), 4348-4358 (gesamt 11), 1460-2075
Language:
English
DOI:
10.1093/emboj/18.15.4348
URN:
urn:nbn:de:101:1-2023120706082619032691
URL:
https://doi.org/10.1093/emboj/18.15.4348
URL:
https://nbn-resolving.org/urn:nbn:de:101:1-2023120706082619032691
URL:
https://d-nb.info/1312446927/34
URL:
https://doi.org/10.1093/emboj/18.15.4348
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