KPNB1 , XPO7 and IPO8 Mediate the Translocation of NF‐κB /p65 into the Nucleus
NF‐κB /p65 is retained in the cytoplasm until it is activated in response to stress. Nuclear import of p65 is regulated by importin α in a nuclear localization signal ( NLS )‐dependent manner. However, the role of importin β family members in the nuclear translocation of p65 is largely unclear. In t...
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Veröffentlicht in: | Traffic (Copenhagen, Denmark) Denmark), 2013-11, Vol.14 (11), p.1132-1143 |
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creator | Liang, Peizhou Zhang, Haiyan Wang, Guoxin Li, Suping Cong, Shujie Luo, Yingyun Zhang, Biliang |
description | NF‐κB
/p65 is retained in the cytoplasm until it is activated in response to stress. Nuclear import of p65 is regulated by importin α in a nuclear localization signal (
NLS
)‐dependent manner. However, the role of importin β family members in the nuclear translocation of p65 is largely unclear. In this study, using high‐content
siRNA
screening, we identified three of 17 importin β family members that are involved in the nuclear import of p65. Our data showed that knockdown of
KPNB1
,
XPO7
and
IPO8
reduced the amount of nuclear p65 following tumor necrosis factor‐α (
TNF
‐α) stimulation, resulting in lower
NF‐κB
activity.
KPNB1
was the major importin β receptor for p65 import, and this import was dependent on the
NLS
of p65. However,
NLS
‐mutated p65 still entered the nucleus and bound to
XPO7
and
IPO8
. Interestingly, among the six members of the importin α family,
KPNA2
was most important for p65 import. Taken together, our results show that the import of p65 mainly relies on the canonical
KPNA2
/
KPNB1
pathway; however, p65 is also imported by an alternative pathway that is independent of its
NLS
. Redundant importin receptors are likely to maintain the important function of p65 according to need
. |
doi_str_mv | 10.1111/tra.12097 |
format | Article |
fullrecord | <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1111_tra_12097</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1111_tra_12097</sourcerecordid><originalsourceid>FETCH-LOGICAL-c159t-17199c48afa42277a8789f2b32a115f7782080c31f37d0fb0aef1c1e66b8dcd83</originalsourceid><addsrcrecordid>eNotkE1OwzAUhC0EEqWw4AbeIpH2PefH9pJWFCpKEqQisYscxxZBIalsd8GOI3AeDsEhOAmlMJuZxadZfIScI0xwl2lwaoIMJD8gI8wAIhBpcrjbsRSRZCiPyYn3LwDA0iQZkYe7Mp8hvaRPZcGp6hu6LAtB703TqmBoeDZ07VTvu0Gr0A49HSzNF9_vH1-fMzrdZClt-zDsuXyrO7P1p-TIqs6bs_8ek8fF9Xp-G62Km-X8ahVpTGWIkKOUOhHKqoQxzpXgQlpWx0whppZzwUCAjtHGvAFbgzIWNZosq0WjGxGPycXfr3aD987YauPaV-XeKoTq10W1c1HtXcQ_yL5QIQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>KPNB1 , XPO7 and IPO8 Mediate the Translocation of NF‐κB /p65 into the Nucleus</title><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Wiley Free Content</source><source>IngentaConnect Free/Open Access Journals</source><creator>Liang, Peizhou ; Zhang, Haiyan ; Wang, Guoxin ; Li, Suping ; Cong, Shujie ; Luo, Yingyun ; Zhang, Biliang</creator><creatorcontrib>Liang, Peizhou ; Zhang, Haiyan ; Wang, Guoxin ; Li, Suping ; Cong, Shujie ; Luo, Yingyun ; Zhang, Biliang</creatorcontrib><description>NF‐κB
/p65 is retained in the cytoplasm until it is activated in response to stress. Nuclear import of p65 is regulated by importin α in a nuclear localization signal (
NLS
)‐dependent manner. However, the role of importin β family members in the nuclear translocation of p65 is largely unclear. In this study, using high‐content
siRNA
screening, we identified three of 17 importin β family members that are involved in the nuclear import of p65. Our data showed that knockdown of
KPNB1
,
XPO7
and
IPO8
reduced the amount of nuclear p65 following tumor necrosis factor‐α (
TNF
‐α) stimulation, resulting in lower
NF‐κB
activity.
