Phosphorylation of p27Kip1 at Thr-157 interferes with its association with importin α during G1 and prevents nuclear re-entry

Incheol Shin, Jeremy Rotty, Frederick Y. Wu, Carlos L. Arteaga

Research output: Contribution to journalArticle

73 Citations (Scopus)

Abstract

We have studied mechanisms of Akt-mediated phosphorylation and regulation of cellular localization of p27. Akt phosphorylates Thr-157 in p27 and retains it in the cytosol. In cells arrested in G1 and then synchronized to enter into S phase, Akt-mediated phosphorylation of Thr-157 p27 occurred in the cytosol during G1 phase of the cell cycle. Both T157A and S10A p27 mutants localized in the nucleus in all phases of the cell cycle regardless of the expression of active Akt. Thr-157 phosphorylation was undetectable in S10A-p27, suggesting that Ser-10 phosphorylation is required for p27 localization in the cytosol and subsequent phosphorylation at Thr-157. Phosphorylation at Thr-157 interrupted the association of p27 with importin α. A T157A-p27 mutant protein exhibited higher association with importin a than wild-type-p27. Treatment of transfected and endogenous p27 with alkaline phosphatase rescued its association with importin α. Leptomycin B inhibited cytosolic Thr-157 P-p27 staining, implying that CRM1-dependent nuclear export is required for Akt-mediated Thr-157 phosphorylation. Heterokaryon shuttling assays with NIH3T3 (mouse) cells transfected with FLAG-p27 and HeLa (human) cells revealed that both wild type and T157A-p27 shuttled from NIH3T3 to HeLa cell nuclei with similar frequencies. However, S10A-p27 was found only in the NIH3T3 nuclei of NIH3T3-HeLa cell fusions. These results suggest that 1) Ser-10 phosphorylation is required for nuclear export of p27, 2) subsequent Akt-mediated phosphorylation at Thr-157 during G1 phase corrals p27 in the cytosol, and 3) Thr-157 phosphorylation inhibits the association of p27 with importin α thus preventing its re-entry into the nucleus.

Original languageEnglish (US)
Pages (from-to)6055-6063
Number of pages9
JournalJournal of Biological Chemistry
Volume280
Issue number7
DOIs
StatePublished - Feb 18 2005

Fingerprint

Karyopherins
Phosphorylation
Reentry
Association reactions
Cytosol
HeLa Cells
Cell Nucleus Active Transport
Cells
G1 Phase
Cell Cycle
Cell Fusion
Mutant Proteins
Cell Nucleus
S Phase
Alkaline Phosphatase
Assays
Fusion reactions

ASJC Scopus subject areas

  • Biochemistry

Cite this

Phosphorylation of p27Kip1 at Thr-157 interferes with its association with importin α during G1 and prevents nuclear re-entry. / Shin, Incheol; Rotty, Jeremy; Wu, Frederick Y.; Arteaga, Carlos L.

In: Journal of Biological Chemistry, Vol. 280, No. 7, 18.02.2005, p. 6055-6063.

Research output: Contribution to journalArticle

@article{d3ca6163ba7141ee993baa2e3a87808b,
title = "Phosphorylation of p27Kip1 at Thr-157 interferes with its association with importin α during G1 and prevents nuclear re-entry",
abstract = "We have studied mechanisms of Akt-mediated phosphorylation and regulation of cellular localization of p27. Akt phosphorylates Thr-157 in p27 and retains it in the cytosol. In cells arrested in G1 and then synchronized to enter into S phase, Akt-mediated phosphorylation of Thr-157 p27 occurred in the cytosol during G1 phase of the cell cycle. Both T157A and S10A p27 mutants localized in the nucleus in all phases of the cell cycle regardless of the expression of active Akt. Thr-157 phosphorylation was undetectable in S10A-p27, suggesting that Ser-10 phosphorylation is required for p27 localization in the cytosol and subsequent phosphorylation at Thr-157. Phosphorylation at Thr-157 interrupted the association of p27 with importin α. A T157A-p27 mutant protein exhibited higher association with importin a than wild-type-p27. Treatment of transfected and endogenous p27 with alkaline phosphatase rescued its association with importin α. Leptomycin B inhibited cytosolic Thr-157 P-p27 staining, implying that CRM1-dependent nuclear export is required for Akt-mediated Thr-157 phosphorylation. Heterokaryon shuttling assays with NIH3T3 (mouse) cells transfected with FLAG-p27 and HeLa (human) cells revealed that both wild type and T157A-p27 shuttled from NIH3T3 to HeLa cell nuclei with similar frequencies. However, S10A-p27 was found only in the NIH3T3 nuclei of NIH3T3-HeLa cell fusions. These results suggest that 1) Ser-10 phosphorylation is required for nuclear export of p27, 2) subsequent Akt-mediated phosphorylation at Thr-157 during G1 phase corrals p27 in the cytosol, and 3) Thr-157 phosphorylation inhibits the association of p27 with importin α thus preventing its re-entry into the nucleus.",
author = "Incheol Shin and Jeremy Rotty and Wu, {Frederick Y.} and Arteaga, {Carlos L.}",
year = "2005",
month = "2",
day = "18",
doi = "10.1074/jbc.M412367200",
language = "English (US)",
volume = "280",
pages = "6055--6063",
journal = "Journal of Biological Chemistry",
issn = "0021-9258",
publisher = "American Society for Biochemistry and Molecular Biology Inc.",
number = "7",

