Molecular biology of Brouton's tyrosine kinase

X-linked agammaglobulinemia (XLA) is caused by an arrest in the B lymphocyte differentiation. XLA patients lack mature B-cells and subsequently antibody production. The defective gene causing XLA is the BTK gene, which codes for the protein Bruton s tyrosine kinase (Btk), a cytoplasmic enzyme related to the Src family of kinases. Btk is only expressed in the hematopoietic cells, except for T lymphocytes and plasma cells.

In an attempt to investigate the function of Btk, we have studied how mutations and other proteins affect the activity, phosphorylation and localization of Btk. XLA causing mutations in the Src homology 2 (SH2) domain of Btk expressed in E. coli were found to disrupt the binding to phosphotyrosine, indicating a necessary function for the Btk protein. Only the mutant directly involved in the binding did not significantly deviate structurally from the native SH2 domain.

Btk can phosphorylate its own tyrosine 223 in the SH3 domain. We found that the site Y223 could also be phosphorylated by c-Abl. Btk and c-Abl did also colocalize and interact in cells. Phosphorylation of Y223 has been suggested to downregulate the activity of Btk. Moreover, we found that the substrate specificity for Btk and the protein family members Itk, Bmx and Tec are different. Btk preferentially phosphorylates the SH3 domain of Btk and Bmx, while Itk phosphorylated Itk and Btk SH3 domains, whereas Tec could phosphorylate the SH3 domain of Btk and Tec, but also with reduced efficiency Bmx and Itk. The phosphorylation sites in the SH3 domains were also mapped. Tec was phosphorylated on a conserved tyrosine, which differs from the conserved Y223, and was the site of phosphorylation in the other family members.

A region in the PH domain binds phospholipids in the cell membrane. Changing negative charged amino acids to positive induce microspikes structures on the cell membrane of the cells. D43R and the previously reported gain-of-function, E41K, showed an increased cell proliferation. These mutations also made IL-5 dependent cells proliferate in the absence of IL-5, indicating a transforming potential. In summary, these studies show some important functions of the Btk protein that are necessary for B-cell development and illustrate the complexity of these mechanisms.

List of scientific papers

I. Mattsson PT, Lappalainen I, Backesjo CM, Brockmann E, Lauren S, Vihinen M, Smith CI (2000). Six X-linked agammaglobulinemia-causing missense mutations in the Src homology 2 domain of Brutons tyrosine kinase: phosphotyrosine-binding and circular dichroism analysis. J Immunol. 164(8): 4170-7.
https://pubmed.ncbi.nlm.nih.gov/10754312

II. Backesjo CM, Vargas L, Superti-Furga G, Smith CI (2002). Phosphorylation of Brutons tyrosine kinase by c-Abl. Biochem Biophys Res Commun. 299(3): 510-5.
https://pubmed.ncbi.nlm.nih.gov/12445832

III. Nore BF, Mattsson PT, Antonsson P, Backesjo CM, Westlund A, Lennartsson J, Hansson H, Low P, Ronnstrand L, Smith CI (2003). Identification of phosphorylation sites within the SH3 domains of Tec family tyrosine kinases. Biochim Biophys Acta. 1645(2): 123-32.
https://pubmed.ncbi.nlm.nih.gov/12573241

IV. Bäckesjö CM, Vargas L, Aints A Christensson B, Berglöf A, Vihinen M, Edvard Smith CI (2003). Transforming effect of pleckstrin homology (PH) domain mutations in Brutons tyrosine kinase (Btk). [Manuscript]