KPNB1
was the major importin β receptor for p65 import, and this import was dependent on the
NLS
of p65. However,
NLS
‐mutated p65 still entered the nucleus and bound to
XPO7
and
IPO8
. Interestingly, among the six members of the importin α family,
KPNA2
was most important for p65 import. Taken together, our results show that the import of p65 mainly relies on the canonical
KPNA2
/
KPNB1
pathway; however, p65 is also imported by an alternative pathway that is independent of its
NLS
. Redundant importin receptors are likely to maintain the important function of p65 according to need
.</description><identifier>ISSN: 1398-9219</identifier><identifier>EISSN: 1600-0854</identifier><identifier>DOI: 10.1111/tra.12097</identifier><language>eng</language><ispartof>Traffic (Copenhagen, Denmark), 2013-11, Vol.14 (11), p.1132-1143</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c159t-17199c48afa42277a8789f2b32a115f7782080c31f37d0fb0aef1c1e66b8dcd83</citedby><cites>FETCH-LOGICAL-c159t-17199c48afa42277a8789f2b32a115f7782080c31f37d0fb0aef1c1e66b8dcd83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Liang, Peizhou</creatorcontrib><creatorcontrib>Zhang, Haiyan</creatorcontrib><creatorcontrib>Wang, Guoxin</creatorcontrib><creatorcontrib>Li, Suping</creatorcontrib><creatorcontrib>Cong, Shujie</creatorcontrib><creatorcontrib>Luo, Yingyun</creatorcontrib><creatorcontrib>Zhang, Biliang</creatorcontrib><title>KPNB1 , XPO7 and IPO8 Mediate the Translocation of NF‐κB /p65 into the Nucleus</title><title>Traffic (Copenhagen, Denmark)</title><description>NF‐κB
/p65 is retained in the cytoplasm until it is activated in response to stress. Nuclear import of p65 is regulated by importin α in a nuclear localization signal (
NLS
)‐dependent manner. However, the role of importin β family members in the nuclear translocation of p65 is largely unclear. In this study, using high‐content
siRNA
screening, we identified three of 17 importin β family members that are involved in the nuclear import of p65. Our data showed that knockdown of
KPNB1
,
XPO7
and
IPO8
reduced the amount of nuclear p65 following tumor necrosis factor‐α (
TNF
‐α) stimulation, resulting in lower
NF‐κB
activity.
