Fig. 6. Gab2 is involved in the activation of ERK MAP kinase. (A) 293T cells expressing the chimeric receptor G277 were transfected with expression vectors for Flag-tagged ERK2, together with either Gab1, Gab2, or a control vector. Cells were stimulated with G-CSF for 30 minutes (+) or left stimulated (−) and the ERK2 activities were determined by an immunoprecipitation kinase assay using myelin basic protein (MBP) as a substrate. The amount of MBP-incorporated32P was quantified by an image analyzer and indicated as the ratios against that from control unstimulated cells. (B) 293T cells were transfected with vectors for Flag-tagged ERK2, together with either Gab1, Gab2, or a control vector. They were also transfected with the expression vectors for v-Src (+) or a control vector (−), as indicated. The ERK2 activities were determined as described above. (C) 293T cells were transfected with vectors for Flag-tagged-Gab1 or Gab2, together with either JAK1, v-Src, Btk, Tec, or a control vector. Gab1 and Gab2 were immunoprecipitated with anti-Flag antibodies and analyzed using anti-phosphotyrosine (upper panel) and anti-Flag antibodies (lower panel).
Fig. 6.

Gab2 is involved in the activation of ERK MAP kinase. (A) 293T cells expressing the chimeric receptor G277 were transfected with expression vectors for Flag-tagged ERK2, together with either Gab1, Gab2, or a control vector. Cells were stimulated with G-CSF for 30 minutes (+) or left stimulated (−) and the ERK2 activities were determined by an immunoprecipitation kinase assay using myelin basic protein (MBP) as a substrate. The amount of MBP-incorporated32P was quantified by an image analyzer and indicated as the ratios against that from control unstimulated cells. (B) 293T cells were transfected with vectors for Flag-tagged ERK2, together with either Gab1, Gab2, or a control vector. They were also transfected with the expression vectors for v-Src (+) or a control vector (−), as indicated. The ERK2 activities were determined as described above. (C) 293T cells were transfected with vectors for Flag-tagged-Gab1 or Gab2, together with either JAK1, v-Src, Btk, Tec, or a control vector. Gab1 and Gab2 were immunoprecipitated with anti-Flag antibodies and analyzed using anti-phosphotyrosine (upper panel) and anti-Flag antibodies (lower panel).

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