}

TY - JOUR

T1 - Phosphorylation of p27Kip1 at Thr-157 interferes with its association with importin α during G1 and prevents nuclear re-entry

AU - Shin, Incheol

AU - Rotty, Jeremy

AU - Wu, Frederick Y.

AU - Arteaga, Carlos L.

PY - 2005/2/18

Y1 - 2005/2/18

N2 - We have studied mechanisms of Akt-mediated phosphorylation and regulation of cellular localization of p27. Akt phosphorylates Thr-157 in p27 and retains it in the cytosol. In cells arrested in G1 and then synchronized to enter into S phase, Akt-mediated phosphorylation of Thr-157 p27 occurred in the cytosol during G1 phase of the cell cycle. Both T157A and S10A p27 mutants localized in the nucleus in all phases of the cell cycle regardless of the expression of active Akt. Thr-157 phosphorylation was undetectable in S10A-p27, suggesting that Ser-10 phosphorylation is required for p27 localization in the cytosol and subsequent phosphorylation at Thr-157. Phosphorylation at Thr-157 interrupted the association of p27 with importin α. A T157A-p27 mutant protein exhibited higher association with importin a than wild-type-p27. Treatment of transfected and endogenous p27 with alkaline phosphatase rescued its association with importin α. Leptomycin B inhibited cytosolic Thr-157 P-p27 staining, implying that CRM1-dependent nuclear export is required for Akt-mediated Thr-157 phosphorylation. Heterokaryon shuttling assays with NIH3T3 (mouse) cells transfected with FLAG-p27 and HeLa (human) cells revealed that both wild type and T157A-p27 shuttled from NIH3T3 to HeLa cell nuclei with similar frequencies. However, S10A-p27 was found only in the NIH3T3 nuclei of NIH3T3-HeLa cell fusions. These results suggest that 1) Ser-10 phosphorylation is required for nuclear export of p27, 2) subsequent Akt-mediated phosphorylation at Thr-157 during G1 phase corrals p27 in the cytosol, and 3) Thr-157 phosphorylation inhibits the association of p27 with importin α thus preventing its re-entry into the nucleus.

AB - We have studied mechanisms of Akt-mediated phosphorylation and regulation of cellular localization of p27. Akt phosphorylates Thr-157 in p27 and retains it in the cytosol. In cells arrested in G1 and then synchronized to enter into S phase, Akt-mediated phosphorylation of Thr-157 p27 occurred in the cytosol during G1 phase of the cell cycle. Both T157A and S10A p27 mutants localized in the nucleus in all phases of the cell cycle regardless of the expression of active Akt. Thr-157 phosphorylation was undetectable in S10A-p27, suggesting that Ser-10 phosphorylation is required for p27 localization in the cytosol and subsequent phosphorylation at Thr-157. Phosphorylation at Thr-157 interrupted the association of p27 with importin α. A T157A-p27 mutant protein exhibited higher association with importin a than wild-type-p27. Treatment of transfected and endogenous p27 with alkaline phosphatase rescued its association with importin α. Leptomycin B inhibited cytosolic Thr-157 P-p27 staining, implying that CRM1-dependent nuclear export is required for Akt-mediated Thr-157 phosphorylation. Heterokaryon shuttling assays with NIH3T3 (mouse) cells transfected with FLAG-p27 and HeLa (human) cells revealed that both wild type and T157A-p27 shuttled from NIH3T3 to HeLa cell nuclei with similar frequencies. However, S10A-p27 was found only in the NIH3T3 nuclei of NIH3T3-HeLa cell fusions. These results suggest that 1) Ser-10 phosphorylation is required for nuclear export of p27, 2) subsequent Akt-mediated phosphorylation at Thr-157 during G1 phase corrals p27 in the cytosol, and 3) Thr-157 phosphorylation inhibits the association of p27 with importin α thus preventing its re-entry into the nucleus.

UR - http://www.scopus.com/inward/record.url?scp=14044276381&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=14044276381&partnerID=8YFLogxK

U2 - 10.1074/jbc.M412367200

DO - 10.1074/jbc.M412367200

M3 - Article

VL - 280

SP - 6055

EP - 6063

JO - Journal of Biological Chemistry

JF - Journal of Biological Chemistry

SN - 0021-9258

IS - 7

ER -