Gene interactions and pathways from curated databases and text-mining

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IL2 — STAT5B

Pathways - manually collected, often from reviews:

Text-mined interactions from Literome

Cohney et al., Mol Cell Biol 1999 : Additionally, in lymphocytes expressing SOCS-3 but not CIS, IL-2 induced tyrosine phosphorylation of STAT5b was markedly reduced, while there was only a weak effect on IL-3 mediated STAT5b tyrosine phosphorylation
Kim et al., Immunity 2001 : Moreover, IL-2 induces the binding of HMG-I(Y), Stat5a, and Stat5b in vivo to PRRIV and PRRIII, which also functions as an IL-2 response element
Xue et al., Int Immunol 2002 : Both Stat5a and Stat5b were rapidly phosphorylated on serine in response to IL-2 and the phosphorylation site in Stat5a was mapped to Ser780, which is not conserved in Stat5b
Bream et al., J Biol Chem 2004 : Within this distal region we found a Stat5-like motif, and in vitro DNA binding assays as well as in vivo chromosomal immunoprecipitation assays showed IL-2 induced binding of both Stat5a and Stat5b to this distal element in the IFNG gene
Lin et al., J Biol Chem 1996 : Reconstitution of interleukin-2 induced Stat5A and Stat5B DNA binding activity in COS-7 cells ... By using specific antisera, we demonstrated that both Stat5A and Stat5B are activated by interleukin-2 (IL-2) in peripheral blood lymphocytes, natural killer-like YT leukemia cells, and human T cell lymphotropic virus type I-transformed MT-2 T cells ... In COS-7 cells, which constitutively express the Janus family tyrosine kinase Jak1, reconstitution of IL-2 induced Stat5A and Stat5B DNA binding activities was dependent on the coexpression of Jak3 along with the IL-2 receptor beta chain and the common cytokine receptor gamma-chain
Rosenthal et al., Cell Immunol 1997 : IL-2 and IL-7 were equivalent in their ability to induce tyrosine phosphorylation of STAT5A and STAT5B and to facilitate binding of these STATs to an immobilized GAS element