Abstract
To elucidate the role of amyloid deposits in the pathogenesis of degenerative disorders of brain, we attempted to develop transgenic mice producing amyloidogenic human variant transthyretin (TTR) in the brain. A minigene, in which the promoter region of the mouse myelin basic protein (MBP) gene was ligated to the human mutant TTR cDNA, was used for microinjection. A transgenic mouse line expressing the human TTR mRNA specifically in the brain was thus derived. However, human TTR was not detected in the brain or in the serum of these mice. These data suggest that the human mutant TTR mRNA is not efficiently translated in the mouse brain.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Amino Acid Sequence
-
Amyloid beta-Peptides / chemistry
-
Amyloid beta-Peptides / genetics*
-
Amyloid beta-Peptides / metabolism
-
Animals
-
Base Sequence
-
Blotting, Southern
-
Brain / metabolism*
-
Electrophoresis, Agar Gel
-
Gene Expression
-
Humans
-
L Cells
-
Mice
-
Mice, Transgenic
-
Molecular Sequence Data
-
Mutation / genetics
-
Myelin Basic Protein / genetics*
-
Plasmids
-
Prealbumin / chemistry
-
Prealbumin / genetics*
-
Prealbumin / metabolism
-
Promoter Regions, Genetic
-
RNA, Messenger / analysis*
-
RNA, Messenger / genetics
Substances
-
Amyloid beta-Peptides
-
Myelin Basic Protein
-
Prealbumin
-
RNA, Messenger