KPNB1
was the major importin β receptor for p65 import, and this import was dependent on the
NLS
of p65. However,
NLS
‐mutated p65 still entered the nucleus and bound to
XPO7
and
IPO8
. Interestingly, among the six members of the importin α family,
KPNA2
was most important for p65 import. Taken together, our results show that the import of p65 mainly relies on the canonical
KPNA2
/
KPNB1
pathway; however, p65 is also imported by an alternative pathway that is independent of its
NLS
. Redundant importin receptors are likely to maintain the important function of p65 according to need
.</description><issn>1398-9219</issn><issn>1600-0854</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNotkE1OwzAUhC0EEqWw4AbeIpH2PefH9pJWFCpKEqQisYscxxZBIalsd8GOI3AeDsEhOAmlMJuZxadZfIScI0xwl2lwaoIMJD8gI8wAIhBpcrjbsRSRZCiPyYn3LwDA0iQZkYe7Mp8hvaRPZcGp6hu6LAtB703TqmBoeDZ07VTvu0Gr0A49HSzNF9_vH1-fMzrdZClt-zDsuXyrO7P1p-TIqs6bs_8ek8fF9Xp-G62Km-X8ahVpTGWIkKOUOhHKqoQxzpXgQlpWx0whppZzwUCAjtHGvAFbgzIWNZosq0WjGxGPycXfr3aD987YauPaV-XeKoTq10W1c1HtXcQ_yL5QIQ</recordid><startdate>201311</startdate><enddate>201311</enddate><creator>Liang, Peizhou</creator><creator>Zhang, Haiyan</creator><creator>Wang, Guoxin</creator><creator>Li, Suping</creator><creator>Cong, Shujie</creator><creator>Luo, Yingyun</creator><creator>Zhang, Biliang</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201311</creationdate><title>KPNB1 , XPO7 and IPO8 Mediate the Translocation of NF‐κB /p65 into the Nucleus</title><author>Liang, Peizhou ; Zhang, Haiyan ; Wang, Guoxin ; Li, Suping ; Cong, Shujie ; Luo, Yingyun ; Zhang, Biliang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c159t-17199c48afa42277a8789f2b32a115f7782080c31f37d0fb0aef1c1e66b8dcd83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liang, Peizhou</creatorcontrib><creatorcontrib>Zhang, Haiyan</creatorcontrib><creatorcontrib>Wang, Guoxin</creatorcontrib><creatorcontrib>Li, Suping</creatorcontrib><creatorcontrib>Cong, Shujie</creatorcontrib><creatorcontrib>Luo, Yingyun</creatorcontrib><creatorcontrib>Zhang, Biliang</creatorcontrib><collection>CrossRef</collection><jtitle>Traffic (Copenhagen, Denmark)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liang, Peizhou</au><au>Zhang, Haiyan</au><au>Wang, Guoxin</au><au>Li, Suping</au><au>Cong, Shujie</au><au>Luo, Yingyun</au><au>Zhang, Biliang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>KPNB1 , XPO7 and IPO8 Mediate the Translocation of NF‐κB /p65 into the Nucleus</atitle><jtitle>Traffic (Copenhagen, Denmark)</jtitle><date>2013-11</date><risdate>2013</risdate><volume>14</volume><issue>11</issue><spage>1132</spage><epage>1143</epage><pages>1132-1143</pages><issn>1398-9219</issn><eissn>1600-0854</eissn><abstract>NF‐κB
/p65 is retained in the cytoplasm until it is activated in response to stress. Nuclear import of p65 is regulated by importin α in a nuclear localization signal (
NLS
)‐dependent manner. However, the role of importin β family members in the nuclear translocation of p65 is largely unclear. In this study, using high‐content
siRNA
screening, we identified three of 17 importin β family members that are involved in the nuclear import of p65. Our data showed that knockdown of
KPNB1
,
XPO7
and
IPO8
reduced the amount of nuclear p65 following tumor necrosis factor‐α (
TNF
‐α) stimulation, resulting in lower
NF‐κB
activity.
KPNB1
was the major importin β receptor for p65 import, and this import was dependent on the
NLS
of p65. However,
NLS
‐mutated p65 still entered the nucleus and bound to
XPO7
and
IPO8
. Interestingly, among the six members of the importin α family,
KPNA2
was most important for p65 import. Taken together, our results show that the import of p65 mainly relies on the canonical
KPNA2
/
KPNB1
pathway; however, p65 is also imported by an alternative pathway that is independent of its
NLS
. Redundant importin receptors are likely to maintain the important function of p65 according to need
.</abstract><doi>10.1111/tra.12097</doi><tpages>12</tpages></addata></record> |
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issn | 1398-9219 1600-0854 |
language | eng |
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source | Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Free Content; IngentaConnect Free/Open Access Journals |
title | KPNB1 , XPO7 and IPO8 Mediate the Translocation of NF‐κB /p65 into the Nucleus |
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