Altered neural cell fates and medulloblastoma in mouse patched mutants

被引:1385
作者
Goodrich, LV
Milenkovic, L
Higgins, KM
Scott, MP
机构
[1] STANFORD UNIV, SCH MED, DEPT DEV BIOL, STANFORD, CA 94305 USA
[2] STANFORD UNIV, SCH MED, DEPT GENET, STANFORD, CA 94305 USA
[3] STANFORD UNIV, SCH MED, HOWARD HUGHES MED INST, STANFORD, CA 94305 USA
关键词
D O I
10.1126/science.277.5329.1109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The PATCHED (PTC) gene encodes a Sonic hedgehog (Shh) receptor and a tumor suppressor protein that is defective in basal cell nevus syndrome (BCNS). Functions of PTC were investigated by inactivating the mouse gene. Mice homozygous for the ptc mutation died during embryogenesis and were found to have open and overgrown neural tubes. Two Shh target genes, ptc itself and Gli, were derepressed in the ectoderm and mesoderm but not in the endoderm. Shh targets that are, under normal conditions, transcribed ventrally were aberrantly expressed in dorsal and lateral neural tube cells. Thus Ptc appears to be essential for repression of genes that are locally activated by Shh. Mice heterozygous for the ptc mutation were larger than normal, and a subset of them developed hindlimb defects or cerebellar medulloblastomas, abnormalities also seen in BCNS patients.
引用
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页码:1109 / 1113
页数:5
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