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
Hauptverfasser: Liang, Peizhou, Zhang, Haiyan, Wang, Guoxin, Li, Suping, Cong, Shujie, Luo, Yingyun, Zhang, Biliang
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container_issue 11
container_start_page 1132
container_title Traffic (Copenhagen, Denmark)
container_volume 14
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 .
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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. 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title KPNB1 , XPO7 and IPO8 Mediate the Translocation of NF‐κB /p65 into the Nucleus
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