The discovery will help researchers better understand Peutz-Jeghers syndrome and the development of the cardiovascular system. Their findings appear in the Aug. 17 issue of Science.
"We found that Lkb1 is very important for regulating the formation of the heart and blood vessels in the embryo," said Dr. Mark Henkemeyer, a professor in the Center for Developmental Biology at UT Southwestern.
Mutations of the Lkb1 gene cause Peutz-Jeghers syndrome, which is characterized by polyps in the intestines and freckle-like spots on the lips, mouth and fingers. People with Peutz-Jeghers syndrome are also at increased risk for cancerous tumors of the colon, rectum, stomach, ovaries and pancreas.
"We wanted to know what Lkb1 does in the mouse," Henkemeyer said. "Is this gene also going to cause Peutz-Jeghers syndrome phenotypes (physical or biochemical characteristics) if we mutate it in the mouse? In other words, can we develop an animal model to study Peutz-Jeghers syndrome?"
Henkemeyer and his colleagues generated mutant mice to breed in order to study their offspring. "Then the question is, 'What happens to the mice that have no Lkb1 protein?'" Henkemeyer said. "The bottom line is: These mice die during embryonic development."
The key reason the Lkb1-deficient mice die at mid-gestation is due to defects in cardiovascular development. Additional experimentation revealed the mice in the study that lacked the Lkb1 gene had difficulty producing VEGF.
"These findings place Lkb1 in the VEGF signaling pathway and suggest that the vascular
Contact: Angela Genusa
UT Southwestern Medical Center