Developmental expression of Pim kinases suggests functions also outside of the hematopoietic system




Eichmann A, Yuan L, Breant C, Alitalo K, Koskinen PJ

PublisherSTOCKTON PRESS

2000

Oncogene

ONCOGENE

ONCOGENE

19

9

1215

1224

10

0950-9232

DOIhttps://doi.org/10.1038/sj.onc.1203355



We have cloned a novel quail cDNA with strong homology to the pint family of proto-oncogenes. The deduced amino acid (aa) sequence of the cDNA, named qpim, is more closely related to Xenopus Pim and to the recently identified rat Pim-3 than to human or rodent Pim-1 or Pim-2. The protein encoded by the qpim cDNA can autophosphorylate itself and share substrates with murine Pim-l, suggesting functional redundancy to other Pim family serine/threonine kinases. We have compared the expression of qpim in avian embryos to mouse pim-1, -2 and -3 by in situ hybridization. qpim shows a highly dynamic expression pattern, particularly at early developmental stages. Surprisingly, its expression pattern is not identical to any of the murine pint genes, which show complementary and/or partially overlapping expression sites both in- and outside of the hematopoietic system. Altogether, our results suggest novel functions for Pim family kinases during embryonic development, in particular in epithelia and in the central nervous system.

Last updated on 2024-26-11 at 22:14