TY - JOUR
T1 - Nuclear translocation of upstream stimulating factor 2 (USF2) in activated mast cells
T2 - A possible role in their survival
AU - Frenkel, Shahar
AU - Kay, Gillian
AU - Nechushtan, Hovav
AU - Razin, Ehud
PY - 1998/9/15
Y1 - 1998/9/15
N2 - Multiple transcription factors are activated in the cytoplasm and translocated to the nucleus where they exert positive or negative control over cellular genes. Such subcellular traffic of transcription factors usually requires the presence of a positively charged nuclear localization sequence (NLS). Upstream stimulating factor 2 (USF2) is one of the few transcription factors that contain two potential domains for nuclear localization. In addition to the conventional basic NLS, USF2 contains a highly conserved USF-specific region that is involved in its nuclear translocation. In the present work, the induction of translocation of USF2 into the mast cell nucleus was observed and found to be dependent on activation of the cells either by IL-3 or IgE-Ag. It was also observed that the prevention of the translocation of USF2 to the nucleus, using a peptide derived from the specific USF-NLS region, significantly inhibited their IL- 3-mediated survival. Thus, our findings show a direct connection between mast cell surface receptor-mediated USF2 nuclear translocation and cell viability.
AB - Multiple transcription factors are activated in the cytoplasm and translocated to the nucleus where they exert positive or negative control over cellular genes. Such subcellular traffic of transcription factors usually requires the presence of a positively charged nuclear localization sequence (NLS). Upstream stimulating factor 2 (USF2) is one of the few transcription factors that contain two potential domains for nuclear localization. In addition to the conventional basic NLS, USF2 contains a highly conserved USF-specific region that is involved in its nuclear translocation. In the present work, the induction of translocation of USF2 into the mast cell nucleus was observed and found to be dependent on activation of the cells either by IL-3 or IgE-Ag. It was also observed that the prevention of the translocation of USF2 to the nucleus, using a peptide derived from the specific USF-NLS region, significantly inhibited their IL- 3-mediated survival. Thus, our findings show a direct connection between mast cell surface receptor-mediated USF2 nuclear translocation and cell viability.
UR - http://www.scopus.com/inward/record.url?scp=0032530948&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.161.6.2881
DO - 10.4049/jimmunol.161.6.2881
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C2 - 9743349
AN - SCOPUS:0032530948
SN - 0022-1767
VL - 161
SP - 2881
EP - 2887
JO - Journal of Immunology
JF - Journal of Immunology
IS - 6
ER -